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The most acidic among the following is...

The most acidic among the following is

A

`CH_(3)CH_(2)`OH

B

`C_(6)H_(5)`OH

C

`CH_(3)`COOH

D

`CH_(3)CH_(2)CH_(2)`OH

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The correct Answer is:
To determine the most acidic compound among the given options, 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 four options as follows: - Option A: CH3CH2OH (Ethanol) - Option B: C6H5OH (Phenol) - Option C: CH3COOH (Acetic Acid) - Option D: CH3CH2CH2OH (Butanol) 2. **Determine the Conjugate Bases**: - For Option A (Ethanol), the conjugate base is CH3CH2O-. - For Option B (Phenol), the conjugate base is C6H5O-. - For Option C (Acetic Acid), the conjugate base is CH3COO-. - For Option D (Butanol), the conjugate base is CH3CH2CH2O-. 3. **Analyze Stability of Conjugate Bases**: - **Option A (Ethanol)**: The negative charge on the oxygen is not stabilized by any resonance or inductive effects. - **Option B (Phenol)**: The negative charge can be delocalized over the aromatic ring, providing significant resonance stabilization. - **Option C (Acetic Acid)**: The negative charge can be delocalized between the two oxygen atoms, providing resonance stabilization. - **Option D (Butanol)**: Similar to ethanol, the negative charge is not stabilized by resonance. 4. **Compare Stability**: - **Ethanol and Butanol** have no resonance stabilization for their conjugate bases, making them weaker acids. - **Phenol** has resonance stabilization due to the aromatic ring, making it more acidic than ethanol and butanol. - **Acetic Acid** also has resonance stabilization, and the presence of two electronegative oxygen atoms allows for effective delocalization of the negative charge. 5. **Conclusion**: - Between **Phenol** and **Acetic Acid**, both have resonance stabilization, but the conjugate base of acetic acid (CH3COO-) is more stable due to the ability to delocalize the negative charge over two electronegative atoms (the two oxygens). - Therefore, **Acetic Acid (Option C)** is the most acidic among the given options. ### Final Answer: The most acidic compound among the given options is **Option C: CH3COOH (Acetic Acid)**. ---

To determine the most acidic compound among the given options, 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 four options as follows: - Option A: CH3CH2OH (Ethanol) - Option B: C6H5OH (Phenol) ...
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NARAYNA-ALDEHYDES, KETONES & CARBOXYLIC ACIDS-EXERCISE -II (C.W.)
  1. In the given reaction CH(3)-CH(2)-COOHunderset((ii)." "Br(2)//Delta)ov...

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  2. In the given reaction :

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  3. In the given reaction CH(3)-COOH underset(underset("(iii) "H(2)O //H^(...

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  4. In the given reactions :

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  5. The reduction of benzoyl chloride with H(2)//Pd-BaSO(4) produces

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  6. Which reaction can produce R - CO-Ar species :

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  7. Which one is a mixed ketone :

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  8. Hydrolysis of an ester gives a carboxylic acid which on Kolbe's electr...

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  9. Reaction of aniline with acety1 chloride in the presence of NaOH gives...

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  10. m-chlorobenzaldehyde on reaction with conc. KOH at room temperature gi...

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  11. In Etard's reaction toluene is oxidised to benzaldehyde using

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  12. Which of the following does not give brick red ppt. with Fehling solut...

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  13. The organic product formed in the reaction C(6) H(5)"COOCH"(3) under...

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  14. The class of compounds that are reduced to primary alcohols and also r...

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  15. Benzoic acid with "SOCl"(2) to give

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  16. Identify X in the sequence, X underset(2H(2)O //H^(+))overset(1.CH(3...

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  17. Identify X, H(3)C - overset(CH(3))overset(|)(C ) = O underset("dry e...

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  18. Pick out the reaction in which formic and acetic acids differs from ea...

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  19. The most acidic among the following is

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  20. Select the strongest acid :

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