Quarterly Journal of the Chemical Society of London, Volume 6 |
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Page 1242
... gives a variety of products depending on the conditions . 2 - Nitrobenzenesulphenyl chloride is reported to react with 2 molar proportions of sodium hydroxide to give the corresponding di- sulphide and thiolsulphonate , but with a ...
... gives a variety of products depending on the conditions . 2 - Nitrobenzenesulphenyl chloride is reported to react with 2 molar proportions of sodium hydroxide to give the corresponding di- sulphide and thiolsulphonate , but with a ...
Page 1565
... give radical anions . At higher tempera- tures these radical anions are unstable and decay to give the corresponding anions . The nature of the substituent markedly affects the rate of the decay which was found to be either of the first ...
... give radical anions . At higher tempera- tures these radical anions are unstable and decay to give the corresponding anions . The nature of the substituent markedly affects the rate of the decay which was found to be either of the first ...
Page 1627
... give stabilized radicals.24 The intermediacy of R , CO - SiMe , radicals is also strongly supported by the nature of the main silicon- containing products and their relative proportions . Dimerization of the radicals R , CO - SiMe ...
... give stabilized radicals.24 The intermediacy of R , CO - SiMe , radicals is also strongly supported by the nature of the main silicon- containing products and their relative proportions . Dimerization of the radicals R , CO - SiMe ...
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