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1. |
THE SYNTHESES OF SUGARS FROM SMALLER FRAGMENTS: PART X. SYNTHESIS OFL-GLUCOHEPTULOSE |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 95-97
J. K. N. Jones,
R. B. Kelly,
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摘要:
L-Glucoheptulose has been prepared by the action of muscle aldolase on a mixture ofL-erythrose and hexose diphosphate.
ISSN:0008-4042
DOI:10.1139/v56-010
出版商:NRC Research Press
年代:1956
数据来源: NRC
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2. |
ORGANIC DEUTERIUM COMPOUNDS: XIV. PREPARATION OF DEUTERATED METHYL BENZENES |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 98-102
R. Renaud,
L. C. Leitch,
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摘要:
The synthesis of toluene-α-d3,o-chlorotoluene-α-d3, andm-xylene-α,α′-d6from benzotrichloride,o-chlorobenzotrichloride, and α,α′ hexachloro-m-xylene respectively is reported using zinc and acetic acid-das the dechlorinating agent. The preparation of acetic acid-dof optimum isotopic purity is described.
ISSN:0008-4042
DOI:10.1139/v56-011
出版商:NRC Research Press
年代:1956
数据来源: NRC
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3. |
THE REACTIONS OF TRIFLUOROMETHYL RADICALS WITH PROPANE,n-BUTANE, AND ISOBUTANE |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 103-107
P. B. Ayscough,
E. W. R. Steacie,
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摘要:
A study of the reactions of trifluoromethyl radicals, produced by the photolysis of hexafluoroacetone, with propane,n-butane, and isobutane has been made. The rate constants of the hydrogen-abstraction reactions have been determined at temperatures between 27 °C and 119 °C and the activation energies found to be 6.5 ± 0.5, 5.1 ± 0.3, and 4.7 ± 0.3 kcal./mole respectively. These values are compared with those obtained for the reactions with methane and ethane, and with the corresponding reactions of methyl radicals.
ISSN:0008-4042
DOI:10.1139/v56-012
出版商:NRC Research Press
年代:1956
数据来源: NRC
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4. |
THE POLYMERIZATION OF STYRENE IN THE PRESENCE OF α- AND β-BROMOSTYRENE |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 108-112
M. H. Jones,
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摘要:
A study of the polymerization of styrene in the presence of either α- or β-bromostyrene at 45 °C and 70 °C has shown that copolymerization does not occur. From the variation of molecular weight and rate of polymerization with bromostyrene concentration it is concluded that the bromostyrenes behave essentially as efficient transfer agents.
ISSN:0008-4042
DOI:10.1139/v56-013
出版商:NRC Research Press
年代:1956
数据来源: NRC
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5. |
THE PHOTOLYSIS OF KETENE IN THE PRESENCE OF HYDROGEN |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 113-122
H. Gesser,
E. W. R. Steacie,
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摘要:
The photolysis of ketene in the presence of hydrogen has been investigated in the temperature range −40° to 207 °C. The main products are CO, C2H4, C2H6, and CH4, with some methyl ethyl ketone at the higher temperatures. Hydrogen and ketene compete for CH2radicals by the reactionswithE3 − E2 = 0.8 kcal. At the higher temperatures the reactionleads to a chain reaction viaThe value ofE6is found to be 10.2 ± 0.5 kcal. in good agreement with previous work.
ISSN:0008-4042
DOI:10.1139/v56-014
出版商:NRC Research Press
年代:1956
数据来源: NRC
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6. |
AN OXYGEN-18 STUDY OF ACETAL FORMATION AND HYDROLYSIS |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 123-127
Fred Stasiuk,
W. A. Sheppard,
A. N. Bourns,
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摘要:
A tracer study has been made of acetal formation and hydrolysis. Benzaldehyde andn-butyraldehyde, enriched in O18, on reaction withn-butyl and allyl alcohols, gave acetals of normal isotopic abundance. The label appeared in the water of condensation. Hydrolysis of benzaldehyde di-n-butyl acetal andn-butyraldehyde di-n-butyl acetal in O18enriched water gave alcohols of normal isotopic content. A slight enrichment due to isotopic exchange was found in allyl alcohol produced by the hydrolysis of benzaldehyde diallyl acetal. These results establish that the reversible reaction proceeds by a fission of the aldehyde-carbon to oxygen bond.
ISSN:0008-4042
DOI:10.1139/v56-015
出版商:NRC Research Press
年代:1956
数据来源: NRC
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7. |
DEPOLARIZATION BY MERCAPTOACETIC ACID DURING ELECTRODEPOSITION OF COPPER |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 128-132
A. J. Sukava,
C. A. Winkler,
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摘要:
Mercaptoacetic acid (MAA) in acid copper sulphate electrolyte decreased the cathode polarization throughout the course of electrolysis at all concentrations up to 20 mgm./liter. Addition of small amounts of chloride caused further depolarization. When present together with cystine, MAA showed an independence of action. The depolarization caused by MAA was ascribed to a decreased activation overpotential due to substitution of a more readily dischargeable MAA–copper complex for the aquo–copper complex. The additional depolarization due to chloride was ascribed to formation of a still more readily dischargeable chloro–MAA–copper complex. The depolarization in both cases increased with time during prolonged electrolysis, apparently due to surface roughening with, presumably, a consequent increase in surface area and decrease in true current density.
ISSN:0008-4042
DOI:10.1139/v56-016
出版商:NRC Research Press
年代:1956
数据来源: NRC
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8. |
THE CRYSTAL STRUCTURES OF SOME INTERMETALLIC COMPOUNDS OF PLUTONIUM |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 133-145
O. J. C. Runnalls,
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摘要:
The crystal structures of the following binary intermetallic compounds of plutonium are reported: PuAl2, PuAl3, PuAl4, PuBe13, PuCo2, PuFe2, PuMn2, PuNi2, PuNi5, and Pu2Ni17. In addition, the unit cell dimensions are reported for PuAg3.
ISSN:0008-4042
DOI:10.1139/v56-017
出版商:NRC Research Press
年代:1956
数据来源: NRC
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9. |
THEORY OF THE TRANSIENT PHASE IN KINETICS, WITH SPECIAL REFERENCE TO ENZYME SYSTEMS: II. THE CASE OF TWO ENZYME–SUBSTRATE COMPLEXES |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 146-150
Ludovic Ouellet,
Keith J. Laidler,
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摘要:
A theoretical treatment is worked out for the kinetic schemein which two enzyme–substrate complexes are formed consecutively. The steady-state rate equations are obtained, and equations are given for the transient phase subject to the condition that the substrate concentration is greatly in excess of that of the enzyme. Some kinetic consequences of the resulting equations are discussed.
ISSN:0008-4042
DOI:10.1139/v56-018
出版商:NRC Research Press
年代:1956
数据来源: NRC
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10. |
VAPOR PRESSURES OF AQUEOUS SOLUTIONS OF SILVER NITRATE, OF AMMONIUM NITRATE, AND OF LITHIUM NITRATE |
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Canadian Journal of Chemistry,
Volume 34,
Issue 2,
1956,
Page 151-159
A. N. Campbell,
J. B. Fishman,
G. Rutherford,
T. P. Schaefer,
L. Ross,
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摘要:
This paper is devoted to the direct determination of the vapor pressures of solutions of the nitrates of silver, of ammonium, and of lithium, at temperatures varying from 30 °C. to 105 °C. and at concentrations varying from 10 to 85 weight % (for lithium nitrate, the limited solubility precluded measurements beyond 65%). From the vapor pressures, the enthalpies of evaporation of water (by a modification of the Clapeyron–Clausius equation), the differential heats of dilution, and the activities of water (as compared with the mole fractions of the solvent) have been calculated. From the results we conclude that the water of hydration of the ammonium and silver ions (if, indeed, these ions are hydrated at all) is very loosely attached, while that of the lithium ion is strongly bound.
ISSN:0008-4042
DOI:10.1139/v56-019
出版商:NRC Research Press
年代:1956
数据来源: NRC
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