Home
Class 12
CHEMISTRY
How is the basic strength of aromatic am...

How is the basic strength of aromatic amines affected by the presence of an electron releasing group on the benzene ring?

Text Solution

Verified by Experts

An electron releasing group increases the electron density on the N-atom. As a result, its tendency to donate an electron pair to a proton increases and hence the basicity of amine increases.
Promotional Banner

Topper's Solved these Questions

  • AMINES

    AAKASH INSTITUTE ENGLISH|Exercise Assignment Section -A Competition Level Questions|50 Videos

  • AMINES

    AAKASH INSTITUTE ENGLISH|Exercise Assignment Section B (Objective Type Questions) one option is correct|23 Videos

  • AMINES

    AAKASH INSTITUTE ENGLISH|Exercise ILLUSTRATION|2 Videos

  • ALDEHYDES, KETONES AND CARBOXYLIC ACIDS

    AAKASH INSTITUTE ENGLISH|Exercise Try Yourself|20 Videos

  • BIOMOLECULES

    AAKASH INSTITUTE ENGLISH|Exercise EXERCISE (ASSIGNMENT) SECTION - D Assertion - Reason Type Questions|5 Videos

Similar Questions

Explore conceptually related problems

Presence of a nitro group in a benzene ring

Which among the following is not an activating group of the benzene ring?

For an electrophilic substitution reaction , the presence of a halogen atom in the benzene ring …..

Basic strength of different alkyl amines depends upon

Acidic and basic nature of organic compound depends upon-Inductive effect. Acidic strength of organic acid increase with increase in electron withdrawing group or - group and decrease with increase in electron releasing group or + group. Basic strength of organic compound having just opposite relationship with inductive effect, i.e. basic strength prop+1 effect Which of the following acid having highest K_(a) value

The typical reaction of benzene and other aromatic compounds are electrophilic substitution. Presence of electron donating group activates the ring towards electrophilic substitution, while presence of electron withdrawing group deactivates the ring towards electrophilic substituion but at the same time activates the ring towards nucleophilic subsituion. Some groups are predominantly meta-directing and all of these are deactivating. Except halogen, most of the o- and p- directing groups are activating groups. Which of the following compound is not formed. X represents mixture of organic compounds. The mixture does not contain

The typical reaction of benzene and other aromatic compounds are electrophilic substitution. Presence of electron donating group activates the ring towards electrophilic substitution, while presence of electron withdrawing group deactivates the ring towards electrophilic substituion but at the same time activates the ring towards nucleophilic subsituion. Some groups are predominantly meta-directing and all of these are deactivating. Except halogen, most of the o- and p- directing groups are activating groups. underset(Delta)overset(C_(2)H_(5)Cl.AlCl_(3))rarr(A) major. A is trisubstituted benzene. The structure of A is :

The typical reaction of benzene and other aromatic compounds are electrophilic substitution. Presence of electron donating group activates the ring towards electrophilic substitution, while presence of electron withdrawing group deactivates the ring towards electrophilic substituion but at the same time activates the ring towards nucleophilic subsituion. Some groups are predominantly meta-directing and all of these are deactivating. Except halogen, most of the o- and p- directing groups are activating groups. underset(Delta)overset(C_(2)H_(5)Cl.AlCl_(3))rarr(A) major. A is trisubstituted benzene. The structure of A is :

Why does the basic strength of the hydroxides of alkali metals increase on moving down the group ?