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Title: Recoil tritium reactions with cyclohexene and alkenes. Determination of rate parameters

Journal Article · · J. Phys. Chem., v. 78, no. 4, pp. 347-354
DOI:https://doi.org/10.1021/j100597a006· OSTI ID:4371995

Kinetic rate parameters can be determined from recoil tritium reaction studies although the energy distribution of the reacting tritium atoms is not known. T is produced by /sup 3/He(n,p)T. Recoil T-for-H substitution on cyclohexene gives excited cyclohexene-t molecules. The dependence of product yield on pressure (in the hexene-t molecules decomposed unimolecularly to give ethylene-t and butadiene-t with an apparent rate constant (at 135 deg ) of 5 x 10/ sup 6/ s/sup -1/. The s parameter in the RRK (Rice, Ramsperger, and Kassel) treatment of the unimolecular decomposition of cyclohexene was determined as s = 24. Similarly, the pressure dependence of product yield showed that cyclohexyl-t radicals which are fornaed by recoil T atom addition to cyclohexene decomposed unimolecularly to give n-hexene-t, 1-butene-t, and methane-t with rate constant 8 x 10/sup 3/, 3 x 10/sup 4/, and 5 x 10/sup 2/ s/sup -1/, respectively . The relative nate of abstraction vs addition of radicals in alkenes was determined from the scavenger dependence of the yields of products with a nadical precursor. (40 references) (auth)

Research Organization:
Univ. of California, Berkeley, CA (United States)
Sponsoring Organization:
USDOE
NSA Number:
NSA-29-018206
OSTI ID:
4371995
Journal Information:
J. Phys. Chem., v. 78, no. 4, pp. 347-354, Other Information: Orig. Receipt Date: 30-JUN-74
Country of Publication:
Country unknown/Code not available
Language:
English