Elimination mechanisms. Position of proton and substituent effects upon geometry in E2 transition states

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Veröffentlicht in:	Journal of the American Chemical Society 1967-11, Vol.89 (24), p.6149-6156
Hauptverfasser:	Steffa, Louis J, Thornton, Edward R
Format:	Artikel
Sprache:	eng
Schlagworte:	AMMONIUM COMPOUNDS, SUBSTITUTED/ dimethylphenethylphenylammonium bromide, reactions in deuterated and normal water, mechanism of isotope eff AMMONIUM COMPOUNDS, SUBSTITUTED/ trimethylphenethylammonium bromide, reactions in deuterated and normal water, mechanism of isotope effects in elimination AMMONIUM COMPOUNDS- ETHYL RADICALS- METHYL RADICALS AMMONIUM COMPOUNDS- ETHYL RADICALS- METHYL RADICALS- ORGANIC CHLORINE COMPOUNDS BENZENE, (2- BROMOETHYL)-/reactions in deuterated or normal water and dioxane mixtures, mechanism of isotope effects in elimination BENZENE- ETHERS- ETHYL RADICALS- SOLVENTS CHEMICAL REACTIONS DEUTERIUM DEUTERIUM/effects on elimination reactions of $beta$-phenethyl derivatives in deuterated and normal water, mechanism of DIOXANE DIOXANE/dioxane-D$sub 2$O, reactions with (2-bromoethyl)benzene, mechanisms of isotope effects in elimination DIOXANE/dioxane-H$sub 2$O, reactions with (2- bromoethyl)benzene, mechanisms of isotope effects in elimination HEAVY WATER ISOTOPE EFFECTS METHYL RADICALS- ORGANIC SULFUR COMPOUNDS N20220 -Chemistry-Inorganic, Organic, & Physical Chemistry-Isotopic Effects ORGANIC BROMINE COMPOUNDS PHENYL RADICALS REACTION KINETICS WATER AMMONIUM COMPOUNDS- METHYL RADICALS WATER-d$sub 2$/dioxane-D$sub 2$O, reactions with (2-bromoethyl)benzene, mechanisms of isotope effects in elimination WATER-d$sub 2$/reactions with $beta$-phenethyl derivatives, mechanisms of isotope effects in elimination
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ISSN:	0002-7863 1520-5126
DOI:	10.1021/ja01000a026