00:01
Okay, this problem is asking us, how do we form my butanoke anhydride starting from my butanolic acid? what is the other reagent that we need? so if we look closely at my butanoke in hydride, we already have a lot of my betanoke acid within it.
00:12
So this is my buttonic acid already right there.
00:15
So the only thing missing from this inhydride is this component.
00:19
So how do we get that? well, let's look at our options.
00:22
One of the options is bettonolic acid, right? just a reaction with another molecule of buttonic acid.
00:27
Okay, so is this a likely one? let's look at it.
00:30
So i know that i have to add four carbons total, right? because i have one, two, three, four carbons.
00:36
Okay, this satisfies that.
00:38
One, two, three, four.
00:39
Okay, so that's a possibility.
00:40
I also have the carbonyl present, but i do have this oh present.
00:44
So that one, we might have to hesitate a little bit if we don't know the mechanism yet, but let's keep it on the table.
00:50
Okay, next step, we have ethanolic acid, right? that's just simply acetic acid.
00:54
So is acetic acid going to be a good contestant for the synthesis of, my butanoga in hydride with butanolac acid.
01:01
The answer is no, right? because we only have 1 -2 carbons, right? we need 4 carbons total.
01:05
Okay, next up we have butanol...