00:01
1 phenyl propon to own is obtained from prope 1 -ianil benzene.
00:05
Consider the reaction.
00:07
This is the structure of prope 1 -i -9 benzene.
00:17
Prope 1 -ianil benzene.
00:24
This is the reactant.
00:26
This when treated with h2 -sophor and water monarchy, h2o, we obtain our required product that.
00:39
That is 1 phenyl propon to 1.
00:52
1 .1.
00:52
1 phenyne propon to o.
00:59
So if you look at the mechanism, this involves mainly two steps.
01:03
One is anol formation.
01:06
The second is the tautomerization.
01:09
So step 1 is enol formation.
01:13
So consider the reactant, that is our probe 1 -i -9, benzene.
01:22
So h2 is our h2 is.
01:24
4 and h2o will convert into these ions to h.
01:36
Oxygen has got two loan pairs on it.
01:39
Now you can see this oxygen attacks this hydrogen.
01:43
Oxygen loan pair attacks the hydrogen.
01:46
The bond between oxygen and hydrogen is shifted towards the oxygen...