The kinetics of the reaction between dimethyldioxirane and 2-methylbut
ane in acetone solutions were studied spectrophotometrically at 25 deg
rees C. The radical-chain induced decomposition of dioxirane proceedin
g with the participation of the carbon-centered radicals follows the f
irst-order kinetic law. The reaction is inhibited by dioxygen. In the
presence of O-2, the dimethyldioxirane consumption is due to the homol
ysis of the O-O bond (at a rate constant of 6.3 . 10(-4) s(-1)) follow
ed by attack of the C-H bond of 2-methylbutane by the biradical formed
. The rate constant of the reaction between the alkyl radical and dime
thyldioxirane was estimated.