00:01
So we have the following reaction here.
00:03
We're given arginosuxinate, and when treated with base, we get the following products.
00:07
We get arginine and fumarate.
00:09
So the question asks us to propose an aeropushing mechanism for something that could explain what's going on here in this biochemical reaction.
00:18
So what's going to happen here is we're going to have an elimination reaction.
00:22
More specifically, we're going to have an e1cb type elimination reaction.
00:27
We're actually going to form a carb anion.
00:29
So i'm going to go ahead and show our base coming in and deprotonating this hydrogen, and then the electrons are going to get pushed towards this carbon to form the carb anion, and we're going to get the following structure.
00:45
All right, it's going to be a long one here, like that.
01:12
So now this carbon has a lone pair here, and it has a negative charge.
01:18
So now it's a carb anion.
01:30
Okay, and then this nitrogen has a hydrogen on it.
01:34
And then we also have ammonium coming, going away from us here, which has a positive charge.
01:43
And then we have hydrogen coming towards us here.
01:52
All right.
01:52
So i believe that's everything there.
01:54
And so the next step in this reaction here is that this loan pair is going to form a bond here.
02:01
It's going to get pushed towards the carbon -carbon bond here.
02:04
And subsequently, oops, sorry...