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- Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol condensation reaction. H Draw Enolate Anion + Draw carbonylDraw the product where the aldol reaction is possible. if there is no reaction then state 'no reaction'.Draw a stepwise mechanism for the following variation of the aldol reaction, often called a nitro aldol reaction.
- Draw the aldol product formed from each compound. See attached file2) 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 reactionDraw the enolate anion and the ketone or aldehyde that would be needed to make this product through an aldol condensation reaction.
- Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol condensation reaction. O oo Draw Enolate Anion QDraw the enol intermediate and the ketone product formed in the attachedreaction.Aldol condensation is a reversible reaction and in fact aldols can be transform into the starting carbonyl compounds. Complete using arrows, the following retroaldol reaction