Quarterly Journal of the Chemical Society of London, Volume 6 |
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Results 1-3 of 83
Page 1436
... analysis of two di - Grignard preparations was carried out ; the results are given in Table 1. The analysis showed that the ratio Mg : Br was close to 1 : 1 . absence of Wurtz coupling and of the mono - Grignard 7 , 17 . The E. C. Ashby ...
... analysis of two di - Grignard preparations was carried out ; the results are given in Table 1. The analysis showed that the ratio Mg : Br was close to 1 : 1 . absence of Wurtz coupling and of the mono - Grignard 7 , 17 . The E. C. Ashby ...
Page 1450
... Analysis of Dihydro - derivatives formed by Reaction of Phenyl- azotriphenylmethane with Furan and Benzene By L. Benati , M. Tiecco , and A. Tundo , * Istituto di Chimica Organica e di Chimica Industriale della Università , Viale ...
... Analysis of Dihydro - derivatives formed by Reaction of Phenyl- azotriphenylmethane with Furan and Benzene By L. Benati , M. Tiecco , and A. Tundo , * Istituto di Chimica Organica e di Chimica Industriale della Università , Viale ...
Page 1450
... analysis . The crystals are orthorhombic , a = 13.886 , b = 12-807 , c = 8-463 A , Z = 4 , space group P212121 . The intensities were measured with a Hilger and Watts automatic four - circle diffractometer using Mo - K radiation . The ...
... analysis . The crystals are orthorhombic , a = 13.886 , b = 12-807 , c = 8-463 A , Z = 4 , space group P212121 . The intensities were measured with a Hilger and Watts automatic four - circle diffractometer using Mo - K radiation . The ...
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