Which one is more reactive towards nucleophiles acetaldehyde or acetone?

Which one is more reactive towards nucleophiles acetaldehyde or acetone?

Acetaldehyde is more reactive than acetone in nucleophilic addition reactions.

Why aldehyde is more reactive than acetone?

Aldehydes are typically more reactive than ketones due to the following factors. The carbonyl carbon in aldehydes generally has more partial positive charge than in ketones due to the electron-donating nature of alkyl groups. …

Why acetaldehyde is more reactive than acetone towards reaction with HCN?

(i) CH3COCH3 is sterically hindered than CH3CHO due to the presence of alkyl group on both sides of the carbonyl carbon, making them less reactive towards nucleophilic attack because both methyl groups have electron releasing tendency due to -I effect. Therefore, acetaldehyde is more reactive towards reaction with HCN.

Why is acetaldehyde more reactive?

Acetaldehyde is more reactive than benzaldehyde. This is because the carbon of the carbonyl group in the benzaldehyde is less electrophilic than the carbon of the carbonyl group in the acetaldehyde.

Which is most reactive towards nucleophilic substitution reaction?

Vinylic halides are reactive towards nucleophilic substitution reaction.

Why acetaldehyde is more reactive than benzaldehyde?

Which of the following is least reactive towards nucleophilic substitution reaction?

Chlorine of vinyl chloride (CH2=CHCI) is non-reactive (less reactive) towards nucleophile (in nucleophilic substitution reaction) because it shows the following resonating structure due to +M effect of −Cl atom.

Which of the following is the most reactive to a nucleophile?

CH3-ΘO is sterically least hindered and hence most reactive nucleophile.

Which acetaldehyde is most reactive towards nucleophilic addition?

Hence, from the above equation we can say that Formaldehyde is more reactive towards nucleophilic addition reaction.