 Okay. So let's try to do this one. So you can see here, hopefully, what kind of molecule do we have here, like functionality-wise? An ether. And what are we making here? What is this? Alcohol or phenol? And alkyl halide. Okay. So how do we take an ether and make an alcohol and an alkyl halide? Okay. So we're going to draw the mechanism. So what do we want to do when we draw the mechanism? Erase everything that's not important, right? So we've got to remember where we're going. So don't forget that. What does this little triangle mean here? Yeah, it's going to, we've got to keep this stuff up. Okay. And I'm actually going to erase the HBR so I can really emphasize that bond in between the H and the L. I also like to write my lone pairs like I always say, you know, so I can remember where the reactive portions of these molecules are. So I'm going to also draw my lone pair over here. Okay. So this, of course, is a strong acid, right? So this is going to act as the what? The base. Very good. Okay. So the base deprotens the acid. Make sure your arrows are going the right way. If I know, I hope that you can get your arrows there. Okay. So we'll do that. So draw what you think the product is. Don't make for me to draw it. You draw it and see if you get it right. Hopefully you drew something that looks like that. Did everybody get to that? Okay. Good. Did you get that, Apple? You didn't have time? Okay. Okay. So what's going to happen next? Can anybody tell me? So this is, if we look here, if we cross, kind of cover that, what compound does that look like? Femal, right? Is that a stable compound on the top? Yeah. So it's a, it would be a good leading group that. So what do you think's going to happen? What reaction? Not SN1, because if it was an SN1, you'd be making a primary carbocation, right? And you can't do that. So it's going to be a what? It's an SN2 reaction. Everybody should be saying so that. So we're going to have the nucleophile attack, that carbon right there. Those electrons are going to go to that oxygen there. Remember, this is a good leading group here. Whenever you can see that good leading group and it's got a positive charge on it, you know, that's going to leave as like an SN1 or an SN2. Okay? So the reason this has to be an SN2 is because it's on the primary carbocation. So when we do that, of course, we're going to make phenol like we've been saying. And the other thing we're going to make is, that's the product mixture there, and none of the steps. Any questions on this one?