 Okay, so I know you guys want to do chemistry and alkenes all night, but I have some desiccate. So this will be the last problem that we do. Very similar to the other ones. How do you make this compound this chlorohydrate from an alkene? So cyclohexene is the only alkene that would be able to be used to synthesize this. Of course. So you're going to have to add the hydroxyl substituent and the chlorine on there. So how would you do this? If you recall, Cl2H2O. So we can do the mechanism too. So Cl2, it looks like that. When it gets into the presence of an alkene, it's going to make this have an instantaneous dipole. So this chlorine will be partially positive, that one will be partially negative, and that will induce that alkene to attack it. Once that happens, these two steps happen at the same time. So all of those really happen at the same time. Concerted reaction. So what are we going to get? We're going to get the chloromium ion. We're also going to get Cl minus, so the chloride ion. And remember, this is in a solvent of water. So there's a ton of water. There's a lot of it relative to the little bit amount of Cl that's in there. So water is going to see this three-membered ring. And remember, three-membered rings are very unstable already. Chlorine being very big and bulky doesn't mind having, you know, is very big and bulky. And these carbons don't like having that strain on that ring. So this is going to see the opening, right, and come in and attack, knocking that bond out like that. So we're going to get the protonated water there, or the protonated alcohol hydroxyl group from water attacking. And then remember, of course, we've got a lot of other water molecules out there. So that's going to give you your final product, H3O plus, which you will wash out. So that's it for the night.