Show how free radical halogenation might be used to synthesize the following compounds. In each case explain why we expect to get a single major product.
b) 2-bromo-2-methylbutane
I have the mechanism figured out but what I can't figure out is why we expect to get a single major product as far as I can tell the only reason why that might be is that the second C is highly substituted making the reactive intermediate more stable. But to me that seems like a flimsy reason to base my answer on.