Alkenes undergo electrophilic addition reactions. Electrophilic addition to unsymmetrical alkenes involve the formation of a more stable carbocation intermediate in the first step which is rate determining and carbocation is then attacked by a nuclephile to form product
Which one of the following alkene reacts most readily with `HCI`?
A. `CH_(2)=CH-Cl`
B. `CH_(2)=CH-O-CH_(3)`
C. `CH_(3)-CH=CH-CH_(3)`
D.
