Organic Chemistry; Or, Chemistry of the Carbon Compounds, Volume 3

acetic acid acetic anhydride acetoacetic ester acetone acid ester acridine action alcohol aldehydes alkali alkaloids alkyl iodides amines ammonia aniline antipyrine atoms bases benzaldehyde benzene benziminazoles benzoyl boiling bromine C.CH C(OH carbon carboxylic acids carboxylic ester caustic potash CH CH CH CH-CH CH-N CH,C CH=CH CH₂ CH₂O chloride cinchonine CO₂ colour compounds condensation product converted COOH corresponding coumarone decomposes decomposition derivatives dicarboxylic dilute dimethyl distillation dyes easily ether formation formed formula furan gives glyoxalines H₂O halogen heating homologues hydrazine hydrochloric acid hydrogen hydroxylamine indazoles indigo blue indole indoxyl iodo-methylate isatin isomeric isoquinoline ketone latter melting methyl iodide N-alkyl N-atom N=CH NaHO NH₂ nicotine nitric nitrous acid oxidation oxime phenyl phenylhydrazine piperidine Potassium permanganate produced pyrazole pyrazolones pyridine pyrrole quinine quinoline reaction reduction ring salts similarly sodium solution split sulphide sulphonic sulphuric acid synthesis thiophen triazoles tropine yields zinc dust