The oxidation of E-5-decene by potassium permanganate in slightly acidic aqueous acetone solutions has been studied. An analysis of the reaction mixture at various time intervals indicates that the ketol, 5-hydroxy-6-decanone, is the initially formed product under these conditions. The other major product, 5,6-decanedione, is formed sequentially from oxidation of the ketol rather than directly from the alkene.
CITATION STYLE
Lee, D. G., & Srinivasan, N. S. (1981). Oxidation of hydrocarbons. X. Concerning the formation of ketols and diones during the oxidation of alkenes by permanganate ion. Canadian Journal of Chemistry, 59(14), 2146–2149. https://doi.org/10.1139/v81-309
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