GRE Subject Test: Chemistry › Carbocations
Which of the following carbocation intermediates requires the least activation energy?
What intermediate is involved in the conversion of compound B to compound C?
If the carbon being pointed to was deprotonated (resulting in a positive charge on it). Would the resonance form (the positive charge being redistributed to the carbon with a bromine) be more stable than a secondary carbocation? Why?
Carbon 1:
Carbon 2:
Let's say we react the given compound with . During the first step of the reaction, will the hydrogen be added to carbon 1 or carbon 2, why?