Please use this identifier to cite or link to this item:
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKumar, J Anil-
dc.contributor.authorSondu, S-
dc.description.abstractThe kinetics and mechanism of oxidation of chalcone and some substituted chalcones by trichloroisocyanuric acid (TCICA) has been investigated at 313 K in HOAc-HClO₄ medium. The reaction has been found to be first order each in [TCICA] and [Chalcone] and fractional order in [H⁺]. There is no kinetic or spectral evidence for the formation of complex between TCICA and Chalcone. The rate increases with increase in percentage of acetic acid and [Cl⁻]. The products of oxidation have been identified as phenyl acetaldehyde and benzoic acid. The reactive species of oxidant have been established as HOCl and H₂OCl⁺. The rate increases with electron releasing groups in the benzaldehyde moety and vice versa with a Hammett’s ρ value of –0.45. A suitable mechanism involving the chalcone molecule and the reactive species of TCICA in the rate determining step has also been proposed.en_US
dc.relation.ispartofseriesInt. Cl. ⁸ C07B33/00en_US
dc.sourceIJCA Vol.46A(11) [November 2007]en_US
dc.titleKinetics and mechanism of oxidation of chalcones by trichloroisocyanuric acid [TCICA] in HOAc-HClO₄ mediumen_US
Appears in Collections:IJC-A Vol.46A(11) [November 2007]

Files in This Item:
File Description SizeFormat 
IJCA 46A(11) 1792-1795.pdf71.12 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.