Why is methylamine a stronger base than aminobenzene?

In methylamine, the lone pair of electrons on the nitrogen atom is more available because of the postive inductive effect of the methyl group, where as in aminobenzene it is less available due to the delocalisation of the benzene ring.

YC
Answered by Young C. Chemistry tutor

6254 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Explain why the 2nd Electron aiffinity of Chlorine is Endothermic whilst the first electron affinity is exothermic


Explain the delocalised model of benzene, and hence why it is less reactive with electrophiles than cyclohexene


Explain the shapes of the molecules NH3 and AlCl3 (using diagrams)


Lead (IV) oxide reacts with concentrated hydrochloric acid as follows: PbO2(s) + 4HCl(aq) -----> PbCl2(s) + Cl2(g) + 2H2O(l) What mass of lead chloride would be obtained from 37.2g of PbO2, and what mass of chlorine gas would be produced


We're here to help

contact us iconContact ustelephone icon+44 (0) 203 773 6020
Facebook logoInstagram logoLinkedIn logo

MyTutor is part of the IXL family of brands:

© 2026 by IXL Learning