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![d. Draw arrow-pushing mechanism for an enzymatic retro-aldol reaction of the following hexose.
Use B: and/or HA as needed.
OH
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OH OH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb52f182a-8cfa-4e43-ab11-a6de061edc39%2F6cad2ace-b3c8-4dd4-9f88-c86a6d2ffefc%2Fltt48un_processed.png&w=3840&q=75)
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- In micxed aldol condensation of acetone with excess benzaldehyde in the presence of MaOH: why benzaldehyde not condense with itself? it's conjugate base is too weak its conjugate base is too strong it contains no a-carbons it contains no a-hydrogensPropose an efficient synthesisDraw a complete stepwise mechanism for the aldol self-condensation reaction shown below. You must show the structures of all intermediates and indicate electron flow with curly arrows
- (a) Draw a mechanism using the curved arrow-formalism for the O-4 methylation of thymine. Is thenucleophilic substitution in the first step an SN1 or SN2 reaction? Explain.Devise a synthesis of CH3CH2CH2CHO from two-carbon starting materials. Draw both the retrosynthesis and the forward synthesis.Q1: Product of aldol condensation H 0^6= + NaOH Ethanol A) B) C) D) ör ör od or
- In micxed aldol condensation of acetone with excess benzaldehyde in the presence of NaOH: it is possible that acetone condense with itself.draw the result from a single such condensationdraw the organic product(s) of the reaction provided.draw both the resonance forms of the acyl cation intermediate. draw the electron arrow mechanism.2) An enolate attacks an aldehyde and the resulting product is subsequently protonated. W type of reaction is this? A) a Fischer esterification B) an acid-catalyzed aldol condensation C) a base-mediated aldol condensation D) a Hell-Volhard-Zelinsky reaction
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