Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism
The reaction of 2,4-dinitrofluorobenzene with o-anisidine (B) in benzene exhibits a quadratic dependence of the observed second-order rate coefficient, kA, with [B], and similar behavior is found in the reaction with p-anisidine, as was previously reported in the literature. The kinetic results are...
Guardado en:
Autor principal: | |
---|---|
Publicado: |
1983
|
Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v48_n10_p1613_Nudelman http://hdl.handle.net/20.500.12110/paper_00223263_v48_n10_p1613_Nudelman |
Aporte de: |
id |
paper:paper_00223263_v48_n10_p1613_Nudelman |
---|---|
record_format |
dspace |
spelling |
paper:paper_00223263_v48_n10_p1613_Nudelman2023-06-08T14:49:26Z Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism Palleros, Daniel Ricardo The reaction of 2,4-dinitrofluorobenzene with o-anisidine (B) in benzene exhibits a quadratic dependence of the observed second-order rate coefficient, kA, with [B], and similar behavior is found in the reaction with p-anisidine, as was previously reported in the literature. The kinetic results are interpreted in terms of a “dimer” nucleophile, B:B, which forms a cyclic intermediate with the substrate. This interpretation is confirmed by the data of the reaction run in the presence of varying amounts of pyridine, where an additional mixed adduct, B:P, is present. © 1983, American Chemical Society. All rights reserved. Fil:Palleros, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1983 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v48_n10_p1613_Nudelman http://hdl.handle.net/20.500.12110/paper_00223263_v48_n10_p1613_Nudelman |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
description |
The reaction of 2,4-dinitrofluorobenzene with o-anisidine (B) in benzene exhibits a quadratic dependence of the observed second-order rate coefficient, kA, with [B], and similar behavior is found in the reaction with p-anisidine, as was previously reported in the literature. The kinetic results are interpreted in terms of a “dimer” nucleophile, B:B, which forms a cyclic intermediate with the substrate. This interpretation is confirmed by the data of the reaction run in the presence of varying amounts of pyridine, where an additional mixed adduct, B:P, is present. © 1983, American Chemical Society. All rights reserved. |
author |
Palleros, Daniel Ricardo |
spellingShingle |
Palleros, Daniel Ricardo Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism |
author_facet |
Palleros, Daniel Ricardo |
author_sort |
Palleros, Daniel Ricardo |
title |
Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism |
title_short |
Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism |
title_full |
Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism |
title_fullStr |
Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism |
title_full_unstemmed |
Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism |
title_sort |
reaction of 2,4-dinitrofluorobenzene with o-anisidine in benzene. further evidence of the “dimer” mechanism |
publishDate |
1983 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v48_n10_p1613_Nudelman http://hdl.handle.net/20.500.12110/paper_00223263_v48_n10_p1613_Nudelman |
work_keys_str_mv |
AT pallerosdanielricardo reactionof24dinitrofluorobenzenewithoanisidineinbenzenefurtherevidenceofthedimermechanism |
_version_ |
1768545130052059136 |