 Let's try this, Mike, and there's some problems. It says, a monoreax with acetyl chloride to give acetamide, identify the bonds broken and formed in each step of the reaction, and draw heart arrows to represent the electrons in each step. So actually, they give you all of the intermediate, but I'm just going to show you how to do it from here. So the first step, remember these carbonyls, especially when they have another electronegative atom next to them, they're very electropositive. So it's a very good Lewis acid, if you will. So you can also think of the resonance structure with the negative charge up on the oxygen. But anyway, so what the electrons are going to do is Pt center and knock those electrons up to the oxygen. So what we're actually going to make is a stereocenter there for reason, because eventually we're going to need to do protonated not yet, though. So does that make sense, so far, the first step? And then this is going to re-collapse, knocking the good leading group away, knocking the good leading group out. So it could knock this one out, or it could knock this one out. We knock this guy out, the ammonia. We just go back to this starting, and it'll just happen again. So to promote the reaction, we're going to draw the mechanism that shows the chlorine getting knocked away. So the chlorine is the leading group. So when we do that, we're going to have this intermediate. And I'm going to continue to draw that with an H now. So if you insist on it, you can put your chlorine out there. It's not a very strong base, though. And you've got a bunch of ammonia in this. The limiting reagent of this reaction is going to be the acetyl chloride. So we've got another ammonia molecule. So what it's going to do, so it's going to see a Bronsted acid, right? So it's a Bronsted base. So what is it going to do? Deep protein. Like that? How do we get it in the hand? Let's see them on it. And then I think in the book, they actually show that in A4 plus, the ammonia mile, and maybe they even show the C l minus r. So does that make sense? So that's the mechanism of how you do this reaction. So this, as you would call this, forming an amide from an acid chloride. This thing is an acid chloride, acetyl chloride, specifically. And this is an amide, acetyl chloride. Any questions on that one? OK. Anybody else? Wonderful.