Table of contents

1. A Review of General Chemistry5h 5m
2. Molecular Representations1h 14m
3. Acids and Bases2h 46m
4. Alkanes and Cycloalkanes4h 17m
5. Chirality3h 39m
6. Thermodynamics and Kinetics1h 22m
7. Substitution Reactions1h 48m
8. Elimination Reactions2h 30m
9. Alkenes and Alkynes2h 9m
10. Addition Reactions3h 19m
11. Radical Reactions1h 58m
12. Alcohols, Ethers, Epoxides and Thiols2h 42m
13. Alcohols and Carbonyl Compounds2h 17m
14. Synthetic Techniques1h 26m
15. Analytical Techniques:IR, NMR, Mass Spect7h 3m
16. Conjugated Systems6h 13m
17. Ultraviolet Spectroscopy51m
18. Aromaticity2h 34m
19. Reactions of Aromatics: EAS and Beyond5h 1m
20. Phenols55m
21. Aldehydes and Ketones: Nucleophilic Addition4h 56m
22. Carboxylic Acid Derivatives: NAS2h 51m
23. The Chemistry of Thioesters, Phophate Ester and Phosphate Anhydrides1h 10m
24. Enolate Chemistry: Reactions at the Alpha-Carbon1h 53m
25. Condensation Chemistry2h 9m
26. Amines1h 43m
27. Heterocycles2h 0m
28. Carbohydrates5h 53m
29. Amino Acids4h 20m
30. Peptides and Proteins2h 42m
31. Catalysis in Organic Reactions1h 30m
32. Lipids 2h 50m
33. The Organic Chemistry of Metabolic Pathways2h 52m
34. Nucleic Acids1h 32m
35. Transition Metals6h 14m
36. Synthetic Polymers1h 49m

25. Condensation Chemistry

Crossed Aldol Condensation

Organic Chemistry

25. Condensation Chemistry

Crossed Aldol Condensation

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Multiple Choice

Give the structure of the aldehydes or ketones used to create the product prepared by a crossed aldol condensation reaction.

Chemical structures of reactants in a crossed aldol condensation reaction.

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Verified step by step guidance

Identify the product structure from the crossed aldol condensation reaction. The product shown in the image is a compound with a furan ring and an α,β-unsaturated ketone.

Recognize that a crossed aldol condensation involves two different carbonyl compounds, typically an aldehyde and a ketone, reacting together.

Examine the product structure to determine the fragments that could have originated from the starting aldehyde and ketone. The α,β-unsaturated ketone portion suggests the presence of an enolate ion formed from a ketone.

Consider the possible aldehyde and ketone combinations that could lead to the observed product. The furan ring suggests that one of the starting materials might be a furan-based aldehyde or ketone.

Analyze the images provided to identify the structures of the aldehydes and ketones. The correct combination will be the one that, when reacted, forms the α,β-unsaturated ketone with the furan ring as seen in the product.