Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/45999
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dc.contributor.authorSikkandar, G-
dc.contributor.authorAhamed, K A Basheer-
dc.contributor.authorKannan, S-
dc.date.accessioned2019-03-18T06:33:04Z-
dc.date.available2019-03-18T06:33:04Z-
dc.date.issued1992-11-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/45999-
dc.description845-848en_US
dc.description.abstractKinetics of oxidation of unsubstituted and substituted γ-oxoacids by acid permanganate in aqueous acetic acid medium have been studied at high and low [H3O+]. At high [H3O+], the reaction is first order each in [oxoacid], [MnO] and [H3O+]. At low [H3O+], the reaction is zero order in [MnO] and first order each in [H3O+] and the [oxoacid].Variation in ionic strength of the reaction medium has no significant effect on the rate of oxidation. But the rate of the reaction is enhanced by lowering the dielectric

constant of the reaction medium. Electron-releasing substituents in the aromatic ring accelerate the reaction rates and electron-withdrawing substituents retard them. The value of the reaction constant (ρ) at 303 K (at [H3O+] = 1M) obtained from the Hammett's plot is -1.49 (corr. coeff. = 0.998). A mechanism consistent with the observed results has been suggested and the related rate laws deduced. Activation parameters have been 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(11) [November 1992]en_US
dc.titleKinetics and mechanism of oxidation of γ-oxoacids by acid permanganateen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.31A(11) [November 1992]

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