00:01
Each of the following reactions has been carried out under these conditions.
00:06
So, nitration of the parynglorobenzoic acid.
00:10
What product we are getting? nitration of the parynglorobanexic acid.
00:20
So, no2 plus will attack on which position with respect to this.
00:25
So this cl is the electron withdrawing group, but less electron withdrawing group.
00:29
That's why we will add electrophile with respect to this cl, not carboxylic acid.
00:35
So cl is the ortho and para directing so but para is the occupied.
00:41
So no2 plus will attack on the ortho position.
00:49
So we are getting this cl and no2 is here.
00:53
In the second part we have brumination of aniline.
00:58
So we have aniline is here.
01:02
It is the ortho and para directing group...