00:01
Hello students, so in this video we are going to perform the following reaction on the following reactant.
00:09
So, we have this reactant and we will react, we will do the intra -aldol condensation.
00:21
So, let us do.
00:23
So, the first one is naoh.
00:26
So, this is a very strong base.
00:28
So, it will take up the most acidic hydrogen here.
00:33
So, it will take up the acidic hydrogen.
00:38
Then what will happen is this o - will attack this carbonyl.
00:44
So, let us number it quickly 1, 2, 3, 4, 5, 6.
00:48
So, we have to draw a cyclopentane.
00:52
So, let us number it 1, 2, 3, 4, 5 and in the second position we have a carbonyl and in the fifth position this will open and an o - will be formed and then the sixth carbon is a substituent...