Quarterly Journal of the Chemical Society of London, Volume 1 |
From inside the book
Results 1-3 of 80
Page 390
... observed as singlets 1 and 2 which are relatively unreactive . 6 However , several observations have been reported which indicate that the intervention of the organic compound in the reaction scheme involves more than its simple ...
... observed as singlets 1 and 2 which are relatively unreactive . 6 However , several observations have been reported which indicate that the intervention of the organic compound in the reaction scheme involves more than its simple ...
Page 394
... observation ; at slower flow rates the radicals are observed after a larger number of cycles and the effects we have described appear in a more ex- aggerated way . The discussion above can be extended to account for the previously ...
... observation ; at slower flow rates the radicals are observed after a larger number of cycles and the effects we have described appear in a more ex- aggerated way . The discussion above can be extended to account for the previously ...
Page 573
... observed are reversible . Similar effects were observed when sodium was the counter - ion . However , when either potassium or caesium was the counter - ion only comparatively small changes in the spectra were observed over the whole of ...
... observed are reversible . Similar effects were observed when sodium was the counter - ion . However , when either potassium or caesium was the counter - ion only comparatively small changes in the spectra were observed over the whole of ...
Contents
Physical organic chemistry | 1 |
Aromatic reactivity Part XXXVIII Protodesilylation of 12dihydrobenzocyclobutene indan and tetralin | 12 |
Aromatic reactivity Part XL Additional substituent effects in protodetrimethylsilylation | 21 |
Copyright | |
6 other sections not shown
Other editions - View all
Common terms and phrases
absorption acetic acid activation added addition alcohol Amer analysis angles appears aqueous atom base benzene bond bromide calculated carbon carbon tetrachloride Chem chemical chloride compared complex compounds concentration conformation constants containing corresponding coupling derived described determined DISCUSSION effect electron energy equation esters ethanol ether expected experimental experiments factor Figure followed formation formed further gave give given hydrogen hydrolysis increase indicate initial intermediate involving kinetic less measured mechanism method methyl mixing mixture mole molecular molecule nitration observed obtained occurs organic oxidation oxygen peaks peroxide Phys plot position possible prepared present pressure proton radical rate constants ratio reaction reactivity reduced relative reported requires resonance respectively ring salts shifts showed shown similar sodium solution solvent spectra spectrum structure studied substituent suggested Table temperature values yield