00:01
Okay, so the reaction that we're shown here is a clear deals alder, right? that may not be immediately obvious, but i'll draw the molecule in such a way as to highlight the dine and the dineophile in blue.
00:20
Oops.
00:39
So we should recognize the shape of basically everything that i've drawn in blue here, which i can highlight as well.
00:48
Right.
00:48
There's our dyene and there's our dienophile.
00:53
Remember that al -kines can also participate in deals -older reactions.
00:58
So what is the product then? well, let's just do the mechanism.
01:02
Right.
01:03
So remember that for a basic diene and dienophile, we do something like this, signetropic rearrangement.
01:15
Okay.
01:17
And nothing changes with this.
01:19
It's just that because we have this extra rest of the molecule, there's going to be like a bridged.
01:29
There's going to be a bridged cycloalking, right? but that's fine.
01:35
Something that will help here is to number these carbons.
01:38
One, two, three, four, five, and six.
01:45
Okay.
01:46
And then we'll go ahead and do our arrow pushing...