Step 1: In the presence of FeCl\(_3\), chlorination of toluene occurs via electrophilic aromatic substitution.
Step 2: The methyl group (\(-\text{CH}_3\)) in toluene is an electron-donating and ortho/para-directing group.
Step 3: Due to increased electron density at the ortho and para positions, substitution occurs mainly at these positions.
Step 4: Hence, the major products formed are ortho-chlorotoluene and para-chlorotoluene.