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प्रश्न
Compare acidity of phenol with that of ethanol.
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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.
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संबंधित प्रश्न
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Reason: m- and p- Nitrophenols exist as associated molecules.
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In the following compounds:
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| (I) | (II) | (III) | (IV) |
The order to acidity is ______.
Which one of the following has the lowest pKa value?
Give the structure of the product you would expect when the following alcohol reacts with SOCl2.
2-Methylbutan-2-ol




