II C. a. II III Br AI Which of the following halides would undergo an SN2 reaction at the fastest rate? Br.

Chemistry
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The image contains a question related to organic chemistry, specifically about Sn2 reaction rates of different alkyl halides. The text is presented upside down:

**Question:**
"Which of the following halides would undergo an Sn2 reaction at the fastest rate?"

**Options:**
- **a. I**: A linear alkyl bromide.
- **b. II**: An alkyl bromide with a terminal alkyne group.
- **c. III**: A secondary alkyl bromide attached to a phenyl group.
- **d. IV**: A tertiary alkyl bromide.
- **e. V**: A different tertiary alkyl bromide.

**Note:**
The correct answer choice is circled: **c. III**.

### Diagram Explanation:
- **I :** Displays a primary alkyl bromide structure.
- **II :** Shows a primary alkyl bromide structure with a terminal alkyne (triple bond).
- **III :** Represents a secondary benzyl bromide.
- **IV :** Illustrates a tertiary bromide.
- **V :** Depicts another tertiary bromide but with a different configuration.

These compounds are analyzed to determine which structure would most readily participate in an Sn2 reaction, known for preferring less sterically hindered substrates.
Transcribed Image Text:The image contains a question related to organic chemistry, specifically about Sn2 reaction rates of different alkyl halides. The text is presented upside down: **Question:** "Which of the following halides would undergo an Sn2 reaction at the fastest rate?" **Options:** - **a. I**: A linear alkyl bromide. - **b. II**: An alkyl bromide with a terminal alkyne group. - **c. III**: A secondary alkyl bromide attached to a phenyl group. - **d. IV**: A tertiary alkyl bromide. - **e. V**: A different tertiary alkyl bromide. **Note:** The correct answer choice is circled: **c. III**. ### Diagram Explanation: - **I :** Displays a primary alkyl bromide structure. - **II :** Shows a primary alkyl bromide structure with a terminal alkyne (triple bond). - **III :** Represents a secondary benzyl bromide. - **IV :** Illustrates a tertiary bromide. - **V :** Depicts another tertiary bromide but with a different configuration. These compounds are analyzed to determine which structure would most readily participate in an Sn2 reaction, known for preferring less sterically hindered substrates.
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