Order the relative base strength of phenyl amine, methyl amine and methylphenyl amine and outline your reasoning.

Phenyl amine is the weakest base- the benzene group has a negative inductive effect on the lone pair on the nitrogen. Therefore it is less availiable for donation.

Methyl amine is the strongest- the methyl group has a positive inductive effect on the lone pair on the nitrogen. Therefore it is more avaliable for donation.

Methylphenyl amine is in the middle as these 2 groups are both attatched to the nitrogen so the inductive effects work in opposition

TF
Answered by Thomas F. Chemistry tutor

5059 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Q1. Two beakers, A and B, each contain 100.0 cm^3 of 0.0125 mol/dm^3 nitric acid. Calculate the pH of the solution formed after 50.0 cm^3 of distilled water are added to beaker A. Give your answer to 2 decimal places.


Calculate the pH of the solution formed when 30 cm3 of 0.150 moldm-3 aqueous sulfuric acid is added to 30 cm3 of 0.200 moldm-3 aqueous potassium hydroxide at 25 C.


why does graphene conduct electricity?


a) How can an element be classified as a transition metal, considering only electronic arrangement? (1 mark) b) In terms of electrons, why is aqueous copper(II) sulphate solution red? (3 marks) c) EDTA is a bidentate ligand. What is a bidentate ligand?(2)


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