What is the major organic product of the following reaction? <img src="https://media.pearsoncmg.com/ph/esm/ecs_mullins_organic1e/msa/content/practice-test/img/Ch05_Q13_QT.jpg" alt="The figure illustrates a reaction. The reaction contains two reactants. The first reactant has the following structure: A 6-carbon hexagonal ring is in a vertical orientation with C 1 occupying the topmost vertex. C 1 is single bonded to C H 3 on the upper right and C H 3 on the upper left, each in the form of a line. C 6 is single bonded to C H 3 in the form of a line. The second reactant has the following structure: B r, single bond, B r. Delta is written under the reaction arrow." />

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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

11. Radical Reactions

Radical Selectivity

Organic Chemistry

11. Radical Reactions

Radical Selectivity

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Multiple Choice

What is the major organic product of the following reaction?

The figure illustrates the structure of a molecule. A 6-carbon hexagonal ring is in a vertical orientation with C 1 occupying the topmost vertex. C 1 is single bonded to B r on the upper right. C 1 is single bonded to C H 3 above and C H 3 on the upper left, each in the form of a line. C 6 is single bonded to C H 3 in the form of a line.

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Verified step by step guidance

Identify the type of reaction: The reaction involves the addition of bromine (Br2) to an alkane under heat, which suggests a radical halogenation process.

Determine the most stable radical: In radical halogenation, the most stable radical is formed preferentially. Tertiary radicals are more stable than secondary or primary radicals due to hyperconjugation and inductive effects.

Locate the tertiary carbon: In the given cyclohexane structure, identify the tertiary carbon atom, which is the carbon bonded to three other carbon atoms.

Predict the major product: The bromine radical will most likely abstract a hydrogen from the tertiary carbon, leading to the formation of a tertiary radical. Bromine will then add to this radical, forming the major product.

Consider stereochemistry: If applicable, consider the stereochemistry of the product, although radical reactions typically do not have stereochemical control.