When toluene reacts with concentrated sulfuric acid under heating conditions, electrophilic aromatic substitution occurs. The sulfonation reaction typically produces a mixture of ortho- and para- products due to the electron-donating methyl group on the toluene ring. The methyl group directs the sulfonic acid group to the ortho and para positions, making a mixture of o- and p-toluenesulfonic acids as the major products.
- Option (A) is incorrect as toluene has a methyl group that directs substitution to the ortho and para positions, not to the benzene ring.
- Option (B) is incorrect as only the para product is favored, but both ortho and para products are formed.
- Option (C) is incorrect as the ortho product is not the only one produced.
Therefore, the correct answer is option (D).