Quarterly Journal of the Chemical Society of London, Volume 1 |
Contents
Physical organic chemistry | 1 |
Molecular conformations Part IV XRay analysis of 3363dimethoxy5ẞ19cycloandrostan17one | 8 |
the form | 15 |
10 other sections not shown
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acetic acid activation added addition alcohol Amer analysis appears aqueous aromatic ation atom band base benzene bond bromide calculated carbon carbon tetrachloride Chem chemical chloride chromatography compared complex compounds concentration conformation containing corresponding dependence derivatives described determined discussed effect electron energy equation ester ether evidence expected experimental experiments factors Figure followed formation formed further gave give greater higher hydrogen hydrolysis increase indicated initial interaction involved isomer kinetic less measured mechanism methanol method methyl mixture mole molecular molecule nitration nitrogen nucleophilic observed obtained occurs oxide peak Ph.D phenyl plot position possible prepared present proton pyridine radical rate constants ratio reaction reactivity reduction relative requires resonance respectively ring shift shown similar sodium solution solvent spectra spectrum steric structure substituents suggested Table temperature transition values yield