Question
Question: Which of the following is most acidic? A. is incorrect.
The 2− methoxy phenol is not most acidic from the given compounds. Hence, option (B) is incorrect.
Among the given compounds 4− methoxy phenol is not the most acidic compound. Hence, option (C) is incorrect.
Among the given options, 3− methoxy phenol is the most acidic compound. Because, the methoxy group is inductive withdrawing and they are mesomeric donating. We know that the mesmeric effect will override the inductive effect. But the mesomeric effect is only valid when the substituent is attached on the para position and the ortho position.
And the addition of an electron donating group to the phenol ring will affect the acidity. Because, the acidity will decrease when an electron donating group is attached to the phenol ring. But the acidity will increase when the electron withdrawing group is attached to the phenol ring. Thus, we can say that the meta- methoxy phenol is more acidic than the others.
Hence, option (D) is correct.
Note:
We need to know that the acidity of the compound increases when an electron withdrawing group is present in that compound. The inductive effect will affect the acidity and basicity of a compound. Because, when the number of negative inductive groups is increasing, there is a chance to increase the acidity. And if the positive inductive group is present, there is a chance to increase the basicity.