Stereoisomerism (AQA AS Chemistry)

Revision Note

Test yourself
Stewart

Author

Stewart

Last updated

Stereoisomerism: Geometrical Isomerism

  • Stereoisomers are compounds that have the same atoms connected to each other, however the atoms are differently arranged in space

E/Z isomerism

  • E/Z nomenclature is used to distinguish between the isomers
    • Z isomers have functional groups on the same side of the double bond/carbon ring
    • E isomers have functional groups on opposite sides of the double bond/carbon ring
  • You may see this type of isomerism referred to in other sources as cis/trans isomerism
    • This is a special case of E/Z isomerism
    • A "cis" isomer would essentially be the same as a "Z" isomer and a "trans" isomer would also essentially be the same as an "E" isomer

 

  • To discuss E Z isomers, we will use an alkene of the general formula C2R4:


20-3-2-general-alkene-c2r4

The general alkene, C2R4

  • When the groups R1, R2, R3 and R4 are all different (i.e. R1 ≠ R2 ≠ R3 ≠ R4), we have to use the E Z naming system
    • This is based on Cahn-Ingold-Prelog (CIP) priority rules

  • To do this, we look at the atomic number of the first atom attached to the carbon in question
    • The higher the atomic number; the higher the priority

  • For example, 1-bromo-1-propen-2-ol has four different atoms or groups of atoms attached to the C=C bond
    • This means that it can have two different displayed formulae:

2-bromo-1-propen-1-ol, downloadable IB Chemistry revision notes

1-bromo-1-propen-2-ol (compounds A and B)

Compound A

  • Step 1: Apply the CIP priority rules
    • Look at R1 and R3:
      • Bromine has a higher atomic number than hydrogen so bromine has priority

    • Look at R2 and R4:
      • Oxygen has a higher atomic number than carbon so oxygen has priority

  • Step 2: Deduce E or Z
    • E isomers have the highest priority groups on opposite sides of the C=C bond, i.e. one above and one below
      • The E comes from the German word "entgegen" meaning opposite

    • Z isomers have the highest priority groups on the same side of the C=C bond, i.e. both above or both below
      • The Z comes from the German word "zusammen" meaning together

    • In compound A, the two highest priority groups are on opposite sides (above and below) the C=C bond
      • Therefore, compound A is E-1-bromo-1-propen-2-ol

Compound B

  • Step 1: Apply the CIP priority rules
    • Look at R1 and R3:
      • Bromine has a higher atomic number than hydrogen so bromine has priority

    • Look at R2 and R4:
      • Oxygen has a higher atomic number than carbon so oxygen has priority

  • Step 2: Deduce E or Z
    • In compound B, the two highest priority groups are on the same side (both below) the C=C bond
      • Therefore, compound B is Z-1-bromo-1-propen-2-ol

More complicated E Z isomers

  • Compound X exhibits E Z isomerism:


20-3-2-compound-x

Compound X

  • Step 1: Apply the CIP priority rules
    • Look at R1 and R3:
      • Carbon is the first atom attached to the C=C bond, on the left hand side

    • Look at R2 and R4:
      • Carbon is the first atom attached to the C=C bond, on the right hand side

    • This means that we cannot deduce if compound X is an E or Z isomer by applying the CIP priority rules to the first atom attached to the C=C bond
      • Therefore, we now have to look at the second atoms attached

    • Look again at R1 and R3:
      • The second atoms attached to R1 are hydrogens and another carbon
      • The second atoms attached to R3 are hydrogens and bromine
      • We can ignore the hydrogens as both R groups have hydrogens
      • Bromine has a higher atomic number than carbon, so bromine is the higher priority
        • Therefore, the CH2Br group has priority over the CH3CH2 group

    • Look again at R2 and R4:
      • The second atoms attached to R2 are hydrogens
      • The second atoms attached to R3 are hydrogens and an oxygen
      • Oxygen has a higher atomic number than hydrogen, so oxygen is the higher priority
        • Therefore, the CH2OH group has priority over the CH3 group

  • Step 2: Deduce E or Z
    • In compound X, the two highest priority groups are on the same side (both below) the C=C bond
      • Therefore, compound X is the Z isomer

Examiner Tip

You may come across the term geometric isomerism in older exam papers and textbooks. The term used to refer to cis/trans isomerism, but is no longer in use and would not be required in exams.

You've read 0 of your 10 free revision notes

Unlock more, it's free!

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

the (exam) results speak for themselves:

Did this page help you?

Stewart

Author: Stewart

Expertise: Chemistry Lead

Stewart has been an enthusiastic GCSE, IGCSE, A Level and IB teacher for more than 30 years in the UK as well as overseas, and has also been an examiner for IB and A Level. As a long-standing Head of Science, Stewart brings a wealth of experience to creating Exam Questions and revision materials for Save My Exams. Stewart specialises in Chemistry, but has also taught Physics and Environmental Systems and Societies.