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Alcohol Phenols and Ethers question

2010 · Q136
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Alcohol Phenols and Ethers question

2010 · Q136

NEETChemistryAlcohol Phenols and EthersMCQ+4 / −1
Given are cyclohexanol (I), acetic acid (II), 2, 4, 6-trinitrophenol (III) and phenol (IV). In these the order of decreasing acidic character will be
  1. A
    III > II > IV > I
  2. B
    II > III > I > IV
  3. C
    II > III > IV > I
  4. D
    III > IV > II > I
View written solutionFree

Correct answer: A

As we know that phenols and carboxylic acids are more acidic than aliphatic alcohols thus cyclohexanol is least acidic.

On the other hand III is more acidic than IV because of the presence of three highly electron with drawing NO2 groups on the benzene ring which makes the OH bond extremely polarized. This facilitates the release of H+.

In acetic acid the electron withdrawing −C∣=O - \mathop C\limits_| = O−∣C​=O

group polarizes the O-H bond and increases the acid strength.

Thus, acetic acid is more acidic than phenol or cyclohexanol.

Thus, the order of acidic strength will be

III > II > IV > I

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