The compound below is treated with $N-$bromosuccinimide $($NBS$)$ in the presence of light.

Draw both resonance structures for the radical produced by reaction of the compound with a bromine atom. Assume reaction occurs only at the weakest $C-H$ bond.

You do not have to consider stereochemistry.

You do not have to explicitly draw $H$ atoms.

Separate resonance structures using the harr symbol from the drop$-$down menu.

Include all valence radical electrons in your answer.