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Cannizzaro reaction does not take place ...

Cannizzaro reaction does not take place with

A

`(CH_(3))_(3)C CHO`

B

C

D

`CH_(3)CHO`

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The correct Answer is:
To determine which compound does not undergo the Cannizzaro reaction, we first need to understand the conditions under which this reaction occurs. ### Step-by-Step Solution: 1. **Understanding the Cannizzaro Reaction**: - The Cannizzaro reaction is a redox reaction that occurs in aldehydes that lack alpha hydrogen atoms. In this reaction, one molecule of aldehyde is oxidized to a carboxylic acid, while another molecule is reduced to an alcohol. 2. **Identifying Aldehydes**: - Aldehydes are compounds with the functional group -CHO. The general structure can be represented as RCHO, where R is a hydrocarbon group. 3. **Alpha Hydrogen Concept**: - Alpha hydrogens are the hydrogen atoms attached to the carbon adjacent to the carbonyl carbon (C=O). For the Cannizzaro reaction to occur, the aldehyde must not have any alpha hydrogens. 4. **Examples of Aldehydes**: - Formaldehyde (HCHO) and benzaldehyde (C6H5CHO) are examples of aldehydes that do not have alpha hydrogens and can undergo the Cannizzaro reaction. - On the other hand, acetaldehyde (CH3CHO) has alpha hydrogens (the three hydrogens on the methyl group) and therefore does not undergo the Cannizzaro reaction. 5. **Conclusion**: - The compound that does not undergo the Cannizzaro reaction is acetaldehyde (CH3CHO) due to the presence of alpha hydrogens. ### Final Answer: **Acetaldehyde (CH3CHO) does not undergo the Cannizzaro reaction.**

To determine which compound does not undergo the Cannizzaro reaction, we first need to understand the conditions under which this reaction occurs. ### Step-by-Step Solution: 1. **Understanding the Cannizzaro Reaction**: - The Cannizzaro reaction is a redox reaction that occurs in aldehydes that lack alpha hydrogen atoms. In this reaction, one molecule of aldehyde is oxidized to a carboxylic acid, while another molecule is reduced to an alcohol. 2. **Identifying Aldehydes**: ...
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