Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/62459
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dc.contributor.authorMeena, Anita-
dc.date.accessioned2023-08-16T13:02:58Z-
dc.date.available2023-08-16T13:02:58Z-
dc.date.issued2023-08-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/62459-
dc.description803-807en_US
dc.description.abstractThe kinetics of oxidation of cinnamyl alcohol by N-chloro-p-toluene sulphonamide (Chloramine-T) in an aqueous acid medium has been studied. The reaction is first order with respect to the oxidant but exhibits rate independence of substrate concentration. Rate is retarded by hydrogen ion concentration due to protonation of Chloramine-T. The product toluene-psulphonamide does not affect the rate of reaction. The cinnamyl aldehyde has been observed to be the oxidation product spectrally.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.62(08) [August 2023]en_US
dc.subjectKinetics, Mechanismen_US
dc.subjectOxidationen_US
dc.subjectCinnamyl Alcoholen_US
dc.subjectChloramine-Ten_US
dc.titleKinetics and mechanism of oxidation of cinnamyl alcohol by N-chloro p-toluene sulphonamide (Chloramine-T) in acid perchlorate mediumen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i8.87en_US
Appears in Collections:IJC Vol.62(08) [August 2023]

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