Chlorobenzene is an electron-withdrawing group through induction (–I), but an ortho/para-directing group due to +R (resonance) effect.
When bromination is carried out using Br\(_2\) in the presence of anhydrous FeCl\(_3\) (a Lewis acid catalyst), electrophilic aromatic substitution occurs.
Since Cl directs the incoming Br to ortho and para positions, the para product is major due to:
- Less steric hindrance
- Better stability
\[
\text{Product: para-bromochlorobenzene}
\]