Draw the product of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. 1. NaCN 2. H20

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Chapter1: Chemical Foundations
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**Transcription for Educational Website:**

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**Reaction Problem Statement:**

Draw the product of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts.

**Reaction Starting Material Diagram:**

- A cyclic ether structure featuring a triangle (epoxide) and a connected carbon chain with a wedge and dash bond indicating stereochemistry.
- An oxygen atom is labeled at the top of the epoxide.

**Reaction Conditions:**

1. NaCN
2. H₂O

**Diagram Explanation:**

- The reaction involves an epoxide opening, which typically undergoes nucleophilic attack.
- NaCN provides the nucleophile (cyanide ion), and water is used for protonation.
- Consider the stereochemical implications of the epoxide ring opening based on the provided wedge and dash bonds.

**Students are expected to:**

- Use knowledge of epoxide reactions to predict product formation.
- Pay attention to stereochemical outcomes due to the nucleophilic attack.
- Draw the resulting organic compound, making sure to clearly depict any stereochemical configurations with appropriate use of wedge and dash bonds.

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Transcribed Image Text:**Transcription for Educational Website:** --- **Reaction Problem Statement:** Draw the product of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. **Reaction Starting Material Diagram:** - A cyclic ether structure featuring a triangle (epoxide) and a connected carbon chain with a wedge and dash bond indicating stereochemistry. - An oxygen atom is labeled at the top of the epoxide. **Reaction Conditions:** 1. NaCN 2. H₂O **Diagram Explanation:** - The reaction involves an epoxide opening, which typically undergoes nucleophilic attack. - NaCN provides the nucleophile (cyanide ion), and water is used for protonation. - Consider the stereochemical implications of the epoxide ring opening based on the provided wedge and dash bonds. **Students are expected to:** - Use knowledge of epoxide reactions to predict product formation. - Pay attention to stereochemical outcomes due to the nucleophilic attack. - Draw the resulting organic compound, making sure to clearly depict any stereochemical configurations with appropriate use of wedge and dash bonds. ---
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