The reactions of 1,1,3,3-tetramethylbutyl (tert-octyl) peroxypivalate (1) with methyl methacrylate (MMA) and styrene in the presence of the free radical scavenger 1,1,3,3-tetramethyl-2,3-dihydro-1H-isoindol-2-yloxyl (2) have been studied at 60 degrees C. tert-Butyl and tert-octyloxyl radicals (3) were generated from the thermolysis of 1. The predominant unimolecular reactions of 3, that is, beta-scission to form neopentyl radicals (14b) and a 1,5-H shift to form 4-hydroxy-2,2,4-trimethylpentyl radicals (14c), were observed in both monomer systems. The resulting alkyl radicals underwent selective addition to the two monomers. The relative reactivities of the alkyl radicals toward addition to the monomers were obtained from competitive addition/trapping reactions. The absolute rate constants for the addition of alkyl radicals 14b and 14c to the two monomers at 60 degrees C were estimated to be 9.5 x 10(5) and 2.6 x 10(5) M-1 s(-1) to MMA and 4.5 x 10(5) and 0.7 x 10(5) M-1 s(-1) to styrene, respectively. The low reactivities of 3 and 14c toward addition to MMA and styrene were attributed to steric effects. Steric effects were also responsible for the low rate of the 1,5-H shift in 3.