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A : In esterification reaction alcohol ...

A : In esterification reaction alcohol act as nucleophile .
R : In this reaction O - H bond of alcohol is broken .

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)

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The correct Answer is:
To solve the question regarding the assertion and reason related to esterification reactions, we can break down the process into clear steps: ### Step-by-Step Solution: 1. **Understanding the Assertion**: - The assertion states that in the esterification reaction, alcohol acts as a nucleophile. - A nucleophile is a species that donates an electron pair to form a chemical bond in a reaction. 2. **Understanding the Reaction**: - In the esterification reaction, a carboxylic acid reacts with an alcohol in the presence of an acid catalyst to form an ester and water. - The general reaction can be represented as: \[ \text{RCOOH} + \text{R'OH} \rightarrow \text{RCOOR'} + \text{H}_2\text{O} \] 3. **Mechanism of the Reaction**: - The carboxylic acid (RCOOH) first gets protonated by the acid catalyst, increasing the electrophilicity of the carbonyl carbon. - The alcohol (R'OH) then acts as a nucleophile, attacking the positively charged carbon atom of the carboxylic acid. 4. **Breaking of O-H Bond**: - As the alcohol attacks the carbon, the O-H bond in the alcohol is broken to stabilize the positive charge that forms on the oxygen atom during the reaction. - This bond breaking is essential for the alcohol to effectively act as a nucleophile. 5. **Conclusion**: - Both the assertion and reason are true. The assertion correctly states that alcohol acts as a nucleophile, and the reason correctly explains that the O-H bond of the alcohol is broken during the reaction, allowing it to act as a nucleophile. - Therefore, the correct option is that both the assertion and reason are true, and the reason explains the assertion. ### Final Answer: - Both Assertion (A) and Reason (R) are true, and R explains A. Thus, the correct option is **Option 1**.
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AAKASH INSTITUTE ENGLISH- ALCOHOLS, PHENOLS AND ETHERS-Assignment Section -D (Assertion - reason type question)
  1. Assertion : Boiling point of p-nitrophenol is greater than that of o-n...

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  2. A : When C(2) H(5) - O- CH(3) is reacted with one mole of Hl then C(2...

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  3. A : When 3,3-dimethyl butan - 2 - ol is heated in presence of concentr...

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  4. A : In esterification reaction , HCOOH is the most reactive acid among...

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  5. A : Ethers can't be distilled upto dryness due to fear of explosion . ...

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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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