Phenol is acidic because of the resonanc...

Phenol is acidic because of the resonance stabilisation of its conjugate base, namely ……….

phenoxide ion

epoxide ion

benzoate ion

none of these

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Phenol is acidic because of the resonance stabilisation of its conjjugate base, namely ……….

Statement- 1 Phenols are more acidic than carboxylic acid Statement -2 Acidity depends on reasonance stabilisation of the conjugate base formed

Phenols are more acidic than aliphatic alcohols acidity of phenols can be further increased by the introduction of electron withdrawing groups in aromatic ring .Acidic nature of phenol is because of the resonance stabilization of phenoxide ion Arrange the given phanols in the increasing order of acidic strength

Phenols are more acidic than aliphatic alcohols acidity of phenols can be further increased by the introduction of electron withdrawing groups in aromatic ring .Acidic nature of phenol is because of the resonance stabilization of phenoxide ion Which of the following will evolve CO_(2) gas with aqueous NaHCO_(3) ?

The compound which is not resonance stabilised

Statement-1: and Statement-2: Conjugate base of phenol is resonance stabilized Statement-2: Conjugate base of phenol is resonance stabilized.

Acid strength is measured by the position of equilibrium of ionization in water. In other words acid strength is the function of the stability of conjugate base of the acid. More is the stability of conjugate base of the acid, more is the acidity of acid. Arrange the given phenols in their decreasing order of acidity:

Which is not a conjugate acid/base pair ?

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The number of resonannce structure for N is
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