Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/39994
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dc.contributor.authorVeeraiah, T-
dc.contributor.authorSondu, S-
dc.date.accessioned2017-02-01T09:34:32Z-
dc.date.available2017-02-01T09:34:32Z-
dc.date.issued1998-04-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/39994-
dc.description328-330en_US
dc.description.abstractThe kinetics and mechanism of oxidation of some heterocyclic aldehydes viz. furan-2-aldehyde, pyrrole-2-aldehyde and thiophene-2-aldehyde by acid bromate in H2SO4 - HOAc medium have been studied. The reaction is first order each in [BrO3 -] and [substrate] and second order in [H+]. The products of oxidation are the corresponding carboxylic acids. From the study of effect of hetero atom of the molecule on rate, HBrO3 and protonated heteroaldehyde have been established as the reactive species. The order of reactivity is found to be furan-2-aldehyde > pyrrole-2- aldehyde> thiophene-2-aldehyde. A suitable mechanism has 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.37A(04) [April 1998]en_US
dc.titleKinetics and mechanism of oxidation of heterocyclic aldehydes by acid bromateen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.37A(04) [April 1998]

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