Halogenoalkanes - Introduction (Edexcel International AS Chemistry)

Revision Note

Richard

Author

Richard

Last updated

Halogenoalkanes - Introduction

Naming halogenoalkanes

  • We use the prefixes 
    • Fluoro for fluorine
    • Chloro for chlroine
    • Bromo for bromine
    • Iodo for iodine
  • The name of the halogenoalkane is based on the orignal alkane
    • So CH3CH2CH2Br would be 1-bromopropane 
  • The position of the halogen atom must be taken into account 
    • So CH3CH(Br)CH3 would be 2-bromopropane 
  • Finally the substituents are listed alphabetically
    • So  CH3CH(Cl)CH2Br would be 1-bromo-2-chloropropane 

Classifying halogenoalkanes

  • Halogenoalkanes can be classified as primary, secondary or tertiary depending on the number of carbon atoms attached to the C-X functional group 
    • A primary halogenoalkane is when a halogen is attached to a carbon that itself is attached to one other alkyl group
    • A secondary halogenoalkane is when a halogen is attached to a carbon that itself is attached to two other alkyl groups
    • A tertiary halogenoalkane is when a halogen is attached to a carbon that itself is attached to three other alkyl groups

Halogen Compounds Halogenoalkanes, downloadable AS & A Level Chemistry revision notes

Primary, secondary and tertiary halogenoalkanes

Examiner Tip

You are also expected to be able to draw structural, displayed and skeletal formulae of halogenoalkanes

You've read 0 of your 5 free revision notes this week

Sign up now. It’s free!

Join the 100,000+ Students that ❤️ Save My Exams

the (exam) results speak for themselves:

Did this page help you?

Richard

Author: Richard

Expertise: Chemistry

Richard has taught Chemistry for over 15 years as well as working as a science tutor, examiner, content creator and author. He wasn’t the greatest at exams and only discovered how to revise in his final year at university. That knowledge made him want to help students learn how to revise, challenge them to think about what they actually know and hopefully succeed; so here he is, happily, at SME.