Issue 16, 1971

The ordering of carbon–hydrogen bond strengths using isotope effects

Abstract

Variations in the tritium isotope effects in the radical addition of R1SH to R2R3C[double bond, length as m-dash]CH2 are interpreted in terms of the transition state symmetry, measured by the difference in bond strengths to hydrogen in the initial state (R1S–H) and the final state (H–CR2R3CH2SR1).

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 941-942

The ordering of carbon–hydrogen bond strengths using isotope effects

E. S. Lewis and M. M. Butler, J. Chem. Soc. D, 1971, 941 DOI: 10.1039/C29710000941

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