00:01
Hi, in this question we need to draw mechanism for this reaction.
00:04
So from this combination we will get no2 plus.
00:09
This is electrophile and this is ortho para or o .p.
00:21
Directing group.
00:28
So and para will be major because in ortho there will be steady hindrance.
00:33
So first loan pair of nitrogen will give in ring and there will be electron density.
00:38
In paraposition.
00:39
So the intermediate will look like this.
00:48
Here is negative charge and here is no2 plus.
00:52
Now this negative charge will attack na2 plus to form no2.
01:00
Here is h, bond, bond, double bond nh positive charge coch3.
01:09
This h will be removed and loan pair of nitrogen will get back.
01:14
The prioritization step is first step.
01:16
Because after it the ring will get back its aromaticity and becomes more stable.
01:23
So, nh co, ch3 and here is no2.
01:28
The last step is actually workup stage in which h2so and h2o will give dilute h plus.
01:39
Now in h and here is c double bonded o coch3...