Quarterly Journal of the Chemical Society of London, Pages 3324-4156 |
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Page 2984
... carbon tetrachloride extremely slowly , the reaction not being complete even after 3 weeks ' refluxing , whereas under comparable conditions acetanilide is chlorinated in less than 40 hours . EXPERIMENTAL Rearrangement of N ...
... carbon tetrachloride extremely slowly , the reaction not being complete even after 3 weeks ' refluxing , whereas under comparable conditions acetanilide is chlorinated in less than 40 hours . EXPERIMENTAL Rearrangement of N ...
Page 3459
... carbon tetrachloride , but the trans - isomer in benzene only . The reference to Puchalik 14 is not available in Australia and the abstracts 14 merely state that μ0 without quoting the polarisations actually found . The entry for Seyer ...
... carbon tetrachloride , but the trans - isomer in benzene only . The reference to Puchalik 14 is not available in Australia and the abstracts 14 merely state that μ0 without quoting the polarisations actually found . The entry for Seyer ...
Page 3630
... carbon dioxide - alcohol freezing bath . A film of solid styrene formed on ... tetrachloride in styrene , previously cooled to the equilibrium temperature ... carbon tetrachloride solution , the temperature was read and stirring ...
... carbon dioxide - alcohol freezing bath . A film of solid styrene formed on ... tetrachloride in styrene , previously cooled to the equilibrium temperature ... carbon tetrachloride solution , the temperature was read and stirring ...
Contents
ii | 2842 |
Catalytic hydrogenation | 2845 |
Garden J F and Thomson R H | 2851 |
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Common terms and phrases
4-triazine absorption acetic acid acetic anhydride acetone acidified added alcohol alkali alkyl Amer amine aqueous sodium atom band benzene benzyl boiling bromine Calc carbonate carbonyl Chem chloroform chromatography CO₂H colourless compound concentration containing cooled crystallised cyclisation decomp derivative diethyl dilute dioxan dioxide diphenyl dissolved distilled dried eluted ester ethanol ethyl acetate evaporated filtered filtrate fluorene formation formed Found fraction gave give H₂O heated hydrochloric acid hydrogen chloride hydrolysis infrared iodide isatin isolated ketone lactone light petroleum b. p. lithium aluminium hydride m. p. and mixed methyl mixed m. p. mixture mole needles nitric acid nitrogen obtained oxidation perchloric phenyl potassium hydroxide precipitate prepared prisms pyridine reaction reagent reduced refluxed requires residue room temperature salt separated sodium hydroxide solid solution solvent spectra structure sulphuric acid Table titration washed yellow yield