The radiolysis of liquid cyclohexane using perfluorocyclohexane as an electron scavenger has been examined at very high dose rates. The dose rates, to lo2* eV/g s, were such that geminate recombination of ions is essentially unaffected by dose rate, but high concentrations of radicals are produced, leading to radical-radical reactions. Up to 0.7 G units of the mixed dimer, C6Fl1.C6Hl1, were produced indicating that large concentrations of C,F1, radicals are formed in the neutralization process. Thus, at conventional dose rates (1016 eV/g s), C6FI 1H is probably produced by reactions of C6F1 radicals rather than by proton transfer to a perfluorocyclohexane or perfluorocyclohexyl anion.