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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 enolate anion and the carbonyl that would be needed to make this product through an aldol condensation reaction. Draw Enolate AnionDraw a stepwise mechanism for the following variation of the aldol reaction, often called a nitro aldol 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 product formed when each dicarbonyl compound undergoes an intramolecular aldol reaction followed by dehydration, when possible.Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol condensation reaction. H O O
- 16. Draw the structure of the aldol self-condensation (followed by dehydration) product for each of the following compounds. If a compound does not undergo aldol self-condensation, explain why it does not. a) || CH3CHCH₂CH T CH₂ b)1. Draw the indicated enols/enolates of the indicated compounds. kinetic enolate thermodynamic enolate thermodynamic enol kinetic enol kinetic enolate thermodynamic enolate thermodynamic enol kinetic enolWhat starting materials are needed to synthesize each compound using an aldol or similar reaction?
- What is the product formed when each dicarbonyl compound undergoes an intramolecular aldol reaction, followed by dehydration.Aldol condensation is a reversible reaction and in fact aldols can be transform into the starting carbonyl compounds. Complete using arrows, the following retroaldol reactionDraw the major product obtained when the compound is heated in the presence of a base to give an aldol condensation.