Quarterly Journal of the Chemical Society of London, Volume 6 |
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Page 1296
... given by equation ( 2 ) . in an inert solvent ( A ) is given by equation ( 5 ) . K = [ DA ] / [ D ] . [ A ] ( 2 ) The effective concentrations of both A and D are given by equations ( 3a and b ) where the concentrations referred ад ...
... given by equation ( 2 ) . in an inert solvent ( A ) is given by equation ( 5 ) . K = [ DA ] / [ D ] . [ A ] ( 2 ) The effective concentrations of both A and D are given by equations ( 3a and b ) where the concentrations referred ад ...
Page 1352
... given isotropic absorption band system have equal areas as well as opposed signs . However , it is found that the two circular dichroism bands connected with a given absorption system do not generally have equal areas , particularly ...
... given isotropic absorption band system have equal areas as well as opposed signs . However , it is found that the two circular dichroism bands connected with a given absorption system do not generally have equal areas , particularly ...
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... given as footnotes at the bottom of the corresponding page in the final printed text . It is thus essential that bibliographic references are numbered in the order in which they will appear . When citation of a paper is repeated the ...
... given as footnotes at the bottom of the corresponding page in the final printed text . It is thus essential that bibliographic references are numbered in the order in which they will appear . When citation of a paper is repeated the ...
Contents
ISCHA 013 | 1034 |
Physical organic chemistry | 1035 |
Studies of the reactions of the anhydrosulphites of ahydroxycarboxylic acids Part IV Steric | 1044 |
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2,4-dinitrophenyl absorption acetic acid aci-anion acid anhydrosulphite addition adducts alcohol Amer amine aqueous aromatic ation atom attack bands benzene benzyl bond buffer calculated carbon carbon tetrachloride carbonyl catalysis Chem chloride compounds concentration conformation corresponding decomposition derived dioxan dipole effect electron electrophilic equation ester ethanol ether ethylene experimental Figure first-order formation hydride hydrogen hydrolysis hydroxide hydroxyl interaction isomer k₁ k₂ kinetic leaving group measured mechanism methyl mixture molar mole mole-¹ molecular molecules nitrogen nitromethane NO₂ nucleophilic observed obtained oxidation oxyanions peroxide persulphate phenyl phenylacetic acid phosphate Phys plot proton pyridine R. J. W. Le Fèvre R. O. C. Norman radical anion rate constants ratio reaction reactivity reduction ring rotation showed similar sodium solution solvent solvolysis spectra spectrum splitting constants steric structure studied substituent sulphate radical anion sulphur Table temperature thiophen titanium(III values yield ΣΔε/Σω