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

18535 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Draw the mechanism for the reaction of an acid chloride with an alcohol to form an ester


Explain the trend in ionisation energies for the group one metals?


What is the optical activity of the product formed when propanone is refluxed with HCN with KCN dissolved in ethanol and why?


What are isotopes?


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:

© 2025 by IXL Learning