Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/41842
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dc.contributor.authorBrahrnaiah, A-
dc.contributor.authorManikyamba, P-
dc.date.accessioned2017-05-18T09:10:47Z-
dc.date.available2017-05-18T09:10:47Z-
dc.date.issued1991-03-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/41842-
dc.description247-251en_US
dc.description.abstractOxidation of diphenylamines (DPA) by iodate in aqueous methanol (70%, v/v) at 303 K is first order in [oxidant] and fractional order in [DPA] and is acid-catalysed. There is a dipole-dipole interaction between the oxidant and DPA. The substituent effect on the rate of reaction shows that electron- releasing groups on the benzene ring enhance the rate and electron-withdrawing groups retard the rate compared to the unsubstituted DPA. The product identified is the corresponding carbazole. Thermodynamic parameters are calculated and a suitable mechanism is proposed.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.30A(03) [March 1991]en_US
dc.titleOxidation of diphenylamines by iodate - A kinetic studyen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.30A(03) [March 1991]

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