 Okay, so let's do this mechanism now. This will be the last mechanism hopefully now or about a real Stay, but anyways, so notice you've got excess ammonia in here, okay? So we're taking acid chloride going to Hema. Okay, so let's erase it and do it So ammonia Makes your solution basic But you will have charge separation So the first step is going to be Attack of the electrophilic carbon By the nucleophilic energy giving you the oxy anion this protonated amine Okay, so we've got a charge difference here. This doesn't like to be that way protonated. This doesn't like to be So what's going to happen here is Well one of two things, you know the probe the proton transfer could happen first or later, you know, but so We're going to knock that back down Okay, I don't one of these is a good leaving group, but if we kick this out, then we just go back to this Yeah, we didn't do anything. So we're going to kick that out like that So that progresses the reaction cl right Minus we that would normally have been the base that removed this last proton But since we've got excess ammonia, but that would make HCO, right? But HCO will make your pH drop like dramatically and if this is a sensitive Material that you're making it's going to decompose it, you know, because it can't be in a very acidic environment So instead of making HCl We're going to use ammonia as the base Do you prove me here? Am I almost got it? Come on neutral molecule there, right? and Which is not as acidic as Yeah, so it's in this it's a complex, you know what I'm saying in fact Oh, we're really talking about is the acid is the ammonia line, you know if you want to look at the difference between The acidity of HCl as opposed to the ammonium ion you couldn't look at that pKa Yeah, it's gonna be very much higher. Yeah, which is good, you know, which makes acidity low, right? Okay, we're cool with that one. Okay. We did