Quarterly Journal of the Chemical Society of London, Volume 1 |
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Results 1-3 of 81
Page 198
... experiments where a phenol was produced , the absorbance contribution from this was measured separately , with a solution prepared by alkaline hydrolysis of ester with identical initial concentration to that used in the main experiment ...
... experiments where a phenol was produced , the absorbance contribution from this was measured separately , with a solution prepared by alkaline hydrolysis of ester with identical initial concentration to that used in the main experiment ...
Page 427
... experiments 15 and 16 ) , the likely explanation being that , while protodeplumbyl- ation is the major route to anisole early in the reaction , it is later superseded by a route involving the p - anisyl radical . Secondly , the yield of ...
... experiments 15 and 16 ) , the likely explanation being that , while protodeplumbyl- ation is the major route to anisole early in the reaction , it is later superseded by a route involving the p - anisyl radical . Secondly , the yield of ...
Page 478
... experiments were carried out with the common splitting J3.5 and also with J. , and the experiments were repeated with com- pounds ( I ) and ( II ) , the results being the same for each compound . The decoupling experiments show that the ...
... experiments were carried out with the common splitting J3.5 and also with J. , and the experiments were repeated with com- pounds ( I ) and ( II ) , the results being the same for each compound . The decoupling experiments show that the ...
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