JV Give the major brief product Hzo 9 explanation and for provide the full arrow predicted regiochemistry pushing mechanism for stereochemistry_ the following...

Provide a mechanism that explains formation of the following products. Indude all intermediates, formal charges, and arrows showing electron flow.

Okay, um, in this problem, we are talking about the mechanisms and predicting the products of alkaline reactions. Specifically, in this case, we are going to be reacting al canes with hell agents, and that's we're going to be going over today, and we're also going to be using stereo chemistry. So for part A, we have this sigh click structure that has an elk in, and we are reacting it with diatonic probing. Remember that our mechanism arrows always go from electron rich to electron poor. This is the idea of a polar reaction using an electoral file and a nuclear file. So we're going to have this double bond. That's electron rich going to our bro Ming and picking up one of the bro means. And then are we? Pardon me, we will return our two electrons of this diatonic roaming bond onto one of our bro means So now we are going to form this ring that has a essentially a a pox side with this bro. Mean Adam And then we have a leftover negatively charged roaming an ion. So these electrons are going to attack are a pox. I'd ring and open it up and this would be our product. We have this ring here. We have a trans relationship between our roaming atoms where 11 would be appointing above the plain. One would be below, and that would be our product for our first reaction. Now, for our second reaction, we have something very similar. But now are all keen is not internal. It is a terminal, Elkin. So we're going to have a terminal, a pox side. So again, we have this benzene ring attached to this Al Kane, and we are reacting it with di atomic chlorine. So again, we're good for electron, rich to electron, poor are double bond is going to pick up one of these chlorine atoms and return the two electrons onto our chlorine. That's how we're getting an anti on. So we're going to have this benzene ring attached to an a pox side. And instead of an oxygen in this case, we're going to have a positively charged chlorine atom and then our leftover and ions we're going to have these electrons attack are a pox. I'd ring, causing it to open up. And this would be our product. Here we have this ring with this Al Caine structure with two chlorine atoms. And now, finally, we have a very similar, um, reaction as in part B, We start with this Al Keen in this case, we have it to be internal. Remember, we go from electron bridge to electron poor Are double bonds going to pick up one of these electrons or partly one of these chlorine chlorine? Return the two electrons onto our chlorine atom. We're going to form an a pox side with our positive charge. Chlorine atom, our chlorine. An ion is going to attack one of the sides of Europe. Oxide. Returning these electrons onto are positively charged chlorine. And then we're going to produce this product. And as we saw in part A, we have a trans relationship between our two chlorine atoms, and that is the end of this problem. I will make sure that all of our reactions are in one screen for you. I hope this made sense. If you have any questions, please comment or feel free to post a question I'm happy to answer. Um, I hope that this helps you in your current studies in organic chemistry

Most rejected Al Qaeda light and strong basic reaction condition favor elimination reaction. There is less of shooting l clear light with the strong nuclear file. Priefer substitution Reaction Question sixty A From Chapter eight, The substrate is to serious alight and the reaction medium is highly basic with a bulky peas this favor elimination over substitution. So this product other than this product elimination product will be favored. Maser product would be the most suspicious and more substituted hell king the sub status family Helen and then and direction condition is strongly nuclear. Filic primary alight with strong clear feli condition Favors sento over l ignition reaction so the product would be a suspicion Productive, not the ignition. This is a tertiary, Helen. Yeah, under strong basic condition. So it will favor elimination over any substitution Porter, But Mr Product would be most shooted Elke Okay, most ofthe uses a cane. Our prudent, technically more unstable this favor part substrate. In this question, it's second relayed. Secondly, her light can undergo either elimination reaction or substitution reaction depending upon reaction condition. In this case, I would die in negative is a weakness. But ah very could nuclear file this this reaction will favor substitution over elimination. So any animation production, I wouldn't be a minor product and Mr products her the substitution product.

Which of the following Let's predict the products or products and provide the complete mechanism for a We're going to start off with two meth Oxy Benzo night trial. This is going to react with ch three m g b are just a little pair minus plus yes, this would come in here. This would come out here and we'd have an intermediate which is an amine and I in minus there. And then this would react with H 20 to produce our products. Fine and NH three and a product here if we name, it would be one gosh to the foxy fennel f a known for be. We're gonna start with three methanol butin night trial and we have okay n g p r. This would be be alone. Pair here. Um minus Plus, this would come over here, this would come out. This was a game produced in a mean and I am And are you mean and I in would be 23 It's carbon. That's a double bond and minus and the presence of H 20 So give us our product here She beat 123 carbon double bond. Oh, and here and this also produce NH three. And if we're to Neymar product, this would be to five di Method hex and three own for C. I'm gonna start with site girl Cyclone Propane. Carbo night Trial on this is going to react with M g p R on benzene. Let's be a minus here. This would come in here, come out gain. We're gonna produce an A mean and iron This would produce see double pond n and we've got a ring here. So there's an intermediate Andi react with each two. Oh, this will give us our product here and N h three. And if we need our product, this is cyclo proposal that long Methadone. Lastly for D true See Triple Bond N on this PMG PR and C H two ch three minus coming here. Come out once again producing an amine and iron See double bond n minus ch two ch three And this is our intermediate react with each too old would produce just a little bit better here. You don't want to own ch two ch three and ammonia and let's name our products here. This is four f o X and three own. There would be the mechanism and the products of the for given reactions

A reaction forms this compound were the E two the mechanism. This compound, on the other hand, is formed by the S and to the mechanism. The reaction forming these two compounds happens B of e two mechanism as well.