Advertisements
Advertisements
प्रश्न
Compare acidity of phenol with that of ethanol.
Advertisements
उत्तर १
Phenol is more acidic than ethanol. This is because the phenoxide ion obtained after the release of a proton from phenol becomes stable through resonance, whereas the ethoxide ion (after the release of a proton from ethanol) is not stable.

उत्तर २
Compared with ethanol, phenols are more acidic. They lose their H atom as H+ more readily than alcohols. The behaviour of phenol can be attributed to resonance stabilisation arising from the contributing structures of the corresponding phenoxide ion.

The resonance stabilisation from the contributing structures (I)-(V) sufficiently offsets the O–H bond dissociation energy, rendering phenol acidic.
No resonance structures exist for the ethoxide ion; hence, the conversion of ethanol to ethoxide is not encouraged under standard conditions. Therefore, ethanol exhibits lower acidity compared to phenol.
APPEARS IN
संबंधित प्रश्न
Write the equation involved in the acetylation of Salicylic acid.
Give the structure of the product you would expect when the following alcohol reacts with HCl–ZnCl2.
Butan-1-ol
Explain how does the −OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?
Account for the following:
o-nitrophenol is more steam volatile than p-nitrophenol.
Phenol is more acidic than alcohol because ____________.
In CH3CH2OH, the bond that undergoes heterolytical change most readily is ____________.
Phenol reacts with Br2 in CS2 at low temperature to give ____________.

What is the correct order of reactivity of alcohols in the following reaction?
\[\ce{R-OH + HCl ->[ZnCl2] R-Cl + H2O}\]
Which of the following statements is true:
Mark the correct order of decreasing acid strength of the following compounds.
| (a) | ![]() |
| (b) | ![]() |
| (c) | ![]() |
| (d) | ![]() |
| (e) | ![]() |
Phenol is used in the manufacture of
Arrange the following in the increasing order of their property indicated:
4-Nitrobenzoic acid, benzoic acid, 3,4-Dinitrobenzoic acid, 4-Methoxy benzoic acid (Acid strength)
For the pair phenol and cyclohexanol, answer the following:
Why is phenol more acidic than cyclohexanol?
Give the structure of the product you would expect when the following alcohol reacts with HCl–ZnCl2.
2-Methylbutan-2-ol
Give the structure of the product you would expect when the following alcohol reacts with HBr.
Butan-1-ol
Give the structure of the product you would expect when the following alcohol reacts with SOCl2.
Butan-1-ol
Give the structure of the product you would expect when the following alcohol reacts with SOCl2.
2-Methylbutan-2-ol





