Quarterly Journal of the Chemical Society of London, Part 4, Pages 3921-5004

absorption acetic acid acetone added alcohol alkaline alumina Amax Amer amine ammonia amylopectin atom band benzene bond bromide Calc carbon CH₂ Chem chloride chloroform chromatography cm.¹ complex compound concentrated cooled crystallised decomp derivative diazomethane dilute dimethylaniline dissolved distilled dried eluted ester ethanol ethylene evaporated extracted with ether filtered filtrate formation formed Found fraction gave H₂O heated hydration hydrazine hydrochloric acid hydrogen hydrolysis hydroxyl hydroxyl group infrared infrared spectrum iodide iodobenzene isolated isomers ketone ligand light petroleum b. p. m. p. and mixed methyl mixed m. p. mixture mole mole-¹ molecules needles nitrate nitrogen nucleophilic obtained oxalate oxidation phenyl potassium precipitate prepared pyridine Raney nickel reaction reduced refluxed requires residue room temperature salt sodium borohydride sodium hydroxide solvent spectra stirred structure sulphuric acid Table tetracyanoethylene ultraviolet values washed yellow yield