00:01
Giant problem, so i wrote a bunch down already.
00:03
We were asked to synthesize each compound by converting benzene and we're told that we can use.
00:10
So you can reference that list.
00:12
And i've written the retrosynthesis.
00:21
And let's see here.
00:30
Let's go.
00:31
So for our first step on this first one here, we're going to start with benzene.
00:51
And here we're going to use bromine, br2, 3.
00:59
That will give me the bromine right here.
01:09
And then with mg, mthf, and this will be mgbr.
01:25
Then we can get benzaldehyde with, okay, it's benzaldehyde.
02:00
Then we're going to take this, the benzeldehyde, put that with mine.
02:25
That will give me, we're going to add pcc.
02:48
And we'll end up with our desire.
03:12
And then we're good with a.
03:15
Now, i'll have some room here, we're gonna do b, and i've done the retro synthesis for b.
03:22
And now we can go ahead and do this with, let's my retro synthesis.
03:32
So let's use the grignard reagent synthesis.
03:52
And then here, okay.
04:06
Then let's synthesize our aldehyde.
04:21
Then we can use our grignard.
04:25
Sure i have room.
04:26
I think i have one more page after this, yes.
04:43
And that will give me.
04:54
And we can oxidize that product.
05:06
That will give me.
05:21
And then we could use eas.
05:23
For this one, that will give me.
05:46
I think that's, yep, that's my product.
05:48
So i'm done.
05:51
And then finally, we've got our last one here.
05:56
And i've done my retrosynthesis.
06:01
And for this one, we're going to start with a, my benzene, obviously.
06:10
We're going to react that with the tertiary butyl alcohol, which we're allowed to use, and this will give me.
06:25
Okay, then we're going to use the fridocrystal acylcalation after we synthesize acet chloride from ethanol, which we can also use, with dichromate and sulfuric.
06:50
Then we'll take that with s -o -c -o -2.
06:58
Okay.
07:00
Now let's take those two that we have two products we just made in aluminum chloro...