Quarterly Journal of the Chemical Society of London, Part 2, Pages 1521-2836 |
Contents
Research to W Z a Fellow of the Fund and the Department of Scientific and Industrial | 1619 |
THE DYSON PERRINS LABORATORY Oxford Received November 24th 1961 | 1837 |
Part VII J 1961 4573 | 2449 |
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absorption acetic acid acetone activity added addition alcohol Amer amount anhydride aqueous atom band benzene bond bromide Calc calculated carbon carbon tetrachloride Chem chloride chromatography complex compound concentration constant containing corresponding crystallised derivative described determined dilute dissolved distilled dried effect electron ester ethanol ether evaporated expected EXPERIMENTAL experiments extracted followed formation formed Found fraction further gave give heated hydrochloride hydrogen hydrogen bromide hydrolysis hydroxide identical increase indicated infrared initial involved isolated light material measured mechanism method methyl mixed mixture mole molecule needles observed obtained occurs oxidation oxygen petroleum position possible potassium precipitate prepared present probably pyridine reaction reduction reflux removed requires residue respectively sample separated showed shown similar sodium solid solution solvent spectra spectrum structure studied substituted suggested sulphuric Table temperature treated values washed yellow yield