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(A) Step $1$: Electrophilic aromatic substitution of $p$-nitrotoluene with $Br_2$ gives $2$-bromo-$4$-nitrotoluene.Step $2$: Reduction of the nitro gr

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$2-$bromo$-1-$methylbenzene

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(A) Step $1$: Electrophilic aromatic substitution of $p$-nitrotoluene with $Br_2$ gives $2$-bromo-$4$-nitrotoluene.Step $2$: Reduction of the nitro group using $H_2/Pd$ yields $2$-bromo-$4$-methylaniline.Step $3$: Diazotization using $NaNO_2/HCl$ at $0^{\circ}C$ converts the amino group into a diazonium salt,forming $2$-bromo-$4$-methylbenzenediazonium chloride.Step $4$: Reduction of the diazonium salt with $H_3PO_2$ replaces the $-N_2^+Cl^-$ group with a hydrogen atom,resulting in $2$-bromo-$1$-methylbenzene (also known as $o$-bromotoluene).

The product $(P)$ formed from the following multistep reaction is :-

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