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Relation of chemical structure to reactivity in complete oxidation on oxide contact catalysts for open-chain hydrocarbons

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Abstract

It is shown that the relative reactivities of alkanes, alkenes, alkynes, and cyclopropane in complete oxidation decreases with increase in the energy of the bond broken in the rate-limiting step: for alkanes from ethane upwards this is a C-C bond, for unsaturated hydrocarbons it is the π-type C-C bond, and for methane it is a C-H bond.

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Golodets, G.I., Pyatnitskii, Y.I. & Goncharuk, V.V. Relation of chemical structure to reactivity in complete oxidation on oxide contact catalysts for open-chain hydrocarbons. Theor Exp Chem 3, 505–507 (1971). https://doi.org/10.1007/BF00523717

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  • DOI: https://doi.org/10.1007/BF00523717

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