Reaction of 2,6-dinitroanisole with cyclohexylamine in toluene-octanol binary solvents. Further support for the 'dimer nucleophile mechanism' in aromatic nucleophilic substitution
The reaction of 2,6-dinitroanisole with cyclohexylamine in toluene, octanol and toluene-octanol mixtures has been studied at several amine concentrations. The reactions in toluene and in octanol-toluene mixtures up to 30% octanol show a third-order kinetic dependence on [amine]. Although the reactio...
Guardado en:
Publicado: |
1993
|
---|---|
Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1472779X_v_n2_p229_Nudelman http://hdl.handle.net/20.500.12110/paper_1472779X_v_n2_p229_Nudelman |
Aporte de: |
Ejemplares similares
-
Reaction of 2,6-dinitroanisole with cyclohexylamine in toluene-octanol binary solvents. Further support for the 'dimer nucleophile mechanism' in aromatic nucleophilic substitution
por: Nudelman, N.S., et al. -
Evidence for A “Dimer” Nucleophile in Aromatic Nucleophilic Substitution
Publicado: (1982) -
Evidence for A “Dimer” Nucleophile in Aromatic Nucleophilic Substitution
por: Sbarbati Nudelman, N., et al. -
The ‘dimer mechanism’ in aromatic nucleophilic substitution by amines in aprotic solvents
Publicado: (1989) -
The ‘dimer mechanism’ in aromatic nucleophilic substitution by amines in aprotic solvents
por: Nudelman, N.S.