7) Using the carbon-containing starting material(s), propose a synthesis the following retrosynthetic analysis. Provide structures for all intermediates. The carbon atoms in the product must originate from the starting material(s), but you may use as many equivalents of each starting material as you would like, and any reagent/reaction you know (note: no mechanisms are required). Br OH racemic ⇒>> -Br

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**Problem 7: Synthesis Proposal**

Using the carbon-containing starting material(s), propose a synthesis for the following retrosynthetic analysis. Provide structures for all intermediates. The carbon atoms in the product must originate from the starting material(s), but you may use as many equivalents of each starting material as you would like and any reagent/reaction you know (note: no mechanisms are required).

**Diagram Description:**

The diagram shows a transformation:

- **Starting Material:** A structure of a racemic mixture of a molecule with a bromine (Br) atom and a hydroxyl (OH) group attached to a central carbon, which is also bonded to two methyl groups.
- **Reaction Arrow:** Indicates the reaction or process that leads from the starting materials to the products.
- **Products:** Indicates the formula representation of the product with an equal sign and loose bromine ion (+ Br⁻).

This exercise involves thinking backward from the product to propose a possible synthetic route to reach the desired product using available starting materials and reagents.
Transcribed Image Text:**Problem 7: Synthesis Proposal** Using the carbon-containing starting material(s), propose a synthesis for the following retrosynthetic analysis. Provide structures for all intermediates. The carbon atoms in the product must originate from the starting material(s), but you may use as many equivalents of each starting material as you would like and any reagent/reaction you know (note: no mechanisms are required). **Diagram Description:** The diagram shows a transformation: - **Starting Material:** A structure of a racemic mixture of a molecule with a bromine (Br) atom and a hydroxyl (OH) group attached to a central carbon, which is also bonded to two methyl groups. - **Reaction Arrow:** Indicates the reaction or process that leads from the starting materials to the products. - **Products:** Indicates the formula representation of the product with an equal sign and loose bromine ion (+ Br⁻). This exercise involves thinking backward from the product to propose a possible synthetic route to reach the desired product using available starting materials and reagents.
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