Kinetic evidence for a methanolysis intermediate in aromatic nucleophilic substitution

The reactions of 2,4- and 2,6-dinitrochlorobenzene and 2,4-dinitroanisole with cyclohexylamine in benzene and in methanol have been examined. Computer analysis of the kinetic data shows the formation and fate of a solvolysis product in the reaction of 2,4-dinitrochlorobenzene in methanol. The result...

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Detalles Bibliográficos
Autores principales:	Nudelman, N.S., Garrido, D.
Formato:	JOUR
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_1472779X_v_n11_p1256_Nudelman
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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