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

17. Ultraviolet Spectroscopy

Woodward-Fieser Rules

Organic Chemistry

17. Ultraviolet Spectroscopy

Woodward-Fieser Rules

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Multiple Choice

Which of the following compounds do you expect to show the largest λ_max?

cyclic alkene

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Verified step by step guidance

Identify the concept of λmax: λmax refers to the wavelength at which a compound absorbs the maximum amount of light. In organic chemistry, this is often related to the extent of conjugation in a molecule.

Analyze the structures: Look at each compound and determine the extent of conjugation. Conjugation occurs when p-orbitals overlap, allowing for delocalization of π-electrons across adjacent double bonds.

Compare the conjugation: The more extensive the conjugation, the longer the wavelength (λmax) at which the compound will absorb. This is because the energy gap between the ground state and the excited state decreases with increased conjugation.

Evaluate the structures: Count the number of conjugated double bonds in each compound. The compound with the most conjugated double bonds will likely have the largest λmax.

Consider aromaticity: If any of the compounds are aromatic, they may have a higher λmax due to the stability and delocalization of electrons in the aromatic system. Compare the aromaticity and conjugation of each compound to determine which has the largest λmax.