Propose a structure for an aromatic hydrocarbon, C9H12, that can form only one C9H11Br product on substitution of a hydrogen on the aromatic ring with bromine.
You do not have to consider stereochemistry.
In cases where there is more than one answer, just give one.
Ignore the ortho, para-directing effects of the alkyl groups in answering this question. Consider only the number of nonequivalent hydrogens on the aromatic ring.
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