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dc.contributor.authorKarunakaran, K.-
dc.contributor.authorGurumurthy, R.-
dc.contributor.authorElango, K. P.-
dc.date.accessioned2017-05-08T08:51:32Z-
dc.date.available2017-05-08T08:51:32Z-
dc.date.issued1997-11-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41659-
dc.description984-986en_US
dc.description.abstractThe kinetics of oxidation of (phenylthio) acetic acid and few para-substituted (phenylthio)acetic acids by vanadium(V) and iron(III) have been studied in acid medium. In both the cases, the order in substrate and oxidant is one each. Both the reactions are catalysed by hydrogen ions and follow a free radical path. A high negative. ρ value (-3.64) is obtained in the case of vanadium(V) oxidation and the product is the corresponding diphenyldisulphide. The ρ value obtained in the iron(III) oxidation is  -1.22 and the identified product is its sulphoxide. On the basis of the kinetic results suitable mechanisms have been proposed and discussed.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.36A(11) [November 1997]en_US
dc.titleDuality on the oxidation of (phenylthio)acetic acids by vanadium (V) and iron (III)en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.36A(11) [November 1997]

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