Determine whether a tertiary halogenoalkane will undergo a SN1 or SN2 reaction. Explain your choice.

Tertiary halogenoalkanes will undergo a SN1 reaction. This means that there is 1 molecule in the rate determining step, which is the slowest step. Because of the bulky alkyl groups surrounding the central carbon attached to the halogen atom, there is very little space for the nucleophile to attack. This is called steric hindrance. Because of this, the weak carbon-halide bond must first be broken without any other molecular interefence and once a carbocation is formed, the nucleophile will be able to attack the now positive carbon atom to form a covalent bond. 

GV
Answered by Ganesh V. Chemistry tutor

19623 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Explain how chromatography is used to separate components in a mixture.


What is a bond?


In d block chemistry, Copper and Chromium electron configuration do not follow the electron filling trend , why is this?


Explain how the electron pair repulsion theory can be used to deduce the shape of, and the bond angle in, PF3


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