Quarterly Journal of the Chemical Society of London

absorption acetic acetone acid activation added addition alcohol Amer appears aqueous aromatic atom band benzene bond bromine calculated carbon carbon tetrachloride cation Chem chloride chromatography complex compound concentration constants containing cooled corresponding crystallised derivatives described determined distilled dried effect electron energy ester ethanol ether evaporated expected extracted filtered followed formation formed Found fraction further gave give heated hydrogen hydrolysis hydroxide identical increase indicated infrared initial involved isolated kinetic light lone pairs material measured mechanism method methyl mixture mole molecule nitrogen observed obtained occur oxidation petroleum position possible potassium prepared present proton reaction rearrangement reduced refluxed removed requires residue respectively ring salt separated showed shown similar sodium solid solution solvent spectra spectrum structure studied substituents suggested sulphuric Table temperature theory transition treated values Vmax washed yield