Q.16 The correct order of acidity is Options: (A) C6H5COOH < CH3COOH < C6H5OH < C2H5OH (B) CH3COOH < C6H5COOH < C2H5OH < C6H5OH (C) C2H5OH < C6H5OH < C6H5COOH < CH3COOH (D) C2H5OH < C6H5OH < CH3COOH < C6H5COOH

Q.16

The correct order of acidity is

Options:

(A) C6H5COOH < CH3COOH < C6H5OH < C2H5OH

(B) CH3COOH < C6H5COOH < C2H5OH < C6H5OH

(C) C2H5OH < C6H5OH < C6H5COOH < CH3COOH

(D) C2H5OH < C6H5OH < CH3COOH < C6H5COOH

 

Correct Order of Acidity – Organic Compounds

The order of acidity of organic compounds depends on the
stability of the conjugate base.
Factors such as resonance and
inductive effect play a major role.

Key Concepts

  • Carboxylic acids are strongest due to resonance stabilization.
  • Phenol is more acidic than alcohol due to resonance.
  • Alcohols are weakest acids.
  • Electron-withdrawing groups increase acidity.

Correct Order of Acidity

C2H5OH <
C6H5OH <
CH3COOH <
C6H5COOH

Correct Answer

Option (D)

Explanation of Options

Option (A): Incorrect order of acids and phenol.

Option (B): Alcohol incorrectly shown more acidic.

Option (C): Benzoic acid wrongly placed before acetic acid.

Option (D): Correct acidity order based on resonance and inductive effect.

Acidity Comparison

Compound Type Acidity
C2H5OH Alcohol Weakest
C6H5OH Phenol Moderate
CH3COOH Carboxylic Acid Strong
C6H5COOH Carboxylic Acid Strongest

Conclusion

The acidity order follows the stability of the conjugate base.
Hence, alcohols are weakest, phenol is moderate, and carboxylic
acids are strongest.

Therefore, the correct answer is Option (D).

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