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Chapter 6 Ionic Reactions-Nucleophilic Substitution and Elimination Reactions of Alkyl Halides

Chapter 6 Ionic Reactions-Nucleophilic Substitution and Elimination Reactions of Alkyl Halides. Introduction The polarity of a carbon-halogen bond leads to the carbon having a partial positive charge

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Competition among S N 2, S N 1, E2, and E1 Reactions

Competition among S N 2, S N 1, E2, and E1 Reactions. S N 2. S N 1. Competition among S N 2, S N 1, E2, and E1 Reactions. E2. E1. Rate-Determining Steps Revisited. S N 2. S N 1. E2. E1. Nucleophile Strength. The Free Energy Diagram. Hammond Postulate.

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Ch 6 Lecture 2 More S N 2

Ch 6 Lecture 2 More S N 2. Synthesis using S N 2 Reactions R ? S conversions We know S N 2 interconverts stereochemistry We can use this to produce the enantiomer we want in one step How would we make the R thiol? (2-steps). If multiple C* present, only the reacting center is affected

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208 views • 9 slides

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Leaving group ability - PowerPoint PPT Presentation

Chapter 6 Ionic Reactions-Nucleophilic Substitution and Elimination Reactions of Alkyl Halides

Competition among S N 2, S N 1, E2, and E1 Reactions

Ch 6 Lecture 2 More S N 2