Quarterly Journal of the Chemical Society of London, Volume 6 |
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Results 1-3 of 77
Page 1687
... experiments gave K values of 2.54 and 2.46 ; with p - methoxy - N - nitroso- acetanilide two experiments gave K values of 1.74 and 1.67 , and with p - methyl - N - nitrosoacetanilide one experiment gave K 2.4 . We thank Dr. D. I. Davies ...
... experiments gave K values of 2.54 and 2.46 ; with p - methoxy - N - nitroso- acetanilide two experiments gave K values of 1.74 and 1.67 , and with p - methyl - N - nitrosoacetanilide one experiment gave K 2.4 . We thank Dr. D. I. Davies ...
Page 1801
... experiments , but in somewhat greater detail , have now been carried out with t - butyl alcohol as the exchanging ... experiments are also reported in the present paper . EXPERIMENTAL The experiments on the effect of added solutes were ...
... experiments , but in somewhat greater detail , have now been carried out with t - butyl alcohol as the exchanging ... experiments are also reported in the present paper . EXPERIMENTAL The experiments on the effect of added solutes were ...
Page 1809
... Experiments . - As a check on the sample isolation and on the lack of significant reduction in the concentration of t - butyl alcohol upon radiolysis , as inferred from the preceding product analysis , solutions of 14C- labelled t ...
... Experiments . - As a check on the sample isolation and on the lack of significant reduction in the concentration of t - butyl alcohol upon radiolysis , as inferred from the preceding product analysis , solutions of 14C- labelled t ...
Contents
ISCHA 013 | 1034 |
Physical organic chemistry | 1035 |
Studies of the reactions of the anhydrosulphites of ahydroxycarboxylic acids Part IV Steric | 1044 |
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absorption acetic acid activation added addition alcohol Amer amine anhydrosulphite anion appears aqueous aromatic assigned atom attack bands base benzene bond buffer calculated carbon carbon tetrachloride Chem chloride compared compounds concentration conformation containing corresponding decomposition derived described determined discussed effect electron energy equation ester ether evidence excess expected experimental experiments factors Figure followed formation formed further gave give given hydrogen hydrolysis increase indicate interaction involving kinetic less measured mechanism method methyl MICHIGAN mixture molecular molecules nitrogen nucleophilic observed obtained occurs organic oxidation phenyl phosphate plot position possible prepared presence proton pyridine radical radical anion rate constants ratio reaction reactivity reduction relative reported requires respectively ring showed shown similar sodium solution solvent spectra spectrum splitting structure studied substituent suggested Table temperature transition University values yield