00:01
Hello students, let's look at the question.
00:02
Iudination is the electrophilic substitution reaction.
00:05
It is esr of ares.
00:10
The substituted product obtained in it according to the ring is activated towards electrophilic substitution or not.
00:17
The functional group present plus minus plus m minus m.
00:22
It influenced the formation of product.
00:25
So here first is iodination of acetyl -cellic acid.
00:30
Acetyl cellic acid.
00:35
So here if this iodination is occur when ki is in the ratio of 1 ratio 1, when ki is in 1 ratio 1 then aspirin aspirin it reacts with ki in ratio 1 ratio 1 and it forms 5 iodospirin.
01:05
5 idiospirin.
01:10
Second is 1 is an ortho and para directing group whereas c -o -o -h is a meta -directing group.
01:18
Major product of mono -hyrination of aspirin is, major product would be 5 idiospirin.
01:27
Next is reaction of aspirin with x's of k -i.
01:33
When aspirin, it reacts with axes of x -a -i.
01:41
Of k .i.
01:44
Then it react to form 3 .5 diido aspirin.
01:51
It forms 3 .5 diido aspirin.
02:04
Next is iodization of valenine...