Journal of the Chemical Society, Part 4Chemical Society., 1962 "Titles of chemical papers in British and foreign journals" included in Quarterly journal, v. 1-12. |
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Results 1-3 of 77
Page 4278
... method in the paper by Gillespie and Solomons 1 was used . The comparison shows : first , that the decrease with concentration of the original basic dissociation constant , ( 4.9 to 3.2 ) × 10-3 mole kg . - 1 , is considerably reduced ...
... method in the paper by Gillespie and Solomons 1 was used . The comparison shows : first , that the decrease with concentration of the original basic dissociation constant , ( 4.9 to 3.2 ) × 10-3 mole kg . - 1 , is considerably reduced ...
Page 4421
... method , and dissociation constants are calculated from these values and the known autoprotolysis constants . The results are compared with those obtained by other methods ; a large discrepancy between the present results and the ...
... method , and dissociation constants are calculated from these values and the known autoprotolysis constants . The results are compared with those obtained by other methods ; a large discrepancy between the present results and the ...
Page 4640
... method 17 gave trans - 9,10 - epithio- octadecanoic acid , although in variable yield ( 15-40 % ) , * identical with our and Kaufmann's compound . The failure of standard methods to afford the sulphide ( II ) led us to explore other ...
... method 17 gave trans - 9,10 - epithio- octadecanoic acid , although in variable yield ( 15-40 % ) , * identical with our and Kaufmann's compound . The failure of standard methods to afford the sulphide ( II ) led us to explore other ...
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Common terms and phrases
absorption acetic acid acetic anhydride acetone acetylacetone added alcohol Amer anhydride aqueous atom b₁ band benzene bond bromide Calc carbon tetrachloride carbonyl CH₂ Chem chloride chloroform chromatography cm.¹ CO₂H complex compound concentration constant cooled Cotton effect crystallised decomp derivative diethyl dilute dioxan distilled dried electron ester ethanol ether ethyl acetate ethylene evaporated experimental extracted filtered filtrate formed Found fraction gave give heated hydrochloric hydrochloric acid hydrogen hydrogen chloride hydrolysis infrared spectrum isomer k₁ ketone lactone ligand light petroleum b. p. measured methyl mixed m. p. mixture mmoles mole molecule molybdenum needles nitrate nitrogen obtained oxidation peroxide phenyl polymer potassium precipitate prepared protons pyridine radicals reaction reduced refluxed requires residue resonance ring room temperature salt sample sodium hydroxide solid solution solvent spectra steric structure sulphide sulphuric acid Table values washed yellow yield