285337
Replacement of Cl of chlorobenzene to give phenol requires drastic conditions, but Cl of 2,4 -dinitrochlorobenzene is readily replaced. This is because
1 \(-\mathrm{NO}_2\) group makes the ring electron rich at ortho and para positions
2 \(-\mathrm{NO}_2\) group withdraws electrons from meta position
3 \(-\mathrm{NO}_2\) donates electrons at meta position
4 \(-\mathrm{NO}_2\) withdraws electrons from ortho and para positions.
Explanation:
(d) \(\mathrm{NO}_2\) withdraws electrons from the carbon bearing chlorine group making the \(\mathrm{C}-\mathrm{Cl}\) bond weak.
Karnataka CET 2016
CHEMISTRY(KCET)
285338
Electrophile that participates in nitration of benzene is
285337
Replacement of Cl of chlorobenzene to give phenol requires drastic conditions, but Cl of 2,4 -dinitrochlorobenzene is readily replaced. This is because
1 \(-\mathrm{NO}_2\) group makes the ring electron rich at ortho and para positions
2 \(-\mathrm{NO}_2\) group withdraws electrons from meta position
3 \(-\mathrm{NO}_2\) donates electrons at meta position
4 \(-\mathrm{NO}_2\) withdraws electrons from ortho and para positions.
Explanation:
(d) \(\mathrm{NO}_2\) withdraws electrons from the carbon bearing chlorine group making the \(\mathrm{C}-\mathrm{Cl}\) bond weak.
Karnataka CET 2016
CHEMISTRY(KCET)
285338
Electrophile that participates in nitration of benzene is
285337
Replacement of Cl of chlorobenzene to give phenol requires drastic conditions, but Cl of 2,4 -dinitrochlorobenzene is readily replaced. This is because
1 \(-\mathrm{NO}_2\) group makes the ring electron rich at ortho and para positions
2 \(-\mathrm{NO}_2\) group withdraws electrons from meta position
3 \(-\mathrm{NO}_2\) donates electrons at meta position
4 \(-\mathrm{NO}_2\) withdraws electrons from ortho and para positions.
Explanation:
(d) \(\mathrm{NO}_2\) withdraws electrons from the carbon bearing chlorine group making the \(\mathrm{C}-\mathrm{Cl}\) bond weak.
Karnataka CET 2016
CHEMISTRY(KCET)
285338
Electrophile that participates in nitration of benzene is
285337
Replacement of Cl of chlorobenzene to give phenol requires drastic conditions, but Cl of 2,4 -dinitrochlorobenzene is readily replaced. This is because
1 \(-\mathrm{NO}_2\) group makes the ring electron rich at ortho and para positions
2 \(-\mathrm{NO}_2\) group withdraws electrons from meta position
3 \(-\mathrm{NO}_2\) donates electrons at meta position
4 \(-\mathrm{NO}_2\) withdraws electrons from ortho and para positions.
Explanation:
(d) \(\mathrm{NO}_2\) withdraws electrons from the carbon bearing chlorine group making the \(\mathrm{C}-\mathrm{Cl}\) bond weak.
Karnataka CET 2016
CHEMISTRY(KCET)
285338
Electrophile that participates in nitration of benzene is