Which of the following products (A-D) represents the correct stereochemical outcome for the reaction shown? Please select all that apply. A. B. H₂/Pt C. D. ||||||*..

Chemistry
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Chapter1: Chemical Foundations
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**Question:**

Which of the following products (A-D) represents the correct stereochemical outcome for the reaction shown? Please select all that apply.

**Reaction:**

- A cyclopentene with a double bond is subjected to hydrogenation using H₂/Pt, indicated by an arrow pointing to the right.

**Products:**

- **Product A:** A cyclopentane with two wedges, both bonds are on the same side of the ring.
- **Product B:** A cyclopentane with one wedge and one dashed bond, indicating opposite sides of the ring. 
- **Product C:** Similar to Product B but with reversed positions for wedge and dashed bond.
- **Product D:** A cyclopentane with two dashed bonds, both on the same side of the ring.

**Explanation:**

This is a stereochemical question evaluating the outcome of a hydrogenation reaction on a cyclopentene. In such reactions, the addition of hydrogen atoms typically occurs on the same side of the molecule, leading to a syn-addition product. The correct stereochemical outcomes should depict added hydrogens on the same side of the ring structure.
Transcribed Image Text:**Question:** Which of the following products (A-D) represents the correct stereochemical outcome for the reaction shown? Please select all that apply. **Reaction:** - A cyclopentene with a double bond is subjected to hydrogenation using H₂/Pt, indicated by an arrow pointing to the right. **Products:** - **Product A:** A cyclopentane with two wedges, both bonds are on the same side of the ring. - **Product B:** A cyclopentane with one wedge and one dashed bond, indicating opposite sides of the ring. - **Product C:** Similar to Product B but with reversed positions for wedge and dashed bond. - **Product D:** A cyclopentane with two dashed bonds, both on the same side of the ring. **Explanation:** This is a stereochemical question evaluating the outcome of a hydrogenation reaction on a cyclopentene. In such reactions, the addition of hydrogen atoms typically occurs on the same side of the molecule, leading to a syn-addition product. The correct stereochemical outcomes should depict added hydrogens on the same side of the ring structure.
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