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A : In esterification reaction , HCOOH i...

A : In esterification reaction , HCOOH is the most reactive acid among carboxylic acid .
R : Alcohol acts as nucleophile

A

If both Assertion & Reason are true and the reason is the correct explanation of the assertion, then mark (1)

B

If both Assertion & Reason are true but the reason is not the correct explanation of the assertion, then mark (2)

C

If Assertion is true statement but Reason is false , then mark (3)

D

If both Assertion and Reason are false statements , then mark (4)

Text Solution

AI Generated Solution

The correct Answer is:
To solve the question, we need to analyze both the assertion (A) and the reason (R) provided. ### Step 1: Analyze the Assertion (A) The assertion states: "In esterification reaction, HCOOH is the most reactive acid among carboxylic acids." - **Explanation**: Esterification is a reaction where a carboxylic acid reacts with an alcohol to form an ester and water. The reactivity of carboxylic acids in esterification is influenced by the stability of the carbonyl carbon. In the case of formic acid (HCOOH), the carbonyl carbon is less hindered compared to other carboxylic acids that have larger alkyl groups. Larger alkyl groups can donate electron density through the +I effect, which reduces the positive character of the carbonyl carbon, making it less reactive. Therefore, HCOOH, having only a hydrogen atom, is indeed the most reactive carboxylic acid. ### Conclusion for Assertion (A): The assertion is **true**. ### Step 2: Analyze the Reason (R) The reason states: "Alcohol acts as a nucleophile." - **Explanation**: In the esterification reaction, the alcohol (R-OH) has a lone pair of electrons on the oxygen atom, which allows it to act as a nucleophile. A nucleophile is a species that donates an electron pair to form a chemical bond. In this case, the oxygen in the alcohol attacks the electrophilic carbon of the carboxylic acid, leading to the formation of an ester. ### Conclusion for Reason (R): The reason is also **true**. ### Step 3: Determine the Relationship Between A and R Now we need to assess whether the reason explains the assertion. - While both statements are true, the reason (alcohol acts as a nucleophile) does not explain why HCOOH is the most reactive acid. The reactivity of HCOOH is due to its structure and the lack of electron-donating alkyl groups, which is not addressed by the reason provided. ### Final Conclusion: - Both the assertion and the reason are true, but the reason does not provide a correct explanation for the assertion. ### Answer: The correct option is **2**: Both assertion and reason are true, but the reason is not the correct explanation of the assertion. ---
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AAKASH INSTITUTE ENGLISH- ALCOHOLS, PHENOLS AND ETHERS-Assignment Section -D (Assertion - reason type question)
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  6. Phenol is less acidic than........... .

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  7. A : CH(3) - underset(O)underset(||)(C)-COOH gives haloform reaction ...

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  8. A : Diphenyl ether is prepared by Williamson synthesis . R : This...

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  9. A : Grignard's reagent is prepared in the presence of ether . R :...

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  10. A : CH(3) - underset(CH(3))underset(|)overset(CH(3))overset(|)(C)-CH=...

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  11. A : Two moles of Grignard reagent is consumed in the formation of ter...

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  12. A : bond angle in ether is slightly greater than normal tetrahedral an...

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  13. A : CH(3)-underset(CH(3))underset(|)overset(CH(3))overset(|)(C)-O-CH...

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  14. A : Ortho - cresol is weaker acidic than meta-cresol . R : It is d...

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  15. A : Among all ortho halophenol , fluorophenol is least acidic . R ...

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  16. A : In esterification reaction alcohol act as nucleophile . R : ...

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  17. A : Phenol is manufactured by Dow 's pocess. R : It involves the ...

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  18. A : Primary alcohol is prepared by the reaction of primary amine with ...

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  19. A : The reactivity order of alcohols is 1^(@) gt 2^(@) gt 3^(@) for ...

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  20. A : The dehydration of ethyl alcohol in presence of Al(2)O(3) at 633 ...

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