Step 1: Nature of isobutylene.
Isobutylene (2-methylpropene) is an unsymmetrical alkene that follows Markovnikov’s rule during addition reactions.
Step 2: Addition of HBr.
In the absence of peroxide, hydrogen bromide adds according to Markovnikov’s rule, forming the more stable tertiary carbocation intermediate.
Step 3: Product formation.
The bromide ion attacks the tertiary carbocation, resulting in the formation of tert-butyl bromide as the major product.
Step 4: Conclusion.
Thus, the major product formed is tert-butyl bromide.