Find the best tutors and institutes for Class 12 Tuition
Search in
Arrange the following compounds in increasing order of their reactivity in nucleophilic addition reactions.
(i)Ethanal, Propanal, Propanone, Butanone.
(ii)Benzaldehyde, p-Tolualdehyde, p-Nitrobenzaldehyde, Acetophenone.
Hint:Consider steric effect and electronic effect.
(i)
The +I effect of the alkyl group increases in the order:
Ethanal < Propanal < Propanone < Butanone
The electron density at the carbonyl carbon increases with the increase in the +I effect. As a result, the chances of attack by a nucleophile decrease. Hence, the increasing order of the reactivities of the given carbonyl compounds in nucleophilic addition reactions is:
Butanone < Propanone < Propanal < Ethanal
(ii)
The +I effect is more in ketone than in aldehyde. Hence, acetophenone is the least reactive in nucleophilic addition reactions. Among aldehydes, the +I effect is the highest in p-tolualdehyde because of the presence of the electron-donating −CH3 group and the lowest in p-nitrobezaldehyde because of the presence of the electron-withdrawing −NO2 group. Hence, the increasing order of the reactivities of the given compounds is:
Acetophenone < p-tolualdehyde < Benzaldehyde
< p-Nitrobenzaldehyde
Predict the products of the following reactions:
(i)
(ii)
(iii)
(iv)
(i)
(ii)
(iii)
(iv)
How helpful was it?
How can we Improve it?
Please tell us how it changed your life *
Please enter your feedback
UrbanPro.com helps you to connect with the best Class 12 Tuition in India. Post Your Requirement today and get connected.
Find best tutors for Class 12 Tuition Classes by posting a requirement.
Get started now, by booking a Free Demo Class