Aldehydes and ketones are amphoteric. Thus they can act both as acids and bases. Under acidic conditions, the carbon of the protonated canbonyl group is much more electrophilic, reacting even with weak nucleopphilie. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack proceeds the elecrophilic attack.
Which one of the carbonyl compounds is more reactive towards `NaCN//H^(+)`?

Aldehydes and ketones are amphoteric. Thus they can act both as acids and bases. Under acidic conditions, the carbon of the protonated canbonyl group is much more electrophilic, reacting even with weak nucleopphilie. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack proceeds the elecrophilic attack. Which of the statements are//is correct?

Aldehydes and ketones are amphoteric. Thus they can act both as acids and bases. Under acidic conditions, the carbon of the protonated canbonyl group is much more electrophilic, reacting even with weak nucleopphilie. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack proceeds the elecrophilic attack. Which of these statements are correct?

Aldehydes and ketones are amphoteric. Thus they can act both as acids and bases. Under acidic conditions, the carbon of the protonated canbonyl group is much more electrophilic, reacting even with weak nucleopphilie. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack proceeds the elecrophilic attack. Which of these statements are correct?

Aldehydes and ketones are amphoteric. Thus they can act both as acids and bases. Under acidic conditions, the carbon of the protonated canbonyl group is much more electrophilic, reacting even with weak nucleopphilie. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack proceeds the elecrophilic attack. Which of the statements are//is correct?

Aldehydes and ketones are amphoteric. Thus they can act both as acids and bases. Under acidic conditions, the carbon of the protonated canbonyl group is much more electrophilic, reacting even with weak nucleopphilie. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack proceeds the elecrophilic attack. Carbonyl compounds gives nucleophilic addition with

Aldehydes and ketones are amphoteric. Thus they can act both as acids and bases. Under acidic conditions, the carbon of the protonated canbonyl group is much more electrophilic, reacting even with weak nucleopphilie. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack proceeds the elecrophilic attack. Carbonyl compounds gives nucleophilic addition with

Aldehydes and ketones are amphoteric. Thus they can react both as acids and bases. Under acidic conditions, the carbon of the protonated carbonyl group is much more electrophilic, reacting even with weak necleophile. Carbonyl compound gives nucleophilic addition reaction. In this reaction the nucleophilic attack precedes the electrophilic attack. Which of the statements regarding nucleophilic addition to carbonyl compounds "is"//"are" correct?

Aldehyde and ketone undergo nucleophilic addition reaction because of polarity between gtC=O group . The reactivity of carbonyl groups toward nucleophile depends upon the nature of inductive effect of froup present at carbonyl carbon. Nucleophilic addition reaction over carbonyl compound is shown by :

Assertion : Carboxylic acids contain a carbonyl group but do not give characteristic reaction of the carbonyl group. Reason : The electrophilicity of the carbonyl carbon is more in carbocylic acids than in aldehydes and ketones.