Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46768
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dc.contributor.authorShunmugasundaram, A-
dc.contributor.authorChandrasekaran, C R-
dc.date.accessioned2019-03-26T09:37:43Z-
dc.date.available2019-03-26T09:37:43Z-
dc.date.issued1989-08-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46768-
dc.description707-708en_US
dc.description.abstractThe second order rate constants in the title reactions in 90% acetone-10% water (v/v) mixture at three different temperatures indicate that electron-releasing substituents accelerate the rate while electron-withdrawing substituents retard the rate. A good Hammett correlation with σp constants is obtained for ortho-substituted cinnamate ions. The rate data have also been analysed using

the method of Charton.
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.28A(08) [August 1989]en_US
dc.titleStructure-reactivity correlations in the reactions of phenacyl bromide and ethyl bromoacetat with ortho-substituted cinnamate ionsen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(08) [August 1989]

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