6 **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).

In NaCN, -CN act as a nucleophile it attacks and the leaving group release.LiAlH4 act as a strong…

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

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

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Question

**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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