Write the aldol condensation mechanism and product for benzaldehyde + cyclohexanone in a base. Then trans-cinnamaldehyde + acetone in base. Then, trans-cinnamaldehyde + cyclohexanone in a base.
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Write the aldol condensation mechanism and product for benzaldehyde + cyclohexanone in a base. Then trans-cinnamaldehyde + acetone in base. Then, trans-cinnamaldehyde + cyclohexanone in a base.
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- Draw the aldol product for the reaction of the aldehyde shown with NaOH. Assume the reaction is run under conditions that allow the reaction to stop before dehydration. NaOHThe compound shown here is the product of a base-catalyzed aldol condensation. Draw the structure of the nonaromatic-containing starting material that is present before the aldol condensation and the aldol addition.please explain how aldol condensation reaction work please
- Can you assist with the complete stepwise reaction mechanism for the following Aldol condensation reaction. curved arrows to show direction of electron flow.Mixed aldol condensations involving benzaldehyde yield typically a single product. Draw the structure of the partner that was used to synthesize this molecule: You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. Do not include lone pairs in your answer. They will not be considered in the grading.need help with the aldol condensation product
- Aldol Condensation- Synthesis of Dibenzalacetone The protocol says that, after adding in all the reactants, stir for an additional 15 minutes. A student swirled for only 8 minutes and then, correctly, stopped and proceeded with isolating the product. What did the student do that gave such confidence and accuracy?Supply the structures of reactant(s) or product(s) for the following aldol and Claisen reactionsDraw the major organic product that forms in an intramolecular aldol condensation. Remember that heat is applied. NaOH/H₂O, heat
- All are true or false a) The initially formed b-hydroxy carbonyl compound loses water in a Aldol condensation. b) Equilibrium favors the starting materials with both aldehydes and ketones for Aldol reactions. c)The Claisen reaction is a type of nucleophilic addition? d) The b-hydroxy carbonyl product of an Aldol reaction is oftentimes not the final isolated product. e)b-Ketoester and an enolate are the two starting materials for a Robinson annulationIn an aldol condensation reaction where dibenzyl ketone is used to produce Tetraphenylcyclopentadienone, the conditions are changed. Suppose instead of using dibenzyl ketone (1,3-diphenyl-2-propanone) we used benzophenone (diphenylmethanone). Would this reaction work? Why or why not? Hint: Does α-carbon to carbonyl group has hydrogen?for the aldo reaction which one is better with solvent or without a solvent? part a used NaoH, benzaldehyde, Acetone, and part b used aceophene, para-methylbenzaldehyde, and NaoH
