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Interpretation:
The product of the base-catalyzed crossed aldol reaction between benzaldehyde and 3-pentanone and the product formed by its dehydration has to be drawn.
Concept introduction:
Aldol reaction is an addition reaction of
If two different carbonyl compound used in an aldol addition, known as a crossed-aldol reaction.
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Chapter 19 Solutions
Organic Chemistry
- What is the product formed when each dicarbonyl compound undergoes an intramolecular aldol reaction, followed by dehydration.arrow_forwardDraw the product formed when each dicarbonyl compound undergoes an intramolecular aldol reaction followed by dehydration, when possible.arrow_forwardDraw the major organic product formed when the benzoyl chloride undergoes a reaction with sodium acetate (sodium ethanoate).arrow_forward
- Draw the product formed when each dicarbonyl compound undergoes anintramolecular aldol reaction followed by dehydration, when possible.arrow_forwardThe 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.arrow_forwardDraw the structure of the aldol that will form when cyclohexanone reacts with one mole ofbenzaldehyde. What is the name of this compound?arrow_forward
- Predict the products of aldol condensation, followed by dehydration, of the followingketones and aldehydes. c) cyclohexanonearrow_forwardWhat 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 compoundarrow_forwardDraw the enol form of the following ketonearrow_forward
- The following molecule can be formed via an intramolecular aldol addition reaction. Draw the organic starting material needed to form the given B-hydroxycarbonyl compound. organic starting material B-hydroxycarbonyl NaOH OHarrow_forwarddraw the product formed if this compound will undergo acid-catalyzed fischer esterificationarrow_forwardDraw out the reaction mechanism for cyclohexanol to cyclohexanone. Sodium hypochlorite oxidation of an alcohol to a ketone with the product being cyclohexanone.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
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