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But over the americans information of this. Mhm. The action starts for recognition. Oh. Uh huh. What? Oh. Oh! They one of our two production groups. That's right. Oh! That organ transfer over is also this spot. We had the formation of a grocery cart at the time. True believes. Oh and the camera guy is attacked by this which floor this disciple, Okay and commission to ensure to the target product.
Hello here we have to describe the mechanism of the following reaction. So I'll the height total. All the heart reacts with profile of mine in the A Cd media forming the mine. So the first step of this reaction is uh protein ation of oxygen. So the other highest reacts with hydrogen and forms the battalion. And this guitar is a strong nuclear file. Sorry, strong electro faisal. This carbon I'll catania carbon I'll atom is a strong nuclear file. So it means that it further reacts with the I mean, which is just a reaction between an electro file and the nuclear file. So again, no nitrogen has uh to undo has a pair of unbounded elections we share interact with electro filic atom. So when it forms the following intermediate, so then this intermediate and it goes proton migration. So ah yeah, yeah, yeah. As a result of the proton migration, this product is formed and then 800 goals ah water elimination of water. So you so it's going to be the fourth step. So this molecule loses water and forms ah they in minimum catan show and lastly, ah the medium catan and the goals of hydrogen abstraction. You can obstruction of hydrogen plus and it forms the final compound. So here is, yeah, here is the mechanism of this reaction. It includes five steps which are shown on the screen. Thank you very much for the submitting this question. I hope I helped you. Bye.
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Okay, So up top. We've got this tie dye ter beautiful bicarbonate. And below, we just have a pretty general amino acid, or I just use ours aside. Group eso The first thing we're gonna do is we notice we have two nuclear files on our amino acid. We've got the nitrogen and the oxygen on. We have several Electra Philip groups on that giant carbonate group s. So what we're gonna have is nitrogen attacking right? Because nitrogen is a better nuclear about the extra so we can have these electrons attacking there, Those electrons being pushed up onto the oxygen. All right, so when I kind of have that attack, what I've got is, um, a larger molecule kind of being formed. Uh oh. Right where I have something like this, it's that, I guess. Okay, So at this point, I have a lot of electron density around this oxygen on, and that's gonna be pushed back to form, Uh, you know, just a normal carbon eel again. And when that happens, we have two groups that can leave eso this second part of the bicarbonate right there is gonna be a substantial better leaving group because it could be stabilized. The residence eso When the electrons get pushed back onto from the carbon eel, this bond will problem onto their to break the Carbonell and thus form a leaving group. All right, so kind of drawing a little sideways area like that. That's how we'll get this final product that looks something like this. All right, Something like this. And that's where a main product, But well, I guess I should probably add my Ohh, there s O that will be the main products. But we'll also have, um this as a side product. It will have, right? Nuttall, former side product eso. What's gonna happen is that since I have so much, uh, electron density on this and I have this pretty acidic hydrogen right here that's gonna just deep throat, Nate. And I'm not gonna draw the mechanism for that since it's just kind of a one aero mechanism. I'm just gonna kind of, um, strategically erase and just draw this as the negative sign that would be used to seeing and draw an eight right there. Uh, now notice those two have a pretty similar PK. Probably eso is very possible those things would exist in equilibrium, kind of just trading that 100 back and forth. But this is the main structure off the product that asked for in the question right there.