Journal of the Chemical Society, Part 3Chemical Society., 1949 |
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Results 1-3 of 79
Page 1947
... carbon monoxide in the two experiments were 85 % and 86 % , respectively . Triphenylacetyl chloride furnished rather less carbon monoxide , the crystalline product yielding triphenylmethane when reduced . The broad inference is clearly ...
... carbon monoxide in the two experiments were 85 % and 86 % , respectively . Triphenylacetyl chloride furnished rather less carbon monoxide , the crystalline product yielding triphenylmethane when reduced . The broad inference is clearly ...
Page 1953
... carbon monoxide was 1073 c.c. ( 65 % ) . Together with unchanged tert . - butylbenzene and di - tert ... carbon disulphide solution . This experiment was carried out in the same way as the first with pivaloyl chloride ( 7 · 7 g ...
... carbon monoxide was 1073 c.c. ( 65 % ) . Together with unchanged tert . - butylbenzene and di - tert ... carbon disulphide solution . This experiment was carried out in the same way as the first with pivaloyl chloride ( 7 · 7 g ...
Page 1967
... carbon monoxide ( 3.6 % ) were formed . ( iii ) Trichloroacetyl chloride . www - Trichloroacetophenone ( 56 % ) , carbon monoxide ( 3.1 % ) , and a tar of high b . p . were produced . Trichloro- Condensations of Other Halogenated ...
... carbon monoxide ( 3.6 % ) were formed . ( iii ) Trichloroacetyl chloride . www - Trichloroacetophenone ( 56 % ) , carbon monoxide ( 3.1 % ) , and a tar of high b . p . were produced . Trichloro- Condensations of Other Halogenated ...
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Common terms and phrases
acetic acid acetic anhydride acetone acetyl added admixture alkaline alkyl aluminium chloride Amer ammonia aqueous solution atoms barium benzene boiling bromine Calc carbinol carbon catalyst Chem Chim chloroform colourless needles compound concentrated condensation cooled crystals cyclohexene decomp derivatives dilute dioxan dissolved distilled dithizone dried equiv ester ethanol ethyl acetate ethyl alcohol ethylene evaporated EXPERIMENTAL filtered filtrate formed Found fraction gave give heated under reflux hydrocarbon hydrochloric acid hydrogen chloride hydrolysis iodide ions isolated ketone Light absorption light petroleum b. p. method methyl mixed m. p. mixture molecule obtained oxide phenyl plates potassium hydroxide precipitated prepared pressure prisms pyridine Q-enzyme R₁ R₂ reaction reagent reduced removed requires residue room temperature salt semicarbazone separated sodium hydroxide solid soluble solvent specimen structure substance sulphate sulphone sulphuric acid synthesis Table unsaturated washed yield