00:01
We're looking at reactions involving 3 -meryl rings with an oxygen inside.
00:09
So remember that when we have an acid catalyst, we're going to attack the more substituted side.
00:15
And here, we'll start with hydrogen and we'll protonate.
00:27
Then you're going to have your methanol come in and attack at your more substituted side, breaking the bond here.
00:41
So then, you have an alcohol coming off here, two methyl groups, and this here.
00:54
And then you can come in with a chlorine and take off that hydrogen.
01:00
So your final product will look like this.
01:10
Now when we then have a base catalyst, we're going to start right away by attacking our less substituted side, breaking our bond here...