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

Related Chemistry A Level answers

All answers ▸

Give the IUPAC name of CH3CH2CH2CH2CH(OH)CN and describe why the formation of this molecule creates 2 enantiomers.


Explain why ethanol has a higher boiling point than ethene (3)


There are two methods of ionisation in a time of flight spectrometer, name and explain one of these methods in detail.


How can you work out, using the changes in oxidation numbers, which compound out of KCl, KBr and KI has the greatest reducing power?