00:01
Okay, so we want to give the alcohols that could form either an aldohide or a ketone, and only a primary alcohol could form an aldahide.
00:07
If we react it with a weak oxidizing agent, it needs a formula c4h10o.
00:13
So we could start with a straight chain alken, putting the alcohol right there.
00:19
If you look at the formula, we're going to have four carbons, two hydrogens there, there, 6, 7, the oxygen.
00:32
If we react this with a mod oxidizing agent like nesmartin, pyridium, which is dmp.
00:39
We'll get butanol with an al ending, a 4 carbon outahide.
00:45
And we can actually shorten the carbon chain by 1.
00:47
We just leave the alcohol as primary.
00:53
Put the methyl group right here.
00:56
Because if you put it right here, this would be carbon 2.
00:59
We do secondary alcohol.
01:03
So this is going to be 2 methyl for italy.
01:07
And we're acting this with, this time using another agent like pcc.
01:14
Get the structure.
01:20
This is carbon 1 and 2.
01:22
Carbon 2 has the method group...