Help with Other Carbonyl Reactions Practice Test

The base-promoted ring-opening of an epoxide using aqueous NaOH will yield a trans glycol

Treatment of an unsymmetrical epoxide with methanol and acid will result in nucleophilic attack at the more hindered carbon

The catalyzed ring-opening of an epoxide in aqueous acid will yield a cis glycol

Treatment of an unhindered epoxide with a Grignard reagent will result in a nucleophilic attack at the less hindered carbon

A nucleophile attacks an epoxide to yield an alcohol