Please showcase whether its a full electron pair being moved or a singular electron moving 2H3C27HArrow-pushing InstructionsH3COHgeHSubmit Answerbase›×™The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination ofnucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to theelectrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes orketones, although aldehydes are more reactive. The product is a B-hydroxy carbonyl compound.OHwalH3CUnder reaction conditions slightly more vigorous than those employed for the aldol reaction, the B-hydroxyl group iseliminated in an E1cB dehydration to give an a,ß-unsaturated carbonyl compound.Draw curved arrows to show the movement of electrons in this step of the mechanism.HонheatH3CH3COHRetry Entire Group 9 more group attempts remainingHH+ H₂OH₂O: 2H3CH3CH3CThe aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination ofnucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to theelectrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes orketones, although aldehydes are more reactive. The product is a ß-hydroxy carbonyl compound.Arrow-pushing InstructionsH:OHSubmit AnswerXTbaseUnder reaction conditions slightly more vigorous than those employed for the aldol reaction, the ß-hydroxyl group iseliminated in an E1cB dehydration to give an a,ß-unsaturated carbonyl compound.Draw curved arrows to show the movement of electrons in this step of the mechanism.:0:-heateleH3CHOHHH3CRetry Entire Group 9 more group attempts remainingH+ H₂OHOH

The mechanism of given reaction can be explained as:

2 H3C ². H OH base H3C H H3C The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination of nucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to the electrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes or ketones, although aldehydes are more reactive. The product is a 3-hydroxy carbonyl compound. H Submit Answer Under reaction conditions slightly more vigorous than those employed for the aldol reaction, the ß-hydroxyl group is eliminated in an E1cB dehydration to give an a,ß-unsaturated carbonyl compound. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions AOC XT H OH OH Retry Entire Group heat H3C OH H3C 9 more group attempts remaining + H₂O i H H₂O:

2 H3C ². H OH base H3C H H3C The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination of nucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to the electrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes or ketones, although aldehydes are more reactive. The product is a 3-hydroxy carbonyl compound. H Submit Answer Under reaction conditions slightly more vigorous than those employed for the aldol reaction, the ß-hydroxyl group is eliminated in an E1cB dehydration to give an a,ß-unsaturated carbonyl compound. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions AOC XT H OH OH Retry Entire Group heat H3C OH H3C 9 more group attempts remaining + H₂O i H H₂O:

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter26: Aldol And Claisen Reactions

Section: Chapter Questions

Problem 5E

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2 H3C H3C H C→XT OH H3C The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination of nucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to the electrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes or ketones, although aldehydes are more reactive. The product is a ß-hydroxy carbonyl compound. base :0: OH H H Under reaction conditions slightly more vigorous than those employed for the aldol reaction, the ß-hydroxyl group is eliminated in an E1cB dehydration to give an a,ß-unsaturated carbonyl compound. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instruct ns H3C heat OH H3C :0: H + H₂O H
base 2 H3C H H3C OH heat H H3C + H₂O H The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination of nucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to the electrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes or ketones, although aldehydes are more reactive. The product is a ẞ-hydroxy carbonyl compound. Under reaction conditions slightly more vigorous than those employed for the aldol reaction, the ẞ-hydroxyl group is eliminated in an E1CB dehydration to give an a,ẞ-unsaturated carbonyl compound. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions X :OH H₂O: а کی H₂C H H₂C H H
I H H3C NOC XT :0: MET H₂C base H3C The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination of nucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to the electrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes or ketones, although aldehydes are more reactive. The product is a ß-hydroxy carbonyl compound. H OH q H3C H₂C H Under reaction conditions slightly more vigorous than those employed for the aldol reaction, the ß-hydroxyl group is eliminated in an E1cB dehydration to give an a,ß-unsaturated carbonyl compound. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions heat H H + H₂O
2 Moin H3C H H₂C C⇒x= base :0: OH Hori H3C H. The aldol reaction is a carbonyl condensation reaction between two carbonyl partners and involves a combination of nucleophilic addition and a-substitution steps. One partner is converted into an enolate ion nucleophile and adds to the electrophilic carbonyl group of the second partner. In the classic aldol reaction, the carbonyl partners are aldehydes or ketones, although aldehydes are more reactive. The product is a B-hydroxy carbonyl compound. Under reaction conditions slightly more vigorous than those employed for the aldol reaction, the ß-hydroxyl group is eliminated in an E1cB dehydration to give an a,ß-unsaturated carbonyl compound. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions H₂C Ἡ :0: heat H Home H3C + H₂O
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