For the given molecule,x,the preferred site f | vedclass

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(C) The molecule $x$ is $N$-phenylbenzamide. It contains two phenyl rings attached to an amide group $(-CONH-)$.In the ring attached to the nitrogen a

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$p$ and $s$

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(C) The molecule $x$ is $N$-phenylbenzamide. It contains two phenyl rings attached to an amide group $(-CONH-)$.In the ring attached to the nitrogen atom,the lone pair on the nitrogen atom is in conjugation with the benzene ring,making it an activating group. This group is ortho/para directing.In the ring attached to the carbonyl carbon,the carbonyl group $(-C=O)$ is a deactivating group and is meta-directing.Therefore,the electrophilic aromatic substitution will occur on the ring attached to the nitrogen atom. The ortho and para positions relative to the nitrogen atom are the most electron-rich sites.In the given structure,$u$ represents the para position and $s$ represents the ortho position relative to the nitrogen atom. Thus,the electrophile will preferentially attack at these positions.

For the given molecule,$x$,the preferred site for the attack of the electrophile is:

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