Page No.:
Arrange the following carbonyl compounds in the
order of their favourability for formation of
nitriles
CH₂ CH₂ CHO , CH 3 CO CH3, HCOH and PhCOCH3,
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The decreasing ease of order of formation of nitriles is :
HCOH , CH₂ CH₂ CHO , CH 3 CO CH3, and PhCOCH3
- Formation of nitriles is a nucleophilic addition reaction.
- Reaction of Aldehydes and ketones with HCN or NaCN, KCN leads to addition of nitrile into the compound.
- We know, Ketones are less reactive towards nucleophilic addition reaction than aldehydes because of i) Steric hinderance ii)Electronic reasons.
- The presence of two bulky groups on the ketonic Carbonyl carbon, hinders the approach of nucleophile towards it.
- Also, the aromatic aldehyde has even lesser reactivity towards nucleophilic addition reaction because of positive charge of carbonyl carbon here is stabilized by electrons of benzene ring.
- So, Formaldehyde is very easy to form Nitrile, than Propanal than Propanone than Benzyl methylaldehyde.
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