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The most acidic of the following is...

The most acidic of the following is

A

`ClCH_(2)`COOH

B

`C_(6)H_(5)`COOH

C

`CD_(3)` COOH

D

`CH_(3)CH_(2)` COOH

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The correct Answer is:
To determine the most acidic compound among the given options A, B, C, and D, we need to analyze the stability of the conjugate bases formed when each compound donates a proton (H+). The more stable the conjugate base, the stronger the acid. ### Step-by-Step Solution: 1. **Identify the Compounds**: - Let's denote the compounds as follows: - A: Compound with Cl (Chlorine) - B: Compound with C₆H₅COOH (Benzoic acid) - C: Compound with CD₃C=O (Deuterated ketone) - D: Compound with C₂H₅COOH (Ethanoic acid) 2. **Understand Acidity**: - Acidity is determined by the ability of a compound to donate a proton (H+). The stability of the resulting conjugate base (A-) is crucial. A more stable conjugate base corresponds to a stronger acid. 3. **Analyze the Conjugate Bases**: - For each compound, we need to consider the stability of the conjugate base formed after losing H+. - **Compound A**: The conjugate base will have a negative charge on oxygen, and the presence of Cl (an electron-withdrawing group) will stabilize this negative charge by pulling electron density away. - **Compound B**: The conjugate base will also have a negative charge on oxygen. However, the stability is not significantly enhanced by any electron-withdrawing groups. - **Compound C**: Similar to B, the negative charge on oxygen is not stabilized by any strong electron-withdrawing groups. - **Compound D**: The presence of an alkyl group (C₂H₅) will increase electron density (due to +I effect), which destabilizes the negative charge on the conjugate base. 4. **Compare Stability**: - **Stability of Conjugate Bases**: - A: Stabilized by Cl (electron-withdrawing) - B: No significant stabilization - C: No significant stabilization - D: Destabilized by alkyl group (electron-donating) - Therefore, the stability order is: A > B = C > D. 5. **Conclusion**: - Since compound A has the most stable conjugate base due to the electron-withdrawing effect of Cl, it is the most acidic among the given options. ### Final Answer: The most acidic compound is **A**.

To determine the most acidic compound among the given options A, B, C, and D, we need to analyze the stability of the conjugate bases formed when each compound donates a proton (H+). The more stable the conjugate base, the stronger the acid. ### Step-by-Step Solution: 1. **Identify the Compounds**: - Let's denote the compounds as follows: - A: Compound with Cl (Chlorine) - B: Compound with C₆H₅COOH (Benzoic acid) ...
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NARAYNA-ALDEHYDES, KETONES & CARBOXYLIC ACIDS-C.U.Q
  1. Which of these do not contain -COOH group

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  2. Carbolic acid is

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  3. The most acidic of the following is

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  4. Which is most reactive towards nucleophilic addition reactions?

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  5. Acetic acid is obtained when:

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  6. Product (P) obtained in the reaction given below CO + NaOHrarr (P)

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  7. Carboxylic acids react with diazomethane to yield :

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  8. The product D of the reaction CH(3)Cl overset( KCN) ( rarr) ( A) overs...

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  9. Which of the following on hydrolysis forms acetic acid

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  10. When benzyl alcohol is oxidised with hot acidic KMnO(4) , the product ...

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  11. Two moles of acetic acid are heated with P(2)O(5). The product formed ...

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  12. o-xylene when oxidised in presence of air and (CH(3)"COO")(2) Mn eatal...

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  13. In esterification, OH^(-) Ion for making comes from

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  14. Heating mxiture of ethyl alcohol and acetic acid in presence of conc. ...

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  15. The vapure of a carboxylic acid HA when passed over MnO at 573 Kyields...

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  16. The acid which reduces Fehling solution is

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  17. The above shown polymer is obtained when a carbonic compound is allowe...

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  18. Which CH(3)COOH reacts with CH(3)-MgX, then

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  19. Base hydrolysis of an ester with NaOH gives a carboxylic acid whose so...

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  20. Acetic anhydride reacts with excess of ammonia to from

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