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. 

Answered by Ganesh V. Chemistry tutor

11843 Views

See similar Chemistry A Level tutors

Related Chemistry A Level answers

All answers ▸

The molecular formula of TCDD is C12H4O2Cl4. Chlorine exists as two isotopes 35Cl (75%) and 37Cl (25%). How many molecular ion peaks are there? What is the mass of the most abundant one?


When vaporised, isotopes of an element can be separated in a mass spectrometer. Name the three processes that occur in a mass spectrometer before the vaporised isotopes can be detected. State how each process is achieved. (6 marks)


If we burn 3 moles of carbon in air (as per the equation), what mass (in grams) of carbon dioxide will be produced? What volume will this gas occupy at standard temperature and pressure?


How does a acid buffer work?


We're here to help

contact us iconContact usWhatsapp logoMessage us on Whatsapptelephone icon+44 (0) 203 773 6020
Facebook logoInstagram logoLinkedIn logo

© MyTutorWeb Ltd 2013–2024

Terms & Conditions|Privacy Policy