00:01
So in this reaction, you have cyclohexene reacting with hbr.
00:08
And so remember in these addition reactions, they're going to occur in two different steps.
00:15
Your first is going to be a nucleophilic attack because this cyclohexene, the pi bonds, these two electrons, and these pie bonds are nucleophilic.
00:27
So this is going to be your nucleophile.
00:32
This is going to be your electrophile, and this bromine is going to be your leaving group.
00:46
So in this reaction, you have these two electrons are going to attack this hydrogen, and you're going to form a new carbon hydrogen bond.
00:56
And then the two electrons from this hydrogen bromine bond are going to go onto your bromine.
01:02
So whereas here, your bromine has three lone pairs of electrons for, six electrons total.
01:12
Now, after this first step, you're going to form a new carbon -hydrogen bond, and you're going to have a carbocation, plus your bromine, which now has a full octet, and a negative charge.
01:30
So in this second reaction, this bromine is going to be your nucleophile, and this carbocation is going to be your electrophile.
01:43
So in the second step, which i'll draw in red, you're going to have this bromine form a new bond with this carbon atom...