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5) Predict the product for the following reaction. Br 1. NaCN 2. LIAIH4 3. H₂O

5) Predict the product for the following reaction. Br 1. NaCN 2. LIAIH4 3. H₂O

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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**Predict the product for the following reaction:** We start with a bromocyclohexane structure with a propyl side chain. **Reactants:** 1. **NaCN (Sodium Cyanide)**: This reagent will likely perform a nucleophilic substitution, replacing the bromine atom with a cyanide group (-CN). The cyanide ion acts as a strong nucleophile. 2. **LiAlH₄ (Lithium Aluminum Hydride)**: This reagent is a strong reducing agent. It will reduce the nitrile group (-CN) to a primary amine (-CH₂NH₂). 3. **H₂O (Water)**: This step is typically to quench the reaction after reduction. **Expected Product:** Starting with bromocyclohexane with a propyl side chain, the final product after all steps will likely be cyclohexane with a propylamine side chain (-CH₂CH₂CH₂NH₂).
Transcribed Image Text:**Predict the product for the following reaction:** We start with a bromocyclohexane structure with a propyl side chain. **Reactants:** 1. **NaCN (Sodium Cyanide)**: This reagent will likely perform a nucleophilic substitution, replacing the bromine atom with a cyanide group (-CN). The cyanide ion acts as a strong nucleophile. 2. **LiAlH₄ (Lithium Aluminum Hydride)**: This reagent is a strong reducing agent. It will reduce the nitrile group (-CN) to a primary amine (-CH₂NH₂). 3. **H₂O (Water)**: This step is typically to quench the reaction after reduction. **Expected Product:** Starting with bromocyclohexane with a propyl side chain, the final product after all steps will likely be cyclohexane with a propylamine side chain (-CH₂CH₂CH₂NH₂).
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