Correct me if im wrong here. At the bottom of destroyer road map #1 it shows cyclohexane double bonded to a CH2 group. It reacts with HBr to produce CH2Br according to destroyer. However, shouldn't it add according to the markovnikov rule to produce cyclohexane with Br and CH3 as substituents?
I dont know if this will make sense to any of you with out pictures, but you could try drawing it out.
THANKS
I dont know if this will make sense to any of you with out pictures, but you could try drawing it out.
THANKS