Abstract:
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.
Referencias:
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Citas:
---------- APA ----------
Nudelman, N.S. & Palleros, D.
(1983)
. Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism. Journal of Organic Chemistry, 48(10), 1613-1617.
http://dx.doi.org/10.1021/jo00158a008---------- CHICAGO ----------
Nudelman, N.S., Palleros, D.
"Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism"
. Journal of Organic Chemistry 48, no. 10
(1983) : 1613-1617.
http://dx.doi.org/10.1021/jo00158a008---------- MLA ----------
Nudelman, N.S., Palleros, D.
"Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism"
. Journal of Organic Chemistry, vol. 48, no. 10, 1983, pp. 1613-1617.
http://dx.doi.org/10.1021/jo00158a008---------- VANCOUVER ----------
Nudelman, N.S., Palleros, D. Reaction of 2,4-Dinitrofluorobenzene with o-Anisidine in Benzene. Further Evidence of the “Dimer” Mechanism. J. Org. Chem. 1983;48(10):1613-1617.
http://dx.doi.org/10.1021/jo00158a008