En:
Molecules 2000;5(3):401-402
Fecha:
2000
Formato:
application/pdf
Tipo de documento:
info:eu-repo/semantics/article
info:ar-repo/semantics/artículo
info:eu-repo/semantics/publishedVersion
Idioma:
eng
Descripción:
The kinetics of the reaction of 2,4-dinitrochlorobenzene (DNClB) with aniline and substituted anilines such as p-anisidine, p-toluidine and N-methylaniline have been studied in toluene. Except for N-methylaniline the reactions have shown a third order in amine rate dependence which is consistent with aggregates of the amine acting as the nucleophile. On the other hand, the reaction of DNClB with N-methylaniline under the same conditions shows a linear dependence of the second order rate coefficient, kA, vs [amine], which is consistent with the previous mechanism.
Derechos:
info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar

Descargar texto: paper_14203049_v5_n3_p401_Alvaro.oai (tamaño kb)

Cita bibliográfica:

Alvaro, C.E.S. (2000). Reaction of 2,4-dinitrochlorobenzene with aromatic amines in toluene: Effect of nucleophile structure  (info:eu-repo/semantics/article).  [consultado:  ] Disponible en el Repositorio Digital Institucional de la Universidad de Buenos Aires:  <http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&cl=CL1&d=paper_14203049_v5_n3_p401_Alvaro_oai>