Quarterly Journal of the Chemical Society of London, Volume 6 |
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Page 1116
... carbon tetrachloride , 15 1.45 D in hexane 16 ) dipole - moment data for these compounds in carbon tetrachloride are not listed by McClellan.17 Because of low solubility in carbon tetrachloride , 1,2 - di- chloro - 1,1,2,2 ...
... carbon tetrachloride , 15 1.45 D in hexane 16 ) dipole - moment data for these compounds in carbon tetrachloride are not listed by McClellan.17 Because of low solubility in carbon tetrachloride , 1,2 - di- chloro - 1,1,2,2 ...
Page 1609
... carbon tetrachloride . should be noted here that the results 14 given in ref . 13 for the α- , B- , 8 - isomers as solutes in carbon tetrachloride are , in fact , those when benzene is solvent . The μ values reported in Table 2 for the ...
... carbon tetrachloride . should be noted here that the results 14 given in ref . 13 for the α- , B- , 8 - isomers as solutes in carbon tetrachloride are , in fact , those when benzene is solvent . The μ values reported in Table 2 for the ...
Page 1671
... carbon tetra- chloride , although in detail there are several differences . First , the B - naphthol is not hydrogen - bonded to carbon tetrachloride . Secondly , acetyl chloride does not have to compete with the solvent for the ...
... carbon tetra- chloride , although in detail there are several differences . First , the B - naphthol is not hydrogen - bonded to carbon tetrachloride . Secondly , acetyl chloride does not have to compete with the solvent for 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