Journal of the Chemical Society, Part 2

absorption acetic acid acetic anhydride acetone added alkali alkyl halide aqueous acetone atoms benzene boiling Calc carbinol carbon CH₂ Chem chloroform colour colourless compound concentration containing cooled corresponding crystallised crystals curve dehydrogenation derivatives dilute dioxide dissolved distilled dried equation equiv ester evaporated excess experimental experiments filtered first-order formation formed formic acid Found fraction gave heated hydrocarbon hydrochloric acid hydrogen chloride hydrolysis initial iodide ionic strength ionisation ions isolated k₁ ketone kinetic light petroleum liquid mass-law effect mercuric method methyl alcohol methyl ester mins mixed m. p. mixture molecular molecule mucic acid naphthalene needles obtained olefin oxidation phenol picrate potassium precipitate prepared pyridine quantity radical rate constants reaction reagent reduced refluxed removed requires residue salt separated sodium hydroxide solid soluble solvent structure substance substitution sulphate sulphuric acid tert.-butyl bromide unimolecular unimolecular mechanism values washed yellow yield