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Abstrakty
The kinetics of oxidation of benzaldehyde by sodium perborate in an acetic acid medium have been studied. The reaction is first order with respect to both oxidant concentration and to the substrate. Hydrogen ion accelerates the rate of reaction. Amechanism involving the formation of an unstable perborate ester, which decomposes to the reaction products, has been suggested. The activation parameters associated with the rate-determining step have been calculated. The effects of various functional groups on the ring at the meta, and para positions of benzaldehyde have also been examined.
Wydawca
Czasopismo
Rocznik
Tom
Strony
437--445
Opis fizyczny
Bibliogr. 31 poz., rys.
Twórcy
autor
- Department of Chemistry, Faculty of Science, Ain Shams University, Cairo, Egypt
Bibliografia
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0023-0190