00:01
So this question says ketones are prepared by oxidation of secondary alcohol.
00:07
So you take a secondary alcohol, okay, you oxidize them, and that will give you ketones.
00:22
So name the alcohol that should be used to prepare three pentanones.
00:29
So that's 5 carbon, 1, 2, 3, 4, 1, 2, 3, 4, 5, 5, 5, 5, and 1, 3, 4, 5, 5, and and it's carbon 3 that is carrying the oxygen.
00:41
So 1, 2, 3.
00:43
1, 2, 3.
00:44
So this is 3 pentanone.
00:48
So what alcohol will produce this by oxidation? so it has to be a secondary alcohol, right? because secondary alcohol, when it gets oxidized, it produce ketone.
01:02
So the secondary alcohol for this would be 3 pentanour.
01:07
Which is going to be this.
01:10
Okay.
01:17
So the next one is mathieu ethyl ketone.
01:24
So, mathieu -hetil -kitone.
01:30
This that looks like.
01:33
So it's going to look like this.
01:41
So this is mathieu -hetil -ele -kitton.
01:49
So on this side, mateo, you have one common.
01:52
On this side at till you have 1 -2, 2 carbons and then the ketone is here.
01:57
So what's i call produce this has to be this, okay? so it has to be 1 -2, 2, 2, 1, 2, 3, 4, 2, butanol.
02:15
Okay? the next one here is 4 oxidation.
02:22
The next one here is 4 -phenoluttonone.
02:28
So 4 fennel button on 4 fennel 2 button on so it's got to be 1 2 3 4 1 2 so that's 2 button on 1 2 2 3 1 2 3 4 let's see again 1 2 3 4 so the phenyl is on carbon 4 it's so long over right okay so this is 4 to butanone.
03:10
So what produce this, it has to be the three, four, the alcohol of this.
03:23
So this should be for phenyl to butanol.
03:52
So then the next question says we should write the structure for each outdoor condensation product that is possible when a mixture of so ethanol is this.
04:11
It's got it is reacted with propanar.
04:17
When i'm a mixture of ethanol, propanar.
04:19
Propanar is this.
04:22
One, two, three, six to c.
04:29
It's reacted with dilute sodium nitroxide.
04:34
Yes, sodium nitoxide...