ynthesis / Retrosy 7) Using the carbon containing starting material(s) provided, propose a synthetic scheme for the following target molecule. 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). НО. OH 20

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Question in Image. Synthesis.

**Synthesis / Retrosynthetic Analysis**

**Question 7:**

Using the provided carbon-containing starting material(s), propose a synthetic scheme for the target molecule. 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 employ any reagent/reaction you know. *(Note: no mechanisms are required).*

**Diagram Explanation:**

The diagram shows a chemical structure with the following features:

- A central carbon chain with two hydroxyl (OH) groups attached.
- An ester linkage (C-O) connecting two parts of the molecule.

**Task:**

Develop a synthetic pathway starting with the given structure to reach the desired target molecule, ensuring all intermediates are clearly drawn. Reagents and reactions can be chosen freely, but all carbon atoms in the final product must be derived from the initial starting materials provided.
Transcribed Image Text:**Synthesis / Retrosynthetic Analysis** **Question 7:** Using the provided carbon-containing starting material(s), propose a synthetic scheme for the target molecule. 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 employ any reagent/reaction you know. *(Note: no mechanisms are required).* **Diagram Explanation:** The diagram shows a chemical structure with the following features: - A central carbon chain with two hydroxyl (OH) groups attached. - An ester linkage (C-O) connecting two parts of the molecule. **Task:** Develop a synthetic pathway starting with the given structure to reach the desired target molecule, ensuring all intermediates are clearly drawn. Reagents and reactions can be chosen freely, but all carbon atoms in the final product must be derived from the initial starting materials provided.
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Synthesis problem. Is there a solution without using the Birch reduction?

Synthesis / Retrosynthetic Analysis
7) Using the carbon containing starting material(s) provided, propose a synthetic scheme for
the following target molecule. 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).
НО.
O
OH
=
2C
Transcribed Image Text:Synthesis / Retrosynthetic Analysis 7) Using the carbon containing starting material(s) provided, propose a synthetic scheme for the following target molecule. 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). НО. O OH = 2C
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Is there a way without Birch Reduction?

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