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tuted diazohydroxylaminocompounds on the above lines the results
saturated with HC1
2 other sections not shown
acetone action added alcoholic solution alkali ammonium amount amygdalin anhydrous aqueous solution benzene boiling bromine c.c. N2 moist carbon dioxide cent chloroform cold colour colourless compound concentrated condensation containing cooling copper corr crystals decomposed decomposition density derivative diazonium dilute dissolved distilled disulphide dried ester ethereal solution ethyl acetate evaporated excess experiments extracted with ether formation formed formula fraction gave glacial acetic acid grams heated hydrochloric acid hydrogen chloride hydrolysis insoluble investigation iodine isomeric light petroleum liquid melting point mercuric method methyl alcohol methyl iodide mixed mixture molecular molecule needles nitrate nitric nitric acid nitrogen observed obtained oxide phenyl potassium hydroxide precipitate prepared pressure pure racemisation reaction readily soluble requires residue rotatory power salt separated silver small quantity sodium carbonate sodium hydroxide solid solvent sparingly soluble substance sulphate sulphide sulphuric acid Trans tube volume washed water-bath whilst yellow yield