Quarterly Journal of the Chemical Society of London, Part 2, Pages 1421-2600 |
Contents
NO PAGE | 1429 |
The relative stereochemistry of the rotenoids | 1448 |
Cocatalysis Part II The relative efficiencies of halogenated acetic acids | 1453 |
111 other sections not shown
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Common terms and phrases
absorption acetic acid acetic anhydride acetone added akuammicine alcohol alkaline allyl Amer ammonia atom azide band benzene benzyl bond bromide buffer Calc carbon tetrachloride cation CH₂ Chem chloride chloroform chromatography cm.¹ colourless complex compound concentration constant crystallised decomp decomposition derivative dilute dioxan dissolved distilled dithizone dried eluted ester ether evaporated EXPERIMENTAL extracted filtered filtrate formed Found fraction frequencies gave give H₂O halides heated hexafluoride hexane hydrochloric acid hydrogen hydrogen chloride hydrolysis hydroxide infrared infrared spectrum iodide isomer ketone liquid lithium lithium aluminium hydride m. p. and mixed methanol method methyl mixed m. p. mixture mole needles nitrate nitrogen obtained olefin oxidation phosphate potassium precipitate prepared pyridine reaction refluxed removed requires residue rhenium room temperature salt sample sodium sodium azide solvent spectra sulphate sulphuric Table Vmax washed yield