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

16. Conjugated Systems

Pericyclic Reaction

Organic Chemistry

16. Conjugated Systems

Pericyclic Reaction

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Multiple Choice

Identify the type of the following pericyclic reaction.

Cycloadditions

Electrocyclic

Sigmatropic shift

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Verified step by step guidance

Examine the structures on both sides of the reaction. Notice that the number of carbon atoms and the overall connectivity remains the same, indicating a rearrangement rather than a reaction that forms or breaks multiple bonds.

Identify the type of pericyclic reaction by considering the changes in the bonding pattern. In this case, observe that a single bond is migrating from one position to another within the molecule.

Recognize that the reaction involves the migration of a sigma bond along with the reorganization of pi bonds, which is characteristic of a sigmatropic shift.

Consider the reaction conditions. The presence of heat (indicated by the delta symbol) is typical for sigmatropic shifts, as they often require thermal activation.

Conclude that the reaction is a sigmatropic shift, as it involves the migration of a sigma bond and the reorganization of pi bonds within a single molecule, without the formation of new rings or the breaking of the molecular framework.