Quarterly Journal of the Chemical Society of London, Volume 1 |
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Page 123
... formed , although the yield decreased substantially with increase in [ P ] . Hydrogen fluoride was observed as a product by the etching of the glass vessel during each experiment . Correlation Between Rate - constants and Product Yields ...
... formed , although the yield decreased substantially with increase in [ P ] . Hydrogen fluoride was observed as a product by the etching of the glass vessel during each experiment . Correlation Between Rate - constants and Product Yields ...
Page 182
... formation , is both formed and oxidised exceptionally rapidly . These radicals are also formed by addition of the hydroxyl radical to oximes , at both pH 1 and 9 , and analogous radicals are formed by the addition of the amino - radical ...
... formation , is both formed and oxidised exceptionally rapidly . These radicals are also formed by addition of the hydroxyl radical to oximes , at both pH 1 and 9 , and analogous radicals are formed by the addition of the amino - radical ...
Page 504
... formed when com- pounds ( I ) and ( III ) are subjected to electron impact . The molecular ions of compounds ( I ) and ( III ) would not be expected to isomerise totally to the molecular ion of compound ( II ) and certain of the ions formed ...
... formed when com- pounds ( I ) and ( III ) are subjected to electron impact . The molecular ions of compounds ( I ) and ( III ) would not be expected to isomerise totally to the molecular ion of compound ( II ) and certain of the ions formed ...
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 | |
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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