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

7. Substitution Reactions

SN2 Reaction

Organic Chemistry

7. Substitution Reactions

SN2 Reaction

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Multiple Choice

Predict the product of the following reaction.

Product structure with hydroxyl and chlorine groups for SN2 reaction.

Chemical structure with hydroxyl and chlorine groups indicating SN2 reaction product.

Chemical structure showing hydroxyl group for SN2 reaction product prediction.

Chemical structure of an alkene for SN2 reaction analysis.

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Verified step by step guidance

Identify the type of reaction: The given reaction involves a secondary alkyl chloride and hydroxide ion (OH-), which suggests a nucleophilic substitution or elimination reaction.

Consider the mechanism: Hydroxide ion (OH-) is a strong base and a good nucleophile, which can lead to either substitution (SN2) or elimination (E2) reactions.

Evaluate the substrate: The substrate is a secondary alkyl chloride, which can undergo both SN2 and E2 reactions. However, with a strong base like OH-, E2 is more likely.

Predict the E2 elimination product: In an E2 reaction, the base abstracts a proton from a β-carbon, leading to the formation of a double bond. Identify the β-hydrogens and predict the most stable alkene product.

Consider Zaitsev's rule: The most substituted alkene is generally the major product in an E2 reaction. Therefore, predict the formation of the more substituted alkene as the major product.