Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/20202
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dc.contributor.authorReddy, S Ranga-
dc.contributor.authorKalyani, P-
dc.contributor.authorManikyamba, P-
dc.date.accessioned2013-07-30T07:09:05Z-
dc.date.available2013-07-30T07:09:05Z-
dc.date.issued2005-09-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/20202-
dc.description1831-1833en_US
dc.description.abstractThe kinetics of the reaction of allyl bromide with benzoyl thiosemicarbazide has been studied in different protic and aprotic solvents. Correlation of rate constants with different solvent parameters applying linear multiple regression analysis indicates that the non-specific solvent parameters Y, P and nucleophilicity, B, influence the rate of nucleophilic substitution. Using these solvent parameters, the linear solvation energy relationship is derived. Study of the reaction with substituted thiosemicarbazides indicates that structural effects on rate of the reaction are minimal.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.44A(09) [September 2005]en_US
dc.titleEffect of solvents and nucleophiles on the reactivity of allyl bromide — A kinetic studyen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.44A(09) [September 2005]

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