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Provide a detailed, arrow-pushing mechanism for the hydrolysis reaction below. [15 points]OCH3HzOCHzOHHCI cat.OH...

Question

Provide a detailed, arrow-pushing mechanism for the hydrolysis reaction below. [15 points]OCH3HzOCHzOHHCI cat.OH

Provide a detailed, arrow-pushing mechanism for the hydrolysis reaction below. [15 points] OCH3 HzO CHzOH HCI cat. OH



Answers

Draw the mechanism for the reaction of cyclohexene with HCI.

Okay, so, I wanted to put the equation for the following reactions. The first one is is reactive for this digester and this is reacting with two equivalents of sodium hydroxide and water. So this would be considered under basic emissions. And the first steps of the O. H. The oxygen on some hydroxide is going to attack the cardinal carbon. We'll get the cocks it on and this is going to reform to expel the fox that I own. So get a Carlos of acid in the fox that I am going to impersonate water to get methanol and wants to get soon my drug step back to. So, if he reacts again, no facts, it will attack that carbon carbon and give us a second car bus of acid and a second equivalent of methanol, as well as a second equivalent of sodium hydroxide. Okay, for B, we're reacting the structure with water and hcl. So this will be under acidic conditions and one of the oxygen's going deeper into the acid. One of the actions of the key tune Earth yester. And then this is going to be calm more lectures silk. So what I was going to attack it. Give us an alcohol edition of O. H two. So we have a rich and the addition of wage to positive church and um, we're gonna get it puts on transfer. So how does your from which to it was going to go to the auction of the ether. Give us this and this is a better leaving group to the alcohol. The auction of the alcohol is going to reform the bond is the more stable than having a single bond. And as a result it's going to expel the ether. Use the oh, it's bad leaving group. We get a car muscle passage and ethanol Cassidy. I mean ethanol And the last step is for so we're still the hydrogen. There I step is for the college base of Hcl. She's scoring. It's a deeper into the key tune. Give us this with Hcl back

YEP. Quarter decks of acid hydrogen Asus. Yeah. Product of acid hide realizes. Has it idolizes. Process has been constantly explored to produce a variety of chemicals. Mhm. To produce a variety of chemicals, such as several doors hang with the windows going to cause, Yeah. Number four fructose. Yeah. Mhm. Number five hydroxy metal. Yeah. Five year old health care. Thank you. Six. Leave your clinic. Mhm. Leave your clinic asset. Right. Miss. I. Lost. And for free five footer. Okay.

Okay. So rest assured mechanism for the hydraulics of Macedo using an acid. And to settle is formed from the addition of two alcohols too a galahad. So we have the addition of two meth oxy groups and we're to treat this with With H 3-plus 2 some acid. It's going to marry draw with us. So one of these auctions is going to do you appreciate the hydrogen and we'll get the formation of a better leaving group. So bonds can form here and it's gonna expel the one group. Next step is for a water molecule to attack at the carbon carbon. Breaking the five armed and screw the addition of O. H. Two positive charge. So this is gonna be is he pregnant about another water molecule serving alcohol and meth oxy group. And the meth oxy group is going to do you appreciate the acid again. So turning itself into a better leaving group. And as a result the oxygen on O. H. Is going to use a pair of electrons to form a bond and expel the oh CH three Go down here. And the last step is for a water molecules to deeper in eight the O. H. Thank you, Mr Kayser. We get our products the key tune from the Seattle and the regeneration of the acid your surplus.

Okay. So restaurant mechanism for the following problems in the first one, we have a reaction with ethel purple in it. And this is this is a high this is a hydraulic this reaction. So it involves water and it's non catalyzed meaning we're not going to use hydroxide. So how hydroxide is is used as a catalyst because it's a stronger based in water that's going to react faster with the carbon carbon. The oxygen is going to attack the carbon carbon the same way hydroxide does but it's not as strong and it's going to expel the Esther. The fox side is going to deeper in the water. And we'll get method also side products. So get purple dark acid. Nothing. All it would be we have the analysis reaction with metal format so reacting with methyl amine. Okay, so the next gin on methyl amine will attack the carbon carbon again and expel the Esther just like an A. So we don't have to use one equivalent of methyl amine here because a fox side or the um be counting a base. So the structure right here is a stronger base than methyl amine. So it's going to deeper detonate the amid as opposed to methyl amine. Which is why we all, I need one equivalent of this and the same with meth oxide as well. It's also a stronger base than a. Nothing. I mean Is there an easy one equivalent? We have fennel as a side project as well?


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