Quarterly Journal of the Chemical Society of London, Volume 6 |
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Results 1-3 of 84
Page 1330
... determined by a single - crystal X - ray analysis . The crystals are orthorhombic , a = 17.781 , b = 8-786 , c = 11.859 Å , Z = 4 , space group P212121 . The intensities were measured with a Hilger and Watts automatic four - circle ...
... determined by a single - crystal X - ray analysis . The crystals are orthorhombic , a = 17.781 , b = 8-786 , c = 11.859 Å , Z = 4 , space group P212121 . The intensities were measured with a Hilger and Watts automatic four - circle ...
Page 1552
... determined signs were not used to determine additional signs until the next pass and ( b ) newly determined signs were used immediately in the determination of signs of reflexions which were lower in the list . 9 The more conservative ...
... determined signs were not used to determine additional signs until the next pass and ( b ) newly determined signs were used immediately in the determination of signs of reflexions which were lower in the list . 9 The more conservative ...
Page 1794
... determination of an initial spectrum , a small quantity of 2,6 - dichlorobenzoic acid was added to the solution and additional spectra were determined as a function of time . For each spectrum , the time ( relative to acid addition ) of ...
... determination of an initial spectrum , a small quantity of 2,6 - dichlorobenzoic acid was added to the solution and additional spectra were determined as a function of time . For each spectrum , the time ( relative to acid addition ) of ...
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