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NH2 1. CH3I (excess) R' R' 2. Ag,0 3. A Alkene Amine

NH2 1. CH3I (excess) R' R' 2. Ag,0 3. A Alkene Amine

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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What is the mechanisms to get from the reactant to the products
**Functional Group Transformations** **Starting Compound Class**: Amine - This section illustrates the transformation starting with an amine group, represented by the structure including \( \text{NH}_2 \) connected to the rest of the molecule (\( \text{R} \) and \( \text{R}' \)). **Typical Reagents and Reaction Conditions**: 1. \( \text{CH}_3\text{I} \) (excess) 2. \( \text{Ag}_2\text{O} \) 3. \( \Delta \) (heat) **Compound Class Formed**: Alkene - The amine undergoes a series of reactions using the above reagents to ultimately form an alkene, where the double-bonded structure is represented by \( \text{R} \) and \( \text{R}' \). This transformation outlines a typical synthetic pathway for converting amines into alkenes using methyl iodide, silver oxide, and heat to facilitate the process.
Transcribed Image Text:**Functional Group Transformations** **Starting Compound Class**: Amine - This section illustrates the transformation starting with an amine group, represented by the structure including \( \text{NH}_2 \) connected to the rest of the molecule (\( \text{R} \) and \( \text{R}' \)). **Typical Reagents and Reaction Conditions**: 1. \( \text{CH}_3\text{I} \) (excess) 2. \( \text{Ag}_2\text{O} \) 3. \( \Delta \) (heat) **Compound Class Formed**: Alkene - The amine undergoes a series of reactions using the above reagents to ultimately form an alkene, where the double-bonded structure is represented by \( \text{R} \) and \( \text{R}' \). This transformation outlines a typical synthetic pathway for converting amines into alkenes using methyl iodide, silver oxide, and heat to facilitate the process.
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