Alkenes (CIE IGCSE Chemistry: Co-ordinated Sciences (Double Award))

Revision Note

Alexandra Brennan

Last updated

Did this video help you?

Catalytic cracking

  • Alkenes are unsaturated hydrocarbons with carbon-carbon double bonds (C=C)
  • They have covalent bonds
  • Their general formula is CnH2n
  • The presence of the double bond, C=C, means they can make more bonds with other atoms by opening up the C=C bond and allowing incoming atoms to form another single bond with each carbon atom of the functional group
  • Each of these carbon atoms now forms 4 single bonds instead of 1 double and 2 single bonds
  • This makes them much more reactive than alkanes

Table of alkenes

Displayed formula Name Molecular formula
ethene ethene C2H4 
propene propene C3H6 
but-1-ene but-1-ene C4H8 
pent-1-ene pent-1-ene C5H10 

The first four members of the alkene homologous series

 

Manufacture of alkenes

  • Although there is use for each fraction obtained from the fractional distillation of crude oil, the amount of longer chain hydrocarbons produced is far greater than needed
  • These long chain hydrocarbon molecules are further processed to produce other products
  • A process called catalytic cracking is used to convert longer-chain molecules into short-chain and more useful hydrocarbons
  • Shorter chain alkanes, alkenes and hydrogen are produced from the cracking of longer chain alkanes
  • Alkenes can be used to make polymers and the hydrogen used to make ammonia
  • Kerosene and diesel oil are often cracked to produce petrol, other alkenes and hydrogen
  • Cracking involves heating the hydrocarbon molecules to around 600 – 700°C to vaporise them
  • The vapours then pass over a hot powdered catalyst of alumina or silica
  • This process breaks covalent bonds in the molecules as they come into contact with the surface of the catalyst, causing thermal decomposition reactions
  • The molecules are broken up in a random way which produces a mixture of smaller alkanes and alkenes
  • Hydrogen and a higher proportion of alkenes are formed at higher temperatures and higher pressure

 

The cracking of decane 

Catalytic crackingDecane is catalytically cracked to produce octane for petrol and ethene for ethanol

 

Examiner Tip

Only extended tier students need to be able to describe the manufacture of alkenes.

Distinguishing from alkanes

  • The presence of the C=C double bond in an alkene but not an alkane allows us to distinguish between them
  • To do this, bromine water is used
  • Bromine water is an orange coloured solution
  • When bromine water is shaken with an alkane the solution remains orange
  • When bromine water is shaken with an alkene, the solution will go colourless, as the bromine can add across the double bond meaning it is no longer in solution

How to distinguish between alkanes and alkenes 

Using bromine water to test for alkanes and alkenes

Alkenes will decolourise bromine water

Examiner Tip

When describing what happens to bromine water in an alkene ensure you say colourless, and not clear. 

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?

Alexandra Brennan

Author: Alexandra Brennan

Expertise: Chemistry

Alex studied Biochemistry at Newcastle University before embarking upon a career in teaching. With nearly 10 years of teaching experience, Alex has had several roles including Chemistry/Science Teacher, Head of Science and Examiner for AQA and Edexcel. Alex’s passion for creating engaging content that enables students to succeed in exams drove her to pursue a career outside of the classroom at SME.