Electrophilic Addition Reactions of Alkenes

Before beginning a detailed discussion of alkene reactions, let’s review briefly some conclusions from the previous chapter.  the alkenes behave as nucleophiles (Lewis bases) in polar reactions, donating a pair of electrons from their electron-rich C=C bond to an electrophile (Lewis acid). For example, reaction of 2-methylpropene with HBr yields 2-bromo- 2-methylpropane. A careful study of this and similar reactions by Christopher Ingold and others in the 1930s led to the generally accepted mechanism shown in below electrophilic addition reactions.

The reaction begins with an attack on the hydrogen of the electrophile

HBr by the electrons of the nucleophilic π bond. Two electrons from the π bond form a new s bond between the entering hydrogen and an alkene carbon, as shown by the curved arrow at the top of Figure 7-7. The resulting carbocation intermediate is itself an electrophile, which can accept an electron pair from nucleophilic Br^-  ion to form a C-Br bond and yield a neutral addition product.

An energy diagram for the overall electrophilic addition reaction (Figure 7-8) has two peaks (transition states) separated by a valley (carbocation intermediate). The energy level of the intermediate is higher than that of the  starting alkene, but the reaction as a whole is exergonic (negative ΔG^ο). The first step, protonation of the alkene to yield the intermediate cation, is relatively slow. But once the cation intermediate is formed, it rapidly reacts to yield the final alkyl bromide product. The relative rates of the two steps are indicated in Figure 7-8 by the fact that ΔG₁^‡ is larger than ΔG₂^‡.

Electrophilic addition to alkenes is successful not only with HBr but with HCl, HI, and H₂O as well. Note that HI is usually generated in the reaction mixture by treating potassium iodide with phosphoric acid and that a strong acid catalyst is needed for the addition of water.