- APhenol < Ethanol < Chloroacetic acid < Acetic acid
- BEthanol < Phenol < Chloroacetic acid < Acetic acid
- CEthanol < Phenol < Acetic acid < Chloroacetic acid
- DChloroacetic acid < Acetic acid < Phenol < Ethanol
Explanation:
Carboxylic acids dissociate in water to give resonance stabilised carboxylate anions and hydronium ion. That is why carboxylic acids are weaker than mineral acids, but they are stronger acids than alcohols and many simple phenols. Electron withdrawing groups (halogens) increase the acidity of carboxylic acids by stabilising the conjugate base through delocalisation of the negative charge by inductive and resonance effects. Ethanol is least acidic because the ethoxide ion formed in not resonance stabilised. Thus, the order of increasing acidic strength is —
Ethanol< Phenol< Acetic acid < Chloroacetic acid.
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$(ii)\, CoBr · SO_4 · 5NH_3$
$(iii)\, FeCl_3 · 6H_2O$
