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A2- Optical Isomerism

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Total cards: 10•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

What is a chiral centre?

Back (Answer)

a carbon with 4 different groups

#2
Front (Question)

What is optical isomerism?

Back (Answer)

a form of stereoisomerism that occurs when there is an asymmetrical carbon

#3
Front (Question)

What can happen is a chiral centre is present?

Back (Answer)

2 isomers that are mirror images of each other

#4
Front (Question)

Why are optical isomers optically active?

Back (Answer)

because they interact with plane-polarised light

#5
Front (Question)

How do optical isomers interact with plane polarised light?

Back (Answer)

rotate it 90 degrees in opposite directions

#6
Front (Question)

What is a racemate?

Back (Answer)

a mixture where a pair of enantiomers are in a 1:1 ration (equal parts of each)

#7
Front (Question)

Why don’t racemic mixtures have an effect on plane polarised light?

Back (Answer)

as the effect of each enantiomer (in opposite directions) cancel out

#8
Front (Question)

Why do racemic mixtures form?

Back (Answer)

as the reagent can attack from above or below (at equal opportunities) so both isomers can be formed, producing optical isomers

#9
Front (Question)

Why might drugs that are enantiomers not be separated?

Back (Answer)

expensive and time-consuming

#10
Front (Question)

Why might drugs that are chiral be separated?

Back (Answer)

• expensive to synthesise • one enantiomer is harmful