Consider this two-step synthesis. Show how compound on the right can be synthesized by providing reagents for each step and the product in the first synthetic step (use the boxes below). step 1 step 2 Br Briefly describe the strategy you outlined above that wil ensure a stereochemically pure product (not a racemic mixture).

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**Title: Two-Step Synthesis Strategy**

**Objective:**

Learn how to synthesize the given compound through a two-step process by identifying appropriate reagents for each step. The goal is to achieve a stereochemically pure product.

**Structure to Synthesize:**
- Target Compound: A molecule with a cyano group (CN) attached to a carbon chain.

**Starting Material:**
- Initial Molecule: A bromo-substituted carbon chain.

**Instructions:**

1. **Step 1:**
   - Provide the reagents required to convert the bromo group to an intermediate structure.
   - Consider factors such as the reaction mechanism and stereochemical outcome.

2. **Step 2:**
   - Identify reagents that will transform the intermediate into the final cyano-substituted compound.
   - Ensure that the product maintains stereochemical purity.

**Diagram Explanation:**

- **Starting Material Illustration:**
  - Chemical structure with a bromine (Br) atom linked to a carbon chain.

- **Intermediate Boxes:**
  - Two empty boxes labeled "Step 1" and "Step 2" for indicating reaction conditions and intermediates.

- **Final Product Illustration:**
  - Chemical structure with a cyano (CN) group linked to the same carbon chain.

**Task: Briefly describe the strategy you outlined:**

- Elaborate on the reagents and conditions selected for each step that ensure a stereochemically pure product rather than a racemic mixture.

---
This exercise emphasizes the importance of understanding reaction mechanisms and stereochemistry in organic synthesis.
Transcribed Image Text:**Title: Two-Step Synthesis Strategy** **Objective:** Learn how to synthesize the given compound through a two-step process by identifying appropriate reagents for each step. The goal is to achieve a stereochemically pure product. **Structure to Synthesize:** - Target Compound: A molecule with a cyano group (CN) attached to a carbon chain. **Starting Material:** - Initial Molecule: A bromo-substituted carbon chain. **Instructions:** 1. **Step 1:** - Provide the reagents required to convert the bromo group to an intermediate structure. - Consider factors such as the reaction mechanism and stereochemical outcome. 2. **Step 2:** - Identify reagents that will transform the intermediate into the final cyano-substituted compound. - Ensure that the product maintains stereochemical purity. **Diagram Explanation:** - **Starting Material Illustration:** - Chemical structure with a bromine (Br) atom linked to a carbon chain. - **Intermediate Boxes:** - Two empty boxes labeled "Step 1" and "Step 2" for indicating reaction conditions and intermediates. - **Final Product Illustration:** - Chemical structure with a cyano (CN) group linked to the same carbon chain. **Task: Briefly describe the strategy you outlined:** - Elaborate on the reagents and conditions selected for each step that ensure a stereochemically pure product rather than a racemic mixture. --- This exercise emphasizes the importance of understanding reaction mechanisms and stereochemistry in organic synthesis.
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