Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 36
... wave is due to a Radiolysis of myo - Inositol Solutions By W. J. Criddle. for the second and third waves were read ... wave at low pH values is in agreement with this theory , but the decrease in the height of the second wave is not ...
... wave is due to a Radiolysis of myo - Inositol Solutions By W. J. Criddle. for the second and third waves were read ... wave at low pH values is in agreement with this theory , but the decrease in the height of the second wave is not ...
Page 89
... wave for the 4 - electron reduction of 4 - nitrotoluene 13 was found to be four times as high as wave I in 18.5-20N- acid and twice as high as wave I in 23-24N - acid . ( Both waves were compared at the same acid concentration or their ...
... wave for the 4 - electron reduction of 4 - nitrotoluene 13 was found to be four times as high as wave I in 18.5-20N- acid and twice as high as wave I in 23-24N - acid . ( Both waves were compared at the same acid concentration or their ...
Page 90
... wave analysis difficult , but it did show that the reduction involves 1 ± 0 · 1 electron . TABLE 2 The dependence of the half - wave potential of wave II on the concentration of triphenylmethanol ethanol , E of AII ' is slightly more ...
... wave analysis difficult , but it did show that the reduction involves 1 ± 0 · 1 electron . TABLE 2 The dependence of the half - wave potential of wave II on the concentration of triphenylmethanol ethanol , E of AII ' is slightly more ...
Contents
Physical organic chemistry | 1 |
Topochemistry Part XXX Crystal and molecular structures of chalcone | 11 |
Conformational studies Part I Crystal and molecular structures of cis12dipchlorobenzoyl and cis | 17 |
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4-nitroaniline A. R. Katritzky acetic acid activation energy alcohol Amer amine anion aqueous aromatic aryl-methyl ation axial benzene bond bond dissociation energies bromination calculated carbanion carbon acids catalyst Chem chemical shifts Chemistry chloride compounds concentration conformation corresponding coupling constants crystal cyclohexane derivatives deviations dilute dimethyl sulphoxide dipole electron equation ether ethylene experimental Figure fluorene formation fraction H₂O hydrocarbons hydroxide increase indicators interactions intermediate ionisation isomer isomerization isotope effect k₁ k₂ kcal kcal./mole kinetic Mc./sec measured mechanism methanol methyl mixture mole mole-¹ molecular molecules n.m.r. spectra nitrogen nucleophilic observed obtained oxide oxygen parameters phenyl Phys piperidine proton pyridines R. P. Bell radical rate constants ratio reaction relative ring selenophen shown shows signal sodium solution solvent spectrum structure substituted t-butyl Table temperature Tetrahedron thiophen transition tri-o-thymotide triethylamine triphenylmethane wave