Identify the product obtained when toluene reacts with chlorine in...

Toluene reacts with chlorine in the presence of a Lewis acid catalyst like $\text{FeCl}_3$ to undergo electrophilic aromatic substitution.

The methyl group ($-CH_3$) attached to the benzene ring is an electron-donating group through hyperconjugation and inductive effect, making it an ortho, para-directing group.

Therefore, the incoming electrophile (Cl^+$) attacks the ortho and para positions, resulting in the formation of a mixture of o-chlorotoluene and p-chlorotoluene.<br><br>Answer: o-Chlorotoluene and p-Chlorotoluene$