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:
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:
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
- Look at R1 and R3:
- 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
- E isomers have the highest priority groups on opposite sides of the C=C bond, i.e. one above and one below
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
- Look at R1 and R3:
- 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
- In compound B, the two highest priority groups are on the same side (both below) the C=C bond
More complicated E / Z isomers
- Compound X exhibits E / Z isomerism:
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
- Look at R1 and R3:
- 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
- In compound X, the two highest priority groups are on the same side (both below) the C=C bond
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.