摘要:

INDEX OF SUBJECTS. TRANSACTIONS A N D PROCEEDINGS. 1907. (Marked T. and P. respectively.) A. Absorption spectra. See under Photo- chemistry. Acetaldehyde, condensation of, and its relation to the biochemical synthesis of fatty acids (RAPER), T., 1831 ; P., 235. Acetanilide, 2:4-dichloro-, preparation of 2:6-dichloro-4-bromo- (REED and OR- 2 :4 :6-trichloro-3-bromo- (REED and ORTON), T., 1552. chloro-p-iodo-, and its dichloride ( CALDWELL and WERNER), T., 246 ; P., 17. p-iodo-, dichloride, action of heat on (CALDWELL and WERNER), T., 240 ; P., 17. thio-, and its homologues, action of ethyl oxalate on (RUHEMANN), T., 797; P., 115. Acetic acid, ethyl ester, purification of Acetic acid, chloro-, and its sodium salt, hydrolytic decomposition of, by water and by alkali, and the influ- ence of neutral salts on the reaction velocities (SENTER), T., 460 ; P., 60.dichloro-, cerous salt (MORGAN and CAHEN), T., 477. Acetoacetic acid, ethyl ester, condensa- tion of, with triacetic lactone (FLEISCHMANN), T., 250 ; P., 16. sodium derivative, production of or- cinol derivatives by the action of heat on (COLLIE and CHRY- STALL), T., 1802 ; P., 231. action of tribromopropane on (GARDNER and PERKIN), T., 848 ; P., 115. (REED and ORTON), T., 1553. TON), ‘r., 1550. (INGLIS and KNIGHT), P., 198. Acetonylazoimide. See Triazoacetone. Acetonylmalonic acid and its semicarb- azone (PERKIN and SIMONSEN), T., 822. Acetophenone, w-mono- and -di-chloro-p- iodo- (CALDWELL and WEP~NER), T., 244 ; P., 17. p-iodo-, dichloride, action of heat on ( C A L D W E L L ~ ~ ~ WERNER), T., 240 ; P., 17.Aceto-p-toluidide, 3-chloro-5-bromo- (ORTON and REED), T., 1570. Acetoxime, inhence of acids and alkalis on the velocity of formation of (BAR- RETT and LAPWORTH), P., 307. Acetyl-. See also Acet-, and under the parent Substance. S-Acetyladipic acid, preparation of, and its ethyl ester, silver salt, and semicarbazone (SIMONSEN), T., 188. B-Acetylbntane-a@-tricarboxylic acid, ethyl ester, preparation of (SIMONSEN), T., 188. Acety lchloroamino-24-dichlorobenzene, preparation of (EEED and ORTON), T., 1554. Acetylchloroamino-26-dichloro-4- bromobenzene (REED and ORTON), T., 1550 ; P., 210. Acetylenedicarboxylic acid, addition of iodine to (JAMES and SUDBOROUGH), T., 1038 ; P., 136. Acetylenic acids, addition of iodine to (JAMES and SUDBOROUGH), T., 1037 ; P., 136.a-Acetylglutaric acid, ethyl ester, pre- paration of (PERKIN and SIMONSEN), T., 1740; P., 197. y-Acetylpentane-ayetricarboxylic acid, ethyl ester ( PERKIN and SIMONSEN), T., 1740; P., 198. y-Acetylpimelic acid and its semicarb- azone and ethyl ester (PERKIN and SIMONSEN), T., 1741 ; P., 198.2104 INDEX OF SUBJECTS. of aminosulphonic acids as deter- mined ,T7 by . the m aid - - . - of methyl-orange - Acid, C6H&N27 from the action of sodium ethoxide on ethyl malonam- ate (DE MOUILPIED and RULE), T., 177 ; P., 13: C8Hl4O4, and its barium salt, from the oxidation of the aldehyde, C,H,,O, (RAPER), T., 1835. Cl0Hi4O2, from limonene ( HENDER- SON), T., 1874 ; P., 247. C,,H,,O,, from the oil of nutmeg (POWER and SALWAY), T., 2056 ; P., 285.C.&t26010, from the interaction of methylene chloride and the sodium derivative of ethyl malonate (TUTIN), T., 1145 ; P., 158. CxH38020, and its potassium and sod- ium salts, from the hydrolysis of the insoluble substance from the inter- action of methylene chloride and the sodium derivative of ethyl malonate (TUTIN), T., 1145 ; P., 158. Aoid chlorides, action of, on thioureas (DJXON and HAWTHORNE), T., 122; (DIXON and TAYLOR), T., 912 ; P., 119,294. Acids, unsaturated, the velocity of reac- tion of bromine with some, in aque- ous solution (BARRETT and LAP- See also Acetylenic acids, Amino-acids, Aminocarboxylic acids, Aminosul- phpnic acids, a-Hydroxycarboxylic acids, and Pseudo-acids. Acridines, synthesis of (SENIER and AUSTIN), T., 1233,1240 ; P., 185,300 ; (SENIER and COMPTON), T., 1927 ; P., 247.Acrylic acids, substituted, esterification constants of (SUDBOROUGH and THOMAS), T., 1033 ; P., 146. Acylamino-compounds, the mechanism of bromination of (COHEN and CROSS), P., 148. Address, congratulatory, to the Geo- logical Society of London, P., 226. tn t h e Snci6t6 rhiminnp de Ti'ranrn WORTH), P., 18. ethylmalonamide (BURROWS and KEANE!, T.,"269,1 p.7 3 5 , . - . AFFINITY, CHEMICAL :- Association of phenols in the liquid condition (HEWITT and WINMILL), T., 441 ; P., 10. Dynamic isomerism, studies in (LOWRY and MAGSON), P., 193, 260. Equilibrium, a method for the deter- mination of the, in aqueous solutions of amines, pseudo-acids, pseudo- bases, and lactones (MOORE), T., 1373 ; P., 154. Hydrolysis of chloroacetic acid and its sodium salt by water and by alkali, and the influence of neutral salts on the reaction velocities (SENTER), T., 460 ; P., 60.of salts, electrometric determination of the (DENHAM), P., 260. Velocity of hydrolysis of the aliphatic amides (CROCKER), T., 593 ; P., 63. by alkali (CROCKER and LOWE), T., 952 ; P., 135. of the I-bornyl and I-menthyl esters of the stereoisomeric mandelic acids (MCKENZIE and THOMPSON), T., 789 ; P., 113. Velocity of oxidation of the side-chain, influence of substitution in the nucleus on the (COHEN and HODS- MAN), T., 970 ; P., 152. Velocity and mechanism of the oxida- tion of hypophosphorous acid by iodine (STEELE), T., 1641 ; P., 213. Velocity of reaction of bromine with some unsaturated acids in aqueous solution ( BARILETT and LAPWORTH), P., 18.Velocity of reduction of the oxides of lead, cadmiuni, and bismuth by carbon monoxide (BRISLEE), P., 286. Alcohol, ClOHl8O, from oil of nutmeg (POWER and SALWAY), T., 2049 ; P., Alcohols, action of metallic calcium on ( PERKIN and PRATT), P., 304. 285. nfthe hvrlmnrnmntir nnd ternpnp qpripf- I., 141. Adipic acid, dihydroxy-derivatives (LE SUEUR), P., 196. Adsorption formula ( MCBAIN), T., 1683 ; P., 209. AFFINITY, CHEMICAL :- Affinity constants of aminocarboxylic --,I - - 2 _ ^ ^ _ _ _ l - l - - - Z - --:>- - _ 2 - allU LUG11 1G:JUlLlbIUll I U L U U ~ ~ L l l ; a l l y active components (PICKAKD and LITTLEBURY), T., 1973 ; P., 262. Aldehyde, C,H,,O,, from the condensa- tion of acetaldehyde (RAPER), T., 1834. C10H140, and its semicarbazone, from I ITT \ rn qnen.. . termine,d_by the-aid - of methyl- I - - - . P., - 24'1. . ,. n ... 1 . (VELEY), 'I., 1240; r., ~ Y Y . conciensation or, with a-IiaphthOl anu a-nanhthvlamine ~SENTRR and ATJS- of bases as determined bv the aid of I =---- ___ ._ --.I ---- --- -- - _ ._ I_ - . ..- - - - - - - I methyl-orange (VELEP), P., 284. 1 TI;), T., 1233 ; P., 185.INDEX OF SUBJECTS. 2105 Amine, C,H,,N, and its platinichloride, from the ketone, C,HI2O, from limonene (HENDERSON), T., 1876 ; P., 247. Ammes, a method for the determination of the equilibrium in aqueous solu- tions of (MOORE), T., 1373 ; P., 154. aromatic, interaction of, with p- diazoimides (MORGAN and NICKLE- THWAIT), T., 1512 ; P., 209. See also Bases and m-Diamines. Amino-acid, CllH1603N2, and its methyl ester, from the oxidation of the lactam, C,,H,,02N2 (LAPWORTH and WECHSLER), T., 982, 1919 ; P., 138, 252.C12H1803N2, from the oxidation of the lactam, C,,H160,N, ( LAPWORTH and WECHSLER), T., 991 ; P., 138. Aminocarboxylic acids, afinity constants 1 of, as determined by the aid of ' methyl-orange (VELEY), T., 153. Aminosulphonic acids, affinity constants of, as determined by the aid of methyl- orange (VELEY), T., 153, 1246 ; P., 179. Amminodiethylauric bromide (POPE and GIBSON), T., 2065 ; E., 295. Ammonia, the " true ionisation con- stants, the hydration constants, and the heats of neutralisation and of solution of (MOORE), T., 1379 ; P., 154. Ammonium compounds, cyclic, optical activity of (BUCKKEY and JONES), T., 1821 ; P., 234. substituted, replacement of alkyl radicles by methyl in (JONES and HILL), T., 2083 ; P., 290.Ammonium salts, interaction of, with the constituents of soil (HALL and GIMINGHAM), T., 677 ; P., 61. Ammonium periodate, specific gravity and solubility of (BARKER), I?., 305. calcium ferrocyanide (BROWN), T., 1827 ; P., 233. Amygdalin, hydrolysis of, by acids (CALDWELL and COURTAULD), T., 666 ; P., '71. hydrolysis of, by emulsin (AULD), P., 7 2. hepta-acetyl derivative (CALDWELL and COUETAULD), T., 675 ; P., 72. isoamygdalin, hepta-acetyl derivativc (CALLJWELL and COURTAULD), T., 675 ; P., 27. Analysis, electrolytic, of metals (SAND), T., 373 ; P., 26. a-Anhydrotrimethylbrazilone, constitu- tion of (PERKIN and KOBINSON), P., 293. Aniline, acetyl derivative. See Acet- anilide.Aldehydes, aromatic: electrolytic reduc- tion of (LAW), T., 748; P., 73. condensation of, with salicylamide (KEANE and NICHOLLS), T., 264 ; P., 36. Alizarin, monomethyl ether of, from the root of Morinda 1ongiJora (BARROW- CLIFF and TUTIN), T., 1913; P., 249. methyl ethers (PERKIN), T., 2068 ; P., 288. Alkali iodates and periodates (BARKER), P., 305. nitrites, double salts with mercuric nitrite (RAY), T., 2031 ; P., 165. Alkalis, caustic, interaction of, with metallic sulphates (PICKERIKG), T., 1981 ; P., 261. Alkaloids of ergot (BARGER and CARR), T., 337 ; P., 27. Alkyl iodides, effect of heat on (KAHAN), P., 307. interaction of, with mercurous nitrite (RAY and NEOGI), P., 246. radicles, replacenient of, by methyl in substituted ammonium compounds (JONES and HILL), T., 2083 ; P., 290.Alkylkairolinium salts, optical activity of (BUCKNEY and JONES), T., 1822 ; P., 234. Alkylqainolinium salts, optical activity of (BUCKNEY and JONES), T., 1822; P., 234. Allylacetic acid (PERKIN and SIMONSEN), T., 829. esterification constant of (SUDBOROUGH and THOMAS), T., 1035 ; P., 146. Allylacetoacetic acid, y-bromo-, ethyl ester (GARDNER and PERKIN), T., 849 ; P., 115. Allylacetone (GARDNER and PERKIN), T., 851. Allylacetone, y-bromo-, and its oxime and semicarbazone (GARDNER and PERKIN), T., 850 ; P., 115. density and magnetic rotation of (PERKIN), T., 851. Allylmalonic acid and y-bromo-, ethyl ester, and its reactions (PERKIN and SIMONSEN), T., 821, 840. Aluminium basic sulphate, formation of (PICKERINO), T., 1987 ; P., 261. h i d e s , molecular weights of, in various solvents (MELDRUM and TURNER), P., 165.fatty, velocity of hydrolysis of (CROCKER), T., 593 ; P., 63. velocity of hydrolysis of, -by alkali (CROCKER and LOWE), T., 952 ; P., 135.2106 INDEX OF SUBJECTS. Aniline, bromo-derivatives, the wander- ing of bromine in the chlorination of (REED and ORTON), T., 1543 ; P., 210. 2 : 6 -dibrom o- 4 -nitro- (SMITH and 0 R- reduction of (HEWITT and WALKER), 2:6-dichloro-4-bromo-, and its acetyl derivative (REED and ORTON), T., 1547 ; P., 210. 24:6-trichloro-3-bromo-, and its acetyl derivatives (REED and ORTON), T., 1552; P., 210. chloro-p-iodo-, and its hydrochloride, picrate, and thiocarbamide (CALD- WELL and WERNER), T., 246 ; P., 17. Aniline-psulphonic acid, cerous salt (MORGAN and CAHEN), T., 477.l-Anilino-6- hydroxynsphthacenequin- one, and its diacetyl derivative (BENTLEY, FRIEDL, THOMAS, and WEIZMANN), T., 419. Anisaldehyde, electrolytic reduction of Anisidines, dinitro-, diazotisation of (MELDOLA and HAY), T., 1474 ; P., 211. o- and p-, 3:5-dinitro-, preparation and dinzotisation O f (MELDOLA and Hay), T., 1474 ; P., 211. Anisil (IRVINE and MOODIE), T., 544. Anisoin, reduction of, and its methyl ether (IRVINE and MOODIE), T., 541 ; P., 62. TON), T., 149 ; P., 14. T., 1141. (LAW), T., 759. Aniayl-. See Rlethoxyphen y l-. Anniversary dinner, P. , 102. Annual General Meeting, T., 615 ; P. ,. 95. Anthragallol methyl ethers ( PERKIN), Anthraquinone, hydroxy-derivatives, methyl ethers of (PERKIN), T. , 2066 ; m-hydroxy-, methyl ether (PERKIN), T., 2070 ; P., 288.1 :2-dihydroxy-. See Alizarin. 1:3-d?hydroxy-. See Purpuroxanthin. 2:3-dihydroxy-. See Hystazarin. 1 :2: 3-trihy droxy-. Anthraquinonea ( BENTLEY, GAKDNER, WEIZMANN, ANDREW, and TEMPER- LEY), T., 1626 ; P., 215. Antimony trihydride (stibine), action of selenium and tellurium on (JONES), P., 164. Arsenic trihydride (arsine), action of selenium and tellurium on (JONES), P., 164. diiodide, preparation, formula, and reactions of (HEWITT and WIN- MILL), T., 962 ; P., 150. T., 2067 ; P., 288. P., 288. See An thragallol. Arsine. See Arsenic trihydride. Aryl haloids, interaction of, with magnesium (SPENCER and STOKES), P., 302. Association. See under Affinity, chem- ical. Atomic weight of tellurium (BAKER and BENNETT), T., 1849 ; P., 240. Atomic weights, report of the Inter- national Committee on, P., 2.table of, P., 7. Atom8 of certain organic compounds a t the melting point, relation between their volumes and valencies (LE BAS), T., 112. Azobenzene, dibromoamino-, and its diacetyl and dibenzoyl derivatives (HEWITT and WALKER), T., 1138; P., 161. Azo-compounds, colour and constitution of (HEWITT and MITCHELL), T., 1251 ; P., 182. amino-, formation of (MORGAN and MICKLETHWAIT), T., 1512 ; P., 209. influence of substitution on the formation of (MORGAN and MICKLETHWAIT), T., 360 ; P., 28. hydroxy-, constitution of (TUCK), T., Azoimides, aromatic (FORSTER and PIERZ), T., 855, 1350, 1942 ; P., 112, 205, 258. o-Azoiminobenzoquinone, 3:5-dibromo-. See Phenylazoimide, 4:6-dibromo-2- hydroxy-. Azoxy-compounds, reduction of aromatic nitro-compounds to., in acid solution (PLURSCHEIM and SIMON), P., 163.449 ; P., 58. B. Balance sheet of the Chemical Society and of the Research Fund. See Annual General Meeting, T., 621. Barbituric acid series, studies i n the (WHITELEY), T., 1330 ; P., 180, 203. Barium salts, an improved form of apparatus for the rapid estimation of (LANG and ALLEN), T., 1370 ; P., 187. Bases, a5nity constants of, as determined by the aid of methyl-orange (VELEY), P., 284. quaternary, hydrates of some (CRICH- TON), T., 1793 ; P., 236. See also Aruines, Diamines, and Pseudo-bases. Benzaldehyde, electrolytic reduction of (LAW), T., 754.INDEX OF SUBJECTS. 2107 Benzamide, absorption spectra of (Ham- LEY and HEDLEY), T., 319 ; P., 31. Benzene derivatives, isomeric change in (ORTON and REED), T., 1554; P., 212.Benzene, s-tribromo-l-nitroamino-, de- composition of (SMITH and ORTON), T., 146 ; P., 14. and its barium salt (REED and OR- TON), T., 1551. p-chloroiodo-, dichloride, action of heat on (CALDWELL and WERNER), T., 528 : P., 64. s-trihalogen-l-nitroamino-derivatives, transformations of (SMITH and ORTON), T., 146 ; P., 14. iodo-, dichloride, action of heat on (CALDWELL and WERNER), T., 528 ; P., 64. m- and p-iodonitro-, dichlorides, action of heat on (CALDWELL and WERN- ER), T., 528 ; P., 64. nitroso-, compound of, with cadmium iodide (PICKARD and KENYON), T., 901. CBenzeneazo- l-acetylamino-3-amino-2- -phenylnaphthalene (LEES and THORPE), T., 1290. 4-Benzeneazo-3-acetylamino-l-amino-2- phenylnaphthalene and its p-nitro- derivative and their hydrochlorides, and their hydrolysis (LEES and THORPE), T., 1295.5-Benzeneazo-l:3-diphenyl-5-benzyl- and -6 - diphenylme thyl- barbituric acids and p-nitro- ( WHITELEY), T., 1345 ; P., 180. Benzeneazo-@naphthol, hydroxy-. See Phenol-2-azo-B-naphthol. Benzene-l-azo-&naphthol, tetrabromo-, 4-chloro-2: 6-dibromo-, 2-chloro- 4 : 6- dibromo-, 2:4-dichloro-6-bromo-, and 2: 6-dichloro- 4-bromo- ( ORTON and REED), T., 1662. Benzene-4-azo-l-naphthol-2-carboxylic acid, 0-. m-, and p-nitro- (HEWITT and MITCHELL), T., 1260 ; P., 183. Benzeneazophenol, 2’:6’-dibromo-4-nitro- (HEWITT and MITCHELL), T., 1262. 4-Benzeneltzophenyl-a-camphoramic acid (WOOTTON), T., 1897 ; P., 250. 4-Benzeneazo-2-phenyl-1: 3-naphthyl- enediamine and its p-nitro-deriva.tive and their hydrochlorides (LEES and THORPE), T., 1290. enedimethyldiamine and p-nitro-, and their hydrochlorides (LEES ana TRORPE), T., 1301. 2:6-dichloro-4-bromo-l-nitroamino-, 4-Benzeneazo-2-phenyl-l:3-naphthyl- XCI. 3enzeneazosalicylaldehyde, p-nitro-, and its acetyl derivative and phenyl- hydrazone (HEWITT and MITCHELL), T., 1262 ; P., 183. 3enzenediazo-as-dimethyl-4:6-diamino- m-xylene, p-nitro- (MORGAN and MICKLETHWAIT), T., 369. 3enzenediazonium salts. See Diazo- benzene salts. Benzenediazotrimethyl-4 6-diamino-?n- xylene, p-nitro- (MORGAN and MICKLETHWAIT), T., 369. Benzenesulphonic acid, cerous salt (MORGAN and CAHEN), T., 477. l’-Benzenesulphonylamino-4-nitrodi- phenyl and its N-methyl derivative (MORGAN and HIRD), T., 1507. Benzenesulphonylbenzidine, azo- and dia,zo-derivatives of (MORGAN and HIRD), T., 1505 ; P., 209.xs-Benzenesulphonylme thylbenzidine and its diazotisation (MORGAN and HIRD), T., 1508 ; P., 209. N-Benzenesulphonyl-a-naphthylethyl- amine (MORGAN and MICKLETHWAIT), T., 1516. Benzenesulphonyl-p-phenylenediazo- imide, interaction of, with benz noid and naphthalenoid amines (MORGAN and MICKLETHWAIT), T., 1512 ; P., 209. Benzoflavol (2:8-dihydroxy-5-phelEyl-3 :7- dimethylacridine), preparation of, and its additive salts, and diacetyl and dibenzoyl derivatives, and anhydro- base (DUNSTAN and CLEAVERLEY), T., 1619 ; P., 206. Benzoic acid, absorption spectra of (HARTLEY and HEDLEY), T., 319 ; P., 31. potassiuni and silver salts, absorption spectra of (HARTLEY and HEDLEY), T., 319 ; P., 31.2-nitro-5-amino-, and its N-acetyl derivative (HEWITT and MITCHELL), T., 1258 ; P., 183. Benzoic anhydride, reactions of, with thioureas (DIXON and TAYLOR), T., 927. Benzoin and its derivatives, application of Baeyer’s reduction to (IRVINE and WEIR), T., 1384 ; P., 205. methylation of, by Fischer’s method (IRVINE and WEIR), T., 1391 ; P., 205. Benzoin synthesis, an extension of the (CLARKE and LAPWORTH), T., 694 ; P., 90. Benzonitrile, condensation of, with the sodium compound of phenylacetonitrile ( ATKINSON, INOHAM, and THORPE), T., 591. 7 A2108 INDEX OF SUBJECTS. o-Benzoqninonediazides, action of hydr- oxylamine on (ORTON, EVANS, and MORGAN), P., 167. Benzoyl-. See also Benz-, and under the parent Substance. Benzoylaoetamide (ATKINSON, INQHAM, and THORPE), T., 591.a-Benzoyl- y-anilino-By diphenylpropane, y-cyano- (CLARKE and LAPWORTH), T., 704 ; P. , 90. Benzoyloyanamide,mercuric salt (AULD), T., 1048 ; P., 152. B-Benzoyldihydrocarvone, formation of, and its cyanohydrin, dioxime, semi- carbazone, and isomeride (CLARKE and LAPWORTH), T., 701 ; P., 90. Benzoylphenylacetamide (ATKINSON, INQHAM, and THORPE), T., 593. Bencyl chlorocarbonate, reaction of, with phenylthiourea (DIXON and HAWTHORNE), T., 144. cyanide. See Phenylacetonitrile. Benrylethylpropylsilicol and its sulphon- ation (KIPPING), T., 726. synthesis of, and its sulphonation and the resolution of the dl-sulphonic derivative into its optically active components ( KIPPING),T., 209 ; P. , 9. Benrylethylpropylsilicyl chloride and ite reactions (KIPPING), T., 722.Benrylethylsilioon &chloride ( KIPPING), T., 720. 2-BenzylhydrindeneY 1 :2‘dihydroxy- (PERKIN and ROBINSON), T., 1089. Benzylideneacetophenone, condensation of, with benzylideneaniline hydro- cyanide (CLARKE and LAPWORTH), T., 704 ; P., 90. Benzylideneaniline hydrocyanide, con- densation of, with benzy lideneace to- phenone and with carvone (CLARKE and LAPWORTH), T., 699 ; P., 90. Benzylidenebis-o-me thoxybenzamide ( K E A N E ~ ~ ~ NICHOLLS),T., 268 ; P., 36. 2-Beneylidenr-l-hydrindone, 2’- hydroxy -, and its potassium and acyl deriva- tives and sulphonic acid (PERKIN and ROBINSON), T., 1087. 2’:4’-dihydroxy-, and its hydro- chloride (PERKIN and ROBINSON), T., 1092. Benzylidenesalicylamides,~~~~- and syn-, preparation and benzoylation of (TITHERLEY), T., 1426; P., 204.dl-Bene ylmethylethylpropylsilicane and experiments on the resolution of its wlphonic derivative (KIPPING), T., 717 ; P., 83. phonic acid, metallic, alkaloidal, and menthylamine salts (KIPPINO), T., 735 ; Y., 83. Benr ylmethyletb ylpropylsilicaneeul- Biology, synthetical chemistry in its rela- tion to (FISCHER), T., 1749 ; P., 220. Bis- I dinaphthacridine dihydride (SENIER and AUSTIN), P., 300. Bismuth oxide, velocity of the reduc- tion of, by carbon monoxide, and the formation of the suboxide ( BRISLEE), P., 286. m-Bistriazobenzene (FORSTER and FIEKZ), T., 1953. Biatrimethylphenonaphthacridine hew- bromide (SENIER and AUSTIN), T., 1242; P., 185. Bordeaux mixture, the chemistry of (PICKERING), T., 1988 ; P., 261. Borneols, preparation of the (PICKARD and LITTLEBURY), T., 1973 ; P., 262.Brazilin and hsematoxylin (PERKIN and ROBrN8ON), T., 1073. Brazilinic acid, synthesis of (PERKIN and ROBINSON), P. , 291. Bromine, the velocity of reaction of, with some unsaturated acids in aqueous solution ( BARRETT and LAPWORTH), P., 18. Butanedicarboxylic acid. See Adipic acid. Butenoic acid. See Crotonic acid. AY-Butinene-a-carboxylic acid and its ethyl ester and salts (PERKIN and SIMONSEN), T., 827 ; (GARDNER and PERKIN), T., 848 ; P., 115. ethyl ester, density, magnetic rota- tion, and refractive power of (PER- KIN), T., 836. Arv-Butinene-aa-dicarboxylic acid and its ethyl ester and salts (PERKIN and SIMONSEN), T., 822. ethyl ester, density, magnetic rota- tion, and refractive power of (PER- KIN), T., 835. Butylenedicarboxylic acid. See Allyl- C.Cadmium oxide, velocity of the reduc- tion of, by carbon monoxide, and the formation of the suboxide ( BRIS- LEE), P., 286. basic sulphate, formation of (PICKER- ING), T., 1986; P., 261. Cadmium, separation of, from zinc, as sultlhide in presence of trichloroacetic acid (FOX), T., 964 ; P., 147. Cmaium iodate and periodate, specific gravity and solubility of (BARKER), P., 305. Calcium, metallic, action of, on alcohols (PERKIN and PRATT), P., 304. action of, on ketones (LAW and PERKIN), P., 308. B--N--B a-CHa malonic acid.INDEX OF SUBJECTS. 2109 Calcium arsenate, note on (PICKERIXG), T., 307 ; P., 35. carbonate, reaction of, with chlorine water (RICHARDSON), P., 118. ammonium and calcium potassium ferrocyanides (BROWN), T., 1826 ; P., 233.Calmatambin and its octa-acetyl deriva- tive and Calmatambetin (PYMAN), T., 1228 ; P., 183. Camphor, mercury derivatives of (NARSH and STEUTHERS), P., 246. Camphor, diiodo- (MARSH and STRU- THERS), P., 119. nitro-, influence of impurities on the mutarotation of (LOWRY and MAG- SON), P., 193. Camphoric acid, aromatic amides and imides of (WOOTTON), T., 1890 ; P., 250. Camphor-B-sulphinic acid and its salts and its condensation with phenol ethers (SMILES and HILDITCH), T., 519 ; P., 35. Camphor-B-snlphonic acid, cerous salt (MORGAN and CAHEN), T., 477. Camphorylazoimide, oxime of (FORSTER and FIERZ), T., 867 ; P., 114. Campboryldi-anisyl- and -phenetyl- sulphonium and its salts (SMILES and WILDITCH), T., 526. d-Camphoryl-a-disnlphone (SMILES and HILDITCH), T., 525.Camphorylphenylhydrazide, N-nitro- and N-nitroso-, and their bromo- derivatives (WOOTTON), T., 1892 ; P., 250. Camphorylphenylthiosemicarbazides (FORSTER and JACKSON), T., 1888; P., 242. Camphorylsemicarbazide, oxime of, and its condensation with aldehydes, and its isomeride (FORSTER and FIERZ), T., 867; P., 114. Camphorylsulphonlum bases, formation of (SMILES and HILDITCH), T., 519; Camphorylthiocarbamic acid, methyl ester (FORSTER and JACKSON), T., 1887. Camphoryldithiocarbamic acid and its methyl ester and benzoyl derivative, and the action of amyl nitrite on (FORSTER and JACKSON), T., 1877; P., 242. Camphorylthiocarbamide and its piper- idyl derivative (FORSTER and JACK- SON), T., 1886 ; P., 242. Camphorylthiocarbimide ( FORSTER and JACKSON), T., 1877 ; P., 242.Carbamic acid, thio.. See Thiocarbarnic acid. P., 35. Carbamic chlorides, disubstitnted, re- action of, with thiourea (DIXON and HAWTHORNE), T., 142 ; (DIXON and TAYLOR), T., 926 ; P., 120. Carbamides, additive compounds of, with acids and salts (PICKARD and KENYON), T., 902 ; P., 138. Carbamidomalonylurea. See $-Uric acid. Carbimides, optically active ( PICKARD and LITTLEBURY), T., 300 ; P., 30. Carbon, the reducibility of magnesia by (SLADE), P., 152. adsorption. of .iodine by (DAVIS), T., dioxide, reduction of, to formaldehvde 1666 ; P., 208. in aqueous solution (FENTON), "T. , 687 ; P., 83. Carbonium salts, structure of (BAKER), T., 1490 ; P., 192. Carbonyl chloride, action of, as an agent for arresting isomeric change Carboetyril, mercury derivative (AULD), T., 1048 ; P., 152.Carboxyalkyl group, preferential saponification of the, in regard to the amino-group ( MOUILPIED and RULE), T., 177 ; P., 14. Carboxyanilinomethylenemalonanil, methyl ester (RUHEMANN), T., 1365 ; P., 196. m-Carboxybenzeneazo-o-nitrophenol, p - nitro- (HEWXTT and MITCHELL), T., 1262 ; P., 183. m-Carboxybenzene-4-azo-a-naphtho1, p - nitro- (HEWITT and MITCHELL), T., 1259 ; P., 183. rn-Carboxybenzeneazophenol, p-nitro- (HEWITT and MITCHELL), T., 1261; P., 183. l-a-Carboxy-n~decyl-A4-cycZopentene'and 1-a-Carboxy -n-decyl-l:4-bicyctopent- am. See Hydnocarpic acid, 1-a-Carboxy-n-dodecyl-A4-cyclopentene and l-a-Carboxy-n-dodecyl-l:4-bi- cyciopentane. See Chaulmoogric acid. 2-Carboxy-4: 6 -dimsthoxyphenylacetic acid (PERKIN and ROBINSON), T., 1082.2-Carboxy-4:6-methylenedioxyphenyl- acetic acid (PERKIN and ROBINSON) T., 1086. 2.Carboxyphenylacetic acid (PERKIN and ROBINSON), T., 1082. o-Carboxyphenylglyceryltropeine, lact- one of, and its additive salts (JOWETT and PYMAN), T., 94. Carvestrene and its derivatives, synthesis of (PERKIN arid TATTERSALL), T., 480; P., 66. (LOWRY and hfAGSON), P., 260.2110 INDEX OF SUBJECTS. Carvone, condensation of, with benzyl- ideneaniline hydrocyanide (CLARKE and LAPWORTH), T., 699 ; P., 90. Carycino-cobaltamine carbonate (GROVES), P., 301. Cerium salts, new (MORGAN aiid CAHEN), T., 475 ; P., 74. Cerous perchlorate, nitrite, and dithion- ate (MORGAN and CAHEN), T., 478. sulphate, spectroscopic examination of (FOWLER), T., 479. Chamaerop humilis, occurrence of quer- citol in the leaves of (MULLER), T., 1766 ; P., 218.Chanlmoogric acid, constitution and oxidation of (BARROWCLIFF and POWER), T., 557 ; P., 70. and its ethyl ester, magnetic rotations of (PERKIN), T., 563. Chemical constitution, relation between absorption spectra and (BAKER and BALY), T., 1122; P., 157; (BALY, TUCK, MARSDEN, and GAZDAR), T., 1572 ; P., 194. and colour of azo-compounds (HEWITT and MITCHELL), T., 1251; P., 182. relation of, to colour and fluorescence (GREEX), P., 12. relation between crystalline form and, of inorganic substances (BARLOW and POPE), T., 1150; P., 142. relation of, to physiological action i n the tropeines (JOWETT and PYMAN), T., 92. and viscosity, relation between (DUNSTAN, THOLE, and HUNT), T., 1728 ; P., 207. equilibrium.See under Affinity, chemical. research, position and prospects of, in Great Britain (MELDOLA), T., 626; P., 101. Chemistry, synthetical, in its relation to biology (FISCHER), T., 1749 ; P., 220. Chloraldiethylmalonamide (BURROWS and KEANE), T., 271 ; P., 37. Chlorine water, reaction of, with calcium carbonate (RICHARDSON), P., 118. Chromium, two volutnetric methods for the estimation of (GREGORY and Mc- CALLUM), T., 1846 ; P., 237. Chromyl dichloride, preparation of (LAW and PERKIN), T., 191 ; P., 11. Cineol, compounds of, with acids, salts, naphthols, and alkyl magnesium haloids (PICKARD and KENYON), T., 900; P., 138. ,in-Cineol (cis-ietrahydrocnrvestrenediol anhydride), synthesis of (PERKIN and TATTERSALL), T., 503; P., 66. Cinnamic acid, esterification constant of (SUDBOROUGH and THOMAS), T., 1034 ; P., 146.velocity of reaction of bromine with (RARRETT and LAPWORTH), P., 18. Cinnamio acid, bornyl and menthyl es- ters, properties of (HLLDITCH), P., 287. Cinhamic acid, bromo- and a- and B- chloro-, and their methyl esters, the addition of bromine to (SUD- BOROUGH and WILLIAMS), P., 146. a- an& B-homo-, velocity of reaction of bromine with ( BARRETT and LAPWORTH), P., 19. aS-diiodo- (JAMES and SUDBOROUGH), Cobalt basic sulphate, formation of (PICKERING), T., 1986 ; P., 261. Cobaltamine compounds (GROVES), P., 301. Cocositol (cocosite) from the leaves of Cocos nescveera and Cocos plzcmosa and its hexa-acetate, benzoatc, nitr- ate, and sulphonic acids, and its reactions (MULLER), T., 1767 ; P., 219. and its hexa-acetate, crystallography of (BARKER), T., 1772.Codeide, bromo- and chloro-, formation of (LEES), T., 1411 ; P., 200. isocodeine and 8-isocodeine, formation of (LEES), T., 1415 ; P., 201. Coerulignone, constitution of (MoIR), P., 308. 8-Collidine. See 2: 4 :6-Trime thylpyrid- me. Colour and constitution of azo-com- pounds (HEWITT and MITCHELL), T., 1251 ; P., 182. arid fluorescence, relation of, to consti- tution (GREEN), P., 12. contribution to the quinonoid theory of (GREEN and KING), P., 228. Colouring matter, new, from Nyctanthes Arbor-tristis (HILL and SIRKAR), T., 1501 ; P., 213. Colouring matters of the oxazine series, a reaction of (THORPE), T., 324; P., 32. of the stilbene group (GREEN, DAVIES, and HORSFALL), T., 2076 ; P., 289. Copper, chemical action of radium eman- ation on solutions containing (CAMER- ON and RAMSAY), T., 1593 ; P., 217.Copper alloys, colorimetric method for the estimation of small percentages of iron in (GREGORY), P., 306. Copper sulphate, interaction, in solution, of, and ferrous sulphate (ELLIS and COLLIER), P., 264. basic sulphates, formation of (PICKEK- IKG), T., 1982 ; P., 261. T., 1040.INDEX OF SUBJECTS. 2111 Copper :- Cnpric salts, colour of, in aqueous solution (SIDGWICK and TIZARD), P., 305. preparation and oxidation of Copper and silver groups, electro- analytical deposition and separation of nietals of the (SAND), T., 373 ; P., 26. Cotton, mercerised, characterisation of (HUBNER), P., 304. isoCoumarincarboxyltropeine and its additive salts (JOWETT and PYXAN), T., 95. p-Cresol sulphoxide and its dibenzoyl derivative, and sulphide (SMILES and HILDITCH), P., 161.o-Creeolphthalein, hydroxy- (BENTLEP, GARDNER, and WEIZMANN), T., 1638. Cresols, o-, m-, andp-, and their methyl ethers, condensations of, with phthalic acid and its derivatives (BENTLEY, GARDNER, and WEIZMANN), T., 1630 ; P., 215. Crotonic acid, B-amino-, ethyl ester, condensation of, with triacetic lact- one (FLEISCHMANN), T., 260 ; P., 16. aS-diiodo- (JAMES and SUDBORGUGH), T., 1041. Crystalline form, relation between chem- ical constitution and, of inorganic substances (BARLOW and POPE), T., 1150 ; P., 142. Crystals, more exact determination of the densities of (EABL of BERKELEY), T., 56. +-Cumidine, 6-broino-, preparation of, and its acetyl derivative (ORTON, COATES, and BURDETT), T., 54.Cuminaldehyde, electrolytic reduction of (LAW), T., 760. Cnpric salts. See under Copper. nitrite (DIVERS), P., 269. (RAY), T., 1405; P., 117. D. wDecanedicarboxylic acid and its methyl ester (BARROWCLIFF and POWER), T., 577 ; P., 71. Dehydracetic acid, isomeric change of (CoLLIEand HILDITCH), T., 787; P., 92. Density of crystals, more exact deter- mination of the (EARL OF BERKELEY), T., 56. Deoxyanisoin and its oxime ( IRVINE and MOODIE), T., 542 ; P., 62. Deoxybenzoin, a-eyano- (ATKINSON, ING- HAM, and THORPE), T., 592. Dextrose, bromo- and chloro-, tetra- methyl ether of (IRVINE and MOODIE), P., 303. Dextrorre guanidine and its properties (MORRELL and BELLARS), T., 1010; P., 87. Diacetanilide, 2:4:6-trichloro-3-bromo- (REED and ORTON), T., 1552.Diacetylacetone, disodium derivative, action of ethvlene dibroniide and propylcne dibrAmide on (BAIN), T., 544 : P., 77. Diacetyl-iitartaric acid, I-menthyl ester, preparation and rotation of (PATTER- SON and KAYE), T., 707 ; P., 89. Diallylacetoacetic acid, yy-dibromo-, ethyl ester (GARDNER and PERKIN), T., 854 ; P., 116. Diallylmalonic acid, yy-dibromo-, ethyl ester, and its reactions (PERKIN and SIMONSEN), T., 842. m-Diamines, aromatic, summary of the interactions of, with diazo-compounds (MORGAN and MICKLETHWAIT), T., 370. Diazoamines, influence of substitution on the formation of (MORGAN and MICKLETHWAIT), T., 360; P., 28. Diazobenzene (beizxenecliaxoniuin), p- amino-, salts, N-benzoyl derivatives of (MORGAN and WOOTTON), T., 1315. chlorobromo-derivatives, replace- ment of halogen by hydroxyl in (ORTON and REED), T., 1554 ; P., 212.4-chloro-2:6-dibronio-, 2-chloro-4:6-di- bromo-, 2 :4-dichloro-6-bromo-, and 2:6-dichloro-4-broino-, hydrogen carbonates and hydrogen sulphates of, replacement of halogen by hydr- oxyl in (ORTON and REED), T., 1562 ; P., 212. Diazo-compounds, constitution of (CAIN), T., 1049 ; P., 158. summary of the interactions of, with aromatic m-diamines (MORGAN and MICKLETHWAIT), T., 370. p-Diazoimides, interaction of, with aro- matic amines (MORGAN and MICKLE- THWAIT), T., 1512 ; P., 209. a-Diazonaphthalene (naphthabene-l-di- axonium), 4-amino-, salts, N-benzoyl derivatives of (MORGAN and WOOT- TON), T., 1317; P., 181. Diazo-reactions, influence of light on (ORTON, COATES, and BURDETT), T., 35.p-Diazotoluene, 3-chloro-5-bromo-,hydro- gen carbonate and hydrogen sulphate, replacement of halogen by hydroxyl in (ORTON and REED), T., 1570 ; P., 212. Dibenzyl disulphide, electrolytic pre- paration of (PRICE and TwIs~), T., 2021 ; P., 263.2112 INDEX OF SUBJECTS. Dibenzyl, 4:4’-dinitro- (GREEN, DAVIES, and HORSFALL), T., 2079 ; P., 289. Dibenzyl-22’-dicarboxylic acid (s-di- phenylethane- 2 : 2’-dicarboxyZic acid), 4:4’-dinitro- (GREEN, DAVIES, and HOESFALL), T., 2082. Dibenzylethylsulphonium mercuric iod- ide ( HILDITCH and SMILES), T., 1399 ; P., 206. Dibenzylmethylsulphonium mercuric iodide (HILDITCH and SMILES), T., 1308 ; P., 206. Dicamphorylthiocarbamide (FORSTER and JACKSON), T., 1887 ; P., 242. Dicarboxyaconitic acid, methyl ester and its reaction with aniline and phenylhydrazine (RUHEMANN), T., 1359 ; P., 195.2:6-Dicarboxybenzoyl- 1:5-dihydroxy- naphthalene ( BENTLEY, FRIEDL, and WEIZMANN), T., 1592 ; P., 216. Dicarboxyglutaconic acid, and its sod- ium salt, from the interaction of metliylene chloride and the sodium derivative of ethyl malonate (TUTIN), T., 1143 ; P., 158, 245. o-Dicresol, 5:5-dibromo-, and its per- bromide (MoIR), T., 1310. Di+ -cumylme thylenediamine and its platinichloride (SENIER and COMPTON), T., 1935 ; P., 248. Diethyl disu1phide;l electrolytic pre- paration of (PRICE and TWISS), T., 2021 ; P., 263. 3-Diethylaminophenonaphthoxazone, formation of, from Nile-blue A and from Nile-blue 2B, and its hydro- chloride (THOEPE), T., 331 ; P., 33. Diethylauric bromide ( POPE and GIBSON), T., 2063 ; P., 245.Diethylmalonamide, condensation of, with aldehydes (BURROWS and KEANE), T., 269 ; P., 36. Diethylnaphthalene, formation of (HOMER), T., 1107 ; P., 88. Diethylthioethylsulphonium dimercuric iodide (HILDITCH and SMILES), T. , 1397 ; P., 206. Dihydrobrazilinic acid, lactone of, syiithesis of (PERKIN and ROBINSON), P., 291. Dihydrocarvestreno1,synthesis of (PER- KIN and TATTERSALL), T., 498. magnetic rotation, refractive power, and dispersion of (PERKIN), T. , 498. Dihydrocarvone, cyano-, interaction of, with amyl nitrite and sodium ethoxide (LAPWORTH and WECHSLEB), T., 977, 1919 ; P., 137, 252. Dihydrochaulmoogric acid, preparation of, and its ethyl ester (BARROWCLIFF and POWER), T., 575. Dihydrochaulmoogric acid, bromo-, ethyl ester, and its reduction (BARROW- CLIFF and POWER), T., 574.a- and B-dihydroxy- ( BARROWCLIFF and POWER), T., 565 ; P., 70. Dihydrohaematoxylinic acid, lactone of, synthesis of (PERKIN and ROBINSON), P., 291. A1’J-Dihydroterephthalic acid. See cycZoHexadiene-l:4-dicarboxylic acid. Dihydroumbelluloneoxime, hydroxyl- amino-, reduction of (TUTIN), T., 275 ; P., 29. 4:6-Diketo-2-cinnamy1-5:5-diethylhexa- hydropyrimidine and its diacetyl deri- vative (BURROWS and KEANE), T., 270 ; P., 37. Diketone, C,H,,02, and its dioxime, from oil of nutmeg (POWER and SALWAP), T., 2049 ; P., 285. a-Diketones, relation between the chemi- cal constitution and absorption spectra of osazones and phenylhydr- azones of ( BALY, TUCK, MARSDEN, and GAZDAR), T., 1572 ; P., 194. hydropyrimidine and its 1:3-diacetyl derivative (BURROWS and KICANE), T., 269 ; I?., 37.3:3’-Diketo- 6: 5:5’:5‘- tetramethyl-A1:” - dicyclohexene and its disemicarbazone (CKOSSLEY and RENOUF), T., 70. o-Dimethoxybenzil(IRv1NE andMooDIE), T., 541. Dimethoxybenzoine, o- and p - , reduction products of (IRVINE and MOODIE), T., 536 ; P., 62. 5 :6-Dimethoxy-2-benzyIhydrindene7 1 :2’- dhydroxy- (PERKIN and ROBINSON), T., 1096. 2:4’- Dime thoxy-2- benz ylidene- 1 -h ydr- indone (PERKIN and ROBINSON), T., 1094. 5:6-Dimethoxy-2-benzylidene-l-hydrind- one, 2-hydroxy-, and its potassium and acetyl derivatives and hydro- chloride (PERKIN and ROBINSON), T., 1095. 2‘:4‘-dihydroxy-, and its diacetyl deri- vative (PERKIN and ROBINSON), T., 1097. o-Dimethoxydibenzyl (IRVINE and MOODIE), T., 540. 22’-Dimethoxydibenzyl (2:2’-dimet11my- s-diphnylethane), 4 :4’-dinitro- (GREEN, DAVIES, and HORSFALL), T., 2081.Dimethoxyeosin ( FRIEDL, W EIZMANN, and WPLER), T., 1587. Dimethoxyfluorercein and its acetyl derivative (FRIEDL, WEIZMANN, and WYLER), T., 1587 ; P., 214. tstrabromo-. See Dimethoxyeosin. 46-Diketo-2-phenyl-5:5-diethylhexa-INDEX OF SUBJECTS. 2113 6:6-Dimethoxy-l:2-hydrindochroman (PERKIN and ROBINSON), T., 1096. 5:6-Dimethoxy-l-hydrindone and {so- nitroso- ( PERKIN and ROBINSON), T. , ‘1 080. 2-anisylidene, 2-benzylidene, 2-piper- onylidene, and 2-veratrylidene derivatives of (PERKIN and ROBIN- SON), T., 1102. o-Dimethoxyhydrobenzoin, preparation and reduction of, and its diacetyl and diphenylurethane derivatives (IRVINE and MOODIE), T., 538 ; P., 62. 5 : 6-Dimethoxy-2:3-indeno- 1 :4-benzopyr- anol hydrochloride, 7-hydroxy- (PERKIN and ROBINSON), P., 150.1: 3-Dimethoxy-2-methylanthraquinone (BARROWCLIFF and TUTIN), T., 1913 ; P., 249. 4:6( 7)-Dimethoxy-l-methyIanthraqnin- one (BENTLEY, GARDNER, WEIZ- MANN, and TEBIPERLEY), T., 1634. benzoic acid ( BENTLEY, GARDNER, WEIZMANN, and TEMPERLEY), T., 1634. 1 :5-Dimethoxynaphthalene and its mom- and di-nitro-derivatives ( BENTLEY, ROBINSON, and WEIZMANN), T., 107. Dimethoxynaphthoylbenzoic acid, hydr- oxy- (BENTLEY, FRIEDL, and WEIZ- MANN), T., 1591 ; P., 215. 1’:5’-Dimethoxy-2-~-naphthoylbenzoic acid ( BENTLEY, FRIEDL, THOMAS, and WEIZMANN), T., 425. 4( or 5) :l‘-Dimethoxy-2-B-naphthoylbenz- oic acid (RENTLEY, FRIEDL, THOMAS, and WEIZMANN), T., 421. 3:4-Dimethoxyphenylpropionic acid (PERKIN and ROBINSON), T., 1079.3:4-Dimethoxyphthalic acid. See Hemi- pinic acid. 45-Dimethoxyphthalic acid. See m- Hemipinic acid. Dimethoxyatilbene and its dibromide (LAW), T., 759. 3-Dimethylaminophenonaphthoxazone, formation of, from New Methylene- blue GG, from New-blue B, and from Meldola’s blue, and its hydrochloride (THoRPE), T., 333 ; P., 33. as-Dlmethyl-46-diamino-m-xylene and the action of diazonium salts on, and its benzenesulphonyl, benzoyl, and azo-B-naphthol derivatives (MORGAN and MICKLETHWAIT), T., 365 ; P., 28. Dimethylaniline, p-nitroso-, compounds of, with acids and salts (PICKARD and KENYON), T., 902. 4( 5):2’-Dimethoxy-5’-methyl-2-benzoyl- 1:3-Dimethylanthraquinone, 4-hydroxy- and 4:6(7)-dihydroxy- ( BENTLEY, GARDNER, and WEIZMANN), T., 1637.Dimethylbenzaldehydes, 2:4- and 3 5 , electrolytic reduction of (LAW), T., 751 ; P., 73. 3’:5’-Dimethyl-2-benzoylbenzoio acid, 2‘-hydroxy- (BENTLEY, GARDNER, and WEIZMANN), T., 1637. 4(5):2’-dihydroxy- (BENTLEY, GARD- NER, and WEIZMANN), T., 1639. ay- Dime thylbu tane- aS6- tricarboxylic acid, preparation of, and its silver salt and anhydro-acid (HENSTOCK and SPRANKLING), T., 354 ; P., 32. 2:2’-Dime thyldibenzyl (s-di. o-toZy2- ethane), 4:4’-dinitro- (GREEN, DAVIES, and HORSFALL), T., 2080. Dimethyldihydrobenzene, iminohydr- oxy-, action of nitrous acid on (HAAS), T., 1444 ; P., 192. 1:l-Dimethyldihydroreeorcin, 4-amino-, and its hydrochloride, platinichlor- ide, and acetyl derivative, and the action of nitrous acid on (HAAS), T., 1443 ; P., 192.4-nitro-, and its salts, and reduction {HAAS), T., 1441 ; P., 192. 4-zsonitroso-, and its oximes and salts, and the action of oxidising and re- ducing agents on (HAAS), T., 1437 ; Dimethylethylenepyrone and its hydro- chloride and platinichloride ( BAIN), T., 549; P., 77. 27-Dimethylflnoranl 4’( 5’)-hydroxy- (BENTLEY, GARDNER, and WEIZ- MANN), T., 1639. 3:6-Dimethylfluoran and 4’( 5’)-hydroxy- (BENTLEY, GARDNER, and WEIZ- MANN), T., 1636. 1 :1- Dime thy1 -3-cyclohexanone (3 -ke:eto- 1 :l-dimethylhexahydrobenzene) and its oxidation and its oxime and semi- carbazone (CROSSLEY and RENOUF), T., 81. l:l-Dimethyl-5-cycZohexanone, 4-oxitn- ino+imino-, and its potassium salt and oxime, and its reduction (HAAS), T., 1445 ; P., 192. 1 :l-Dimethyl-A4-cycZohexenone-3 (3- keto- 1 : 1 -dimethyl- A4-tetrahydrobenz- ene) and its oxidation and its oxime and semicarbazone (CROSSLEY and RENOUF), T., 78.5-chloro-, action of reducing agents on (CROSSLEY and RENOUF), T., 63. Dimethylpheno- ZKi- and -$Ff-naph- thacridinea, 8:ll- and 9 : l l - , and their platinichlorides (SENIER and COMP- TON), T., 1935 ; P., 248. P., 191.2114 INDEX OF SUBJECTS. 1 :2-DimethylcycZopropane-l :2-dicarb- oxylic acid (l:2-dimethyZtrimethyZ- enene-1:2-dicarboxylic acid), chemical and physical properties of ( HENSTOCK and WOOLLEY), T., 1954 ; P., 235. ethyl ester, optical properties of (PER- KIN), T., 1957. Dimethylstilbene dibromide (LAW), T., 757. 2:5-Dimethyltetrahydroqninolinoline. See Tetrahydro-p- tolu yuinaldine. Dimethylthetine menthyl ester, nitrate of (SMILES), P., 291.p-Dimethyltolane (IRVINE and MOODIE), T., 540 ; P., 62. Dimethylumbelliferone and its acetyl derivative and methyl ether (COLLIE and CHRYSTALL), T., 1804 ; P., 232 ; (COLLIE), T., 1811. 3:7-Dimethyluric acid, mercuric salt (AULD), T., 1046 ; P., 152. Dimethylvioluric acid, mercury salt (AULD), T., 1048; P., 152. Dimethyl-m-4-xylidine, nitro-, picrate of (MORGAN and MICKLETHWAIT),T., 365. B-N-B I -Dinaphthacridine and its addi- u-CHU (SENIER and b--N-B I -Dinaphthacridine, attempted B-CHB synthesis of (SENIER and AUSTIN), Dinaphthacridines, 7-aryl derivatives, synthesis of (SENIER and AUSTIN), T., 1233; P., 185. ’ BB-Dinaphthyl, preparation of (HOMER), T., 1103; P., 88. Dipentene, spectroscopic constants of (BRUHL), T., 120. Diphenetole, sulphonation of (MoIR), T., 1308.Diphenol and its dibenzoate and di-, tri-, and tetra-sulphonic acids and their salts and its nitration (MoIR), T., 1305. Diphenol, 3‘-bromo-3-nitro-, 5:5’-di- brnmodinitro-, and di- and tetra-nitro- (MoIR), T., 1310. “ Diphenoquinone, tetrabromo-,” action of reducing agents on (MoIR), P., 308. 1:3-Diphenylalloxan-diphenyl-, -phen- 91-, pnitrophenyl-, -phenylbenzyl-, and -phenylmethyl-hydrazones (WHITELEV), T., 1344; P., 180. 1:3-Diphenylbarbituric acid and its acetyl derivative and 5-amino-, and S-isonitroso- and its metallic and amine salts, and its reactions (WHITELEY), T., 1338. tive salts and 7-bromo- AUSTIN), P., 300. P., 300. 1:3-Diphenylbarbiturio acid, 5:5-di- bromo-, and its condensation with phenylhydrazine or its B-substituted derivatives (WHITELEY), T., 1347 ; P., 180.1:3-Diphenyl-5-benzyL7 -5-benzylidene-, -5-cinnamylidene-, -5-diphenylmeth- ylene-, and -5-diphenylmethyl-barbit- uric acids (WHITELEY), T., 1342 ; P., 203. as-Diphenylethane, 8-imirro-a-cyano-, and the action of sulphuric acid on (ATKINGON, INGHAM, and THORPE), T., 592. s-Diphenylethane-2:2’-dicarboxylic acid. See Dibenzgl-2:2’-dicarboxylic acid. Diphenylethylsilicyl chloride ( KIPPING), T., 218. Diphenylhexatriene, synthesis of and allied hydrocarbons, refractive Diphenyloxaluric acid, ethyl and methyl esters, ethyl and methyl iso- ethers of (LANDER), T., 970; P., 149. Diphenylsalicylthetine, di-p-hydroxy-, and its platinichloridc (SMILES and BAIN), T., 1121 ; P., 161. Diphenylsulphoxide, compounds of, with acids and salts (PTCKARD and KEN- YON), T., 901 ; P., 138.s-Diphenylthiocarbamide (thiocarbanil- ide), action of acyl chlorides on (DIXON and HAWTHORNE), T., 137. 1:3-Diphenyluramil. See 1 :3-Diphenyl- barbituric acid, 5-amino-. 1:3-Diphenyluric acid, synthesis of (WHITELEY), T., 1338. 1:3-Diphenyl-+uric acid, synthesis of (WHITELEY), T., 1341. 1:3-Diphenylvioluric acid. See 1:3-Di- phenylbarbituric acid, 5-isonitroso-. Diisopropylstilbene and its dibromide (LAW), T., 760. Disalicylamide and its dibenzoyl deriva- tive (MCCONNAN), T., 196 ; P., 18. Disalicylic acid, dibromo- (MoIR), T., 1311. Dissolved substance, liquid volume of a (LUMSDEN), T., 24. Disulphides, electrolytic preparation of (PEICE and TWISS), T., 2021 ; P., 263. s-Di-o- to1 ylethane. See 2: 2’-Dimethyl- dibenzyl.Di-o-tolylthiocarbamide, action of acetyl chloride on ( DIXON and HAWTHORNE), T., 138. Dixylylmethylenediamines, m-4- and p-5-, synthesis of (SENIER and COMP- TON), T., 1929 ; P., 247. (SMEDLEY), P., 162. power of (SMEDLEP), P., 295.INDEX OF SUBJECTS. 2115 n-Dodecanedicarboxylic acid and its methyl ester (BARROWCLIFF and POWER), T., 568 ; P., 70. Dyeing, experimental investigation into the process of (HUBNER), T., 1057 ; P., 144. Dynamic isomerism. See under Affinity, chemical. E. Earths, rare, chemistry of the (ESPO- Electrolytic preparation of disulphides (PRICE and TWISS), T., 2021 ; P., 263. reduction of aromatic aldehydes (LAW), T., 748 ; P., 73. Emodin methyl ether from Yentilago maderaqatnna (PERKIN), T., 2074 ; P., 288. Emulsin, hydrolysis of amygdalin by (AULD), P., 72.Emulsions (PICKERING), T., 2001 ; P., 256. Eosin, hydroxy- (FGIEDL, WEIZMANN, and WYLER), T., 1586. Equilibrium, chemical. See under A% nit y, chemical. SITO), P., 64. Ergot, aikaloids of (BARGER and CARR), T., 337 ; P. 27. Ergotinine and its composition and pro- perties (BARGER and CARR), T., 341 ; P. 27. Ergotoxine and its salts (BAKGER and CARR), T., 347 ; P., 27. Eriodictvol and the action of acetic anhydiide on (POWER and TUTIN), T., 895 : P., 134. Esterification .constants of substituted acrylic acids (SUDBOROUGH and THOMAS), T., 1033 ; P., 146. 6-Ethoxy-1: 1-dimethylhexahydrobeno- ene, 3-hydroxy-, and its acetyl and benzoyl derivatives (CROSSLEY and RENOUF), T., 74. B-Ethoxy-7-phenylcrotonic acid, a- cyano-, ethyl ester and anilide (SMITH and THORPE), T., 1905 ; P., 249.Ethyl B-bromoallyl ether (PERKIN and SIMONSEN), T., 833. chlorocarbonate, reaction of, with phenyl- and tolyl-thioureas (DIXON and TAYLOR), T., 914 ; P., 119. B-Ethylacrylic acid, esterification con- stant of (SUDBOROUGH and THOMAS), T., 1035 ; P., 146. Ethylauric dzhomide (POPE and GIB- SON), T., 2064 ; P., 295. Ethylbutylmalonic acid, ethyl ester (RAPER), T., 1837. Ethylene dibromide, action of, on the disodium derivative of diacetylacetone (RAIN), T., 544 ; P., 77. a-Ethylhexoic acid, synthesis of (RAPER), T., 1837. Ethylidenepropionic acid, esterification constant of (SUDBOROUGH and THOMAS), T., 1036 ; P., 146. Ethylsilicon trichloride, preparation of (KIPPING), T., 214. F. Faraday lecture (FISCHER), T., 1749 ; P., medal, presentation of, to Prof.Emil Ferrocyanides, double, of ammonium, calcium, and potassium (BROWN), T., 1826 ; P., 233. Ferrous sulphate. See under Iron. Fluorescein, tetmbromohydroxy-. See Eosin, hydroxy-. hydroxy-, and its triacetate (FRIEDL, WEIZMANN, and WYLER), T., 1585 ; P., 214. Fluorescence and colour, relation of, to Formaldehyde, forniation of, by the re- duction of carbon dioxide in aqueous solution (FEXTON), T., 687 ; P., 83. tests for (FENTON), T., 693. Freezing point, depression of the, of aqueous solutions of hydrogen peroxide by potassium persulphate and other compounds (PRICE), l’., 531 ; P., 75. &Fructose. See Lzcvulose. Fumaric acid, d- and I-bornyl and I - mentliyl esters, preparation and oxida- tion of (MCKENZIE and WREN), T., 1218; P., 188.220. Fischer, P., 223. constitution (GREEN), P., 12. G. Gases, chemical changes indnced in, by the action of ultra-violet light (CHAPMAN, CHADWICK, and RAMS- BOTTOM), T., 942 ; P., 136. influence of non-electrolytes and elec- trolytes on the solubility of sparingly soluble, in water (PHILIP), T., 711 ; P., 85. apparatus, with stirrer, for treating a liquid at its boiling point with two or more (GICBHARD), P., 34. Gas generator, simple, for analytical operations (SANDERS), P. , 232. Glucose. See Dextrose. Glutaconic acid (TUTIN), T., 1144 ; P., 158, 246.2116 INDEX OF SUBJECTS. Qold, alkyl compounds of (POPE and GIBSON), T., 2061 ; P., 245, 295. Gnanidine, some compounds of, with sugars (MORRELL and BELLARS), T., 1010 ; P., 87. Guncotton, evolution of nitrogen per- oxide in the decomposition of (ROBERT- SON and NAPPER), T., 764 ; P., 91.H. Hsematoxylin and brazilin (PERKIN and Halogen, replacement of, by hydroxyl in chlorobromodiazobenzenes ( ORTON and REED), T., 1554 ; P., 212. salts. See Perhalogen salts. Halogens, displacement of, by hydroxyl (SENTER), T., 460 ; P., 60. estimation of, in organic substances (MoIR), P., 233. Heats of combustion. See under Thermo- chemistry. Eedeoma p l e g i o i d e s . See Pennyroyal, American. Hemipinic acid, the fluoresceins and eosins from (FRIEDL, WEIZMANN, and WYLER), T., 1584 ; P., 214. m-Hemipinic acid (PERKIN and ROBIN- SON), T., 1083. Hentriacontane from the leaves of Mor- inda longiflora (BARROWCLIFF and TUTIN), T., 1916 ; P., 249. a(-Heptadiene-88-dicarboxylic acid.See Diallylacetic acid. Aaf-Heptadi-inene-8-carboxylic acid ($- m-toluic acid), formation of, and its ethyl ester and silver salt, and its reactions (PERKIN and SIMONSEN), T., 840 ; (GARUNER and PERKIN), T., 854 ; P., 116. ultra-violet absorption spectra of (BALY). T., 846. Ad-Heptadi-inene-6-carboxylic acid, ethyl ester, density, magnetic rotation, and refractive power of (PERKIN), T., 844. Heptanedicarboxylic acid. See Ethyl- butylmalonic acid. Heptanetricarboxylic acid. See aayy- Tetramethyltricarballylic acid. Hevea brasiliensis, constituents of the seeds of (DUNSTAN), P., 168. A1:4-cycZoHexadiene- 1:4-dicarboxylic acid (PERKIN and TATTERSALL), T., 494. Hexahydro-m-toluic acid, cis- y-hydroxy-. See cis-l-Methylcyclohexanol-3-carb- oxylic acid. ROBINSON), T., 1073.1: %46: 7:9-Hexamethylacridine ( SENIER and COMPTON), T., 1934 ; P., 248. cycZoHexanecarboxylic acid, 3:4-di- bromo- (PERRIN and TATTERSALL), T., 490. cycZoHexanecarboxylic acids, cis- and trans-3-bromo- (PERKIN and TAT- TERSALL), T., 488. Hexanetricarboxylic acids. See ay- Dimethyl butane-USE-tricarboxylic acid and aay-Trimethyltricarballylic acid. cis-cycZoHexano1-3-carboxylic acid and its ethyl ester and lactone (PERKIN and TATTERSALL), T., 486. trans-cycZoHexano1-3-carboxylic acid (PERKIN and TATTERSALL), T., 489. cycZoHexanone - 3- carboxylic acid and its ethyl ester, silver salt, oxime, and semicarbazone ( PERKIN and TAT- TERSALL), T., 491. Hexatriene, magnetic rotation of, and its relation to benzene and other aromatic compounds, and its refrac- tive power (PERKIN), T., 806 ; P., 110. derivatives, synthesis of (SMEDLEY), P., 162.Aa-Hexene, B-hydroxy- (methylcrotonyl- carbind) (GARDNER and PERKIN), T., 851 ; P., 116. A3-cycZoHexenecarboxylic acid (PERKIN and TATTERSALL), T., 490. Homatropine alkyl salts ( JOWETT and PYMAN), T., 97. Homoeriodictyol, constitution of, and its tetra-acetyl derivative (POWER and TUTIN), T., 887 ; P., 133, 243. Eomophthalic acid. See 2-Carboxy- phenylacetic acid. Homoterpenylic acid, synthesis of, and its ethyl ester (SIMONSEN), T., 184. Hydnocarpic acid, constitution and oxidation of (BARROWCLIFF and POWER), T., 557 ; P., 70. Hydrastic acid (PEEKIN and ROBINSON), T., 1086. Hydrates in solution, question of of some quaternary bases (CRICIITON), Hydrazines, oxidation of, by free oxygen (CHATTAWAY), T., 1323 ; P., 183.2:3-Hydrindochroman (PERKIN and ROBIXSON), T., 1090. 1:2-Hydrindo-4’-methoxychroman (PER- KIN and ROBINSON), T., 1092. Hydroanisoin and its methyl ether (TRVINE and MOODIE), T., 543. Hydrobenzoin and its mono- and di- methyl ethers, application of Baeyer’s reduction to (IRVINE and WEIR), T., 1390. (PHILIP), T., 711; P., 85. T., 1793 ; P., 236.INDEX OF - XJBJECTS. 211 7 _ _ Hydrocarbon, C26H22t from the action of aluminium chloride on naDhthalene (HOMER), T., 1111 ; P., 8 s C,H,, from the action of aluminium chloride on naphthalene (HOMER), T., 1112 ; P., 88. Eydrocarbons, relation between the val- ency and heats of combustion of (LE BAS), P., 134. of the benzene series, oxidation of (LAW and PERKIN), T., 258; Hydroergotinine.See Ergotoxine. Hydrogen chloride, density of (GRAY), peroxide, depression of the freezing point of aqueous solutions of, by potassium persulphate and other compounds (PRICE), T., 531 ; experiments on the oxidising action of (PERKIN), P., 166. action of, on potassium cyanide (MASSON), T., 1449; P., 117. Hydrotoluoin and isoHydrotoluoin (LAW), T., 750. a-Hydroxycarboxylic acids, action of heat on (LE SUEUR), T., 1365; P., 196. Hydroxyl, displacement of halogens by (SENTER), T., 460 ; P., 60. replacement of halogen by, in chloro- brornodiazobenzencs (ORTON and REED), T., 1554 ; P., 212. Hydroxylamino-, See under the parent Hydroxyloin and isoRydroxyloin ( LAW), Hyponitrous acid. See under Nitrogen. Hypophospharous acid. See under P., 11. P., 119.P., 75. Substance. T., 752. Phosphorus. Hystazkin methyl ethers (PERKIN), T., 2070 ; P., 288. I. Imino-compounds, formation and re- actions of (ATKINSON, INGHAM, and THORPE), T., 578 ; P., 76 ; (THORPE), T., 1004; P., 151; (ATKINSON and THORPE), T., 1687 ; P., 216. 2S-Indeno-l:4-benzopyranol hydrochlor- ide, 7-hydroxy-, and its salts (PER- KIN and ROBINSON), P., 149. Indican and its reactions (PERKIN and BLOXAM), T., 1715 ; P., 116, 218. Indigo, Java, occurrence of isatin in some samples of (PEKKIX), P., 30. natural, some constituents of ( PERKIN and BLOXAM), T., 279 ; P., 30 ; (PERKIN), T., 436 ; P., 62. Indigo-brown, constituents of (PERKIN and BLOXAM), T., 280 ; P., 30. Indigofera szbmatrana, amount of in- dican obtainable from (PERKIN and BLOXAM), T., 1727 ; P., 116, 218.Indoxyl-brown (PERKIN and RLOXAM), T., 1725 ; P., 218, Inorganic subthmces, relation between the crystalline form and chemical Constitukn of (BARLOW and POPE), T., 1150 ; P., 142. Inositol (inosite) acetates, bromo-deriva- tives and their reactions (MULL- ER), T., 1781 ; P., 219. bromo-derivatives of, and dibromo- hydrin, crystallography of (BARK- ER), T., 1781. dibromohydrin (MULLER), T., 1788 ; P.. 219. Intramolecular change, new method for studying (PATTERSON and MCMILL- AN), T., 504 ; P., 60. Iodine, adsorption of, by carbon (DAVIS), T., 1666 ; P., 208. addition of, to acetylenic acids (JAMES and SUDBOROUGH), T., 1037, P., 136. the velocity and mechanism of the reaction between, and hypophos- phorous acid (STEELE), T., 1641 ; P., 213. multivalent, derivatives of (CALDWELL arid WERNER), T., 240, 528 ; P., 17, 64.Iron, rusting of (DUNSTAN), P., 63. mechanism of the rusting of (MOODY), P., 84. Iron basic sul hate, formation of (PICK- ERING), $, 1985 ; P., 261. Ferrous sulphate, interaclion, in solution, of, and copper sulphate (ELLIS and COLLIER), P., 264. Iron, colorimetric method for the estimation of small percentages of, in copper alloys (GREGORY), P., 306. Isatin, occurrence of, in some samples of Java indigo (PERKIN), P., 30. Isomeric change, carbonyl chloride as an agent for arresting (LOWRY and MAGSON), P., 260. Isomerism, dynamic, See under Affinity, chemical. K. Kaempferitrin froin natural indigo (PERKIN), T., 438. Kaem~ferol and its acetvl derivative fro& natural indigo (PERKIN), T., 436; P., 62.2118 INDEX OF SUBJECTS.Keten and its reactions (WILSMORE), T., 1938 ; P., 229. Keten group, multiple, derivatives of (COLLIE), T., 1806 ; P., 230. Ketodihydrochanlmoogric acid, hydr- oxy-, and its methyl ester and its semicarbazone ( BARROWCLIFF and POWER), T., 567 ; P., 70. 5-Keto- I: l-dimethylhexahydrobenzene. See 1 :1 -Dimethyl-3-cycZohexanone. S-Ke to- I :l-dimethyl-A4- tetrahydro- benzene. See 1 :1 -Dime thyl- A4-c yc Zo- hexenone-3-. y-Ketohexahydrobenzoic acid. See cyeZoHexanone-3-carhoxylic acid. y-Ke to-8-methyl-n-pentadecane-aa'di- carboxylic acid and its methyl ester and OXime(BAPROWCL1FF and POWER), T., 575 ; P., 70. Ketone, C,H120, and its semicarbazone, from limonene (HENDERSON), T., 1875 ; P., 247. Ketones containing the group 'CH;CO* CH:, condensations of, with esters in presence of sodium ethoxide (CLARKE, LAPWORTH, and WECHS- LER), P., 294.action of metallic calcium on (LAW and PERKIN), P., 308. See also Diketones. y-Keto-n-pen tadecane-aa'-dicarboxylic acid and its oxidation (BARROWCLIFF and POWER), T., 573 ; P., 70. y-Keto-y-phenylbutyric acid, a-cyano- (phenacylcyanoacetic acid), ethyl ester, preparation of (THORPE), T., 1005. L. Lactam, CllH1402N2, from the inter- action of cyanodihydrocarvone, amyl nitrite and sodium ethoxide, and its isomeride and N-methyl derivative(LAPW0RTH and WECHS- LER), T., 981,1919 ; P., 137, 252. constitution of (LAPWORTH an2 WECHSLER), T., 1920 ; P., 252. C12Hl,0,N2, from the lactam C11H14 02N2 (LAPWORTH and WECHSLER), T., 990; P., 138. Lactones, a method for the determination of the equilibrium in aqueous solutions of (MOORE), T., 1373 ; P., 154.Lactonic acid, Cl,HI7OSN, from the hydrolysis of tho lactam, C11H1,02N2 (LAPWORTH and WECHSLER), T., 989 ; P., 138. constitution of, and its bromo- derivative, and oxidation of ( LAPWORTH and WECHSLER), T., 1921 ; P., 252. Lactonic base, C12Hl,0,N2, from the amino-acid, Cl,HI,03N2 (LAPWORTH and WECHSLER), T., 992 ; P., 138. Lactonic bases, CllH,,03N2, from the lactam, CllH,,O2N2 (LAPWORTH and WECHSLER), T., 985 ; P., 138. constitution of, and the action of acids on (LAPWORTH and WECH- SLER), T., 1921 ; P., 252. Laevulose (d-fructose), alkylation of (PURDIE and PAUL), T., 289 ; P., 33. Laevulose guanidine and its properties (MORRELL and BELLARS), T., 1011 ; Lead, chemical action of radium emana- tion on solutions containing (CAMERON and RAMSAY), T., 1593 ; P., 217.Lead arsenates, note on (PICKERING), T., 307 ; P., 35. oxide, velocity of the reduction of, by carbon monoxide, and formation of the suboxide (BRISLEE), P., 286. sulphate, solubility of, in concentrated solutions of ammonium acetate (Fox), P., 199. P., 87. Light. See under Photochemistry. Limonene, oxidation of, with chromyl dichloride (HENDERSON), T., 1871 ; P., 247. Limonenes, d- and 1-, spectroscopic con- stants of (BRUHL), T., 120. Liquid mixtures, viscosity of ( DUNSTAN and WILSON), T., 83. Liquids, molecular complexity of (DUX- STAN and THOLE), P., 19. apparatus, with stirrer, for treating, at their boiling points with tFo or more gases (GEBHARD), P., 34. Lithium mercuric nitrites (RAP), T., 2033 ; P., 165.116. Magnesium, action of, on aryl haloids (SPENCER and STOKES), P., 302. oxide (magnesia), the reducibility of, by carbon (SLADE), P., 152. Hagnesium organic haloids, reaction of, with nitro-compounds (PICKARD and KENYON), P., 153. Malonic acid, ethyl ester, sodium deriva- tive, interaction of, with methylene chloride (TUTIN), T., 1141 ; P.., 158, 245. action of, on tribromopropane (PERKIN and SIMONSEN). T.. I. , 816, 840. Yandelic acid, racemisation of, bv alkali, and resolution of the racemic acid, into its optically active isomerides (MCKENZIE and MULLER), T., 1814; P., 234.INDEX OF SUBJECTS. 2119 Mandelic acids, stereoisomeric, measure- ments of the velocities of saponifi- cation of the 2-bornyl and 1- menthyl esters of (MCKENZIE and THOMPSON), T., 789 ; P., 113.menthyl esters, freezing point curves of (FINDLAY axid HICKMANS), T., 905 ; P., 132. Mandelonitrile glucoside, Fisch er’s, pre- paration of (CALDWZLL and COURTAULD), T., 670 ; P., 71. tetra-acetyl derivative of (CALD~ELL and COURTAULD), T., 675; P., 71. Mandelonitrile glucosides (CALDWELL and COUHTAULD), T., 671 ; P., 71. Mannose guanidine and its properties (MORRELL and BELLARS), T., 1012 ; P., 87. Medal from the Sociktk chiniique de France in commemoration of its Jubilee celebration, present of, to the Society, P., 255. A1:8(9)-,-Menthadiene. See Carvestrene. m-Menthane-l:8-diol. See Tetrahydro- carvestrenediol. A1-m-Menthenol(8). See Diliydrocar- vestrenol. d-isoMenthone in the oil of American pennyroyal (BARROWCLIFF), T., 875 ; P., 114.Henthylamine, l-amino-. See Tetra- hydroumbellulylamine, amino-. 2-Menthylcarbamic acid, aryl esters and amides of (PICKARD and LITTLEBURY), T., 300 ; P., 30. Mercurous and Mercuric salts. See under Mercury. Mercury, univalent, isomorphous re- placement of, by silver (RAY), T., 2033 ; P., 165. Mercury nitrite, double salts with the alkali metal nitrites (RAY), T., 2031 ; P., 165. Mercurous nitrite, interaction of, with alkyl iodides (RAY and NEOGI), P., 246. preparation of, and dissociation of an acid solution of (RAY), T., 1404 ; P., 89. decomposition of, by heat (DIVERS), P., 265. decomposition of, by heat, and constitution of (RAY and GA%- GULI), T., 1399 ; P., 89. ates and the isomorphous replace- ment of iinivalefit mercury by silver (RAY), T., 2033 ; P., 165.hyponitrite (DIVERS), P., 264. Mercuroso-mercuric-silver oxynitr- Mercury :- Mercuric iodide, influence of, on the formation of sulphonium iodides (HILDITCH and SMILES), T.,1394 ; P., 206. oxychloride, new ( HEWITT), P., 10. Mercury derivatives of pseudo-acids con- taining the group .CO*NH. (AULD), T., 1045 ; P., 151. Mesityl oxide (methyl isobutenyl ketone; isopropylideneacetone), formation of (LAW and PERKIN), P., 308. Metallic sulphates, interaction of, with caustic alkalis (PICKERIXG), T., 1981 ; P., 261. Metals, rapid electro-analytical deposition and separation of (SAKD),T. ,372; P. ,26. Methoethylheptanonolide and its optical isomerides, formation of (LAPWORTH and WECHSLER), T., 1924; P., 252. 4’-Methoxy-2-benzylhydrindeoe, 1 :2’- dihydroxy- (PERKIN and ROBINSON), T., 1092.4‘-Methoxy-2-benzylidene-l -hydrindone, 2’-hytlroxy-, and its acetyl derivative (PERKIN and ROBIKSON), T., 1091. 6- He thoxy -2 -benz ylidene - 1 -hy drindone (PERKIN and ROBINSON), T., 1094. 4-Methoxy-l:3-dimethylanthraquinone ( BENTLEY, GARDNER, WEIZMANN, and TERIPERLEY), T., 1635. 2’-Methoxy-3’:5’-dimethyl-2-benzoyl- benzoic acid (BENTLEY, GARDNER, WEIZMANN, and TEMPEELEY), T., 1634. Methoxyeosin (FRIEDL, WEIZMANN, and WPLER), T., 1586. Methoxyfluorescein and its diacetate (FRIEDL, WEIZMANN, and WPLER), T., 1586 ; P., 214. tetrabrom o-. Methoxymethylanthraquinone, hydr- oxy-, and its acetyl derivative from the root of Morinda ZongiJora ( BAP~ROW- CLIFF and TUTIN), T., 1912 ; P., 248. 2-Methoxy-l-methylanthYaquinone, and its amino- and its acetyl derivative, hromo-, and nitro-derivatives (BENT- LEY, GARIINER, and WEIZMANN), T., 1631.4-Methoxy-1-methylanthraquinone and 6(7)-hydroxy- ( BENTLEY, GARDXER, WEIZMAXN, and ANDREW), T., 1633. Methoxy-3-methyl-8-benzoylacrylic acid (BENTLEY,GARDNER, and WEIZMANN), T., 1640. 2-Methoxy-5’-methyl-2-benzoylbenzoic acid (BENTLEY, GARDNER, WEIZ- MANN, and ANDREW), T., 1633. 4‘-Methoxy-5‘-methyl-2- benzo ylbenzoic acid and bromo- (BENTLEY, GARDNER, and WEIZMANN), T., 1630. See A1 e thoxy eosin.2120 INDEX OF SUBJECTS. Methoxymethyl-B-benzoylpropionic acid (BENTLEY, GARDNER, and WEIZ- MA”), T., 1640. Methoxynaphthacenequinane, trihydr- oxy- (BENTLEY, FRIEDL, and WEIZ- MANN), T., 1592 ; P., 215. 5 -Methoxynaphthacenequinone, 1 -hydr- oxy- (BENTLEY, FRIEDL, THOMAS, and WEIZMANN), T., 425.8( or 9)-Methoxynaphthacenequinone, 1- hydroxy- ( BENTLEY, FRIEDL, THOMAS, and WEIZYANN), T., 423. 3(or 6)-Methoxy-2-B-naphthoylbenzoic acid, 1‘-hydroxy- (BENTLEY, FRIEDL, THOMAS, and WEIZMANN), T., 420. 29-Methoxyphenyl- 1:3-benzoxazone and its acetyl derivative (KEANE and NICHOLLS), T., 268 ; P., 3.6. 7 - p - l e t h o x y ~ h e n y l - ~ ~ ~ ~ ~ -dinaph- thacridine and its additive salts (SEN- IER and AUSTIN), T., 1237 ; P., 186. Methoxyphenyl-m-meconine, hydroxy- (PERKIN and ROBINSON), P., 292. 3-Methoxyphthalanilic acid ( BENTLEY, ROBINSON, and WEIZMANN), T., 110. 4-Methoxyphthalanilic acid ( BENTLEY and WEIZMANN), T., 104. 3-Methoxyphthalic acid and its anhy- dride, a d , and imide (BENTLEY, ROBINSON, and WEIZMANN), T., 110.4-Xethoxyphthalic acid and its methyl ester, anhydride, anil, and imide (BENTLEY and WEIZMANN), T., 102. the fluoresceins and eosins from (FRIEDL, WEIZMANN, and WYLER), T., 1584 ; P., 214. 3-Methoxyphthalonic acid and its anhydrophenylhydrazone ( BENTLEP, ROBINSON, and WEIXMANN), T., 109. Methyl, replacement of alkyl radicles by, in substituted ammonium com- ounds (JONES and HILL), T., 2083 ; g., 290. Methyl-46-diamino-m-xylene and the action of diazonium salts on (MORGAN and MICKLETHWAIT), T., 363 ; P., 28. 2-Methylanthranol, dihydroxy- (BAR- ROWCLIFF and TUTIN), T., 1913 ; P., 249. 1-Methylanthraquinone, 2-hydroxy- and nitro-2-hydroxy-, and their methyl ethers (BENTLEY, GARDNER, and WEIZMANN), T., 1631. 4-hydroxy- and its methyl ether (BENTLEY, GARDNER, WEIZMANN, and ANDREW), T., 1633.4:6( 7)-dihydroxy- ( BENTLEY, GARD- NER, and WEIZMANN), T., 1639. 2-Methylanthraquinone, 1- and 4-hydr- oxy-, and their potassium salts (BENTLEY, GARDNER, and WEIZ- MAKE), T., 1635. 4:7(8)-dihydroxy (BENTLEY, GARD- NER, and WETZMANN), T., 1638. trihydroxy-. See Emodin. 4’-Yethyl-2-benzoylbenzoic acid, 4( 5) :2’- dihydroxy- ( RENTLEY, GARDNER, and WEIZMANN), T., 1638. 6’-Methyl-2-benzoylbenzoic aoid, 4(5):2’- dihydroxy- ( BENTLEY, GARDNER, and WEIZMANN), T., 1639. Methyl-2-bensoylbenzoic acids, 3’-, 4‘-, and 5‘-, 2’-bydroxy- (BENTLEY, GARD- NER, and WEIZMANN), T., 1635. Methyl-y-bromoallylacetoacetio acid, ethyl ester ((XARDNER and PERKIN), T., 853 ; P., 116. Methyl-y-bromoallylmalonic acid, ethyl ester (PERKIN and SIMONSEN), T., 830.Methyl isobntenyl ketone. See Mesityl oxide. Methyl AY-bnthene ketone and its oxime and semicarbazone (GARDNER and PERKIN), T., 851 ; P., 116. density, magnetic rotation, and re- fractive power of (PERKIN), T., 852. Methylcrotonylcarbinol. See A-Hex- Methylene chloride, interaction of, with the sodium derivative of ethyl malonate (TUTIN), T., 1141; P., 158, 245. condensation of, with 1 -bromo- and 1-chloro-2-naphthylamines (SENIER and AUSTIN), P., 300. 5:6-Methylenedioxy-2-benzylidene-l -hy- drindone, 2’-hydroxy-, and its acetyl derivative (PERKIN and ROBINSON), T., 1097. 5:6-Methylenedioxy-l- hydrindone and its oxime and .isonitroso- and S-benz- ylidene derivatives (PERKIN and ROBINSON), T., 1084. Methylethylthetine menthyl ester, ni- trate of (SMILES), p., 291. Methylfrnctoside and its methylation (PURDIE and PAUL), T., 290 ; P., 33.y-Methyl-Ay-heptene-eone (LAW and PERKIN), P., 308. 1 -Methyl yclohexane-3-carboxylic acid, cis-1-bromo-, preparation of (PERKIN and TATTERSALL), T., 495. cis-1-Methylcyclohexanol-5-carboxylic acid, lactone of, and its conversion into cis-l-bromo-l-methylcyclohexane-3- carboxylic acid (PERKIN and TATTER- SALL), T., 495. ene, B-hydroxy-.INDEX OF SUBJECTS. 2121 l-Methyl-A1-cycZohexene-3-osrboxyIic acid and its ethyl ester (PERKIN and TATTERSALL), T., 496. Methylhexylcarbinol, See sec. -0ctyl alcohol. Methylhomoeriodictyol (POWER and TUTZN), T., 895. Methylmorindanol ( BARROWCLIFF and Tu-rrN), T., 1918 ; P., 249. Z-Methyl-6:8-naphthylenediamhe and its additive salts and diacetyl deriva- tive and 7-carboxylic acid and its ethyl ester (ATKINSON and THORPE), T., 1708 ; Y . , 216.Methyl-5:7-naphthylenediamines, 1- and 2-, and their additive salts and diacetyl derivatives and 6-carboxylic acids and their ethyl esters (ATKINSON and THORPE), T., 1700 ; P., 216. l-Me thyl-4-isopropylcycZohexane, 1 :3-di- amino-. See Tetrahydroumbellulylam- ine, amino-. 2-Methylpyrone-6-acetic acid (COLLIE aud HILDITCH), T., 789 ; P., 92. N-Methylsalicylamide, preparation of, and its benzoyl derivatives (MCCONNAN and MARPLES), T., 194 ; P., 18. Methyluracyl, mercuric salt (AULD), T., 1047 ; P., 152. Methyluric acids, 3- and 7-, mercuric salts (AULD), T., 1046 ; P., 152. Molecular aggregation in solution as exemplified in aqueous mixtures of sulphuric acid with inorganic sul- phates (HOLMES and SAGEXIAN), T., 1606 ; P., 210.complexity of liquids (DUNSTAN and THOLE), P., 19. weight. See Weight. Morinda ZongiJEora, chemical examina- tion of the leaves and root of (RAR- ROWCLIFF and TUTIN), T., 1907 ; P., 248. Morindanol from the leaves of Morindn Zongzpora (BARROWCLIFF and TUTIN), T., 1917 ; P., 249. Morphide, chloro-, methylation aud hydrolysis of (LEES), T., 1411 ; P., 200. Morphine, researches on (LEES), T., 1408 ; P., 200. B-isoMorphine, formation and methyla- Mutarotation. See under Photochem- tion of (LEES), T., 1413 ; P., 200. istry. N. Naphthacenequinone derivatives (BENT- LEY, FRIPDL, THOMAS, and WEIZ- MANX), T., 411 ; (BENTLEY, FRIEDL, and WEIZMANN), T., 1588 ; P., 215. Naphthaoenequinone derivatives, absorp- tion spectra of (BALY and TUOK), T., 426.Naphthacenequinone, 7(10)- and S(9)- amino-l-hydroxy-, and 1:5-di- and 1:4:5-tri-hydroxy- ( BENTLEY, FRIEDL, and WEIZMANN), T., 1591. Naphthacene-4(?)-sulphonic acid, 1 :5- THOMAS, and WEIZMAXN), T., 425. B-Naphthacinchonhic acid (m.p. 248”) from an aldehyde from oil of nutmeg (POWER and SALWAY), T., 2053; P., 285. Naphthalene, action of aluminium chloride on (HOMER), T., 1103 ; P., 88. 1:5-dihydroxy-, and its methyl ethers, and their oxidation (BENTLEP, ROBINSON, and WEIZMANN), T., 106. amino-, N-benzoyl derivative of (MOR- GAN and WOOTTON), T., 1322. Naphthalene-l:2’-azo-l’:4’-naphthylene- diamine, 4:4‘-N-dibenzoyl derivative of (MOIWAN and WOOTTON), T., 1392. 4-a-Naphthaleneazo-2-phenyl-1:S-naph- thylenediamine (LEES and THORPE), T., 1291.Naphthalenediazonium salts. See Di- azonaphthalene salts, Naphthionio acid, cerous salt (MORGAN and CAHEN), T., 477. a-Naphthol, condensation of with alde- hydes (SENIER and AUSTIN), T., 1233 ; P., 185. B-Naphthol, molecular weight of, in solution in solid naphthalene (PEE- MAN and DAVIES), T., 1114 ; P., 162. a- Naphtholresor cinelp h thalein anhydr- ide and its acetyl derivative and methyl ether (FRIEDL, WEIZMANN, and WYLER), T., 1587. B-Naphthol-6-sulphonic acid, cerous salt (MORGAN and CAHEN), T., 476. Naphtholsulphonic acids, amino-, affinity constants of, as determined by the aid of methyl-orange (VELEY), T., 1246 ; P., 179. 3-B-Naphthoylbenzoic acid, 3(6)- and 4( 5)-amino-, and -nitro-1’-hydroxy- MA”), T., 1590 ; P., 215.4‘-amino-l’-hydroxy-, 4‘-amino-l‘:4(or 5)-dihydroxy-, 6’(!)-bromo-l’:4(or 5 ) - dihydroxy-, and 4(or 5):l’- and 1’:5’- dihydroxy- ( RENTLEY, FRIEDL, THOMAS, arid WEIZMANK), T., 416. a-Naphthylamine, condensation of, with aldehydes (SENIER and AUSTIN), T., 1233 ; P., 185. dihydroxy- (HENTLEY, FRIEDL, Naphthalene-l-aeo-B-naphthol, 4- (BENTLEY, FRIEDL, and WEIZ-2122 INDEX OF SUBJECTS. 2-Naphthylamine, l-bromo- and 1- chloro-, condensation of, with methyl- ene dichloride (SENIER and AUSTIN), P., 300. Naphthylazoimides, a- and B-, and their nitro-derivatives (FORSTER and FIERZ), T., 1942 ; P., 258. 1:s-Naphthylenediamine and its deriva- tives, formation of, from o-toluo- nitrile (ATKINSON, INGHAM, and THORPE), T., 578 ; P., 76. formation of methyl derivatives of, from the three tolylacetonitriles (ATKINSON and THORPE), T., 1687 ; P., 216.acid, ethyl ester, formation of, from ethyl 8-imino-a-cyano-6-o-tolylpro- pionate (ATKINSON, INGHAM, and THORPE), T., 587 ; P., 76. 1 :4-Naph thylenediamine, benzoyl deriva- tive, coloured diazo-salts from, and azo- derivatives of (MORGAN and WOOT- TON), T., 1311 ; P., 180. 1:4-Baphthylenediamine and its S-carb- oxylic acid and its ethyl ester, for- mation of (THORPE), T., 1005 ; P., 151. a-Naphthylnitrosoamine, 4-amino-, N- benzoyl derivative of (MORGAN and WOOTTON), T., 1322. Neoisocodeine, formation of (LEES), T., 1414; P., 200. Xeoisomorphine, formation and methyla- tion of, and its hydrochloride and methiodide (LEES), T., 1413 ; P., 200. Nickel basic sulphates, formation of (PICEERING), T., 1985 ; P., 261.Nitro-compounds, reaction between or- gano-magnesium haloids and (PICK- ARD and KENYON), P., 153. aromatic, reduction of, to azoxy-com- pounds in acid solution (FLURSCHEIM and SIMON), P., 163. fatty, preparation of, by the inter- action of alkyl iodides and mercurous nitrite (RAY and NEOGI), P., 246. Nitrogen trioxide (nitrous anhydride), gaseous (H. B. and M. BAKER), T., 1862 ; P., 239. peroxide, evolution of, in the decom- position of guncotton (ROBERTSON and NAPPER), T., 764 ; P., 91. estimation of small quantities of' (ROBERTSON and NAPPER), T,, 761; P., 91. Hyponitrous acid, decomposition of, in presence of mineral acids (RAY and GAGGULI), T., 18.66 ; P., 184. Nitroso-derivatives, compounds of, with acitls and salts (PICKARD and KENYON), T., 896 ; P., 138.l:3-Naphthylenediamie-2-carboxylic Nomenclature of the proteins, recom- meridations as to the, P., 55. Nonoic acid. See a-isoPropy1-n-hexoic acid. Nopinone, attempted synthesis of (PER. KIN and SIMONSEN), T., 1736 ; P., 198. Nutmeg oil, constituents of (POWER and SALWAY), T., 2037 ; P., 285. Nyctanthin from Nyctanthes Ar6or- trijtis, and its acetyl derivative (HILL and SIRKAR), T., 1501 ; P., 213. 0. Obituary notices :- George Bowdler Buckton, T., 663. Frederic Just Claudet, T., 660. Hermaiin Johann Philipp Sprengel, T., 661. Octadecapeptide, preparation of an (FISCHER), P., 82. Octanedicarboxylic acids. See y-iso- Propylpimelic acid and Sebacic acid. Octane-8-01. See sec. -0ctyl alcohol. Octinenedicarboxylic acid. See y-iso- Propylidenepimelic acid.Octoic acid. See a-Ethylhexoic acid. sec. -0ctyl alcohol (meMylhelmjlcarbinoZ; octane-2-oZ), resolution of (PICKARD aiid KENYON), T., 2058 ; P., 286. Optical activity, influence, and super- position and Optically active com- pounds. See under Photochemistry. Orcinol derivatives, production of, by the action of heat on the sodium salt of ethyl acetoacetate (COLLIE ' and CHRYSTALL), T., 1802 ; P., 231. Organic compounds, offect of a white-hot platinum wire on (WILsMoRE and STEWART), P., 309. estimation of halogen in (MoIR), P., 233. Oxalic acid, ethyl ester, action of, on thioacetanilide and its homologues (RUHEMANN), T., 797 ; P., 115. Oxazine series, a reaction of colouring matters of the (THORPE), T., 324 ; P., 32. Oxime formation and decomposition in presence of mineral acids (LAP- WORTH), T., 1133; P., 168.influence of acids and alkalis oc the velocity of (BARRETT and LAP- WORTH), P., 307. Oxygen ctompounds, chemistry of (PICK- ARD and KENYON), T., 896 ; P., 138. P. Palmityl chloride, reaction of, with thioureas (DIXON and TAYLOR) T., 923; P., 120.INDEX OF SUBJECTS. 2123 Pennyroyal, American, oil of, constituen t s of (BARROWCLIFF), T., 875 ; P., 114. n-Pentadecane-aa’y-tricarboxylic acid and its esters (BARROWCLIFF and POWER), T., 569 ; P., 70. Pentanedicarboxylic acid. See Tri- methylsuccinic acid. Pentenoio acids. See Allylacetic acid, &Ethylacrylic acid, and Ethylidene- propionic acid. As-Pentinene-8-carboxylic acid and its ethyl ester and silver salt (PERKIN and SIMONSEN), T.: 832 ; (GARDNEIL and PERKIN), T., 848 ; P., 116.ethyl ester, density, magnetic rotation, and refractive power of (PERKIN), T., 836. As-Pentinene-8B-dicarboxylic acid and its ethyl ester and silver salt (PRR- KIN and SIMONSEN), T., 830. ethyl ester, density, magnetic rotation, and refractive power of (PERKIN), T., 836. Peptides. See Octadecapeptide. Perhalogen salts, studies on the (TINK- LER), T., 996 ; P., 137. Permanganic acid (MuIR), T., 1485; P., 195. Petroleum from Borneo, chemical com- position of (JONES and WOOTTOS), T., 1146 ; P., 184. Phenacylcyanoacetic acid. See y-Keto- y-pheuylbutyric acid, a-cyano-. X-Phenetyl-N-methylphenazothionium salts (SMILES and HILDITCH), P., 306. X-Phenetyl-3:3’-dinitrophenazothionium salts (ShiILEs and HILDITCH), P., 306. Phenol, 2:3-dinitro-4-amino-, and its diazotisation and 2:3:5-trinitro- 4 - amino- (MELDOLA and HAY), T., 1481 ; P., 211. Phenols, association of, in the liquid condition (HEWITT and WINMILL), T., 441 ; P., 10.Phenol-2-azo-&naphthol, tribromo- and 3:5-dichloro- (ORTON and REED), T., 1566. Phenolphthalein salts, constitution of (GREEN and KIXG), P., 228. Phenol p-sulphone (SMILES and BAIN), Phenol-p-sulphonic acid, cerous salt (MORGAX and CAHEN), T., 476. Phenol p-sulphoxide and its diacetyl and dibenzoyl derivatives and reactions (SMILES and BAIN), T., 1118; P., 161. Phenonaphthacridines, synthesis of (SENIER and AUSTIN), T., 1240 ; P., 185 ; (SENIER aud COMPTON), T., 1927; P., 247. pr., 1120. XCI. Phenyl chlorocarbonate, reactions of, with thioureas (DIXON and ‘TAYLOR), T., 920 ; P., 120.y-Phenylacetoacztic acid, a-cyano-, ethyl ester, and its salts and reactions, and nnilide (SMITH and THORPE), T., 1899 ; P., 249. Phenylacetonitrile, sodium compound of, contiensation of, with berizonitrile (ATKINSOX, ISGHAM, and THORPE), T., 591. Phenylacetyl chloride, reaction of, with thioureas ( DIXON and TAYLOR), T., 924 ; P., 120. 5-Phenylacridine and its halogen deriva- tires, action of bromine on, and the nietliylntion alid salts of the products (DUKSTAX and HILi)I*rCH), T., 1659 ; P., 206. Phenylazoimide, s-tribronio- ( VORSTER and FIERZ), T., 1952. 4:6-dibromo-2-hydroxy- (ORTON, EVANS, and MORGAN), P., 167. o- and m-hydroxy-, and their nietallic and acyl derivatiws (FORSTER and FIERZ), T., 1350 ; P., 205. p-hydroxy-, and its benzoyl, m-nitro- benzogl, and potassium derivatives, and methyl cther, and 3-nitro-4- hyclroxy-, and its benzoyl and potassiunl derivatives (FORSTEIL and FIERZ), T., 859 ; P,, 112.2-Phenyl-l:4-benzopyranol hydroclilor- ide, 7-hydroxy- (PERKIN and ROBIX- SON), P., 149. Phenyl-l:3-benzoxazone, preparation and reactions of (TITHE~LLEY), T., 1425 ; P., 203. 2-Phenyl- 1: 3- benzoxazone and its 1 - acetyl derivative (KEANE and NICHOLLS), T., 266; P., 86. Phenylbenzylcarbamic chloride, reaction of, with phenylthionrea (DIXON and TAYLOR), T., 926; P., 120. Phenylbenz ylethylpropylsilicane, pi e- paration of (KIPPIKG), T., 221. l-Phenyl-3-benzylethylpyrazolone, 4- cyano- (SMITH aiid THORYE), T., 1907. l-Phenyl-3-benzylpyrazolone, 4-cyano- ( S w m and THORPE), T., 1903. Phenyl-2’:6’-di- and -2‘:4’:6’-tri-bromo-4’- hydroxyphenylamines, 2:4 :6-t ri- bromo- (SMITH and ORTOX), T., 151 ; P., 14.y-Phenylbutyric acid, y-imin0.a-cgano-, ethyl ester, formation and conilensatioii of (THORPE), T., 1007 ; P., 151. Phenyl-a-camphoramic acid, 4-aniino-, 4-bromo-, 4-bromo-3-amino-, and its acetyl derivative, and 4-bronro-3-nitro- (WOOTTON), T., 1895 ; P., 250. ? B21 24 IKDEX OF SUBJECTS. 11‘- Phenylcamphorimide, 4 - bromo-, 4 - bronio-3-amino-, and 4-bromo-3-nitro- (Woor~on.), T., 1898 ; P., 250. Phenylisocrotonic acid, esterification constant of (SUDBOKOUGH a i d TIIOM- AS), T., 1034 ; P., 146 ..,. 5- Phenyl-3:7- dimethylacricme, 2 : 8 -cli- hydroxy-. See Benzoflavol. 7 - P h e n y l - ~ ~ ~ ~ ~ - d i n a p h t h a c r i d i n e , m-nitro-, and its additive salts (SEXIER aiid AUSTIN), T., 1238 ; P., 186.p-Phenylenediamine, benzoyl derivative, diazo-derivatives of (MORGAN m d WOOTTOR), T., 1315. 2:6-dibromo-, preparation of (HETVITT and WALKER), T., 1141 ; P., 161. y-Phenyl-a-ethylacetoacetio acid, a- cyano-, ethyl ester, and its hydrolysis, and anilide (ShlITH and THORPE), T., 1905 ; P.; 249. Phenylethylpropylsilicol and its chlor- ide, preparation of (KIPPIXG), T., 218. Phenylethyl-silicon dichloride and -silicone, preparation of ( KIPPING), T., 215. d-Phenylglucosazone, melting point of (TUYIN), P., 250. Phenylhydraaine and p-lmrno-, oxidx- tion of, by free oxygen (CHATTAWAY), T., 1326 ; P., 183. Phen ylhydrazinodicarbox ytricarball ylic acid, methyl ester (RUHEM.4NS), T., 1363 ; P., 195. B-Phen y liminobenzo yldihydrocarvone and its cyanohydrili (CLARKE and LAPWORTH), T., 699 ; P., 90.Phenylimino-di- and 4ri-bromobenzo- quinones, 2:4:6-t.ribroino- (SMITH and ORTON), T., 150 ; P., 14. l-Phenyl-2-methylbenziminazole, 7- nitro-6-hydroxy- (MELDOLA and HAY), T., 14S2. Phenylmethylethylpropylsilicane, pre- paration of (KIPPING), T., 221. 2-Phenylnaph t halene, 1 -amino - 3 - hydr- oxy-, and its hydrochloride, 3-amino- l-hydroxy-, and its F-acetyl deriva- tive, and 1 :3-dihgdroxy- (LEES and TIIOKPE), T., 1302. 2-Phenylnaphthalene- 1 - azo- 8-naphthol, 3-amino-, and its N-acetyl derivative (LEES and TIIORPE), T., 1293. 2-Phenylnaphthalene-3-azo-P-naphtho1, l-amino- (LEES and THORPE), T., 1289. 2-Phenylnaphthalene- 1:4’-azo-2’-phenyl- 1’:3’-naphthylenediamine, 3-aniino-, and its N-acetyl derivative and their hydrochlorides (LEES and TIIORPE), T., 1294.Phenglnaphthols, amino-. See 2- 1 -ainino-3- hydr- 2-Phenyl-l:3-naphthylenediamine, pre- paration of, and its acetyl, benzylid- ene, and methyl derivatives and their diazotisation and its com- pounds with diazonium salts (LEKS and T~~ortre), T., 1282 ; P., 189. fornixtion of, from b-imino-a-cyano- a-phenyl-0-o-tolylethane (ATKTX- sox, IKGHAM, and THORPE), T., 2-Phenyl- 1:3-naphthylenedimethyldiarn- ine, a- and 8- forms, and their dihydro- chlorides and dinitrosoamines (I,EEs and THORPF,), T., 1296. diamine and its dihydrochloride and 4-nitroso-derivative (LEES and THORPE), T., 1300. amine and its hydrochlorides antl nitrosoarnine (LEES and THORPE), T., 1299. X-Phenylphenazothionium, derivatives of (SMILFS and HILDITCH), P., 306.Phenylpropiolic acid and o- antl p - nitro-, additioii of iodine to (JAMES and SUDBOROUGH), T., 1041 ; P., 136. borriyl and menthgl esters, properties of (HILDITCH), P., 287. 8-Phenylpropionic acid, bornyl and inenthyl esters, properties of (HIL- DITCH), P., 287. 8-Phenylpropionic acid, aaS- and aPB- tribromo-, and their methyl esters, and P-chloro-ab-c2ibronio- (SUD- 8-iniino-a-cyano-, ethyl ester, and the action of snlpliniic acid on (ATKIN- SON, IKGHAM, and THORPE), T., 590. 1- Phenyl-5-pgrazolone-3-carboxylic acid ( ~ U H E M A S N ) , T., 1364 ; P., 196. l-Phenyl-5-pyrazolone-3:4-dicarboxylic acid, 4-methyl ester, and.its pheiiyl- hydrszide (RUHEIIANN), T., 1363 ; P., 196. Phenylthiourea, reaction of, with nwtyl chloride and benzyl chlorocarbonate (DIXON and HATVTHOIXE), T., 128.a-Phenyl-8-o-tolylethane, 8-imino-a- cyano-, aiid the forniation of 1:3- diamino-2-phenylr1aplithalene from (ATKINSON, ISGHAM, aiid THORPE), T., 588 ; P., 76. Phosphates. See under Phosphorus. Phosphorus, atomic volumes of (PRI- DEAUX), T., 1711 ; P., 207. coefficient of expansion of ( PRIDEAUX), T., 1712 ; P., 207. Phenyl napli t halene, oxy-, and 3-aniino-l-hydroxy-. 589 ; P., 76. Z-Phenyl-1:3-naphthylenetetramethyl- 2-Phenyl-l:3-naphthylenetrimethyldi- BOROUGH all& WILLIAMS), p., 146.INDEX OF SUBJECTS. 21 25 Phosphorus pentachloride, coefficient of expansion of (PRIDEAUX), T., 1713 ; P., 207. Phosphates, action of yeast juice on soluble (YOUNG), P., 65. Hypophosphorous acid, the velocity and mechanism of the reaction be- tween iodine and (STEELE), T., 1641 ; P., 213.Light, ultra-violet, chemical changes induced in gases submitted to the action of (CHAPMAN, CHADWICK, and RAarsBoTroM), T., 942 ; P., 136. influence of, on diazo-reactions (ORTON, COATEB, and BummrT), T., 35. Optical activity and unsaturation, relation be tween ( HILDITCH), P., 287. of cyclic ammonium compounds (BUCIINEY and JONES), T., 1821 ; P., 234. influence of contiguity of un- saturated groups ( BRUHL), ‘1’. , 115. superposition, studies in (PATTER- SON and KAYE), T., 705 ; I?., 89. Optically active compounds, influence of solvents on the rotation of (PAT- TERSON and MCMILLAN), T., 504; and FAIRLIE), T., 1838 ; P., 236 ; (PATTERSON and THOMSON), P., 263. Refractive power of diphenylliexa- trieiie and allied hydrocarbons (SMEDLEY), P., 295.Rotation of the aryl esters and amides of Z-menthylcarbaniic acid (PICK- ARD and LITTLEBURY), T., 303 ; P., 30. of optically active compounds, influ- ence of solvents on (PATTERSON and MCMILLAN), T., 504 ; P., and FAIRLIE), T., 1838 ; P., 236 ; (PATTEBSON and THOMSON), P., 263. Rotatory power and absorption spectra, relation between (STEW- ART), T., 1537 ; P., 197. relation between absorption spectra and, and the effect of unsaturation and stereoisonierism (STEWART), T., 199 ; P., 8. Mutarotation of nitrocamphor, influ- ence of impurities on the velocity of (LOWRY and MAGSON), P., 193. PHOTOCHEMISTRY : - P., 60 ; (PATTERSON, HENDERSON, 60 ; (PATTEESON, HESDERSON, PHOTOCHEMISTRY :- Absorption spectra, relation between chemical constitution and (BAKER and BALY), T., 1122 ; P., 157 ; ( KALY, TUCK, MARSDEN, and GAZDAR), T., 1572 ; P., 194.relation between opticnl rotatory power and (STEWART), T., 1537 ; P., 197. relation between optical rotatory power and, and the effect of unsataration and stereoisornerism (STEWARY), T., 199 ; P., 8. of beiizoic acid and its salts and aniide (HARTLEY and HEDLEY), T., 319 ; P., 31. of naphthacenequiiione derivatiyes (BALY and TUCK), T., 426. of phthalic, isophthalic, and tere- phthalic acids, phthalicanhydride, and phthalimide (HARTLEY and HEDLEY), T., 314 ; P., 31. Phthalanilic acid, 3-hydroxy- ( BENTLEY, ROBIKSON, a i d WEIZMANN), T., 112. 4-hydroxy- (P,EP;TLEY and WEIZ- MANN), T., 101. Phthaleins, researches on (BENTLEY, GARDNER, WEIZMANN, ANDHEW, and TEMPERLEY), T., 1626 ; P., 215.Phthalic acid and its derivatives, condensations of, with o-, m-, and p - cresol and m-4-xylenol and their methyl ethers (BENTLEY, GARDNER, and WEIZMANN), T., 1630; P., 215. absorption spectra of ( HARTLEY and HEDLEY), T., 314 ; P., 31. Phthalic acid, 3-hydroxy-, and its an- hydride and anil (BENTLEY, ROBIN- SON, and WRIZMANN), T., 111. 4-hydroxy-, aiid its methyl ester, anhydride, anil, and imide (BENTLEY and WEIZMANN), T., the fluoresceins and eosins from structure of (GREEN), P., 12. 98. (FRIEDL, WEIZMANN, and WY- LER), T., 1584 ; P., 214. isoPhthalic acid, absorption spectra of (HARTLEY and HEDLEY), T., 314 ; P., 31. Phthalic anhydride, absorption spectra of (HARTLEY and HEDLEY), T., 314 ; P., 31.Phthalimide, absorption spectra of (HARTLEY and HEDLEY), T., 314; P., 31. Physiological action, relation of, to chemical constitution in the tropeines (JOWETT and PYMAN), T., 92.2126 INDEX OF SUBJECTS. Pinene nitrolamine and its reactions, and its additive salts, acetyl, dibenzoyl, and diphenylearbamide derivatives, and its conipouiids with aldehydes (LEACH), T., 1. preparation of, from the substance, C,,H,,O,N, (LEACH), T., 15. Pinyl-#-carbamide and its nitroso- derivative and -#-semicarbazide and its additive salts and compouncls with aldehydes anti ketones ( LEACII), T., 16. Piperidine, the “ true ” ionisation con- stants, the hydration constants, and the heat of neutralisation of (MOORE), T., 1379 ; P., 154. Platinichlorides, abnormal, formation of (DUNSTAN and CLEAVERLEY), T., 1622 ; P., 206 ; (DUNSTAN), P., 290.Platinum organic compounds (POPE and PEACHEY), P., 86. Polypeptides, synthesis of (FISCHER), See also Octadecnpeptide. Portraits of Faraday and Daniell, presents of, to the Society from Professor Meldola, P., 255. Potassium periodate, specific gravity and solubility of (BARKER), P., 305. mercuric nitrites (RAY), T., 2032 ; P., 165. sulphite, action of, on potassium tetrathionate in aqueous solution (COLEFAX), P., 207. sodium double sulphites, isomerism of (GPDRY), P., 241. Potassium cyanide, action of hydrogen peroxide on ( MASSON), T., 1449 ; P., 117. calcium ferrocyanide (BROWN), T., 1826 ; P., 233. Propane, tribromo-, action of, on the sodium derivative of ethyl aceto- acetate (GARDNER and PERKIN), T., 848 ; P., 115.action of, on the sodiuni derivative of ethyl malonnte (PEHKIN and SIMONSEN), T., 816, 840. y 4soPropenolpimelic acid, ethyl hydro- gen ester, lactone of (PERKIN and SIMONSEN), T., 1742 ; P., 198. Propiolic acid and its ethyl ester (PERKIN and SIMOKSEN), T., 833. densities, magnetic rotations, and refractive powers of (PEKKIN), Propylene dibromide, action of, on the disodium derivative of diacetylacetone (BAIN), T., 544 ; P., 77. Propylenedicarboxylic acid. See Glut- aconic acid. P., 82. T., 837. Propylenetetracarboxylic acid. See Dicnrlsoxyglu tnconic acid. a-isolropyl-72-hexoic acid, 2-6-hydroxy-, formation and oxidation of, and its lactone (TUTIM), T., 272; P., 29. isoPropylideneacetone. See Mesityl oxide. 4-isoPropylidenec~cZohexane and its seniicarbazone and B-bromo-, and their 2-carboxylic acids, ethyl esters, synthesis of (PERKIN arid SIMONSEN), T., 1736; P., 197.y-isoPropylidenepimelic acid and its ethyl ester and reactions (PERKIN and SIMONSEN), T., 1743 ; P., 198. y-iso-Propylpimelic acid, broino-, ethyl and ethyl hydrogen esters (PERKIN and SIMONSEN), T., 1742 ; P., 198. Proteins, recommendations as to the nomenclature of the, P., 55. Prulaurasin and its tetm-acetyl deri- vative (CALDWELL and Coua-rAuLD), T., 671 ; P., 71. Pseudo-acids, a method for the deter- mination of the equilibrinm in aqueous solutions of (MOOICE), T., 1373; P., 154. containing the group .CO.NH*, mer- cury derivatives of (AULD), T., 1045 ; P., 151. Pseudo-bases, a method for the deter- mination of the equiliLrium in aqueous Bolutions of (MOORE), T., 1373; P., 154.Purpuroxanthin, 2-methyl ether (PER- y-Pgranol derivatives (PERKIN and Pyridine and some of its derivatives, relation betwecn absorption spectra and chemical constitution of (BAKER and RALY), T., 1122 ; P., 157. solutions, viscosity of ( DUNSTAN, THOLE, and HUNT), T., 1728 ; P., 207. Pyro enic reactions, certain ( M T ~ ~ ~ ~ RE KIN), T., 2072. ROBINSON), P., 149. a n 8 STEWART), P., 303. Q. d-Quercitol (quercite), occnrrence of, in the leaves of C’hamnerops humilis (MULLER), T., 1766 ; I?., 218. Quinoline, 2-hydroxy-. See Carbcstyri). Quinolphthalein salts, constitution of (GREEI~ and KING), P., 228. Quinoneanil, bromo-derivatives. See Phenyliminobr omobenzoquinones. o-Quinonediazide, 3-chloro-5-bromo- (ORTON and REED), T., 1569.INDEX OF SUBJECTS.2127 Quinonediazides, chlorobromo-, forin- ation of (OXTON and REED), T., 1564 : P., 212. R, Racemisation by alkali as applied to the resolution of r-mandelic acid into its optically active isomerides (MCKENZIE and MULLER), T., 1814 ; P., 234. Radium emanation, some properties of (CAMERON and RAMSAY), T., 1266 ; P., 178. chemical action of, on solutions con- taining copper, a,nd lead, and on water (CAMERON a d RAMSAY), T., 1593 ; P., 217, actiou of, on distilled water (RAMSAY), T., 931 ; P., 132. Refractive power. See Iulder Photo- chemistry. Research fund, gift of $1,000 to thc, from the Worshipful Conipany of Goldsmiths, P., 53. balance sheet. See under Balance sheet. Rotation and Rotatory power. See Rubber tree, Para.See IIeven bmsi- Rubidium iodate and periodate (BARKER), under Photochemistry. Zicnsis. P., 305. S. Salicylamide, condensation of, with aryl aldehydes ( KEANE and NICHOLLS), T., 264 ; P., 36. Salicylidene-l-hydrindone. See 2- Benzylidene-l-hydrindone, 2’-hydr- oxy-. O-Salicylsalicylamide’ (MCCONNAN), T., 196 ; P., 18. Salts, electrometric determination of the hydrolysis of (DENHAM), P., 260. Sebacic acid, aa‘-dihydroxy-, and its diacetyl derivative, action of heat on (LE SUEUR), T., 1365 ; P., 196. Selenium, action of, on arsine and stibine (JONES), P., 164. Selenonium bases, aromatic (SMILES and HILDITCH), P., 12. Semi-ortho-anilidotri-ethyl and -methyl- oxalates and their transformations (LANDER), T., 968 ; P., 149. Semi-ortho-oxalic compounds, mixed (LANDER), T., 967 ; P., 148.Silicon organic compounds (KIPPING), T., 209, 717 ; P., 9, 83. Silver, isomorphous replacement of univalent mercury by (RAY), T., 2033 ; P., 166. Silver nitrite, constitution o f ; a cor- hyponitrite, decomposition of, by heat (DIVERS), P., 265. decompositioii of, by heat, and con- stitution of (RAY and GA~~GULI), T., 1399 ; P., 89. Silver-mercuroso-mercuric oxynitrates and the isomorphous replacement of univalent mercury by silver (RAY), T., 2033 ; I’., 165. Silver and copper groups, electro- analytical deposition and separatioii of inetals of the ( S ~ s n ) , T., 373 ; P., 26. Sodium periodate, specific gravity and solubility of ( BAILKKR), P., 305. mercuric nitrites (RAY), T., 2032 ; P., 165. potassium double sulpliites, isomerisni of (GODBY), P., 241.thiosulphate, constitution of (PRICE and Twss), T., 2024 ; P., 263. pentahydrate, volunie changes which accompany transformation in the system (DAWSOS and JACKSON), T., 552 ; P., 75. Soil, interaction of ammonium salts with the constituents of the (HALL and GIBIINGHAM), T., 6f7 ; P., 61. Solubility of sparingly soluble gases in water, influence of non-electrolytes a d electrolytes on the (PHILIP), T., 711 ; P., 85. Solvent, effect of configuration and degree of saturation of the, on the rotation of optically active com- pounds (PATTERSON, HENDERSON, a d FAIRLIE), T., 1838 ; P., 236. Solvents, influence of, on the rotation of optically active compounds (PATTKIL- SON and MCMILLAN), T., 504 ; P., 60 ; (PATTERSON, HENDERSON, and FAIRLIE), T., 1838; P., 236; (PATTER- SON a d THOMSON), P., 263.Spectra. See under Photochemistry. Starch, xanthogenic esters of (CROSS, BEVAN, and BRIGGS), T., 612 ; P., 90. alkali, interaction of, with carbon clisulphide (CROSS, BEVAN, and BBIGGS), T., 612 ; P., 90. Stibine. See Antimony trihydride. Stilbene, 4:4’-dinitro- (GEEEN, DAVIES, arid HOBSFALL), T., 2079 ; P., 289. (GEE EN, DAVIES, a d HORSFALL), T., 2083. Htilbene group, colouring matters of the (GREEN, DAVIES, and HORSFALL~, T., 2076 ; P., 289. Suberic acid, dialdehyde of, and its dioxime, formation of (LR SUEUR), T., 1366 ; P., 196. rection (DIVERS), P., 11. 4:4’-dinitro- 2 :2’-cZicy nno-2128 INDEX OF SUBJECTS. Llnbstance, C,HlpO,N,, from the action of nitrous acid on aminodimethyldi- hydroresorcin (HAAS), T., 1444 ; P., 192.C,Hl10N3, and its platinichloricle, froin the reduction of 4-oxiinino-3-imino- 1 :l-dimethyl-5-cyclohexanone and of the oxirne of isonitrosodiinethyldi- hydroresorcin (HAAS), T., 1447, 1448. CRZ!1002, from the action of ethylene dibromide on the disodium drriva- tive of diacetylacetoiie (BAIN), T., 548 ; P., i f . C,,H,O,, and its reactions, from the condensation of triacetic lactone with ethyl acetoacetate (FLEIscIr- MANN), T., 251 ; P., 16. CloH,,O,, from the action of propyletre dibromide on the disodium deriva- tive of diacetylacetone (BAIN), T., 550. C,,H,,O,,, froin the actiaii of dilute acids on calmatambetin (YYMAN), T., 1232 ; P., 184. Cl1Hl5ONS,, from the action of amyl nitrite 011 camphoryldithiocarhaniic acid (FORSTI+:H arid JACKSON), T., 1885 ; P., 242.C1&t&N3, and its reactions, from pinene nitrosochloride and potassium cyanate (LEACH), T., 10. C1,H,,06, anti its bromo-derivative, froin the action of hcat on the sod- ium salt of ethyl acetoacetate (COLLIE and CHEYSTALL), T.: 1803 ; P., 231 ; (COLLIE), T., 1811. C16H,0,, from the condensation of the aldehyde, C,H,,O, (RAPEX), T. ,1834. Cl6Hl2O3N2, from natural indigo (PERKIN a i d BLOXAM), T., 281 ; P., 30. C16Hi40,N2, from indigo-brown (PERKTN and BLOXAM), T., 284 ; I?., 30. CleH,,06N, from the con_deiisation of triacetic lactone and cthyl p- aminocrotonate, T., 256 ; P., 16. C,7H,,?U',S., from carnpliorylphenyl- thiosemicarbazide (FORWER and JACKSON), T., 1890 ; P., 242. CmHI5Ol8Br6, from the flowers of Ngctanthes Abor-tristis (HILL and SIRKAR), T., 1505 ; P., 213.CmH190,N, from benzoflavol (DUN- STAN and CLEAVERLEY), T., 1624 ; P., 206. C,H,06N3, from indigo-brown (PER- KIN and BLOXAM), T., 284 ; P., 30. C,H,O, from the root of Mori?zda 2ongiJos.a ( BABROWCLIFF and TUTIN), T., 1915 ; P., 249. Substance, C3,,HDO4, from the methyl- ation of benmin by Fischer's rwthod (IRVIXE and WEIR), T., 1392. C,,H,,O,N,, from the benzoylation of syiz-benzylidenesalicylamide (TITH- ERLEY), T., 1432. Substitution, influence of, in the nucleus on the rate of oxidation of the side-_chain (COIIEN and HODS- MAN), T., 970 ; P., 152. influence of, on the formation of diazo- amines and aminoazo-compounds (MORGAN and MICKLETH WAIT). T., 360 ; P., 28. of alkvl radicles bv methvl in substi- tutid amnioniuli cornpcknds (JONES and HILL), T., 2083 ; P., 290.of halogens by hydroxyl (SENTER), T., 460 ; P., 60. of lialogen by hydroxyl in chlorobromo- diazobenzenes (ORTON a i d REED), T., 1554 ; P., 212. Succinic acid and its potassium salts and their crystallography (MARSHALL and CAMERON), T., 1519 ; P., 214. Sucrose, estimation of, by Fehling's so- lution (LANG and ALLEN), T., 1372 ; P., 187. Sugars, compounds of, with gumiidine (MORRELL and BELIAIW), T., 1010 ; P., 87. Sulphanilic acid. See Aniline-p-sul- phonic acid. Sulphates. See under Sulphuric acid. Sulphonium iodides, inflnence of mor- curie iodide on the formation of (HILDI'rcir and SMILES), T., 1394 ; P., 206. Sulphuric acid, molecular aggregation in aqueous mixtures of, with inor- ganic sulphates (HOLMES and SAGE- MAN), T., 1606 ; P., 210.Sulphates, an iinproved form of ap- paratus for the rapid estimation of (LANG and ALLEN), T., 1370 ; P., 187. Thiosnlphates, constitution of (PRICE and TWISS), T., 2024 ; P., 263. Synthesis, asymmetric, studies in (MC- KENZIE and WREX), T., 1215 ; P., 188. T. Tartaric acid, ethyl ester, rotation of, in aliphatic halogen derivatives (PATTERSON and THOMSON), P., 263. influence of solvents on the rotation of (PATTERSON and MCMILLAN), T., 504 : P., 60 ; (PAI'TERSON, HENDERSON, and FAIRLIE), T., 1838; P., 236.INDEX OF SUBJECTS. 2129 Tartaric acids, optically active, asym- metric synthesis of (MCICENZIE nnd WREN), T., 1215 ; P., 188. relation between the absorption spectra and optical rotatory power of the (STEWART), T., 1537 ; P., 197.Tellurium, atomic weight of (I~AKER and BENNETT), T., 1849 ; P., 240. action of, on arsine and stibine (JONES), P., 164. Terebic acid, synthesis of (SIhIossEN), T., 184. Terephthalic acid, absorption spectra of (HARTLEY and HEDLEP), T., 314 ; P., 31. Terpenes, contributions to the chemistry of the (HENDERSON), T., 1871 ; P., 247. experiments on the synthesis of the (KAY and PERKIN), T., 372 ; (PEE- KIN and TATTERSALL), T., 480 ; P., 66 ; (PERKIN and SIMONSEN), T., 1736 ; P., 197. Terpenylic acid, synthesisof (SIMONSEN), T., 184. Terpin, direct synthesis of, from ethyl cyclohexanone-4-carboxylate, and its hydrate (KAY and PERKIN), T., 372. Terpineol, density, magnetic rotation, refractive power, and dispersion of (PERKIN), T., 499. Tetraethvlammonium hvdroxide. tetra- and hexa-hydrates of ~CRICHTON), T., 1794 ; P., 236.A8-Tetrahydrobenzoic acid. See A3- CycloHexeriecarboxylic acid. Tetrahydrocarves trenediol (m -nzenth- am-1 :8-diol), cis- and tram-, syn- thesis of (PERKIN and TATTERSALL), T., 501 ; P., 66. Tetrahydrocarvestrenediol anhydride. See m-Cineol. Tetrahydro-y-toluquinaldine, resolution of, into its ontically active components (POPE and I ~ I T C K ) , T., 455 ; P., 15. Tetrahydroumbellulylamine, amino-, and its sulphate, dibenzoate, dihydro- chloride, and dibenzoyl derivative (TUTIX), T., 276 ; P., 2% Te€raketopiperazine, formation of, and its hydrazone 2nd salts (DE MOUILPIED and RULE), T., 176 ; P., 13. 2':4':5:6-Te tramethoxy-2-benzyl- 1 -hydr - indone (PERILIN and ROBINSOX), T., 1101. 2':4':5:6-Tetramethoxy-2-benzylidene-l- hydrindone (PEEKIN and ROBINSON), T., 1101.Tetramethylacridines, 1 :3:7:9- and 1:4:6:9-, and their additive salts (SF,NIER and COMPI'OII), T., 1929 ; P., 247. 6:6:5':5'-Tetramethyldicyc?ohexane, 1:l'- and 3:3'-dihytlroxy-, and their diacetyl and clibenzoyl derivatives (CI~OSSLEY and RRNOUF), T., 71. ene, 1:l'-dihydroxy-, and its bromo- derivative (CROSSLEY and REh'ouF), T., 76. Tetramethyldinaphthanthracene, forni- ation of (HOMER), T., 1107; P., 2:4:S:7-Tetramethylfluoran (BENTLEY, GA~LDNER, aiitl WEIZMANN), T., 1637. Tetramethyl fructose, crystalline (PUR- DIE and PAUL), T., 295 ; P., 33. Tetramethyl glucose, derivatives of (IRVINP and MOODIF,), P., 303. Tetramethyl methylfructoside and its hydrolysis (PUI:DIE and PAUL), T., 293 ; P., 33.Tetramethylnaphthalene, preparation of (HOMER), T., 1107 ; P., 88. Tetramethylstilbene dibromide (LAW), T., 752. aayy-Tetramethyltricarballylic acid, preparation of, and its salts arid anhydro-acid (HENSTOCK and SPRANK- LING), T., 354 ; P., 32. Tetranaphthyl, formation of (HOMER), T., 1112; P., 88. Tetraphenylpyrrole (CLARKE and LAP- WORTH), T., 704 ; P., 90. Tetrapropylammonium hydroxide, heptahydrate of (CRICHTON), T., 1796 ; P., 236. Tetrolic acid, addition of iodine to (JAMES and SUDBOROUGH), T., 1039 ; I'., 136. Heats of combustion and valency, relation between ( LE BAS), P., 134. rhiocarbamic acid, imino-, acyl-JI-deriva- tives of, and their isomerides (DIXON and TAYLOR), T., 912 ; P., 119. rhiocarbanilide. See s-Diphenylthio- carbamide. rhiosulphates. See under Sulphuric acid.rhiourea, action of acyl chlorides on (DIXOX and HAWTHORNE), T., 124 ; ( D r x o ~ and TAYLOR), T., 923; P., 120. rhioureas, action of acyl chlorides on (DIXON and HAWTHORNE), T., 122 ; (DIXON and TAYLOR), T., 912; P., 119, 294. >-Tolidhe, 5:5'-dibromo- (MoIR), T., 1310. Colualdehydes, electrolytic reduction of 5: 5: 5':s' -Tetramethyl-A2:"'-dicycZohex- 88. rHERMOCHEMISTRY :- (LAW), T., 7 5 0 ; P., 73.2130 INDEX OF Toluene, chloronitro- and nitro-deriva- tives, rate of oxidation of (COHEN and HODSMAN), T., 970 J P., 152. o-, m-, and p-iodo-, dichlorides, action of heat on (CALDwELLand WERNER), T., 240; P., 17. p-nitro-, and its derivatives, action of caustic alkalis on (GREEN, DAVIES, and HORSFALL), T., 2076 ; P., 289. p-nitro-o-cyano-, action of caustic alkalis and air on (GREEN, DAVIES, and HOKSFALL), T., 2082.p-Tolneneazo-/?-naphthol, 3-chloro-5- bromo- (ORTON and REED), T., 1571. Toluenediazonium salts. See Diazo- toluene salts. Toluene-p- diazotrimethyl-4:6-diamino- wt-xylene (MORGAN and MICKLE- 4-Toluene-p-sulphonyl-4-meth 1-4:B-di- amino-mxylene and its hy Aochlorid: and acetyl and azo-/?-naphthol deriva- tives (hfORGAN and MICKLETHWAIT), T., 364. Toluene-p-sulphonyl-6-nitro-4-amino-~~t- xylene and its N-methyl derivative (NORGAN and MICKLETHWAIT), T., 363. o-Toluic acid, p-nitro-, action of caustic alkalis and hypochlorites on (GREEN, DAVIES, and HORSFALL), T., 2081. nt-Toluic acid, ultra-violet absorption spectra of (BALY), T., 846. ethyl ester, density, magnetic rotation, and refractive power of (PERKIN), T., 845.+-?n-Toluic acid. See AaS-Heptadi-inene- 8-carboxylic acid. p-Toluidine, acetyl derivative. See monohydrate (WALKER and BEVE- p-Toluidine, 3-chloro-5-bromo-, and its acetyl derivative (ORTON and REED), T., 1570 ; P., 212. Tolyl chlorocarbonatee, reactions of, with thioureas (Drxox and TAYLOR), T., o-Tolyl methyl ether, p-nitro-, action of caustic alkalis and air on (GREEN, DAVIES, and HORSFALL), T., 2080. Tolylacetonitriles, o-, m-, and p - , pre- paration of, and formation of methyl derivatives of 1 :3-naplithylenediamine from (ATRIKSON and TIronm), T., 1699 ; P., 216. 7-Tolylbutyric acida, o-, m-, and p-, 6- imlno-a-cyano-, ethyl esters, and the action of cold concentrated sulnhuric ‘I‘HWAIT), T., 370. Aceto-p- toluidide.RIDGE), ‘r., 1797 ; P., 236. 821 ; P., 120. acid on (ATKINSON and THORP;), T., 1699; P., 216. SUBJECTS. 7-Tolyl- ;:&I> dinaphthacridines, o-, m-, andp,, and their additive salts (SENIERandAUSTIN),T., 1235 ; P.,186. Tolylhydrazinee, o- and p - , oxidation of, by free oxygen (CHATTAWAY), T., 1330; P., 183. 8-o-Tolylpropionic acid, 8-irnino-a- cyano-, ethyl ester, and its conversion in to ethyl 1 :3-n aph thylen edianiine-2- carboxylate (ATKINSON, INGHAM, and THORPE), T., 585 ; P., 76. Tolylthioureae, o- and p - , action of acyl chlorides on (DIXON and HAWTHORNE), T., 136 ; (DIXON and TAYLOR), T., 919; P., 120. Triacetic lactone, condensation of, with ethyl acetoacetate and with ethyl B- aminocrotonate (FLEISCHMANN), T., 250 ; P., 16. Trianisylselenonium salts and hydroxide (SMILES and HILDITCH), P., 12.Triazoacetic acid and its salts, ethyl ester, and amide (FOHSTER and FIEEZ), P., 258. Triazoacetone (acetonylnzoimide) and its sernicarljazone (FORSTER and FIERZ), P., 259. Triazo-groups, the (FORSTER and FIERZ), P., 258. n-Tridecane-aa’y-tricarboxylic acid and its methyl ester (BARROWCLIFF and Triethylamine and its mixtures with water, vapour pressures of (LATTEY), T., 1959 ; P., 243. the “ true ’) ionisation constants, the hydration constaiits, and the heat of neutralisation of (MOORE), T., 1379 ; P., 154. liquid (LATTEY), T., 1971 ; P., 243. Triethylaulphonium and its mercuric iodides (HILDITCH and SMILES), T., 1397 ; P., 206. Trimethoxybenzoylbenzoic acid, hydroxy- (PERKIN and ROBINSON), P., 292. 4’:5 :6-Trimethoxy-2-benzylhydrindene, 1:2’-dihydroxy- (PERKIN and KOBIN- SON), T., 1100.4‘: 6:6 -Trimethoxy-2-benzylidene-l-hydr- indone, 2’-hydroxy-, and its potass- ium, acetyl, and acetylbromometh- oxy derivatives and hydrochloride ( PERKIN and ROBINSON), T., 1098. 4’:5 : 6-Trimethoxy- k2-hydrindochroman (PERKIN and ROBINSON), T., 1100. Trimethyl-4:6-diamino-nt-xylene and the action of diazonium salts on and its nitrosoamine and benzenesulphonyl derivative (MORGAN and MICKLE- THWAIT), T., 366; P., 28. POWEP.),’T., 577 ; P., 71.INDEX OF SUBJECTS. 2131 1:2:4-Trimethylbenzene, 5-ami~o-. See +Cumidine. 2:3:6-Trimethylbenzoic acid, formation of (LAYWOETH and WECWSLER), T., 994, 1919 ; P., 138. Trimethylbraeilone and +Trimethyl- brazilone, constitution of (PERICIX and ROBINSON), P., 293. Trimethylphenonaphthacridines, s y i - thesis of, and their additive salts (SENIER and AUSTIX), T., 1240 ; P., 185. Trimethylplatinimethyl hydroxide and salts (POPE and PEACHEY), P., 86. 246-Trimethylpyridine (8-collidirw) and its mixtures with water, vaponr pressures of (LATTEY), T., 1959 ; P., 243. Trimethylsuccinic acid, hydroxy-, ethyl ester, action of phosphorus penta- chloride on (HENSTOCK and WOOLLEY), T., 1954 ; P., 235. Trimethylsulphine hydroxide, prepar- ation of (CRICHTOX), T., 1797; P., 236. aay-Trimethyltricarballylic acid, pre- paration of, and its salts and the aiihydro-acid (HENSTOCK and SPRANK- LING), T., 354 ; P., 32. Triphenetylselenonium salts and hydroxide (SMILES and HILDITCII), P., 12. Triphenylarsine, formation of (HEWITT and WINMILL), T., 964 ; P., 150. 2:46-Triphenyl yrimidine, 6-nmino- (ATKINSON, PNCHAM, and THORPE), T., 592. Tropeinea, relation between chemical constitution and physiological action in the (JOWETT and PYMAN), T., 92. Tropine niethonitrate (JOWETT and PYMAN), T., 98. U. Umbellulone. constitution of (TUTIN), T., 271 ; P., 28. Umbellulonic acid, reduction of ( TUTIN), T., 271 ; P., 28. n-Undecanedicarboxylic acid (BARROW- CLIFF and POWER), T., 568 ; P., 70. Unsaturated compounds, addition of bromine to (SUDBOROUGH and THOMAS), P., 147. Uneaturation and optical activity, relation between (HILDrrcW), P., 287. Urea, thio-. See Thiourea. Uric acid, mercuric salt (AULD), T., 1046 ; P., 152. +Uric acid (carbamidonznlonylz~rea), mercuric salt (AULD), T., 1046 ; P., 152. V. Valencies and volumes of atoms of certain organic compounds a t the melting point, relation between (LE BAS), T., 112. Valency, note on the theory of (BARLOW relation between heats of combustion Valeric acid, yy- and y8-dibromo- and yy-diiodo- (PERXIN and SIMOKSEN), T., 828. Veratralaldehyde, preparation of (PERKIN and ROBINSON), T., 1079. Violuric acid, mercuric salt (AULD), T., 1047. Viscosity and chemical constitution, relation between ( DUNSTAN, THOLE, and HUNT), T., 1728 ; P., 207. of liquid mixtures (DUNSTAN and WILSON), T., 83. of pyridine solutions (DUNSTAN, THOLE, and HUNT), T., 1728 ; P., 207. Volume, liquid, of a dissolved substance ( LUMSDEN), T., 24. Volumes of atoms of certain organic compounds a t the melting point and their valencies, relation between (LE HAS), T., 112. Volume changes which accompany transformations in the system Na,S20, : 5H,O (DAWSON and JACKSON), T., 552; P., 75. and POPE), P., 15. and (LE BAS), P., 134. W. Water, chemical action of radium emanation on (CAMERON and RAMSAY), T., 1593 ; P., 217. Weights, molecular, of amides in various solveiits (MELDRUM and TURNER), P., 165. X. Xanthoxalanil, thio- and dithio- and its isomel-ide (RUHEMANK), T., 800 ; P., 115. Xanthoxalo-B-naphthylanil and -m- xylidil, dithio- ( RUHEMANN), T., 803. Xanthoxalo-p-toluidil, mow- and di- thio- (RUHEMAKN), T., 802 ; p., 802. m-Xylene, 6-nitro-4-amino-, preparation and methylation of (MORGAN and MICKLIWHWAIT), T., 363. o-Xylem, p-nitro-, action of caustic alkalis and air on (GREEN, DAVIES, and HORSFALL), T., 2080.2132 INDEX OF SUBJECTS. Xylenes, o-, ?it-, and p - t bromination of (ATKINSON and THORPE), T., 1695. m-4-Xylenol a i d its methyl ether, condensations of, with phthalic acid and its derivatives ( BENTLEY, GARDNER, and WEIZMANN), T., 1634 ; Y., 215. m-Xylylene-as-dimethyl-4:6-diamine. See as-Dimethyl-4:6-~i~inino-,,z- xylene. in-Xylylenemetbyl-46-diamine. See Methyl-4:6-diamino-ni-xylene. ?n-XylylenetrimethyI-4:6-diamine. See Trimethyl-4:6-diiamino-?n-xylene. Y. Yeaet juice, action of, on soluble phosphates (Yoma), P., 65. 2. Zinc, electrolytic deposition and separa- tion of, from metals of the silver and copper groups (SAND), T., 373 ; P., 26. Zinc basic sulphate, formation of (PICPEHING), T., 1986 ; P., 261. Zinc, separation of cadmium as sulphide from, in presence of trichloroacetic acid (Fox), T., 964 ; P., 147.

ISSN:0368-1645    

DOI:10.1039/CT9079102103

出版商:RSC    

年代:1907

数据来源: RSC

摘要:

FORMULA INDEX OF NEW COMPOUNDS . TRANSACTIONS . 1907 . PAGE C2 Group . CgHaO .................... 1940 C ~ H ~ B ~ ~ A U .............. 2065 (I. Qroup . C4 Group . C.H. OBr .................... 54 C.H.,, B.Aa .............. 2064 (2.0. N2Ag2 ................ 183 0404NaNa, ......... .182. 183 0,HO.N.Ag ............... 183 CpH0.N3Hg ............. 1047 C.H04N.Na ....... .182. 183 C4Hl3N B . An ............ 20 65 C.O. N.HgK ............. 1047 C. Group . C5H.0 ,. ....... 827. 848. 849 C6H.02Ag.AgOH . 827. 828 C5H80. Br. ................ 829 C.H.O.1. .................. 829 C.H.O.N.Hg ............ 1046 C3H70N2ClS .............. 125 C.H.O.N. ................. 1 8 2 C4H180.N.C1. P t ......... 9 02 c. Group . C6H.N. ................... 1953 0.H.O. .............. 823. 824 C6H80 ...................... 852 C6H802 ..............832. 85: c6H806 ............. .822. 82f C.H..O. ................... 1774 C6H403N ................... 861 C6H.0.Ag..AgOH ....... 821 C.H.O.Ca.2H. 0 ......... 82: C&€.ON. ..859. 1353. 13% 06H.20. ................... 172f c6H4c13 I .................. 5 3 ( PAGE J.H.O.Ag. ................ 826 &H702hg.AgOII ........ 832 Y,H, ON ................... 852 3,H, OBr .................. 850 I,H.,O,Br, .............. 1789 J6H1103W8 ................ 827 l,H,,O,Nn. H,O ........ 1775 3,Z130,N,C1 ............. 1483 16H30.N,I ...... .1483. 1484 3,H, N GI.. 13r ............. 1 5 5 2 ?,H,ON,Na ............. 13 55 3.H,O2N,I3r, ............ 1 4 9 C,H,NCl,Br .... 1545. 1550 C,H,NClI ................. 246 C,H, N C 1 ,I ................2 4 6 C6H,N, Cave ............ 1828 C, HIoO NBP ............... 850 C6H151. SHg2 ............ 1397 C6Hl.15Q2Hg, ........... 1396 C,N,K. CaFe ............ 1827 C6H,0N,Cl13r ........... 1570 C,H30,N,Cl,13r ......... 1551 C,H,O, ............. .830. 832 C7H,N. H20 ............. 1798 C7H,,0, ...... .488. 490. 829 C,H,,O, ............ .492. 494 C7H.,0, ..................... 80 C7H.20, ...... .487. 488. 489 C7H.0,1 ............ .248. 249 C7HOOBrz ................... 55 C,H,O,N, ................ 125s C7 Oroup . C7HGO,Ag,.AgOW ....... S31 C,H,ClI’. ............ .248. 24: C7H6C131 ................... 24t C7HvCI2I ................... 24E C,H,O,’A g ................. 49: PAQE $H904N3 ................. 902 I,H,,0N3 .................. 852 >7Hl,02Br ......... .488. 489 j,H,.O,N, ................ 826 J7H.0.N,I ......1478. 1480 J7H. O.NI ............... 1484 :, H7NCI B .............. 1570 J7H.0N. Cl ............... 902 :.H..ON. Rr .............. 850 3.13.0. ..................... 112 I.H.O. ..................... 101 I.H.O. ............. .843. 854 1.H.. 0 ...................... 78 I.H120. ...... .495. 496. 833 l.H120. .................... 189 J.H.. 0 ................ .SO. 81 3.H1.0. ......... .2049. 2050 3.H1.0. ...... .82. 101. 886. 3.H.O. N .................. 101 C.H,O.Ag. AgOH ....... 844 C.H70.Ag.2AgOH ...... 844 C.H70.N. ................ 1481 C.H.. OSi .................. 218 C.H..O.N. ..... .1441. 1444 C.H..Cl. Si ................ 217 C,Hl1O,N., ..... .1440. 1441 C.H..O.N. ............... 1445 C.H.. ON .................... 79 C.Group . I. H7Br3 ..1696. 1697. 1698 3.H.O. ..................... 494 1836 C.H. 0.N .................. 195 C8H..0.Ag. ............... 189 C.H..ON. ................ 1447 C.H..O. N ................ 1437 C.H.2O.N. ............... 14382134 PAGE C.H..O. N , ............... 1446 C8Hl,0,Br ................. 495 C,H,,0,N3 ........ .492. 1439 C8HI40,N, ............... 1438 C8Hl,0N .................... 81 0, H1602N, ............... 205 1 C8Hz10N,4H,0 ......... 1794 C8H,,0N. 6H,O., ....... 1795 C8H50Cl, I ................ 245 C8H,OC1, 1 ................ 245 C8H6OClI .......... .244. 245 C,H60C1, I ................ 245 C8H, ,02N3K ...... .863. 863 C8Hl0O,NK .............. 1438 C,Hlo04NK .............. 1442 C8H1004N K. H, 0 ....... 1442 C8Hl,0,N2K ............. 1446 C,H,,O,NCl .............1443 C,H,ONCI,Rr .. .1551. 1552 C&,404??2 ............... 1442 C8H7ONCII ............... 246 C8H70NCI3I .............. 247 C, Group . C,H604 ..................... 11 0 C,H,,O, .................... 548 CgHIZO ........... 1875. 1876 C,H,,O5 .................... 357 C,H,, O ................... 1745 C9H140, .................... 487 C,Hl,O, .................. 1741 C,H1406 ...... .356. 357. 359 C0Hl4N, ................... 364 COH,, N ................... 1876 C9H805 .............. 103. 110 C,H&, .................... 273 C&&4 .................. 1837 CoH70,N ........... .104. 110 C,H805N ,. ............... 1259 C,H,,ON .................. 5 50 CgH,,06Ag, ..356. 357. 359 C,H,, C 1, Si ................ 7 2 1 CgH,,O,Br ................ 849 C9H150 Br ................17 4 6 CoHl,06N,.H, 0 .......... 189 CoHi, NBr .................. 54 CoH,,ON, ................... 79 CgH170N3 ................... 81 COH1703Ag ................ 273 C,HlB04N, .................. 98 FORMULA INDEX . PAGE C.H.O.NC1. .............. 968 C9H90.N. C1 .............. 974 C.H. 0.N.S ............... 127 C.HloON. S ............... 132 C.H..O,N.Cl.. ............ 271 C.H. ONClEr ........... 1570 C.H..O.N.S ............... 143 C.H..ON. CIS ..... .128. 924 C.H..ON. C IS ............. 143 Cl0 Group . C1.H.. ..................... a499 C.oH7N. ........ ..1916. 1950 C..H. 0. .................. 1084 CloH804 .................... 251 C.oH.0. .................... 109 C1.H.oO. ................... 102 C.oH1.O. .... .497. 550. 844. 994 C..H.. 0 ..................1873 C..H..O. ................. 1874 C.oH.40. ................... 823 C..H..O. ................... 360 C1.H.. O. ................. 1743 C.OH1.O. ................... 359 C..H..N. ................... 365 883. 2049 C. 0H.80 ..... .498. 508. 882. C.oH..CI. .................. 500 C1.H.. Br. .................. 500 C..H, 0 6 ........... .294. 295 Cl0H..O. ...... .74. 501. 502 C10H.002. H. 0 ............ 373 C..H,N. .................. 276 1949. 1950. 1951. 1952 C.0H.O.N. ..... .1947. 1948. C.oH7O.N ................ 1085 C10H7O4Br ................ 253 C..HvO. N ................. 254 C.0H.O.N. ............... 1364 CloH80. N. ................ 183 C.oH9O.N ................ 1085 CIoH. oO.Ra. ............... 252 C..H..O.Ag .............. 1874 Cl0Hl5ON. ...............1876 C..H..O.N ............... 1443 C10H1603h' ............... 853 CloHl. 04Br ............... 821 C1.H. 3 0 . Ag. .............. 360 CloHiGON4 ................ 874 PAGE ~lo~160,s ................. 523 C.oH.yON3 ............... 1746 CloH., 05N ............... 1741 CloH180N, ............. .4. 16 C..H,N. C 1. ............... 277 C..H..O.N. C 1 ............. 902 C..H.. 0 N.. 4H. 0 ........... 4 C..H..O. N.Hg ......... -10 47 C..H..O.N.CI. ............ 903 ClOH..O.N.S .............. 915 ClOHl4O.N4S .............. 143 C..H..O.SN~. H. 0 ...... 523 C..H?O.NCI. Br ........ 1553 C..H.ON.ClBr ......... 1568 C..H..ON. C 1s ............ 143 C.. H 4. ................... 108 C..H..ON. CIS ..... 136. 137 C.. Group . C..HloO. ................... 107 C..H..O. ..1081. 1228.1232 C..H..O. ................... 103 C..H..N ,..1702. 1706. 1710 CllH1604 ................... 831 C..H..O. ................... 190 C11H1.N. ................... 367 C..H,O. ............ .293. 297 C..W70.Ag. H. 0 ......... 109 C..H..O.N. ..... .1009. 1904 C..H..O.N ............... 1081 C..H..02N. ..981. 982. 1920 C..H..N.CI. .... 1702. 1707. 1710 CllH1504N ................ 969 C..H.60.N. . .982. 985. 987. C1.H. 7ON.3 ....... .367. 1874 C..H.70,N. ................. 18 C1.Hl7O.Br ................ 830 C.1H.vO.N ................. 989 C..H..ON. .................. 17 C.. HISOSi ................. 220 C..H.sON. .................. 20 C..H.oO.N. ........ .870. 871 CllH.O.N, I< ............ 1009 C1.H.ION. CI ............. 903 C..H..O.N.S .............. 919 C..H..ONS ..............1886 1921 C..H..N.CI.Pt . .1702.1703. 170?. 1710FORMULA INDEX . PAGE PAQE 2135 C.H. O.NBr ............ 1310 C14H..0N. S ............. 1316 Cl.H140.N4S .............. 142 1709 C..H..O.N.ClS ........... 920 CI4Hl40N.C1S ............ 142 C..HI7O2N.CI.Au ........ 902 C15 aroup . CI5H..0. ..1631. 1633. 1636 PAGE Cl4H1.O.N.S .............. 920 CI4Hl80.N.C1. . .1701.1705. C15H1.O. ......... .1638. 1639 C1.H.20. ......... .1912. 1913 C1.H.20. .. 1635. 1636. 1637 C15H..0 ,. ........ .1638. 1639 C15H1206 .................. 895 Ul5Hl6O2 ................. 1390 C..H.O.N ................ 1632 3..Hl.0.N ........ ..104. 111 &HI 302N ................ 593 J15H..0.N ......... .195. 268 J..H..O.N ......... .104. 111 1710 C1.HNO. ................... 188 C)15Hl10N .................592 31.HI.O.N. .............. 1263 Z1.H.. O.Np .... 1703. 1707. 3l.H.70. N. ............... 368 Jl.H.70.N ....... 1905. 1906 C). H17C1Si ................ 218 &jH1g02?? .................. 82 Sl.H,O. N. .................. 8 3..H1.08N.S .............. 129 3.5H140N. S .............. 9% 3.. H1402N2S ...... .921. 922 ?15H1604N4S ....... 144. 363 I..H..I. SHg ............ 1398 j15H. .O.N.CI ............. 368 924 1.. H1502N2C1S ... .921. 922 c16 Group . ..5H150N.C1S .... 138. 139. .16H120. ................. 1087 ... Hl.O ,..lo%. 1631.1633. 1637 !16H1201., 1634.1640.1908. 1912. 2070 C..H..ONS. ............. 1881 Ol1Hl6O5N Br., .......... 192. C..H..ONS. ............. 1881 C..H.TO.N.Cl ............. 981 01. H..ON.S ............. 188t O1.H..ON. C'l ................! C..H..ON..C:l ............... 2. C.. Group . Cl.H.O ,. .................. 10. C12H..0. ................. 180f C.H. 0. ................. 164( C.H.O. ................. 161( C1.H. 0. ................. 174: C12H. .Si ................... 221 C12H,0. .................... 74 C..H.N.R . ,. ............. 113s C..H..O.S ................ 112C 012H1803 ................. 1744 C1.H. 0 0 . .................. 18E C1.H.oO.N. .............. 1362 C..H..O.N. ............... 107 C.H.O. N ................ 107 C.H.O.N. ..... .590. 1702. 1706. 1709 CI.H..O. N. ............... 990 Cl.Hl.O.N. ................. 14 C.H.O. Br ............ 1745 C.H. C1Si ................ 723 Cl.H, OSi ................. 727 C..H.,,O.N. ............ .6. 18 C..H..O.Br .............. 1742 C..H.ONEr. ..............151 C..H.ONBr. .............. 152 C1.H.ONBr. .............. 151 CI.2H,0,2CIl,Ce,, 3H.O .. 477 C..H70.N. Br. .......... 1262 C.. Hg0..S3K. ........... 1307 Cl.HloO.S.Na..H. 0 ... 1306 Cl2HI60.N. K .............. 15 CI2HlgONS. ............. 1883 C..H..O. N S ............. 1888 C.2H608Br.S.K. ........ 1308 C..H..o.B1.2 ............... 854 C.H.O.N. . .984. 991. 993 C..H. 0 N R1.6. ............. 1 53 Cl.H.01.S. Ba. .. 1305. 1307 C1:< Group . C.. Hl2O4 ................. 180! C13H1803 ........ .2056. 205: C..H..O..~H.O .. 1228. 1231 C..H, 0. ................ 17 4 I C..H.O.N. ..862. 865. 1354. 1358. 1359 C..H.O7N. ............... 1265 C13H.0.N4 ............... 14 79 C..H90.N. ............... 1263 C..H.O.N. ............... 1261 C.3H1.O.N. ..585. 586.587 1007. 1008 C.H.O.N. H20 ....... 1903 C..H1804Br. ............... 842 J.H,NI ................. 1825 J..Hg0.N2Hr. ............ 867 J..H..O.N. S ............ 13 5 5 31.H12OsNAg ........... 1903 C)..H..O.N.CI. .......... 1008 JI3H..O.N.I. H. 0 ....... 992 3.. HloN2ClIS ........... 246 CI4 Group . C.H, Si ................... 73( C.H.O.N. .. 86 1.1354. I 358 31.H1.O.N.S ............ 1008 3. H.6 ............. 1107. 1109 2.4Hl.O. ................. 1792 I.H, 0. ................. 1368 JI4H,O. ................. 1743 3..Hg0.N .......... .102. 112 ~..H1.O8N4 .............. 1479 >l.H1OO.N @ . ............ 1316 3..H..O.N . 267. 1425.1426. 1427. 1429 H1. O.N. .............. 1482 ~l.H.lO.N ......... .101. 198 314HloOZBr4 ............. 1311 f14HI.iOSN5 ............... 902 I14H..CISi ................ 218 !14H.60.N. .... .1699. 170'1. 1703. 1704. 1705. 1707. 1709 i4H1802Np ............... 270 '..H1808Br. ..... 1784. 1787 14H.104N ................. 968 i14H2504Br .............. 1742 ~..H.O1.S. N a4 .......... 13072136 FORMULA INDEX . PAaE CI6H1,9, . .541. 16.3 1. 1633. 1637 Cl6Hl,O .................. 1090 Cl6HI4O5 ................. 1639 C16H.,06 ........... .891. 892 CI6Hl4N 2. .................. 588 CI6H.,O,. . ..540. 759. 1090 C., HI6O6 ......... 1803. 1811 C16Hl6Hrp .......... 7 50. 757 C16H., O, .... 510. 750. 751. 1 a90 C1,Hl,O, ................... 539 C16H,0, ................... 70 C]GH26 0, .................... 'I 6 C.,H,,O, ................. 1934 C.,H, O7 ................. 1740 C16H. o02 .......... 7 1. 72. 7 7 C., HgOgN............... 1633 C16H,06 ............. 5 7 7. 5 7 8 C16H804N. ............... 2083 C16H1102K ............... 1087 C.,jH..O,Br .............. 1632 C16H..0,?!f, .............. 1310 C.,H..O.N ............... 1632 C1,HI2O, N2 ............... 28 1 C..H.,O.N, ............... 109 c16Hlz~8N2 .............. 2082 Cl6H1.ON ....... .1303. 130 1 Cl6H.&, N ........ 267. 1632 C16Hl,0,N. .............. 1340 C.6H.$,Cl ............... 1094 Cl6H1,O, Br .............. 1631 c16H1404N2 ............... 'L 8 4 C.6H.. 0 6 Br3 ............. 1803 C.6H.,N&l .............. 1304 C.EH.~O~BI; ............... 759 c.6H.60.N~ .............. 2080 C.6H.40,N. ................ 183 C16H14058 ............... 1120 C.,H160,S. ............... 1309 C.,H.6O,jN2 .............. 208 1 C.6H.@gN, ...............365 &.902N5 ............... 369 C.GH.,O,N, .............. 1892 C.,H19O,N3 .............. 18 92 C16H1g06N ................ 256 C..HmO, N2 ............... 270 Cl6HaOIQBr ............. 1784 Cli Group . C17H12O3 ................. 1085 C.7H.. 0. ................. 1097 CITH.. 0; ................. 1095 C.&..O. .......... 1091. 1635 C17Hl.0 ,. ........ .163f. 1913 C.7H.. 0. ................. 2068 C.7H.60. ................. 1092 C17H1604 ................ 1635 ol7Hl605 ................ 1634 C17H1606!H20 ............ 895 C17H1606 .................. 895 PAGE C.7H.pN ..1930. 1931. 1333 C17H1803 .................. 1092 C17Hl, Od .................. 543 C17H,, 0 2 ........... .701. 702 Cl7H,.O, ................... 543 CliH,N, ................. 1932 C.?H,,O.................... 573 C.7H1.O.N.3 ..... .1260. 1261 C.VH1,O.N. ..... .1319. 1311 C.7H.,O,N, .............. 1318 C.7H.,O,N, ..... .1'178. 1480 C,iH.,ON, ............... 1904 C.7Hl,0, N3 ............. 1321 C.?H,, 02N2 ............. 1908 C,7Hl,O,N4 ............. 1341 C.~HI,O,N ....... 141 3. 1414 C17H210,N3 ................. 24 C.7€€,.O2N.. 1 3 2 0 .......... 24 Cl7H,.N, S ............... 1890 C17HB0,N, ........... .8. 703 C17H,06N2 ................. 98 CI7H,.O, N ................ 573 C17H.ZON301 ............ 1317 C17Hl, ON3Br ........... 1318 Cl7HI3O6N3Q ............ 1318 C.,H,ON, R ............. 1889 C17H,, ON,Ci Br ......... 1571 C.7H8.ON.ClS ............ 923 C.7H.,O4N ................ 268 C.7H.GO,N, ............... 970 C.7H,oOXy, ............... 366 C..H210,N................ 3 i 0 C17H2, ON, ................... 7 C ~ ~ H ~ ~ N C I ~ A U .. 1930. 1933 C.7H,O,N, S ............. 367 C.7H1QON, C IS ............ 138 C17~260N2016Pt ....... 1932 ClS Qroup . Cl8€Il0O4 ... .421. 422. 1593 C..H.. 0. ........... .421. 424 Cl8Hl4O3 ................. 1088 C..H.. O. ........ .1094. 1102 C. H..O. ................. 1095 C..H1605. 2H20 ......... 1098 ClRH1805 ................. 1097 C..H..N. ........ .1297. 1298 Cl8HIoG. ... .418. 424. 1593 C.8Hl.O. ................. 1912FORMULA INDEX . PAOF: O18Haa04 ................ -1096 CIsHmBr2 .......... .752. 753 2137 PAGE l,Hl,ON,S. ............ 1319 &&iOa- ........... .751. 752 Cls&Ola ................ 1 7 7 6 C18&X4 ................... 3 7 0 ClBHe4Si ...................2 2 2 C18HalL04 ................... 56 7 ClSH,O, .. I ......... 575. 576 C18H,0 B. .................. 5 6 9 Q,H, O, ........... .565. 566 (&,Ha 04Ag2 ............... 887 C, H807N2 ................ 4 19 C18H90, C1 ................ 4 1 8 C1BHuOaN ................ 4 15 e18Hl103N ....... .417. 1591 C18Hl104N ................ 4 2 4 C18Hl10,Br ................ 424 C18Hl10,N ...... .1590. . 1591 C18Hl,0N4 ............... 1320 C18Hl,04N .. 416. 1590. 1591 ClsHBOsN ,. ............. 1340 Cl8Hl4o2N2 .. .333. 335. 336 C18E1403Br, ............. 1088 ClsHl6Q2N ............... 1303 48H1806N ................ 42 3 C18H1404N. ..... .1339. 1365 C18H1604N ............... 1635 C I ~ H , ~ O ~ K ............... 1 O9t C2SH,BON, ............... 129: ClsH,,O2N4 ..... .1298. 129E ClsH,,O4Nd ..., .......... 136! Cl,H,,04Cl ............... 1 O 9; ClSH1gO4N .................. 9f C18HmO3Np ............. 192f ClsH,N2C12 ..... 1297. 12% Cl8&102N ................ io: ClsH,O,N ............... 14 1 i Cl$,1O.CI. 21320 ........ 5.1: cl8H2.O.N .................. 9< Cl8H&,N, ................. 2. C1&&04N2 ............... 27( C18HBO8N. ................. 9; C18Hmo12Ca3. H.0 ....... 35( c,,H,ON. .................. 21 C18H,O&, ............... 8 71 Cl8& 02N3 ......... .22. 70; C18&04N5 ............... 87; C18HBO.N ,. ................ 7 ‘18H..0.N.S.211.0 .... 1510 !.8Hl.0.N.S ............ 16 08 ‘..H..O.N.S. ........... 1509 .l.H.60.N. S ............ 1508 I..H..ON.CI. ........... 1293 ... H170.N S ............. 1 5 16 .18H.00.N Cl ............... 9 6 71.H200.NI ................. 96 >18H.00. N I. H.O. ......... 96 4. IT..O.NS. ............ 1884 ... H, 03NI ............. 1414 ’18H..0. NC1 ............. 416 I..H..O.N.CI ..... .33S. 335 >..H,O.NBP ............... 96 :..H,O.NCI ............... 94 ..SH,O.NRr.H.O ........ 94 >..H,O. N I ................ 95 2..H..O. NB ................ 9 ’I ... H,O.CI.Pt ............ 550 :.8H.12N.CI.Pt .......... 1877 ~..H..O.N. C1S ......... 1509 218H140.NjKr8 ......... 150s 2..H..O.NCl. An .......... 97 2..H, 0 jNCI. Au .......... 9i CIg Group . :‘lgHl.O. ............ .423. 42! Cl9Hl2O6 ................. 1591 C..H..O. .......... .421. 109; ClgH..;1\7 ..1035. 1336. 1937 1931 ClgH1604 ................. 109. C19H..0. ................. 11 Of C..H..O. .................1 lo: Cl.H.oN. ................. 139. C..H,O. ................. 1101 C.gH.60. ................. 11 0: C19H1805 ................. 109: C..H,N. ................. 193. ClgH..O. ................... 56 C..H,01..2H. 0 .1228. 122’ ClgH3.0. ................... 5’1 Cl.H360 ,. ................. - 5 6 C..H120.N ,. ............. 13 11 ClgHl2NBr., ............. 166 C..H12NBrg ..... .1663. 166 C.,H..O, S ............. 112 PAGE !19H1503N5 .............. 1263 !19H1606S ................ 1121 jl9Hl6O6S, H, 0 ......... 1121 &9H1,0N3 ............... 1907 ?1gH1705K ............... 1099 :,, H1802N2 .............. 1906 .,gHl,02N ,. ............... 365 319H190N3 ............... 1299 >,,H,,O, CY .............. 1102 31,H1g0, C1 .............. 1099 >lgH,oO,N, ............... 970 21gH,N,CI, .............1299 21,H,010N, ............. 1363 I,, HmNSi ................. 725 &H,,O,N,CI, .......... 1319 I19H1604N, S ............ 1508 IlgHSO, Np ................ 23 21gH1706N3S2 ........... 1510 21,H,oON, C1 ............ 1299 2,,Hu0, NI .............. 1415 C19H2405NHr .............. 95 ClgH,N,C16Pt. T-I, 0 ... 1935 JlgH,O, N Br ............... 97 01gH1602N, CIS ......... 1510 C,CJH@~N~I<~S ......... 1510 .. Group . CmH3. ...................... 905 C,H2. ...................... 760 C..H..O. ................. 1585 C,H..O. ........... .422. 425 C20H16O6 ................. 1592 C2.Hi.N ......... .124‘2. 1244 C.oH.80. ................. 1096 C.oH.00. ........ .1101. 1102 C..H,O. ................... 539 C..H,N. ................. 1300 C..H,BI.. .................760 C,H,O.. ................ 1145 C.oH.70. ................. 1504 C2.H3.0. .............. .73. 77 C,H3. O .................... 575 C20H806Br.p ............. 1586 CmHlo08N2 ............... 420 C20Hl10. Cl ................ 418 O18Br6 ............ 15052138 FORMULA INDEX . PAGE CmH1.O. N* ............... 805 CmH1.0.N. ......... .... 332 C,H.. N I .................. 4 5 C,H..ON. ....... .366. 1301 C,H..O.N. ............... 271 C,HaN.CI. ............. 1300 C,H,ON. .................. 23 C,H2.O..C3.. 813.0 ..... 360 C&&.O. N. ............... 872 C,H,O..N ..... 1011. 1012 C,Hl10N2C1 ............ 1484 C,H..O.N.S .............. 802 C,H.. NC1 I .............. 1662 CmH.7NCl.Hg .......... 1242 C,H190.N. Cl ............. 3 . C,H,O.N. S ............ 1514 C,H3.07NS ..............524 C,H3.0.1. Z ............... 900 CmH..0X.C1S ............ 141 CmH,O.N.C1. P ............. 5 C21H.. 0. ................. 1586 C.. H,O. ................. 1099 C..H..O. ................... 570 C,H..O.S. ................ 525 C..H370. Br ............... 574 C, H1203N2S2 ............ 801 C,H..NCl. Au ..1242. 1245 C,H..O.S~ZII ..... .523. 524 C,H3. 021.CJ ............. 900 Czl Group . C..H1.0.Br. ............. 1586 C2.H..0.N ...... .1428. 1429 C..H1702N ............... 1621 C,H,O.Br. ............. 1099 C..H,O.N. ............... 9 88 C,H, O7N. ............... 988 Cz1H..0.N ...... .1976. 1980 C,H..O.N.S ................. C. H..O. N 8 ............. 1621 C..H,O.N. ................. C..H,O.N. S ............ 1887 C,,H,O.N .............1340 C2.H.80. NSC1 .......... 1663 C2lH1.0. NS Br .......... 1665 C..H..O.N.CI. P .......... 903 CflH3.03NBrS ............ 459 C, Group . CBH1. O. ................... 422 PAOE C.H.60. ................. 1636 C,H..O. ................. 1639 C,H..O ,. ................ 1587 C,H..O. ................. 1638 CBH.7N. ................... 5 92 C.2Hl.N. ................. 1290 CBH.00, ................. 1098 CnHBO11 ................ 1812 C,H290 ,. ........ .1504. 1505 CBHI.O.Ba. 2H.O ....... 108 C..H..O.N. .............. 13 44 C,H.7O.N. .............. 1291 CBH.70. N ................ 195 CBH1207Br4 ............. 1587 Cz2Hl.O.N. .............. 1345 C..H.. 0.N. ............. 1340 C,H..O.N ............... 1625 C,H..N.Cl .............. 1290 C,H,07Br .............. 109 9 c2aH2.O.N............... 1897 C,H,O.. N ............... 676 C,H..O.N. .................. 3 C,H..O.N . S,. ............ 802 C,H..O.N.S .............. 803 C..H.. 02N5C1 .......... 1291 CBH1.O.N. S .... 1515. 1518 CBH.10. NS ............. 1624 C,H..O1.Nl.C'n ............ 21 C,H4.0.NSSi ............ 734 C,H..O.TMg ............. 904 C23 Group . CsH..O. ................. 1088 C,H..O.N. ............. 1342 C,H..O.N ,. ............. 1342 C,H..07N. .............. 1930 CBH,O.N. ............... 2 68 C..H, ON ................. 7 00 CsH..O.. .................. 896 CsH..OBN. .............. 1348 C,H,,ON,S., ............. 924 C,H,O. NBrS .......... 1823 C,H..ON. CIS ............ "23 C,H,O.NSSi ..... .732. 736 C%H..O. ................. 1587 C2rH..03 ................. 1638 C,HBO.. ..................894 CNHBN 4. ................ 1301 CN Group . PAOE 024H&, ................... 571 CaH.. 0.N. ............... 420 CuH1503N ................ 419 C,H..ON. ............... 1317 C..H..O.N. .............. 1296 C24H..ON. ...... .1291. 1296 CsH..O.N.. ............. 1302 CNHB0.N. ................ 284 C24HN04Np ............. 1364 CaH26ON2 ................ 701 C,H.. O.N. .................. 7 CaH3.0. N. ............... 278 CNH.. 0.N. ...... .... 6 CaH3.OSi. ................ 223 C..H..O.N.S. ............. 804 C,H.oO.N.CI ........... 1296 CaH,02N. S .... 15 1 7. 1 51 8 C%H,O.N.CI ........... 1302 C2hHaO.N. S ............ 1516 CNHaO.T.S. Cd .......... 901 CNH..O.C1. S2Au ........ 901 C,H..O.N.CI.Pt ......... 902 C.H. 0. ................. 1588 C,H180. .................1586 C..H,O.. .................. 896 C,H..O.N ,. ............. 1343 C2.H..0N. ............... 1293 C..H..O.N ............... 1623 C..H..O.N.CI ........... 1662 C25H1507NjB ............. 1664 C2jH3002N2 ............... 278 C23 Group . C..H..O. ................. 1090 Ca6 Group . C..H. ,. ............ 1107. 1111 C.. H1.O. ................. 1588 C..H..O. ................. 1592 C..H..O. ................. 1585 C2.H2.N. ................. 1291 C..H..O. S ............... 1120 C..H..ON. ...... .1289. 1294 C,H,07N. ...... .1243. 1245 C,H,O.Br. ............... 253 C,H..O.N.Hr. .......... 1141 C..H..O.N.S .............. 364 C2.H2. 0.N I .............. 1625 CZ7H,N. ........... .703. 704 C., Group .PAGE (&Ha014 .................. 438 Q&O ..................1915 CdHMO, .................. 571 CmHmOfi, ............. 1239 C&E€mO&, ............ -13 22 C&B&OgN& ............. 1623 C ~ H ~ O ~ B ~ .............. 253 C&,H&$iSHg .......... 1048 C, Qroup . W l 9 N ... 1235. 1236. 1237 CSHMO ,. .................. 707 hH,ON ................ 1238 %H,O ,N ................ 4 1 9 C,EIIgO, N ................ 199 w o $ p ............. 1294 C A O S N k ............. 1349 Q&O*N ............... 1979 GH&N& ............. 804 OaeH,NC&Au .. 1235. 1236. 1237 o,&OsrS&l ............ 15 1 1 C,H, ON C1,Au ........ 1 2 3 8 C, Qroap . C&OSN, ............. 1 3 4 3 CW%O6N ,. ............. 1346 OpeHasO,N, ..... .1345. 1350 Cs&Os ........ .1387. 1391 C,HsOsN ,. ............. 1 3 4 4 -OsNsS ............15 1 1 OmHMO, .............. .72. 7 7 O,H~O, ............... 53 9 CaHNONa ................ 704 C, Qroap . C m h O .......... 1387. 1392 O~H~OsN1~CO ........... 902 C,&OaN6S.$e ......... 9 O 1 OmH, 06N6L$d ......... 901 C, Qroup . t&HuO14N,Brs ......... 1665 C, Group . Cm&N6., ............... 1295 CaHaOa ................ 1146 C)slHcnN&l~ ............. 1295 QmH&mKs ............. 1 1 4 5 C, Qroap . UsHmO, N% ........... 1 14 5 0% Hm07N , .............. 1237 CMH,02N6 .............. 1323 CaGONS ............... 1295 XCI . FORMULA INDEX . PAGE 2.H.1O1.N ................ 675 >.Ha 0N.Cl ............ 1294 23. H.6N.Cl.Pt .......... 1930 2..H,O.. N2S .............. 98 &.H,02N.Cl.Pt ....... 1318 ....... .1228. 1230 C. Group . CI,H,O.N ...............1624 C3,H.&,N4. ............. 1346 ZsH, 0.N. .............. 1347 CSHBO5N2 ..... .1432. 1433 C35H4106N5 ............... 347 C~H44010N.P ............. 350 C35H,010N5P.H20 ..... 349. C35H4206N5C1 ............ 3 5 0 350 c36 Group . C36H,014N4. €3.0. ......... 96 C,H..O..S.Ce.. 23H.O .. 477 C36H,0O.&ce2,12H20.476 C.6H3oO~S.Ce.. I7H2O . 476 C..H4o0~N.Br2. H.0 ...... 96 CsH. .O..N.CO ........... 901 C36H.7O.N.CO ............ 900 C.6H,O.N.C&Pt .......... 97 C.6H.60.sN.S6Ce 2 16HJO 477 C~~H.OO~N.C~.P~. H.0 ... 97 C.6H4.010N2C16Pt. 2H2O 95 C. Group . C37HeO .ON. ............... 3 5 1 CsHM0.N. .............. 1980 C38 Group . C,H,04.H20 ........... 1917 C,HmN2C18Pt .......... 1661 C,H~O.N.Cl.Cr ....... 1662 1665 C,H,o7N2Br6Cr2 ... .1664. C~H.oOloC16S.Pt. ...... 1121 C,H,02N.Cl.Pt ....... I938 C38H3.0N2C16Pt . 1936. 1937 C,H,07N2C12Br.Cr. .. 1663 C, Group . C39Hg404 ................. 19 1 8 C,H%OJ?8 ............. 1240 C40 Group . C..H2,5. ........... 11 08. 1112 C..H,O.. Np .... 1236. 1237 C.oHmO1.N. ............. 1238 2139 PAGE z4,-,H,N&ir6 ............. 1243 C4H,N2CI6Pt. 2H20 . . 1242 C41HBO11 ................ 1777 CaH&!&&Pt .......... 1245 Cq, Group . C42 Group . C4 Group . S42H,011N2Cr2 ......... 1622 C44H4008NaCr .......... 1625 C,,H,07N, S2Si2 ......... 229 C,H, O13S2Cr2 ........... 527 C,H, 06C16S4Pt ......... 527 C,HUOl5N2Cr2 ......... 1623 C,H,o02N4Cl, Fe ........ 903 C52HssOl, S2Cr2 ........... 528 C,H6, 06C16S2Pt ......... 527 C5,H,, 04N4C14Au ...... 1239 C,HJ40,N, C1,P t ....... 1239 C,H,007N2S2Si2. 4H,o . 229 Ca Group . C, Group . C52 Group . C54 Group . c56 Group . C,H40N&16Pt ..1236. 1237 C36H4~N2C&Pt. 2H2O 1235, 1236 C,6H40N2C16Pt, 3H2O . . 1235 1238 1238 Cm Group . CmH,0,S6Ce2, 20H20 .. 476 C,H4oO,N,Cl,Pt, 2H2O C,6H,02N2Cl&%, 3H2O CGOH,0,S6Ce2,20H20 .. 477 (&H,O18N6S6Ce2. 32H2O 477 C60H5205C16S5P t ......... 901 C7,,H5,O1, N2Cr2 ......... 1624 c72H&$?, 0 ............. 351 C~H&8N4C&Pt ....... 1623 CmH7808N4C16Pt. ...... 1625 Cl~H&16N4C16Pt ..... 1624 C70 Group . C72 Group . Csa Group . Cse Group . CIM) Group . 7 C

ISSN:0368-1645    

DOI:10.1039/CT9079102133

出版商:RSC    

年代:1907

数据来源: RSC