Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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**Text Transcription for Educational Website:**

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**Chemical Transformations Challenge**

*How would you accomplish the following transformations? Each reaction will require several steps.*

**Transformation 1:**
- **Starting Material:** Cyclopentane ring
- **Product:** A straight chain with a five-carbon backbone, featuring two ketone groups (C=O) at the second and fourth carbon. The structure includes a terminal aldehyde group (O=CH-) at the first carbon.

**Transformation 2:**
- **Starting Material:** A linear alkene with three carbons, featuring a double bond between the first and second carbon.
- **Product:** A saturated three-carbon chain with a ketone group at the second carbon.

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**Detailed Explanation:**

The task involves the conversion of cyclopentane to a linear molecule containing ketones and an aldehyde, and an alkene to a ketone. Both transformations require understanding of organic synthesis routes, such as oxidation, functional group interconversion, and possible ring-opening reactions.
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Transcribed Image Text:**Text Transcription for Educational Website:** --- **Chemical Transformations Challenge** *How would you accomplish the following transformations? Each reaction will require several steps.* **Transformation 1:** - **Starting Material:** Cyclopentane ring - **Product:** A straight chain with a five-carbon backbone, featuring two ketone groups (C=O) at the second and fourth carbon. The structure includes a terminal aldehyde group (O=CH-) at the first carbon. **Transformation 2:** - **Starting Material:** A linear alkene with three carbons, featuring a double bond between the first and second carbon. - **Product:** A saturated three-carbon chain with a ketone group at the second carbon. --- **Detailed Explanation:** The task involves the conversion of cyclopentane to a linear molecule containing ketones and an aldehyde, and an alkene to a ketone. Both transformations require understanding of organic synthesis routes, such as oxidation, functional group interconversion, and possible ring-opening reactions.
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