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Amines as leaving groups in nucleophilic aromatic substitution reactions. II. Hydrolysis of N ‐(2,4,6‐trinitrophenyl)amines
Author(s) -
De Vargas Elba B.,
De Rossi Rita H.
Publication year - 1989
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/poc.610020703
Subject(s) - chemistry , picrate , morpholine , piperidine , stoichiometry , reaction rate constant , nucleophile , hydrolysis , amine gas treating , nucleophilic substitution , medicinal chemistry , substitution reaction , decomposition , kinetics , equilibrium constant , ion , kinetic energy , photochemistry , inorganic chemistry , organic chemistry , catalysis , physics , quantum mechanics
The hydrolysis reactions of N ‐(2,4,6‐trinitrophenyl)piperidine ( 2 ) and N ‐(2,4,6‐trinitrophenyl)‐morpholine ( 3 ) were studied. Two kinetic processes well separated in time are observed in both reactions. The fastest process, which is reversible, leads to the formation of a species of λ max 260 and 410 nm and is attributed to the formation of a σ complex of stoichiometry 1 : 2 due to the addition of a second HO − to the σ complex of 1 : 1 stoichiometry. The slowest process leads quantitatively to picrate ion. The equilibrium constants for the formation of the σ complexes of 1:1 and 1:2 stoichiometries and the rate of formation and decomposition of the latter complex were determined. The kinetic data for the slow process lead to the conclusion that the picrate ion is formed from the attack of HO − on the two σ complexes, confirming previous findings. There are some differences in the calculated rates for 2 and 3 which may be an indication that the elimination of the amine is partially rate determining.