Q.
The compound C7H8 undergoes the following reactions
C7H8→3Cl2/ΔA→Br2/FeB→Zn/HClC
The product ‘C’ is
1375
151
NTA AbhyasNTA Abhyas 2020Hydrocarbons
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Solution:
First toluene undergoes side chain halogination to give compound A. In compound A - CCl3 group is meta directing so meta product B is formed. B on reaction with Zn/HCl gives meta bromo toluene (C) .