Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/45972
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dc.contributor.authorManikyamba, P-
dc.date.accessioned2019-03-18T04:29:15Z-
dc.date.available2019-03-18T04:29:15Z-
dc.date.issued1992-12-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/45972-
dc.description959-962en_US
dc.description.abstractThe kinetics of nucleophilic substitution on benzyl bromide by s-triazole has been studied in different pure (protic and aprotic) solvents. The reaction is overall second order, with first order dependence on [benzyl bromide] and the [nucleophile].The rate data is correlated with different solvent parameters using linear multiple regression analysis. From the regression coefficients, information on the solvent-reactant and the solvent-intermediate interactions is obtained and the solvation models are proposed. The reaction has also been studied at different temperatures and the thermodynamic parameters H≠, S≠ and G≠ are computed.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.31A(12) [December 1992]en_US
dc.titleSolvation models in the reaction between benzyl bromide and s-triazole dictions of the reaction mechanisms have been obtained from such studies.en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.31A(12) [December 1992]

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