Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 267
... prepared by reduction of the methyl ester with lithium aluminium hydride , 30 and for the preparation of [ xx - 2H2 ] ... prepared by exchanging the 9 - methyl ester of fluorene several times with a solution of potassium carbonate in DO ...
... prepared by reduction of the methyl ester with lithium aluminium hydride , 30 and for the preparation of [ xx - 2H2 ] ... prepared by exchanging the 9 - methyl ester of fluorene several times with a solution of potassium carbonate in DO ...
Page 366
... prepared by dehydration of Cu ( salgly ) , 5H2O and 1.56 B.M. when prepared by dehydration of Cu ( salgly ) , 1.5H2O , and suggested that antiferromagnetic spin interaction by way of dimeric structures could explain these anomalously ...
... prepared by dehydration of Cu ( salgly ) , 5H2O and 1.56 B.M. when prepared by dehydration of Cu ( salgly ) , 1.5H2O , and suggested that antiferromagnetic spin interaction by way of dimeric structures could explain these anomalously ...
Page 622
... prepared by the method of Ziegler and his co - workers , 24 1 - chloro - 2 - trichloromethylcyclohexane following Goldwhite , Gibson , and Harris , 25 and 3,3 ' - bicyclohexene by Berlande's procedure.26 3 - Cyclohexenylisobutylamine ...
... prepared by the method of Ziegler and his co - workers , 24 1 - chloro - 2 - trichloromethylcyclohexane following Goldwhite , Gibson , and Harris , 25 and 3,3 ' - bicyclohexene by Berlande's procedure.26 3 - Cyclohexenylisobutylamine ...
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