For the given molecule, "x", the preferred site for the attack of the electrophile is:
(A)Predominantly at "r"
(B)"r" and "u"
(C)"p" and "s"
(D)Predominantly at "u"✓ Correct
Answer: (D)
Solution
The right-hand ring carries an −NH−CO− (anilide) nitrogen whose lone pair is donated into that ring, directing electrophiles to its ortho and para positions. The left-hand ring bears the carbonyl, −CO−NH−, an electron-withdrawing group that deactivates it, so substitution is confined to the nitrogen-bearing ring. Among its activated sites the para position marked u is free and sterically unhindered, making it the predominant site of electrophilic attack.
JEE Main · 2026 · 02 Apr 2026 · Shift 1 · Single correct option