Monosubstituted product 'P' would be:

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Solution

The correct option is C
Electrophile attacks on that ring which has more +M effect.
$N$ atom can increase the electron density in the ring and makes it o/p directing.

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Similar questions

It is given that when (±)-2,3-dibromobutane reacts with $K O H$ , some of the products formed are:

Explain via mechanism and then choose the correct ones from the following.

Monosubstitution of (2S,3S)-2,3-dibromobutane using $O H^{-}$ yields a mixture of products.
Monosubstitution of (2S,3S)-2,3-dibromobutane using $O H^{-}$ yields a single major product.
Monosubstitution of (2R,3R)-2,3-dibromobutane using $O H^{-}$ yields a mixture of products.
Monosubstitution of (2S,3S)-2,3-dibromobutane using $O H^{-}$ yields a mixture of products.

C H_{2} = C H - C H_{2} - C H_{2} - C H = C H_{2}

C_{5} H_{10}

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