00:01
So what we have here is a butanol, one, two, three, four, but we had a methyl on the four position, or the three positions, so three methyl butanol with a two methyl propane.
00:20
And we're just going to go over the reaction mechanism here.
00:25
So knowing that we're working in acidic environments, one of the first things we form is parination at the most.
00:32
Basic site which is right here seeing on this hydroxy will protonate this to form a cation and i'll write in a different color to show that this is actually sort of a step and not really a part of the reagent so we protonate at that site there and now what basically happens if i just literally show it there is the sbt2 electrons here and want to pick up this proton there and to form this compound here.
01:18
And that's how we get our carburekaryone.
01:21
And what we're now left with is the butanol.
01:29
Okay.
01:31
So with that, the most negative nucleophilixate now is the hydroxy.
01:36
And it is able then to come in here and basically nucleophile, fill of the attack onto this tertiary site.
01:47
There we have.
01:48
Also to just go over this reach inside the electrons here, and this bond are able to come up there to receive this neutral charge...