Quarterly Journal of the Chemical Society of London, Part 3 |
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Page 2328
... alkaline solution are not oxidised by molecular oxygen , probably because of the much smaller concentration of the carbanions ( II ; R = alkyl ) than of the aryl analogue ( II ; R = Ph ) . However , the great electron- attraction of the ...
... alkaline solution are not oxidised by molecular oxygen , probably because of the much smaller concentration of the carbanions ( II ; R = alkyl ) than of the aryl analogue ( II ; R = Ph ) . However , the great electron- attraction of the ...
Page 2329
... alkaline indicated the presence of two ionising NH groups . 10 Finally , removal of MeHC — NH R'N - CO SC - NH CHR - CO -co .NH – CHMe CR - N CS - NR ' ( IX ) ( X ) SC -NH CO - NH SC – NH CC = CH - C HN- -Có INH - CS H - CS HN- C = CCO ...
... alkaline indicated the presence of two ionising NH groups . 10 Finally , removal of MeHC — NH R'N - CO SC - NH CHR - CO -co .NH – CHMe CR - N CS - NR ' ( IX ) ( X ) SC -NH CO - NH SC – NH CC = CH - C HN- -Có INH - CS H - CS HN- C = CCO ...
Page 2711
... Alkaline Media . Part I. By H. R. GERSMANN and A. F. BICKEL . The autoxidation of substituted 2,6 - di - t - butylphenols in alkaline media has been studied at various temperatures . 2,4,6 - Tri - t - butylphenol and 4 - methyl - 2,6 ...
... Alkaline Media . Part I. By H. R. GERSMANN and A. F. BICKEL . The autoxidation of substituted 2,6 - di - t - butylphenols in alkaline media has been studied at various temperatures . 2,4,6 - Tri - t - butylphenol and 4 - methyl - 2,6 ...
Contents
ABEL E W Bennett M A and Wilkinson G | 2323 |
Bourne E J Hartigan J and Weigel H | 2332 |
Clark E R | 2344 |
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1,3,5-trinitrobenzene absorption acetic acid acetic anhydride acetone added alcohol alkaline alkyl Amer amine ammonia anhydride atom benzene boiling bond bromide Calc carbon Chem chloride chloroform chromatography complex compound concentration constant cooled crystallised crystals curve decomp derivatives diethylamine dilute dimer dioxan dioxide dissolved distilled dried eluted ester ethanol evaporated filtered filtrate formation formed Found fraction gave give glycollic acid glyoxylic acid heated hydride hydrochloric acid hydrolysis hydroxide infrared infrared spectrum iodide isolated isomer K₁ light petroleum b. p. lithium lithium aluminium hydride m. p. and mixed methyl methyl iodide mixed m. p. mixture mole molecular molecule nitrogen obtained oxidation oxygen perchlorate picrate polymer potassium precipitate prepared prisms pyridine reaction reduced refluxed requires residue room temperature salt sodium hydroxide solid solvent spectra stirred structure sulphuric acid Table titration ultraviolet values washed yield