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

Substitution Comparison

Organic Chemistry

7. Substitution Reactions

Substitution Comparison

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2:58 minutes

Problem 5

Textbook Question

Would you expect the following substitution reaction to proceed with inversion or racemization? Why?

Verified step by step guidance

Identify the type of substitution reaction (SN1 or SN2) by analyzing the substrate, nucleophile, solvent, and leaving group. SN1 reactions typically occur with tertiary substrates and polar protic solvents, while SN2 reactions favor primary substrates and polar aprotic solvents.

Understand the stereochemical outcome of each mechanism: SN1 reactions proceed through a carbocation intermediate, which allows for planar geometry and can lead to racemization. SN2 reactions involve a backside attack by the nucleophile, leading to inversion of configuration.

Examine the substrate structure. If the carbon undergoing substitution is chiral, the stereochemical outcome will depend on the mechanism. For SN1, the planar carbocation intermediate allows the nucleophile to attack from either side, leading to a mixture of enantiomers (racemization). For SN2, the backside attack ensures inversion of configuration.

Consider the role of the nucleophile and solvent. A strong nucleophile and polar aprotic solvent favor SN2, while a weak nucleophile and polar protic solvent favor SN1. This will help determine the likely mechanism and stereochemical outcome.

Conclude whether the reaction proceeds with inversion or racemization based on the mechanism determined in the previous steps. If SN1 is favored, expect racemization. If SN2 is favored, expect inversion of configuration.

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Nucleophilic Substitution Mechanisms

Nucleophilic substitution reactions can occur via two primary mechanisms: SN1 and SN2. In SN2 reactions, the nucleophile attacks the electrophile in a single concerted step, leading to inversion of configuration at the chiral center. In contrast, SN1 reactions involve a two-step process where the leaving group departs first, forming a carbocation, which can then be attacked by the nucleophile from either side, potentially resulting in racemization.

Stereochemistry

Stereochemistry is the study of the spatial arrangement of atoms in molecules and how this affects their chemical behavior. In substitution reactions, the stereochemical outcome is crucial; inversion occurs in SN2 reactions due to the backside attack of the nucleophile, while racemization can occur in SN1 reactions due to the planar nature of the carbocation intermediate, allowing for attack from either side.

Chirality and Optical Activity

Chirality refers to the property of a molecule that makes it non-superimposable on its mirror image, often due to the presence of a chiral center. Molecules that are chiral can exhibit optical activity, rotating plane-polarized light. In substitution reactions, the outcome—whether inversion or racemization—affects the optical activity of the product, which is essential for predicting the behavior of the resulting compounds.

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