Adolph Strecker's Short Text-book of Organic Chemistry

acetic acid acetone action alcohol and ether alcohol radicals alcoholic solution aldehyde alkalies alkylic allyl amines ammonia ammonic aqueous solution argentic baric benzene benzoic bodies boiling point bromine C₂H C₂H5 cacodylic calcic carbon atoms carbonic anhydride CH₂ CH3 CH3 CmH2m+1 CnH2n+1 CO.OH colour colourless liquid compounds converted crystals cyanide decomposed decomposition derivatives dibromide dichloride diethyl difficultly soluble dilute dissolves dry distillation ethylamine ethylene ethylic evaporation formation formed formula glycerine glycol glycollic acid H₂O halogen haloid heating hydric hydriodic acid hydrochloric acid hydrogen atoms insoluble iodide iodine isomeric ketone latter melting mercuric metallic mixed mixture molecules nitrate nitric acid obtained odour oxalic oxide oxidising oxygen phenyl phosphine plumbic potassic cyanide precipitated prepared prisms quantity reaction readily soluble salts separates sodic sodium sodium amalgam soluble soluble in alcohol soluble in water sulphate sulphide sulphuric acid temperature triethyl tube urea whilst yellow yields zinc