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- What is the reactant that would give the following Aldol Condensation product? 01 0 | 0 ||| O IV OV H H تبار نہید لبد بد مبد IV :O: ة :0: :0: :O:Synthesis Reaction for Organic Chemistry Can you go from the starting material to the product using mostly aldol reactions@GMU 73765 What is the expected product A for the following intramolecular aldol reaction? O CH3 O NaOH A H3C EtOH H
- The reaction below is a base-catalyzed aldol reaction. O || CH₂-C-H CH3-C-H Ethanal (Acetaldehyde) H I CH3-C-H Ethanal (Acetaldehyde) NaOH Draw curved arrows to show the movement of electrons in the step of the mechanism shown below. Arrow-pushing Instructions AC⇒x= :O: || :CH₂-C-H OH Bl CH3-CH—CH2-CH -CH₂-1-1 a 3-Hydroxybutanal (B-hydroxyaldehyde; formed as a racemic mixture) :0: :0: || CH3—CH—CH2-C-H A tetrahedral carbonyl addition intermediate XDraw the product for the following reaction.Draw the structure for the nucleophilic substitution product.
- 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 HReaction of the given D-aldose below with Ac₂0 can be catalyzed by BF3-Et20. Which of the following is the B-furanose structure of the product upon acetylation of the given aldose? Select one: CH₂OAc Aco OAc CH₂OAc OAC AC OAc O CH₂OAC OAc ỌAc ACO OAC OAc O CH,OAc ỌAC OAc HO CHO -OH -ОН CH₂OHGive the product of the aldol condensation in Figure 3
- Subject: chemistryWhat are the products of an aldol cyclization for the following compound?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