Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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**Predict the product in the following reactions:**

1. **Reaction 1:**
   - **Reactant:** A brominated cyclohexane with one methyl (CH₃) and one trifluoromethyl (CF₃) group.
   - **Reagent:** DBU

2. **Reaction 2:**
   - **Reactant:** A cyclohexanol with a hydroxyl (OH) group.
   - **Reagent:** Concentrated sulfuric acid (H₂SO₄)

3. **Reaction 3:**
   - **Reactant:** A 1-bromo-2-chloro-3-fluorocyclohexane.
   - **Reagent:** Sodium azide (NaN₃) in DMSO.

4. **Reaction 4:**
   - **Reactant:** A cyclohexanol with a hydroxyl (OH) group.
   - **Reagent:** Hydrochloric acid (HCl)

Each reaction set involves cyclohexane derivatives with different substituents, subjected to various reagents, requiring the prediction of the resulting chemical structure for each transformation.
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Transcribed Image Text:**Predict the product in the following reactions:** 1. **Reaction 1:** - **Reactant:** A brominated cyclohexane with one methyl (CH₃) and one trifluoromethyl (CF₃) group. - **Reagent:** DBU 2. **Reaction 2:** - **Reactant:** A cyclohexanol with a hydroxyl (OH) group. - **Reagent:** Concentrated sulfuric acid (H₂SO₄) 3. **Reaction 3:** - **Reactant:** A 1-bromo-2-chloro-3-fluorocyclohexane. - **Reagent:** Sodium azide (NaN₃) in DMSO. 4. **Reaction 4:** - **Reactant:** A cyclohexanol with a hydroxyl (OH) group. - **Reagent:** Hydrochloric acid (HCl) Each reaction set involves cyclohexane derivatives with different substituents, subjected to various reagents, requiring the prediction of the resulting chemical structure for each transformation.
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