Relative rate constants for the reactions of hydroxyl radicals with a series of alkyl substituted olefins were measured by competitive reactions between pairs of olefins a t 298 r 2 K and 1 atmospheric pressure. Hydroxyl radicals were produced by the photolysis of H,O, with 254-nm irradiation. The o
Rate constants for the reactions of alkyl radicals with 1,4-cyclohexadiene
β Scribed by J. A. Hawari; P. S. Engel; D. Griller
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 220 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
An electron paramagnetic resonance (EPR) technique was used to show that simple alkyl radicals readily abstract hydrogen from l,4-cyclohexadiene. Rate constants for the reaction were ca. 104-105 M-' s-' at 300 K and activation energies 5-7 kcal mol-'. For the stabilized radicals, ally1 and benzyl, the rate constants were <lo2 M-' s at 300 K. The data suggest that 1,4-cyclohexadiene could be used as an effective trap to probe rearrangement reactions of carbon centered radicals and biradicals.
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## Abstract Rate constants for the reactions of Cl atoms with two cyclic dienes, 1,4βcyclohexadiene and 1,5βcyclooctadiene, have been determined, at 298 K and 800 Torr of N~2~, using the relative rate method, with __n__βhexane and 1βbutene as reference molecules. The concentrations of the organics