 Okay, so this is an elimination reaction as well, but this is a bimolecular elimination reaction, right, an E2 reaction. Why is that? Yeah, so what do we got? We got a good leaving group. What else do we have? What is it called? Strong faiths. Strong faiths in this case. Not a nucleophile, right? Okay, because why? It's held on. Because it cannot do an SN2 reaction, it can't do a nucleophilic attack on that thing, so in this case it's going to be a strong base, okay? So we have a strong base and we can't do that nucleophilic attack, okay? If it was, if that wasn't, it would do an SN2, okay? So, like we said, tertiary. The thought side is a strong base. So what's going to happen is the one step bimolecular reaction elimination, or E2 is one step, E1 is two steps, okay? Same thing with SN1 and SN2, okay? So it's all going to happen at once, one, two, three, I guess I shouldn't say one right after the other. They're all going to induce each other with it. Of course, that's an all-is-form there, and we've got also a plus and a minus, so there's your E2 reaction, again, just to go over, good leaving group, tertiary alkyl halide, strong base, right? That's all the recipe for an E2 reaction, okay? Any questions on that one?