Quarterly Journal of the Chemical Society of London, Part 5, Pages 5005-6079
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absorption acetate acetone acid activity added addition alcohol Amer amount anhydride aqueous atoms bands benzene boiling bond calculated carbon tetrachloride carbonate Chem chloride chloroform chromatography complexes compound concentration constants containing cooled corresponding crystallised crystals decomposition derivative described determined dilute distilled dried effect electron ester ethanol ether evaporated expected experiments extracted filtered followed formation formed Found fraction further gave give heated hydration hydrogen hydrolysis hydroxide increase indicated infrared spectrum isolated less light material measured method methyl mixed mixture mole needles nitrogen observed obtained occurred oxide peaks peroxide petroleum possible potassium prepared present pressure pyridine radicals reaction reduction reflux relative removed requires residue resonance respectively ring room temperature salt sample separated showed shown similar sodium solid solution solvent spectra stirred structure studied substituent suggested Table treated values washed yellow yield