 So let's do the last mechanism of the day, we'll do transesterification, so notice what we're doing is we're taking one ester and we're making a different ester of it, okay? So what we're having is a small concentration of this stuff, okay, a small concentration and a high concentration of ethanol that's the solvent, okay, that's the promoter of this reaction. If you didn't have a high concentration of one and not the other then this reaction would be an equilibrium, okay, there's no favoritism over one or the other. What's more favor, the methyl or an ethyl, they're essentially the same, right? So the first step of the reaction is going to be sulfuric acid reacting with ethanol, okay? I don't think I need to do that mechanism, so I'm going to draw the product of it. Remember the mechanism, what happens, donating those electrons first, these electrons go over there, like that, this is a resonance structure, molecule there, that's the molecule we're going to use to react the ethanol with, okay, these are the same molecules, ethanol here, electrophilic carbonyl carbon. Then what's going to happen is we're going to have the proton transfer, I'm not going to show that mechanism because it's two steps, so we're just going to show the proton transfer here. What happens next? Collapse, knock out the leaky group, last step we'll have another ethanol molecule from the solvent, deprotonate that, and the last thing I should say is that all of these are acid-base and nucleophile-electrophile steps, so they're all in equilibrium. So what's the promoter of the reaction to go forward? It's because we've got a lot of ethanol and no methanol in this reaction, okay? The only methanol that's being produced is from this, so we're right there, we're not producing a tiny bit of methanol, which cannot compete in sheer numbers against as much ethanol, because ethanol is salt, okay? So we're going to get out of here, okay guys, so watch it on your own.