Quarterly Journal of the Chemical Society of London, Volume 1 |
From inside the book
Results 1-3 of 76
Page 922
... reaction mixture . However , if the reaction is heated under reflux for 2 days triethylenediamine hydrochloride , chloro- form , and 2 - chlorotriethylenediamine can be identified in the mixture . Reaction of NN - Dimethylbenzylamine ...
... reaction mixture . However , if the reaction is heated under reflux for 2 days triethylenediamine hydrochloride , chloro- form , and 2 - chlorotriethylenediamine can be identified in the mixture . Reaction of NN - Dimethylbenzylamine ...
Page 923
... reaction and are best interpreted as arising from the reaction of the trichloromethyl radical with cyclo- hexene . The reaction of triethylenediamine was investigated to observe what effect the rigid cage structure had on the rate and ...
... reaction and are best interpreted as arising from the reaction of the trichloromethyl radical with cyclo- hexene . The reaction of triethylenediamine was investigated to observe what effect the rigid cage structure had on the rate and ...
Page 924
... reaction of NN- dimethylbenzylamine which suggests that reactions involving dichlorocarbene are of no significance in the reactions of secondary amines and carbon tetrachloride . The secondary reactions of tertiary amines resemble those ...
... reaction of NN- dimethylbenzylamine which suggests that reactions involving dichlorocarbene are of no significance in the reactions of secondary amines and carbon tetrachloride . The secondary reactions of tertiary amines resemble those ...
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 |
23 other sections not shown
Other editions - View all
Common terms and phrases
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