00:01
Draw the products, including the sterochemistry of each reaction.
00:04
All right.
00:05
So we have some mechanisms that we need to draw and just make sure that we are aware of where the sterochemistry is and how we're going.
00:13
All right.
00:13
So first one, hbr and alkyne.
00:17
So this alkyne will donate inward to the most stable carbon.
00:21
One electron goes outwards.
00:23
This h, that h donates both to the br.
00:25
So we then lose our alkyne.
00:30
But we now have a carbocatinine.
00:32
We have a new hydrogen bond that will draw right there just so we know where it is, but we're not going to keep drawing him.
00:39
And we have a negative br who is looking for something.
00:45
So his, we're going to have a electron pair will attack right here at this carbocatin because there's no rearrangements that are favorable for it.
00:54
It's already the most stable it can be at that point.
00:58
So we now have a br group.
01:02
Okay, so now it's important to identify stereochemistry for this.
01:09
Do we have chirocentres that we need to be aware of? we do have a carol center right here.
01:16
All right, so let's go ahead and draw like sterechemistry for this.
01:19
So there is a same addition, and there's anti -edition.
01:23
So let's draw our base structure, start by drawing your base chain.
01:29
There's our base chain.
01:31
So we're going to consider this coming out to the front for hydrogen.
01:38
That's the hydrogen we added...