1,4-dimethylcyclopentene gives a mixture of 2 alcohols upon hydroboration (BH3) followed by oxidation (H2O2, OH-). How and what are they?
I thought it would just be 2,4-dimethylcyclopentanol and I understand how, but I have no idea what else it could be if the boron always attaches at the less substituted double-bonded carbon atom.