1. |
SYNTHESE DES ACIDES AMINES A PARTIR DE LA RHODANINE |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 427-438
Roger Gaudry,
Robert A. Mcivor,
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摘要:
The Gränacher method has been investigated to discover its applicability to the synthesis of a variety of natural amino acids. The procedure has been simplified for phenylalanine and tyrosine, and extended to valine and isoleucine. An unusual product of the oximation of α-thioketo-β-(p-methoxyphenyl)propionic acid is described.
ISSN:0008-4042
DOI:10.1139/v51-051
出版商:NRC Research Press
年代:1951
数据来源: NRC
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2. |
CONDUCTANCE MEASUREMENTS IN WATER – NITRIC ACID – NITROGEN PENTOXIDE MIXTURES AT VARIOUS TEMPERATURES |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 439-451
Edward G. Taylor,
L. Murray Lyne,
Alan G. Follows,
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摘要:
Conductance measurements in the system water – nitric acid – nitrogen pentoxide have been made over a range of temperatures. The results are in accordance with the findings of Veley and Manley (12) as regards (1) the presence of a minimum in the specific conductance at about 96% by weight nitric acid (2) the existence of a negative temperature coefficient of specific conductance for solutions rich in nitric acid. As reported by Berl and Saenger (1) the specific conductance of solutions of nitrogen pentoxide in nitric acid at first increases with increasing concentration of the former, ultimately attaining a maximum and then decreasing with further increase in the nitrogen pentoxide content. Some viscosity and density data for nitric acid – nitrogen pentoxide mixtures are included.
ISSN:0008-4042
DOI:10.1139/v51-052
出版商:NRC Research Press
年代:1951
数据来源: NRC
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3. |
CONDUCTANCE OF AMMONIUM NITRATE IN WATER – NITRIC ACID – NITROGEN PENTOXIDE MIXTURES AT VARIOUS TEMPERATURES |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 452-460
Edward G. Taylor,
Charles A. N. Baker,
L. Murray Lyne,
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摘要:
Conductance measurements have been made with ammonium nitrate in water – nitric acid – nitrogen pentoxide mixtures at various temperatures and over a wide range of concentrations. For all solutions except those rich in nitrogen pentoxide the variation of the specific conductance with the concentration of ammonium nitrate is similar to that observed for many electrolytes in a variety of solvents. With nitrogen-pentoxide-rich solvents however the specific conductance of ammonium nitrate is observed to decrease with increasing salt concentration. This is regarded as indicative of an interaction between the salt and one or more of the components of the nitric acid – nitrogen pentoxide system. The variation of conductance with temperature is normal in all cases. It is shown that ammonium nitrate confers a considerable degree of thermal stability on anhydrous nitric acid.
ISSN:0008-4042
DOI:10.1139/v51-053
出版商:NRC Research Press
年代:1951
数据来源: NRC
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4. |
SOME FREEZING POINT AND CONDUCTANCE MEASUREMENTS IN THE SYSTEM NITRIC ACID – ACETIC ACID |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 461-468
Edward G. Taylor,
Alan G. Follows,
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摘要:
An independent investigation of the phase diagram for the solid–liquid system nitric, acid – acetic acid has confirmed the findings of Miskidzh'yan and Trifonov (4), namely, that a 1: 1 molecular compound exists. Conductance measurements at 0°, 25°, and 40°C. have been made for the same system. It does not appear possible to predict compound formation from the conductance measurements alone. A preliminary investigation of the liquid–vapor equilibrium for the system nitric acid – acetic acid indicates the existence of a maximum boiling azeotrope. Diacetylorthonitric acid—(CH3COO)2N(OH)3—discovered by Pictet and Genequaud (8) is, in all probability, identical with this binary azeotrope. Some molecular weight measurements tend to confirm this view.
ISSN:0008-4042
DOI:10.1139/v51-054
出版商:NRC Research Press
年代:1951
数据来源: NRC
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5. |
DROPPING AMALGAM ELECTRODES |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 469-477
R. C. Turner,
C. A. Winkler,
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摘要:
The anodic limiting current at a lead amalgam dropping electrode is shown to be proportional to the concentration of the lead in the amalgam, at constant flow rate. The original Ilkovic equation does not apply to the anodic limiting current from dropping amalgam electrodes.The anodic limiting currents with lead and cadmium amalgams have been found to agree with the 2nd approximation of the Ilkovic equation, as derived by Strehlow and Stackelberg for this process, for flow rates in the region below approximately 1.2 mgm. per sec. With flow rates greater than this, the lead amalgams gave a linear relation between the anodic limiting current divided by concentration and the mass flow rate. With cadmium amalgams no such linear relation was evident and the magnitude of the limiting current depended on the size of the drops as well as on the mass flow rates. The half wave potentials of lead and cadmium were found to depend on the flow rate of the dropping electrode.
ISSN:0008-4042
DOI:10.1139/v51-055
出版商:NRC Research Press
年代:1951
数据来源: NRC
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6. |
PREPARATION OF N-SUBSTITUTED UREAS FROM NITROSOMETHYLUREAS |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 478-481
Jean L. Boivin,
Paul A. Boivin,
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摘要:
Good yields of N-substituted ureas were obtained by reacting amines with N-nitroso-N-methylurea in aqueous solution. It has been shown that N-nitroso-N-methylurea decomposed into methylnitrosamide and isocyanic acid. Similarly, N-nitroso-N, N′-dimethylurea and amines gave rise to good yields of N-substituted-N′-methylureas.
ISSN:0008-4042
DOI:10.1139/v51-056
出版商:NRC Research Press
年代:1951
数据来源: NRC
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7. |
6-IODOMETAMECONINE AND 3–IODOMETAHEMIPINIC ACID |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 482-489
J. A. McRae,
R. B. VanOrder,
F. H. Griffiths,
Thelma Eskin Habgood,
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摘要:
6-Iodo-m-meconine has been prepared fromm-meconine by several steps and oxidized to 3-iodo-m-hemipinic acid. The orientation of the iodo-m-meconine is based on its conversion to 4, 5, 6-trimethoxyphthalide. The identity reported by Rây and Robinson of the bromo-m-meconine made directly by similar steps fromm-meconine with that from 2-bromoveratric acid and formaldehyde could not be confirmed. The former substance has the orientation ascribed to it by Rây and Robinson but the identity and orientation of the latter substance is left in doubt. Attempts to form a substituted diphenyl ether from dimethyl 3-iodo-m-hemipinate and the potassium salt of methyl vanillate failed.
ISSN:0008-4042
DOI:10.1139/v51-057
出版商:NRC Research Press
年代:1951
数据来源: NRC
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8. |
HYDROGEN PEROXIDE AND ITS ANALOGUES: III. ABSORPTION SPECTRUM OF HYDROGEN AND DEUTERIUM PEROXIDES IN THE NEAR ULTRAVIOLET |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 490-493
M. K. Phibbs,
Paul A. Giguère,
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摘要:
The absorption of ultraviolet light between 3000 and 4000 Å by solutions of hydrogen peroxide in water and of deuterium peroxide in heavy water has been measured at various concentrations. Both peroxides show slight but real deviations from Beer's law at high concentrations. Substitution of hydrogen by deuterium shifts the absorption continuum by about 390 cm.−1towards shorter wave lengths. This shift is of the same order as that calculated from the difference in zero-point energy of the two isotopic molecules.
ISSN:0008-4042
DOI:10.1139/v51-058
出版商:NRC Research Press
年代:1951
数据来源: NRC
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9. |
THE DIELECTRIC CONSTANT OF DISULPHUR DECAFLUORIDE |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 494-507
N. R. S. Hollies,
R. L. Mcintosh,
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摘要:
A method is described for obtaining the dielectric constant and conductivity of disulphur decafluoride in both liquid and gaseous forms. The freezing point of the liquid and the molecular weight of the vapor are established as criteria of purity. All the measurements lead to the conclusion that disulphur decafluoride is non-polar. Its molar polarizations in the two forms are compared with those of other members of the sulphur fluoride and carbon fluoride homologous series as well as with hexane, benzene, and toluene.
ISSN:0008-4042
DOI:10.1139/v51-059
出版商:NRC Research Press
年代:1951
数据来源: NRC
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10. |
THE KINETICS OF THE THERMAL DECOMPOSITION OF DISULPHUR DECAFLUORIDE |
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Canadian Journal of Chemistry,
Volume 29,
Issue 6,
1951,
Page 508-525
W. R. Trost,
R. L. McIntosh,
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摘要:
The thermal decomposition of the gas disulphur decafluoride has been studied in a metal reactor. Analytical evidence showed that the reaction proceeds according to the equation S2F10 = SF6 + SF4.The reaction was found to be largely homogeneous, as the heterogeneous reaction accounted for less than 5% of the total process. The homogeneous reaction was shown to be first order, and in the temperature range investigated the rate is given by ln k = 47.09 − 49,200/RT. A chain reaction is postulated to explain the observed rate of the reaction. The effect of nitric oxide and acetylene dichloride on the rate and products of the reaction was investigated.
ISSN:0008-4042
DOI:10.1139/v51-060
出版商:NRC Research Press
年代:1951
数据来源: NRC
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