1. Provide structures for the products and/or starting materials for the following reactions.DonorAcceptorNaOHCH₂CH₂OHheatloss of H₂OH3Cmixed-aldol condensation productNaOHCH₂OHheat*) NOEEtOH#402) H₂O*ΕΙΟCH₂mixed-Claisencondensation product+HgC.H3CCHSHloss of H₂Omixed-aldol condensation productH3CлюдетеCH3 NaOEtloss of H₂Ointramolecular aldol condenstationcyclization product

The objective of the question is to provide the structures for the products and/or starting…

Answered: 1. Provide structures for the products…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter23: Carbonyl Condensation Reactions

Section23.SE: Something Extra

Problem 56AP

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Fill in the missing reagents a-e in the following scheme:
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resource from Cengage Learning - Google Chrome ssignment/takeCovalentActivity.do?locator=assignment-take e by the Aldol Condensation (References) OH base + H,0 heat H. 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. In the mixed aldol reaction, the best results are obtained when one of the partners does not have an a-hydrogen. It cannot form an enolate anion and can therefore not undergo self-reaction. The enolizable aldehyde is added slowly to a basic solution of the first aldehyde so that the mixed product is preferentially formed. Under reaction conditions slightly more vigorous…
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