Draw the organic product(s) of the following reaction. CH3 1. OsO4 2. NaHSO3 CH2 • You do not have to consider stereochemistry. • The aromatic ring, when present, is unreactive in

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Draw the organic product(s) of the following reaction.

 
 
**Reaction Description:**

The task is to draw the organic product(s) resulting from the reaction of a given alkene with osmium tetroxide (OsO₄) followed by sodium bisulfite (NaHSO₃).

**Chemical Structure:**

The reactant is a cyclopentene derivative, featuring a five-membered ring with a double bond adjacent to a methyl group (CH₃).

**Reagents:**

1. **OsO₄ (Osmium Tetroxide):** A reagent commonly used for syn-dihydroxylation of alkenes, which adds OH groups to both carbons of the double bond.
2. **NaHSO₃ (Sodium Bisulfite):** Utilized to reduce and stabilize the osmium reagent, typically aiding in the formation of diols.

**Instructions Provided:**

- Consideration of stereochemistry is not required.
- The aromatic ring, when present, remains unreactive in this reaction.

This information would typically be used in an educational setting to teach about syn-dihydroxylation reactions and the use of OsO₄ in organic chemistry.
Transcribed Image Text:**Reaction Description:** The task is to draw the organic product(s) resulting from the reaction of a given alkene with osmium tetroxide (OsO₄) followed by sodium bisulfite (NaHSO₃). **Chemical Structure:** The reactant is a cyclopentene derivative, featuring a five-membered ring with a double bond adjacent to a methyl group (CH₃). **Reagents:** 1. **OsO₄ (Osmium Tetroxide):** A reagent commonly used for syn-dihydroxylation of alkenes, which adds OH groups to both carbons of the double bond. 2. **NaHSO₃ (Sodium Bisulfite):** Utilized to reduce and stabilize the osmium reagent, typically aiding in the formation of diols. **Instructions Provided:** - Consideration of stereochemistry is not required. - The aromatic ring, when present, remains unreactive in this reaction. This information would typically be used in an educational setting to teach about syn-dihydroxylation reactions and the use of OsO₄ in organic chemistry.
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