1.

Explain the following behaviours:Ortho-nitrophenol is more acidic than ortho-methoxyphenol.

Answer»

Nitro being the electron withdraning group stabilises the phenoxide ion.

Detaited Answer

Nitro-group is an electron-withdrawing group. The presence of this group in the ortho position decreases the electron density in the O-H bond resulting in  easier loss of proton. The o-nitrophenoxide ion formed after the loss of protons is stabilsed by resonance. Hence, orthonitrophenol is a stronger in  acid. Whereas, methoxy is an electron-releasing the b-u bond. Thus, proton is released easily. Thus ortho-nitrophenol is more acidic that orthowhereas methoxyphenol.



Discussion

No Comment Found