Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/46779
Title: Structure-reactivity correlations in the reaction of substituted N-methyl- 2-styrylpyridinium iodides with alkaline hydrogen peroxide
Authors: Shunmugasundaram, A
Thanulingam, T Lekshmana
Murugesan, R
Issue Date: Aug-1989
Publisher: NISCAIR-CSIR, India
Abstract: The kinetics of reaction between N-methyl-2-styrylpyridinium iodides and alkaline hydrogen peroxide have been studied spectrophotometrically in 1:1 (v/v) water-methanol mixture. The reaction is first order in [substrate], [H2O2] and [OH-]. Structure-reactivity study with various 2'- and 4'-substituted N-methyl-2-styrylpyridinium iodides shows that the reaction is accelerated by electron-withdrawing substituents and retarded by electron-releasing substituents. A Hammett ρ-value of +0.916 ± 0.064 (r = 0.988; s = 0.063) is obtained. A suitable mechanism involving the attack of hydroperoxide ion on the β-carbon atom of the substrate to form epoxide in a slow step followed by cleavage of epoxide is proposed. Analysis of ortha-effects using multiparameter extensions of the Hammett equation in the reaction of 2'-substituted-N-methyl-2-styrylpyridinium iodides with alkaline hydrogen peroxide shows that both localised and delocalised effects are important and the steric effect is insignificant.
Page(s): 666-669
URI: http://nopr.niscair.res.in/handle/123456789/46779
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.28A(08) [August 1989]

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