00:01
Okay, the best thing to do with this problem is think about the stem of the enzyme and then also look at if there's anything else.
00:11
So in this case, we see that fad is going to fadh2.
00:15
So that means we know that two hydrogens are going to be lost.
00:20
We can also see that from the stem of this dehydrogenase.
00:24
So let's go ahead and draw out just the skeleton structure.
00:30
So we're going to have one, two, three, four, five, six, and then this is going to be s -c -o -a.
00:51
Great.
00:52
So the acyl -coa dehydrogenase is actually going to oxidize the alkanase to oxidize the alkan to an alken.
01:07
So i know oxidation, usually you think of adding more oxygens, but this can also be removing hydrogen.
01:16
So in this case, causing an al -quine to become an al -cane.
01:19
And this specific enzyme is going to have this done between the alpha and beta carbons of this chain.
01:28
So in order to find the alpha and beta carbons, we start here at the carbonyl carbonal carbon, and then the next one is going to be our alpha.
01:36
And then that means that this one is going to be beta.
01:40
So that means we know that these two hydrogens are coming off, and we can corroborate that.
01:48
Oops, gosh, i cannot.
01:50
With fad going to fadh2, and then this would cause a double bond here.
01:57
So that is our first product.
02:00
All right, going on to b.
02:04
Again, let's see what we're adding.
02:05
So we're adding h2o, which usually means.
02:07
Means we're hydrating the compound, and that makes sense since we have a double bond here.
02:13
So you can add things to a double bond to introduce a new functional group...