Quarterly Journal of the Chemical Society of London, Volume 6 |
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Page 1241
... molecule was the species being reduced requires that the equilibrium between protonated and non - protonated molecules be very rapid at all pH values . Alternatively , the neutral molecules must be the species being reduced . The fact ...
... molecule was the species being reduced requires that the equilibrium between protonated and non - protonated molecules be very rapid at all pH values . Alternatively , the neutral molecules must be the species being reduced . The fact ...
Page 1322
... molecules . Molecule ( 1 ) Cl ... N ( 1 ) Cl ・・・ N ( 11 ) 3.33 3.38 Molecule ( 2 ) Cl ... N ( 1 ) 3.41 Cl . ... N ( III ) 3-42 ( ii ) between 1,1,4,4 - tetraethylpiperazinium and p - nitro- aniline molecules . Molecule ( 1 ) C ( 3 ) ...
... molecules . Molecule ( 1 ) Cl ... N ( 1 ) Cl ・・・ N ( 11 ) 3.33 3.38 Molecule ( 2 ) Cl ... N ( 1 ) 3.41 Cl . ... N ( III ) 3-42 ( ii ) between 1,1,4,4 - tetraethylpiperazinium and p - nitro- aniline molecules . Molecule ( 1 ) C ( 3 ) ...
Page 1535
... molecule suggest that there ON ( 2 ) Quinoid ring of bcdh molecule 179-1 ( 3 ) Complete hmb molecule ( 4 ) Phenyl ring of hmb molecule 122-6 114-7 117-3 Direction cosines ( x 104 ) of planes relative to Perpendicular distance ( Å ) of ...
... molecule suggest that there ON ( 2 ) Quinoid ring of bcdh molecule 179-1 ( 3 ) Complete hmb molecule ( 4 ) Phenyl ring of hmb molecule 122-6 114-7 117-3 Direction cosines ( x 104 ) of planes relative to Perpendicular distance ( Å ) of ...
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