3.7 Optical Isomerism
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What property must a carbon atom have for the molecule to display optical isomerism about that carbon atom?
4 different substituents attached to one carbon atom
What are the similarities and differences between two optical isomers?
Same atoms and bonds, but they are non-superimposable mirror images of one another. NOT IDENTICAL in chemical properties necessarily. Differ in the way they rotate plane polarised light - rotate plane of polarisation by the same angle but in different directions
What word is used to describe optically active molecules?
Chiral
What are the pair of isomers called?
Enantiomers
What is a chiral centre ?
The carbon that has four different substituents attaches to it
How is the chiral centre denoted
C*
Give two examples of chiral molecules. Draw one of them (both enatiomers)
all alpha amino acids, except glycine Lactic acid / 2-hydroxypropanoic acid
How is light polarised
By passing it through a Polaroid filter, so oscillations are only in one plane
What effect does the racemic mixture have on plane polarised light?
None, as the rotation by each enantiomer cancels out to nothing
What effect does the + isomer have on plane polarised light?
Rotates plane of polarisation by X0 clockwise
What effect does the - isomer have on plane polarised light?
Rotates plans of polarisation by X0 anti-clockwise (same angle, opposite direction)
What is the structure of a polarimeter?
Light source (unpolarised light) —> polarising filter (polarised light) —> polarised light passes through compartment containing sample —> detector determines the angle of rotation of the plane polarised light
What are the polariimeters used for?
To identify which enantiomer is present, the purity of the sample, the concentration of the sample
What is the first stage of the synthesis of lactic acid (2-hydroxypropanoic acid) from ethanal? (Equation)
(Reagents are KCN and HCl but it is acceptable to write HCN in the balanced equation as this is the H+ from the HCl and -CN from KCN)
Why is the CH3CH(OH)CN molecule formed chiral?
H,CH3,OH and CN groups attached to the central chiral carbon atom - 4 substituents
What is the second stage of the synthesis of lactic acid (2-hydroxypropanoic acid) from ethanal?
Hydrolysis: CH3CH(OH)CN + HCl +2H2O—> CH3CH(OH)COOH + NH4Cl
How does this second stage affect the chirality?
Does not affect it - still racemic as chirality not affected by this stage
Are racemic mixtures formed in nature? Why?
Not often, as enzyme mechanisms are 3D so only form one enantiomer
Why is optical isomerism a problem for the drug industry?
Sometimes, only one enantiomer is effective due to enzyme’s active site/cell receptors being 3D
What are the options to resolve the issue of only one enantiomer being effective?
• Separate enantiomer- difficult and expensive as have very similar properties 2.sell racemate - wasteful as half is inactive 3.design alternative synthesis to only produce one enantiomer
Examples of optically active drugs
Ibuprofen, Thalidomide
Why is ibuprofen able to be sold as a racemate, even though the + isomer is needed to treat inflammation?
Sold as 50% racemate But body converts 60% of R - isomer to S+ isomer —> end up with 80% S+ isomer