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Chapter 25 - Optical Isomerism

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Total cards: 9•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

define optical isomerism

Back (Answer)

a form of stereoisomerism where there are 4 groups bonded to a central atom, forming 2 molecules with non-superimposable mirror images of each other

#2
Front (Question)

what are enantiomers

Back (Answer)

a pair of optical isomers which correspond to eachother

#3
Front (Question)

whats a chiral carbon

Back (Answer)

the carbon with 4 different groups

#4
Front (Question)

whats a racemic mixture or racemate

Back (Answer)

a 50/50 mixture of an enantiomer pair

#5
Front (Question)

describe the optical effects of enantiomers

Back (Answer)

when polarized light is shone through a sample of enantiomers, one will rotate the plane of polarization in the clockwise direction and one in the anticlockwise direction the + isomer is clockwise, the - isomer is anticlockwise

#6
Front (Question)

why does a racemate have no optical effect on polarised light

Back (Answer)

because the effects of each isomer cancel out

#7
Front (Question)

what is lactic acid

Back (Answer)

2-hydroxypropanoic acid

#8
Front (Question)

what is stage one in the synthesis of lactic acid

Back (Answer)

ethanal undergoes nucleophilic addition with a CN group to form 2-hydroxypropanenitrile

#9
Front (Question)

what is stage two in the synthesis of lactic acid

Back (Answer)

hydrolysis of 2-hydroxypropanenitrile with a mixture of water acidified with dilute HCl the nitrile group is replaced with a carboxylic acid group. the products are lactic acid and ammonium chloride