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...

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Autores principales: Nudelman, N.S., Palleros, D.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00223263_v48_n10_p1613_Nudelman
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
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spelling todo:paper_00223263_v48_n10_p1613_Nudelman2023-10-03T14:31:17Z Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism Nudelman, N.S. Palleros, D. 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar 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.
format JOUR
author Nudelman, N.S.
Palleros, D.
spellingShingle Nudelman, N.S.
Palleros, D.
Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism
author_facet Nudelman, N.S.
Palleros, D.
author_sort Nudelman, N.S.
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
url http://hdl.handle.net/20.500.12110/paper_00223263_v48_n10_p1613_Nudelman
work_keys_str_mv AT nudelmanns reactionof24dinitrofluorobenzenewithoanisidineinbenzenefurtherevidenceofthedimermechanism
AT pallerosd reactionof24dinitrofluorobenzenewithoanisidineinbenzenefurtherevidenceofthedimermechanism
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