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Which of the following on treatment with...

Which of the following on treatment with aqueus sodium hydroxide will give corresponding alcohol and acid?

A

`C_(6)H_(5)CH_(2)CHO`

B

`C_(6)H_(5)CHO`

C

`CH_(3)CH_(2)CH_(2)CHO`

D

`CH-overset(O)overset(|)(C)-CH_(3)`

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we need to identify which compound, when treated with aqueous sodium hydroxide, will undergo the Cannizzaro reaction to produce an alcohol and a carboxylic acid. The Cannizzaro reaction occurs with aldehydes that do not have alpha-hydrogens. ### Step-by-Step Solution: 1. **Identify the Compounds**: We need to analyze the given compounds to check for the presence of alpha-hydrogens. The compounds provided are: - (a) C6H5CH2CHO (Benzaldehyde) - (b) C6H5CHO (Benzaldehyde) - (c) C6H5C(OH)CH3 (an alcohol) - (d) C6H5C(O)CH3 (an acetophenone) 2. **Check for Alpha-Hydrogens**: - **Compound (a)**: C6H5CH2CHO has alpha-hydrogens (the CH2 group has hydrogens). Therefore, it cannot undergo the Cannizzaro reaction. - **Compound (b)**: C6H5CHO (Benzaldehyde) does not have any alpha-hydrogens. Thus, it is a candidate for the Cannizzaro reaction. - **Compound (c)**: C6H5C(OH)CH3 is an alcohol and does not have the aldehyde functional group, so it is not applicable for the Cannizzaro reaction. - **Compound (d)**: C6H5C(O)CH3 (acetophenone) has alpha-hydrogens and will not undergo the Cannizzaro reaction. 3. **Determine the Reaction for Compound (b)**: - When benzaldehyde (C6H5CHO) is treated with aqueous sodium hydroxide, it undergoes the Cannizzaro reaction. - In this reaction, one molecule of benzaldehyde is oxidized to form sodium benzoate (C6H5COONa), and another molecule is reduced to form benzyl alcohol (C6H5CH2OH). 4. **Write the Products**: - The products formed from the Cannizzaro reaction of benzaldehyde are: - **Benzyl Alcohol**: C6H5CH2OH - **Sodium Benzoate**: C6H5COONa 5. **Conclusion**: The compound that undergoes the Cannizzaro reaction to give the corresponding alcohol and acid is **option (b) C6H5CHO (Benzaldehyde)**. ### Final Answer: The correct answer is **option (b)**.

To solve the question, we need to identify which compound, when treated with aqueous sodium hydroxide, will undergo the Cannizzaro reaction to produce an alcohol and a carboxylic acid. The Cannizzaro reaction occurs with aldehydes that do not have alpha-hydrogens. ### Step-by-Step Solution: 1. **Identify the Compounds**: We need to analyze the given compounds to check for the presence of alpha-hydrogens. The compounds provided are: - (a) C6H5CH2CHO (Benzaldehyde) - (b) C6H5CHO (Benzaldehyde) - (c) C6H5C(OH)CH3 (an alcohol) ...
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