Quarterly Journal of the Chemical Society of London, Volume 1 |
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Results 1-3 of 81
Page 293
... containing sodium ( 0-04 g . ) was electrolysed in cell A until the electrolyte became slightly alkaline ( after passage of ca. 2 faraday equiv . ) . Work - up as in the preceding electrolysis yielded a liquid residue ( 2-3 g . ) . This ...
... containing sodium ( 0-04 g . ) was electrolysed in cell A until the electrolyte became slightly alkaline ( after passage of ca. 2 faraday equiv . ) . Work - up as in the preceding electrolysis yielded a liquid residue ( 2-3 g . ) . This ...
Page 438
... containing an excess of 2 - chloropropene , perchloric acid ( 0-10м ) , and silver perchlorate ( 0.00 , 0.01 , and 0.05M ) . Chloroacetone was extracted from each and the activity was determined by counting a standard solution in ...
... containing an excess of 2 - chloropropene , perchloric acid ( 0-10м ) , and silver perchlorate ( 0.00 , 0.01 , and 0.05M ) . Chloroacetone was extracted from each and the activity was determined by counting a standard solution in ...
Page 501
... containing the endocyclic bond and perpendicular to the benzene ring ; BF ' , containing the exocyclic bond and per- pendicular to the mean plane through atoms ABCF'A'E ' close to the centres of the bonds are 0.16 , 0.12 , 0.10 , and ...
... containing the endocyclic bond and perpendicular to the benzene ring ; BF ' , containing the exocyclic bond and per- pendicular to the mean plane through atoms ABCF'A'E ' close to the centres of the bonds are 0.16 , 0.12 , 0.10 , and ...
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