3. Which of the compounds shown below will yield a carboxylic acid when reacted with chromic acid? HO- HO A' B' C' D'

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which of the compounds shown below will yield a carboxylic acid when reacted with chromic acid?
**Transcription for Educational Website**

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**Question 3:** Which of the compounds shown below will yield a carboxylic acid when reacted with chromic acid?

**Compounds:**

- **A’**: A linear chain with an alcohol group (-OH) at the end.
- **B’**: A linear chain with an alcohol group (-OH) attached to the second carbon.
- **C’**: A cyclohexane ring with an alcohol group (-OH) attached to one of the carbons.
- **D’**: A branched structure with an alcohol group (-OH) attached to a tertiary carbon.

**Explanation:**

The question focuses on identifying which of the given alcohol compounds will be oxidized to form a carboxylic acid upon reaction with chromic acid. Primary alcohols will typically oxidize to carboxylic acids, whereas secondary alcohols oxidize to ketones and tertiary alcohols do not get oxidized by chromic acid.

**Diagrams:**

Each compound is represented as a structural drawing:

- **A’**: Depicts a straight carbon chain ending with -OH.
- **B’**: Shows a straight chain with -OH on the second carbon.
- **C’**: Represents a hexagonal (cyclohexane) ring with -OH attached.
- **D’**: Illustrates a branched carbon chain with a tertiary -OH group.

For educational purposes, it is significant to recognize that compound **B’** (a primary alcohol) will yield a carboxylic acid when reacted with chromic acid.
Transcribed Image Text:**Transcription for Educational Website** --- **Question 3:** Which of the compounds shown below will yield a carboxylic acid when reacted with chromic acid? **Compounds:** - **A’**: A linear chain with an alcohol group (-OH) at the end. - **B’**: A linear chain with an alcohol group (-OH) attached to the second carbon. - **C’**: A cyclohexane ring with an alcohol group (-OH) attached to one of the carbons. - **D’**: A branched structure with an alcohol group (-OH) attached to a tertiary carbon. **Explanation:** The question focuses on identifying which of the given alcohol compounds will be oxidized to form a carboxylic acid upon reaction with chromic acid. Primary alcohols will typically oxidize to carboxylic acids, whereas secondary alcohols oxidize to ketones and tertiary alcohols do not get oxidized by chromic acid. **Diagrams:** Each compound is represented as a structural drawing: - **A’**: Depicts a straight carbon chain ending with -OH. - **B’**: Shows a straight chain with -OH on the second carbon. - **C’**: Represents a hexagonal (cyclohexane) ring with -OH attached. - **D’**: Illustrates a branched carbon chain with a tertiary -OH group. For educational purposes, it is significant to recognize that compound **B’** (a primary alcohol) will yield a carboxylic acid when reacted with chromic acid.
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