Question 4 of 14Write the structure of the products formed in the following acyl group transfer reactions. Identify the reagents as esterificationsor thioesterifications.EDс728RF7V96OH5C Search or type URLTGcatalystBSiv6YMacBook ProHDraw the major organic product of reaction A. Draw nonbonding electronpairs where applicable.Select Draw Templates MoreN/////SUJ8MCHTEZAO9IKH<0✓O***LOcommandPA.T****optionQ2Q74{[?AaI+1"1Erase1deletereturnshift EC728RFV:0: IClassify the reactions.OH265SHTO Search or type URLGcatalystBtv6YHDraw the major organic product of reaction B. Draw nonbonding electronpairs where applicable.MacBook ProNSelect Draw Templates More/ ||||||3 CUJ8MC H S 0THZAOIK9<OLcommandPV;IoptionQ2 Q[~~?AaErase1deletereturnshift

Esterification is a chemical reaction between an alcohol and a carboxylic acid or a derivative of a…

Question 4 of 14 Write the structure of the products formed in the following acyl group transfer reactions. Identify the reagents as esterifications or thioesterifications. Macmillan Learning 28 :0: catalyst Draw the major organic product of reaction A. Draw nonbonding electron pairs where applicable. Draw Templates More Select S MacBook Pro e CH 0 TRZAO Q2Q Aa Erase

Question 4 of 14 Write the structure of the products formed in the following acyl group transfer reactions. Identify the reagents as esterifications or thioesterifications. Macmillan Learning 28 :0: catalyst Draw the major organic product of reaction A. Draw nonbonding electron pairs where applicable. Draw Templates More Select S MacBook Pro e CH 0 TRZAO Q2Q Aa Erase

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter26: Biodiesel

Section: Chapter Questions

Problem 1Q

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Complete and balance the following methesis reaction in aqueous solution.Answer Entery Instructions• Parentheses are only required around polyatomic ions and only when more than 1 of those ions is present.K3PO4 (no parentheses required).Mg3(PO4)2 (parentheses required).• In each case one product is soluble (aq) and one insoluble (s). Use solubility rules to determine which product appears in each box.***Answer*** Na2S (aq) + ***Answer*** FeCl3 (aq) ➝ ***Answer*** ***Answer*** (s) + ***Answer *** ***Answer*** (aq)
When some sugars dissolve in water they spontaneously undergo changes in optical rotation called mutarrotation. The Mutarrotation of D-glucopyranose is catalyzed by acid and bases. 2-Hydroxypyridine is a more effective catalyst than phenol and pyridine for this reaction because: a.Both oxygen and N in 2-hydroxypyridine act as bases increasing the rapid interconversion of sugar b. The OH of 2-hydroxypyridine serves as the base while the current N as the acid. c. 2-hydroxypyridine acts both as a base to remove the proton from the hydroxyl group in the hemiacetal and as an acid to provide a proton to the oxygen in the hemiacetal. d.Phenol and pyridine are very expensive.
pls match them with the options, thats all What is the purpose of using the following chemicals in the preparation of n-butyl acetate? 1. Na2CO3 2. H2SO4 3. MgSO4 4. CH3COOH options: It is used as a dehydrating agent It is used as a catalyst It is used as a neutralizing substance for excess acid It is one of the reactant
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When the ammonium salt (CH3CH2CH2)3NHCl is treated with NaOH, the products are water, NaCl, and an organic product. Provide the product in an attached file.
A student decided to run the esterification reaction between p-toluic acid (p-methylbenzoic) and ethanol but found that the stockroom had only just enough ethanol left to react with her carboxylic acid, that is, a stoichiometric amount of alcohol. Furthermore, the only concentrated acid the stockroom had left was hydrochloric acid (a non-dehydrating acid ). What other method (s) could she use to drive the esterification reaction to completion ?
Rewrite the saponification reactions using bond line formula. Also include the names and molecular mass of each molecule. I NEED HELP WITH THIS QUESTION- Sketch the mechanism of the reaction and show what part of the triglyceride becomes the glycerol molecule and what becomes sodium palmitate.
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PLEASE ANSWER COMPLETELY.1. Write an equation showing the esterification reactions that would produce these followingcompounds:a. Butyl ethanoateb. Ethyl propanoate2. Complete each of the following reactions by supplying the missing portion indicated with a blankspace.(PLEASE REFER TO IMAGES)3. Design the synthesis of the following esters from organic alcohols. Write the IUPAC name of thecompounds involved.a. Methyl butanoateb. Propyl methanoate4. Complete each of the following reactions by drawing the structures of the missing product(s).Write the IUPAC nomenclature system to name each of the products.(PLEASE REFER TO IMAGES)
Draw the product of the reactions of succinic anhydride with each of the listed reagents. Assume in all cases that the reagent is present in excess and an aqueous workup takes place after each reaction. A. Reaction with (CH3)2CHOH. \table[[Select,Draw,Templates More,,],[/,//,I//,H,Erase]] B. Reaction with NH3. \table[[Select,Draw,tes More,Erase],[/,//,III,C,H,N,0]] Question Source: Vollhardt 7e0 Organic Chemistry: Structure And Function Publishęr: W. Freemar C. Reaction with phenylmagnesium bromide in THF, followed by H+,H2o. \table[[Select,Drav,v T,lates,,,Erase],[1,II,III,C,H,0,]] D. Reaction with LiAlH4 in ether, followed by H+,H2O \table[[Select,Draw,Templates More],[/,//,III]] \table[[3,0]] \table[[,2,Q
Draw the missing organic structures or select the missing reagents in the following multistep synthesis. Ignore any inorganic byproducts formed.
so we know that fischer esterification is a type of organic reaction that involves the formation of an ester from a carboxylic acid and an alcohol in the presence of an acid catalyst. am I correct to assume that a fisher esterification mechanism would look different than the above nucleophilic addition reaction? If they are different you you present the Fisher esterification mechanism of the reaction of acetic acid with pentanol in the presence of an acid catalyst, sulfuric acid and explain the mechanism