= APPLICATIONS OF SUBSTITUTION AND ELIMINATION Predicting the products of nucleophilic epoxide ring opening Add the necessary reaction conditions above or below the arrow in this organic reaction. Also, if a major product is missing from the right-hand side, draw it in. Å ccc + T X Ś HO *** Br

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Chapter1: Chemical Foundations
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**Predicting the Products of Nucleophilic Epoxide Ring Opening**

**Instructions:**
Add the necessary reaction conditions above or below the arrow in this organic reaction. If a major product is missing from the right-hand side, draw it in.

**Reaction Diagram:**

- **Reactant:** On the left, there is an epoxide (three-membered cyclic ether) structure shown with an oxygen atom forming a triangle with two carbon atoms.

- **Reaction Arrow:** A right-pointing arrow indicates the progression of the reaction.

- **Product:** On the right, there is a structure showing a two-carbon chain with a hydroxyl group (–OH) on the first carbon and a bromine atom (Br) on the second carbon.

**Tools Provided:**

- Drawing tools are shown below the diagram to modify or complete the reaction.

**Note:**
This exercise involves understanding how an epoxide ring opens through nucleophilic attack, typically under acidic or basic conditions. Be sure to specify the conditions that facilitate this transformation.

**Buttons:**

- “Explanation” for additional guidance.
- “Check” to verify the accuracy of your solution.
Transcribed Image Text:**Predicting the Products of Nucleophilic Epoxide Ring Opening** **Instructions:** Add the necessary reaction conditions above or below the arrow in this organic reaction. If a major product is missing from the right-hand side, draw it in. **Reaction Diagram:** - **Reactant:** On the left, there is an epoxide (three-membered cyclic ether) structure shown with an oxygen atom forming a triangle with two carbon atoms. - **Reaction Arrow:** A right-pointing arrow indicates the progression of the reaction. - **Product:** On the right, there is a structure showing a two-carbon chain with a hydroxyl group (–OH) on the first carbon and a bromine atom (Br) on the second carbon. **Tools Provided:** - Drawing tools are shown below the diagram to modify or complete the reaction. **Note:** This exercise involves understanding how an epoxide ring opens through nucleophilic attack, typically under acidic or basic conditions. Be sure to specify the conditions that facilitate this transformation. **Buttons:** - “Explanation” for additional guidance. - “Check” to verify the accuracy of your solution.
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