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

19733 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

Calculate Gibbs free energy when S = 131 J mol-1 and H = 155 kJ mol-1 at 25 C, stating whether or not the reaction is feasable.


Flask Q (volume = 1.00 x 103 cm3 ) is filled with ammonia (NH3) at 102 kPa and 300 K. Calculate the mass of ammonia in flask Q. (Gas constant R = 8.31 J K−1 mol−1 )


Draw an Alkane with the molecular formula C4H8 as well as a possible functional group isomer and state a chemical test you can use to differentiate between the two.


Why is SiO2 a solid whereas CO2 is a gas at room temeperature?


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