Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/41469
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dc.contributor.authorKamble, D L-
dc.contributor.authorChougale, R B-
dc.contributor.authorNandibewoor, S T-
dc.date.accessioned2017-04-27T05:45:55Z-
dc.date.available2017-04-27T05:45:55Z-
dc.date.issued1996-10-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41469-
dc.description865-869en_US
dc.description.abstractThe title reaction is carried out in aqueous alkaline medium and is first order in (NBS] both in the presence and absence of ruthenium(III) catalyst. However, the order in [allyl alcohol] is unity in the absence and fractional in the presence of Ru(III) catalyst. Increase in [OH-] accelerates the reaction rate while the added succinimide retards the reaction rate in both the cases. Increase in the ionic strength and t-butanol content in the reaction medium have negligible effect in both the cases. A mechanism involving the hypobromate ion as the reactive species of the oxidant has been proposed. The reaction constants of individual steps of reaction mechanism have been evaluated.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.35A(10) [October 1996]en_US
dc.titleKinetics and mechanism of uncatalyzed and ruthenium(lll) catalyzed oxidation of allyl alcohol by N-bromosuccinimide in aqueous alkaline mediumen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.35A(10) [October 1996]

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