Ive got to leave really quick here, but the short answer I can give is that when you look that the stability of the product, a radical, an ethyl radical is more stable than a methyl radical (hyperconjugation and such). The relative stability in this case means that homolytic cleavage would not be favorable for either, but it would be more unfavorable for a methyl compared to ethyl. The same logic can be used in both cases.