2. Propose a mechanism and predict the product(s) for each reaction. For reactions where more than one product can form, draw all possible products and predict which would be the major product. a) Br NaCl SN1

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Propose a mechanism and predict the products for each reaction. For reactions where more then one product can form, draw all possible products and predict which would be the major product.

**Reaction Mechanism and Product Prediction**

**Task:**
Propose a mechanism and predict the product(s) for each reaction. For reactions where more than one product can form, draw all possible products and predict which would be the major product.

**Reaction:**

a) The reaction starts with the compound that contains a bromine (Br) substituted cyclohexane. It's shown reacting with NaCl under S<sub>N</sub>1 conditions.

**Mechanism Explanation:**

- **Step 1:** The bromine (Br) will leave, forming a carbocation intermediate on the cyclohexane ring.
- **Step 2:** Chloride ion (Cl<sup>-</sup>) from NaCl will attack the carbocation, forming various stereochemical products depending on the specific conditions.

**Product Prediction:**

Consider all possible stereochemical outcomes, and determine major and minor products based on stability and reaction conditions.
Transcribed Image Text:**Reaction Mechanism and Product Prediction** **Task:** Propose a mechanism and predict the product(s) for each reaction. For reactions where more than one product can form, draw all possible products and predict which would be the major product. **Reaction:** a) The reaction starts with the compound that contains a bromine (Br) substituted cyclohexane. It's shown reacting with NaCl under S<sub>N</sub>1 conditions. **Mechanism Explanation:** - **Step 1:** The bromine (Br) will leave, forming a carbocation intermediate on the cyclohexane ring. - **Step 2:** Chloride ion (Cl<sup>-</sup>) from NaCl will attack the carbocation, forming various stereochemical products depending on the specific conditions. **Product Prediction:** Consider all possible stereochemical outcomes, and determine major and minor products based on stability and reaction conditions.
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