2) By the Reactivity-Selectivity principle, as the bromine free radical is less reactive than the chlorine radical, it is more selective on which hydrogen site it will attack. Thus a greater activation energy is required for the desired product.
1)Iodine free radicals are very unstable, and they combine to form molecular iodine instead. Also, by the RS principle, iodine is least reactive/not reactive at all.
3)PhCH3 leads to the formation of a benzylic radical, which is stabilised by resonance. Tert-butyl radical is stabilised by hyperconjugation.
As hyperconjugation is given more preference, tert butyl radical is more stable than benzyl radical, and the stability order follows that of carbocations. Additionally tert-butyl radical has the most hyperconjugation structures, and is most stable.