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THE EFFECT OF THE BASE STRENGTH UPON THE STRUCTURE OF THE TRANSITION STATE IN E2 REACTIONS. KINETICS OF ELIMINATIONS FROM 2-ARYLETHYLTRIMETHYLAMMONIUM BROMIDES PROMOTED BY SODIUM PHENOXIDE AND SODIUM M-NITROPHENOXIDE IN N,N-DIMETHYLFORMAMIDE.

Author
ALUNNI S; BACIOCCHI E; PERUCCI P
DEP. CHIM., UNIV. PERUGIA, PERUGIA, ITAL.
Source
J. ORG. CHEM.; U.S.A.; DA. 1977; VOL. 42; NO 2; PP. 205-207; BIBL. 18 REF.
Document type
Article
Language
English
Keyword (fr)
MECANISME E2 CINETIQUE ELIMINATION AMMONIUM QUATERNAIRE COMPOSE SOLVANT ORGANIQUE EFFET ISOTOPIQUE HYDROGENE ISOTOPE DEUTERIUM ETAT TRANSITION FONCTION HAMMETT EFFET SUBSTITUANT REACTION CHIMIQUE EFFET MILIEU SOLUTION BASIQUE AMMONIUM(ARYL-2 ETHYL TRIMETHYL) BROMURE SODIUM PHENOLATE SODIUM PHENOLATE(NITRO-3) DMF CHIMIE ORGANIQUE
Keyword (en)
E2 MECHANISM KINETICS ELIMINATION QUATERNARY AMMONIUM COMPOUND ORGANIC SOLVENT ISOTOPE EFFECT DEUTERIUM TRANSITION STATE HAMMETT FUNCTION SUBSTITUENT EFFECT CHEMICAL REACTION MEDIUM EFFECT BASIC SOLUTION ORGANIC CHEMISTRY
Keyword (es)
QUIMICA ORGANICA
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry

Discipline
General chemistry and physical chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
PASCAL7760267108

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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