Home
Class 12
CHEMISTRY
Assertion: Esters which contain alpha-hy...

Assertion: Esters which contain `alpha-`hydrogens undergo Claisen condensation.
Reason : `LiAIH_(4)` reduction of esters gives acids

A

a. If both assertion and reason are true and reason is the correct explanation of assertion

B

b. If both assertion and reason are true but reason is not the correct explanation of assertion

C

c. If assertion is true but reason is false

D

d. If both assertion and reason are false.

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we will analyze the assertion and the reason provided separately. ### Step-by-Step Solution: 1. **Understanding the Assertion**: - The assertion states that "Esters which contain alpha-hydrogens undergo Claisen condensation." - Claisen condensation is a reaction between two esters or an ester and a carbonyl compound in the presence of a strong base, resulting in the formation of a β-keto ester or a β-diketone. - For Claisen condensation to occur, the ester must have at least one alpha-hydrogen. This is because the alpha-hydrogen is necessary for the formation of an enolate ion, which acts as a nucleophile in the reaction. 2. **Understanding the Reason**: - The reason states that "LiAlH₄ reduction of esters gives acids." - Lithium aluminum hydride (LiAlH₄) is a strong reducing agent that can reduce esters to primary alcohols, not acids. The reduction of esters by LiAlH₄ results in the formation of alcohols and not acids. Therefore, this statement is incorrect. 3. **Conclusion**: - The assertion is true because esters with alpha-hydrogens do undergo Claisen condensation. - The reason is false because the reduction of esters by LiAlH₄ yields alcohols, not acids. - Based on this analysis, the correct answer is that the assertion is true, but the reason is false. ### Final Answer: Assertion is true, but the reason is false. Therefore, the correct option is **C**. ---

To solve the question, we will analyze the assertion and the reason provided separately. ### Step-by-Step Solution: 1. **Understanding the Assertion**: - The assertion states that "Esters which contain alpha-hydrogens undergo Claisen condensation." - Claisen condensation is a reaction between two esters or an ester and a carbonyl compound in the presence of a strong base, resulting in the formation of a β-keto ester or a β-diketone. - For Claisen condensation to occur, the ester must have at least one alpha-hydrogen. This is because the alpha-hydrogen is necessary for the formation of an enolate ion, which acts as a nucleophile in the reaction. ...
Promotional Banner

Similar Questions

Explore conceptually related problems

Which of the following does not give claisen condensation reaction :

Reduction by LiAIH_(4) of hydorlysed product of an ester gives:

Reduction by LiAlH_4 of hydrolysed product of an ester gives

Which one of the following esters cannot undergo self Claisen condensation?

Ester gives nucleophilic addition reaction followed by elimination reaction with carbon nucleopile. When carbon nucleophile is of an ester then the reaction is known as Claisen condensation reaction. This reaction is also carried out between ester and a ketone. A suC Cessful Claisen condensation requires an ester with two alpha- hydrogens and an equivalent amount of base rather than a catalytic amount of base. Intramolecular Claisen condensation given diester is known as :

Ester gives nucleophilic addition reaction followed by elimination reaction with carbon nucleopile. When carbon nucleophile is of an ester then the reaction is known as Claisen condensation reaction. This reaction is also carried out between ester and a ketone. A suC Cessful Claisen condensation requires an ester with two alpha- hydrogens and an equivalent amount of base rather than a catalytic amount of base. Consider the given reaction CH_(3)-COOC_(2)H_(5)underset(C_(2)H_(5)OH)overset(C_(2)H_(5)ONa)rarr"enolate ion"underset("Claisen condensation")overset("ether(X)")rarr Product For the above reaction the most reactive ester is :

Assertion : All aldehydes donot take part in aldol condensation. Reason : In th aldol condensation, carbanion is generated by the abstraction of alpha -H atopm by the base.

Assertion (A) The alpha -hydrogen atom in carbonyl compounds is less acidic. Reason (R) The anion formed after the loss of alpha -hydrogen atom is resonance stabilised.