Quarterly Journal of the Chemical Society of London |
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Page 65
... compound with optically active forms merely to record one more optically active compound . Yet it must always be remembered that the optical activity of a compound is a physical property which throws much light on the configuration ...
... compound with optically active forms merely to record one more optically active compound . Yet it must always be remembered that the optical activity of a compound is a physical property which throws much light on the configuration ...
Page 143
... compound in view of its bearing on the problem of the mechanism by which carcinogenic compounds are detoxified in the animal body . A possible route to the desired compound was indicated by the observation of Vollmann , Becker , Corell ...
... compound in view of its bearing on the problem of the mechanism by which carcinogenic compounds are detoxified in the animal body . A possible route to the desired compound was indicated by the observation of Vollmann , Becker , Corell ...
Page 531
... compound , m . p . 154 ° ( Borsche's compound ) , obtained when Fischer's indole ynthesis is applied to cyclohexanone - m - nitrophenylhydrazone ( Borsche , Witte , and Bothe , loc . cit .; Perkin nd Plant , loc . cit . ) , was shown by ...
... compound , m . p . 154 ° ( Borsche's compound ) , obtained when Fischer's indole ynthesis is applied to cyclohexanone - m - nitrophenylhydrazone ( Borsche , Witte , and Bothe , loc . cit .; Perkin nd Plant , loc . cit . ) , was shown by ...
Contents
An Investigation of the Occurrence of the Coordinate or Dative Link by Electric Dipolemoment | 38 |
Electrolytic Dissociation Processes Part IV The Ionisation of a CarbonHalogen Bond | 129 |
By J SHERIDAN | 133 |
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4-benzthiazine absorption acetic anhydride acetone acetyl acetylene added addition adsorbed alkali Amer ammonia aqueous atoms benzene boiling bond Calc carbinol carbon catalyst CH₂ Chem chloroform colourless needles compound concentrated condensation cooling crystallised from alcohol crystals cyclisation D.Sc decomp derivative described dilute dissolved distilled dried ester ethanol ether ethylene evaporated EXPERIMENTAL extracted filtered filtrate formation formed Found fraction gave give heated hydrocarbons hydrochloric acid hydrogen bromide hydrogen chloride hydrolysis iodide isolated ketone light petroleum liquid methiodide method methyl alcohol mixed m. p. mixture molecule nickel nitric nitrogen obtained optically oxide oxychloride phosphate phosphorus picrate potassium potassium hydroxide precipitate prepared pressure prisms pyridine reaction reduced refluxed requires residue ring room temperature salt saturated separated sodium carbonate sodium hydroxide solid soluble solution solvent structure substance sulphate sulphuric acid vacuum washed yellow needles yield zinc