00:01
Okay, so we're asked to give the products in the perkin condensation reaction and the novanagle condensation reaction.
00:10
And we're starting with benzodiaodod.
00:18
So reacting the structure with this ester.
00:29
And this is reacting with the conjugate base of acetic acid.
00:35
So this is going to depurtenate the alpha hydrogen on this ester.
00:46
So we'll get a carbana iron here.
00:48
And this carbonyon is going to attack the carbonyl carbon.
00:53
So this is going to be r1.
00:59
So we have the alcoxid ion.
01:01
And we're adding two more carbons.
01:04
So these two carbons, which is bound to the rest of the chain.
01:08
So one, two, three.
01:10
And then here's the ester.
01:11
And the rest of the ketone.
01:13
I mean the rest of the structure.
01:19
So the alcoxylide ion is going to deperinate acetic acid to get the conjugate base again.
01:37
So we get an alcohol...