What would be the product if one molecule of cinnamaldehyde reacted with one molecule of acetone in an aldol condensation reaction vesus two molecules of cinnamaldehyde reacting with one molecule of acetone?
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What would be the product if one molecule of cinnamaldehyde reacted with one molecule of acetone in an aldol condensation reaction vesus two molecules of cinnamaldehyde reacting with one molecule of acetone?
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- Draw the structure of the aldol that will form when cyclohexanone reacts with one mole ofbenzaldehyde. What is the name of this compound?4. Give the structures of the aldol products that form when each of the following compounds or mixtures is treated with NAOH. a) Butanal b) Cyclopentanone c) Acetophenone d)-Chlorobenzaldehyde and 2,2-dimethylcyclohexanoneGive the IUPAC name of the reactants that would give the following aldol condensation product.
- What is the general name for the reaction product formed in an aldol addition reaction? O y-Hydroxy carbonyl compound a,B-Hydroxy carbonyl compound O a-Hydroxy carbonyl compound O B-Hydroxy carbonyl compoundWhat is the major intramolecular aldol product formed when dicarbonyl compound A is treated with base?Why is the Aldol reaction often called an Aldol condensation? 1) The initially formed b-hydroxy carbonyl compound loses an oxygen atom 2) The initially formed b-hydroxy carbonyl compound loses a hydrogen atom 3) The initially formed b-hydroxy carbonyl compound loses water 4) The initially formed b-hydroxy carbonyl compound loses a hydroxyl group
- Draw the product formed when each dicarbonyl compound undergoes anintramolecular aldol reaction followed by dehydration, when possible.The following molecule is formed in a mixed aldol condensation reaction. organic starting materials B-hydroxycarbonyl HO NaOHWhat is the reaction mechanism for formaldehyde and phenol under acidic conditions.
- The following molecule is formed in an intramolecular aldol condensation reaction. Draw the organic starting material needed to form the given α,β-unsaturated carbonyl compound.An enolate attacks an aldehyde and the resulting product is subsequently protonated. What type of reaction is this? an acid-catalyzed aldol condensation a Fischer esterification. a Grignard reaction. a base-mediated aldol condensationWhat steps use in Malonic ester synthesis?