 Okay, let's start this one over again. So we'll take an acid chloride to an anode, okay? So it's the same mechanism that you know from before, okay? But remember, this one is going to make HCl1. So let's get it going. So I'm gonna erase. So we've got a secondary amine here, okay? We've got our acid chloride, make a tertiary amine, okay? So remember, just like last time, chlorine takes negative charge away from that positive center, that electrophilic carbon. So that nitrogen, it wants to donate those electrons so bad already, you know? So it sees that positive, it's gonna attack, okay? So it's again the same mechanism as when the sodium ethoxide attack. Remember, this is what we've been saying. I don't know if we formally written it down on any of these things, but that's an SP2 center. Gotta go from the SP2 to the SP3, which is what we're about to do here. There's our SP3 center, tetrahedral intermediate. That nitrogen still has its proton on it. So what's going to happen now? What's gonna happen, guys? Somebody tell me. The electrons go back down, and create that opon, and they throw that chlorine away. What he's saying, right? I was trying to tell him. Which one's gonna, which one's going to leave? The chlorine, but it's actually questionable which one will leave, because this is a protonated amine, right? So that's a pretty good leaving group, too. But if that happened, it would just go back this way, and then it would start the reaction again, okay? So the only way to promote the reaction to go forward is to have the chlorine be the leaving group. So remember, it went from an SP2 to an SP3, back to an SP2, okay? So that's what it's doing now, because we can't have that charge still in there. So what's gonna happen, the chlorine's going to remove that proton, yeah? Putting those electrons back there, and give us a product. So hopefully, again, I said this a few times already, you've all been doing this, but I hope you guys can see that all of these kind of esters, formation, amine formation, all of those, they're almost the same mechanism, right? So this one you gotta watch. If you put excess of the secondary amine in there, that will take the pH higher, okay? Of pH higher, okay? This, obviously the HDL is gonna make your pH low, so if you've got a sensitive molecule, you're gonna destroy it, so you gotta watch out. If you put excess amine in there, that will alleviate that problem. Is there any questions about that one?