Please correct answer and don't use hend raiting(Step by step solutions) Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the aldol or enone below.geHOOHCitrate coenzyme ADisconnect the C-C bond nearer the SCOA group.Represent SCOA by drawing SCH3.SCOA(This is a step in the glyoxylate metabolic pathwaycatalyzed by the enzyme citrate synthase.SCOA is coenzyme A.)You do not have to consider stereochemistry.• Draw the enolate ion in its carbanion form.• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Separate multiple reactants using the + sign from the drop-down menu.0▾+ChemDoodleⓇ√ F5c

The formation of citrate coenzyme A typically involves the condensation of oxaloacetate with…

Answered: Draw structures for the carbonyl…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter19: Eas: Electrophilic Aromatic Substitution

Section: Chapter Questions

Problem 25E

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Similar questions

Draw the product formed (after dehydration) in the crossed aldol condensation of phenylacetaldehyde (C6H5CH2CHO) with CH2(CO2Et)2 in the presence of sodium hydroxide.
(b) Why is the Claisen-Schmidt reaction a special type of aldol condensation? one of the reactants does not have a β hydrogen one of the reactants is acetone the reaction is base-catalyzed one of the reactants does not have an α hydrogen (b) Aside from having a carboxylic acid functional group, salicylic acid also has which of the following functionality? aldehyde alcohol ester phenol
Predict the products of aldol condensation, followed by dehydration, of the followingketones and aldehydes. c) cyclohexanone
Draw the enone product of aldol self- condensation of benzaldehyde. If self- condensation fails, tell OWL by drawing ethane, CH3CH3.
An enolate attacks an aldehyde and the resulting product is subsequently protonated. What type of reaction is this? an acid-catalyzed aldol condensation a Fischer esterification. a Grignard reaction. a base-mediated aldol condensation
Define Dehydration of the Aldol Product ?
ArSO,H Draw curved arrows to show the movement of electrons in the following step of an acid-catalyzed aldol condensation reaction. Arrow-pushing Instructions Hjö: H-Ö- -Ar H. Ar O=h=0
2) Provide the structure of the two organic starting materials that are required to produce cinnamaldehyde (PhCH=CHCHO) via a crossed aldol condensation followed by dehydration?
During the second reaction of glycolysis, the carbonyl group is moved from carbon 1 to carbon 2 forming the ketose fructose-6-phosphate. This is a necessary step in glycolysis because O this is an energetically favorable reaction that drives the first step in glycolysis forward the carbonyl in this position stabilizes the subsequent formation of the enediol intermediate the position of the carbonyl will determine the cleavage point in the reverse aldol condensation two steps later this allows transfer of the phosphate group from fructose to ADP to form ATP in the next step
D) 2) What two organic starting materials are required to produce cinnamaldehyde (PHCH=CHCHO) via a crossed aldol condensation followed by dehydration? A) PHCH3 and CH3CHO B) PHCHO and CH3CH2CHO C) PHCHO and CH3CH2OH D) PHCHO and CH3CHO uart "nolizable ketone to its enolate
This reaction shows that an aldol-type reaction can be performed with a deprotonated imine as the nucleophile. On hydrolysis, the product is the normal B-hydroxycarbonyl compound. Notice that LDA is used H3C N. 1. LDA Но ? as the base instead of HO¯. H3C H. H. (a) Explain why HO¯ cannot be used as a base for this 2. reaction. (b) Provide a detailed mechanism for this reaction, including the structure of the intermediate species not shown.
ArSO;H Draw curved arrows to show the movement of electrons in the following step of an acid-catalyzed aldol condensation reaction. Arrow-pushing Instructions :ÓH :OH ö:

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