ISOMERISM
A guide for A level students
KNOCKHARDY PUBLISHING
2015
SPECIFICATIONS
KNOCKHARDY PUBLISHING
ISOMERISM
INTRODUCTION
This Powerpoint show is one of several produced to help students
understand selected topics at AS and A2 level Chemistry. It is based on the
requirements of the AQA and OCR specifications but is suitable for other
examination boards.
Individual students may use the material at home for revision purposes or it
may be used for classroom teaching using an interactive white board.
Accompanying notes on this, and the full range of AS and A2 topics, are
available from the KNOCKHARDY SCIENCE WEBSITE at...
www.knockhardy.org.uk/sci.htm
Navigation is achieved by...
either
or
clicking on the grey arrows at the foot of each page
using the left and right arrow keys on the keyboard
ISOMERISM
CONTENTS
• Prior knowledge
• Types of isomerism
• Structural isomerism
• Stereoisomerism
• Geometrical isomerism
• Optical isomerism
• Check list
ISOMERISM
Before you start it would be helpful to…
• know the functional groups found in organic chemistry
• know the arrangement of bonds around carbon atoms
• know what affects the boiling point of organic molecules
TYPES OF ISOMERISM
CHAIN ISOMERISM
STRUCTURAL ISOMERISM
Same molecular formula but
different structural formulae
POSITION ISOMERISM
FUNCTIONAL GROUP
ISOMERISM
GEOMETRICAL ISOMERISM
STEREOISOMERISM
Same molecular
formula but atoms
occupy different
positions in space.
Occurs due to the restricted
rotation of C=C double bonds...
two forms… E and Z (CIS and
TRANS)
OPTICAL ISOMERISM
Occurs when molecules have a
chiral centre. Get two nonsuperimposable mirror images.
STRUCTURAL ISOMERISM - INTRODUCTION
COMPOUNDS HAVE THE SAME MOLECULAR FORMULA
BUT DIFFERENT STRUCTURAL FORMULA
Chain
different arrangements of the carbon skeleton
similar chemical properties
slightly different physical properties
more branching = lower boiling point
STRUCTURAL ISOMERISM - INTRODUCTION
COMPOUNDS HAVE THE SAME MOLECULAR FORMULA
BUT DIFFERENT STRUCTURAL FORMULA
Chain
different arrangements of the carbon skeleton
similar chemical properties
slightly different physical properties
more branching = lower boiling point
Positional
same carbon skeleton
same functional group
functional group is in a different position
similar chemical properties - slightly different physical properties
STRUCTURAL ISOMERISM - INTRODUCTION
COMPOUNDS HAVE THE SAME MOLECULAR FORMULA
BUT DIFFERENT STRUCTURAL FORMULA
Chain
different arrangements of the carbon skeleton
similar chemical properties
slightly different physical properties
more branching = lower boiling point
Positional
same carbon skeleton
same functional group
functional group is in a different position
similar chemical properties - slightly different physical properties
Functional Group different functional group
different chemical properties
different physical properties
• Sometimes more than one type of isomerism occurs in the same molecule.
• The more carbon atoms there are, the greater the number of possible isomers
STRUCTURAL ISOMERISM - CHAIN
caused by different arrangements of the carbon skeleton
similar chemical properties
slightly different physical properties
more branching = lower boiling point
There are two structural isomers of C4H10. One is a straight chain molecule where all
the carbon atoms are in a single row. The other is a branched molecule where three
carbon atoms are in a row and one carbon atom sticks out of the main chain.
BUTANE
straight chain
2-METHYLPROPANE
branched
C4H10
STRUCTURAL ISOMERISM - CHAIN
DIFFERENCES BETWEEN CHAIN ISOMERS
Chemical
Isomers show similar chemical properties because
the same functional group is present.
Physical
Properties such as density and boiling point show trends according
to the of the degree of branching
Boiling Point
“straight” chain isomers have higher values than branched ones
the greater the degree of branching the lower the boiling point
branching decreases the effectiveness of intermolecular forces
less energy has to be put in to separate the molecules
- 0.5°C
straight chain
- 11.7°C
branched
greater branching
= lower boiling point
STRUCTURAL ISOMERISM - POSITIONAL
molecule has the same carbon skeleton
molecule has the same same functional group... BUT
the functional group is in a different position
have similar chemical properties / different physical properties
Example 1
POSITION OF A DOUBLE BOND IN ALKENES
1
2
PENT-1-ENE
double bond between
carbons 1 and 2
2
3
PENT-2-ENE
double bond between
carbons 2 and 3
There are no other isomers with five C’s in the longest chain but there are three
other structural isomers with a chain of four carbons plus one in a branch.
STRUCTURAL ISOMERISM - POSITIONAL
molecule has the same carbon skeleton
molecule has the same same functional group... BUT
the functional group is in a different position
have similar chemical properties / different physical properties
Example 2
POSITION OF A HALOGEN IN A HALOALKANE
1
1-CHLOROBUTANE
halogen on carbon 1
2
2-CHLOROBUTANE
halogen on carbon 2
BUT
2
is NOT
3-CHLOROBUTANE
Moving the chlorine along the chain makes new isomers; the position is measured from
the end nearest the functional group... the third example is 2- NOT 3-chlorobutane.
There are 2 more structural isomers of C4H9Cl but they have a longest chain of 3
STRUCTURAL ISOMERISM - POSITIONAL
molecule has the same carbon skeleton
molecule has the same same functional group... BUT
the functional group is in a different position
have similar chemical properties / different physical properties
Example 3
RELATIVE POSITIONS ON A BENZENE RING
1,2-DICHLOROBENZENE
ortho dichlorobenzene
1,3-DICHLOROBENZENE
meta dichlorobenzene
1,4-DICHLOROBENZENE
para dichlorobenzene
STRUCTURAL ISOMERISM – FUNCTIONAL GROUP
molecules have same molecular formula
molecules have different functional groups
molecules have different chemical properties
molecules have different physical properties
ALCOHOLS and ETHERS
ALDEHYDES and KETONES
ACIDS and ESTERS
MORE DETAILS FOLLOW
STRUCTURAL ISOMERISM – FUNCTIONAL GROUP
ALCOHOLS and ETHERS
Name
ETHANOL
METHOXYMETHANE
Classification
ALCOHOL
ETHER
Functional Group
R-OH
Physical properties
polar O-H bond gives rise
to hydrogen bonding.
get higher boiling point
and solubility in water
Chemical properties
Lewis base
Wide range of reactions
R-O-R
No hydrogen bonding
low boiling point
insoluble in water
Inert
STRUCTURAL ISOMERISM – FUNCTIONAL GROUP
ALDEHYDES and KETONES
Name
PROPANAL
PROPANONE
Classification
ALDEHYDE
KETONE
R-CHO
R-CO-R
Functional Group
Physical properties
polar C=O bond gives
dipole-dipole interaction
polar C=O bond gives
dipole-dipole interaction
Chemical properties
easily oxidised to acids of
same number of carbons
undergo oxidation under
extreme conditions only
reduced to 1° alcohols
reduced to 2° alcohols
STRUCTURAL ISOMERISM – FUNCTIONAL GROUP
CARBOXYLIC ACIDS and ESTERS
Name
PROPANOIC ACID
Classification
CARBOXYLIC ACID
Functional Group
R-COOH
METHYL ETHANOATE
ESTER
R-COOR
Physical properties
O-H bond gives rise
to hydrogen bonding.
get higher boiling point
and solubility in water
No hydrogen bonding
insoluble in water
Chemical properties
acidic
react with alcohols
fairly unreactive
hydrolysed to acids
STEREOISOMERISM
Molecules have the SAME MOLECULAR FORMULA but the atoms are
joined to each other in a DIFFERENT SPACIAL ARRANGEMENT - they
occupy a different position in 3-dimensional space.
There are two types...
• GEOMETRICAL ISOMERISM
• OPTICAL ISOMERISM
GEOMETRICAL ISOMERISM IN ALKENES
Introduction
•
•
•
•
an example of stereoisomerism
found in some, but not all, alkenes
occurs due to the RESTRICTED ROTATION OF C=C bonds
get two forms...
GEOMETRICAL ISOMERISM IN ALKENES
How to tell if it exists
Two different
atoms/groups
attached
Two different
atoms/groups
attached

Two similar
atoms/groups
attached
Two similar
atoms/groups
attached

Two similar
atoms/groups
attached
Two different
atoms/groups
attached

Two different
atoms/groups
attached
Two different
atoms/groups
attached

GEOMETRICAL ISOMERISM
Once you get two similar
atoms/groups attached to
one end of a C=C, you
cannot have geometrical
isomerism
GEOMETRICAL ISOMERISM
GEOMETRICAL ISOMERISM IN ALKENES
Introduction
•
•
•
•
an example of stereoisomerism
found in some, but not all, alkenes
occurs due to the RESTRICTED ROTATION OF C=C bonds
get two forms...
CIS (Z)
Groups/atoms are on the
SAME SIDE of the double bond
TRANS (E)
Groups/atoms are on OPPOSITE
SIDES across the double bond
GEOMETRICAL ISOMERISM IN ALKENES
RESTRICTED ROTATION OF C=C BONDS
Single covalent bonds can easily rotate. What appears to be a different structure is
not. It looks like it but, due to the way structures are written out, they are the same.
ALL THESE STRUCTURES ARE THE SAME BECAUSE C-C BONDS HAVE ‘FREE’ ROTATION
Animation doesn’t
work in old
versions of
Powerpoint
GEOMETRICAL ISOMERISM IN ALKENES
RESTRICTED ROTATION OF C=C BONDS
C=C bonds have restricted rotation so the groups on either end of the bond are
‘frozen’ in one position; it isn’t easy to flip between the two.
Animation doesn’t
work in old
versions of
Powerpoint
This produces two possibilities. The two structures cannot interchange easily
so the atoms in the two molecules occupy different positions in space.
GEOMETRICAL ISOMERISM IN ALKENES
E/Z or CIS-TRANS
CIS /
TRANS
Should only be used when there are two H’s and two nonhydrogen groups attached to each carbon.
cis
non-hydrogen groups / atoms on the
SAME SIDE of C=C bond
trans
non-hydrogen groups / atoms on
OPPOSITE SIDES of C=C bond
GEOMETRICAL ISOMERISM IN ALKENES
E/Z or CIS-TRANS
CIS /
TRANS
Should only be used when there are two H’s and two nonhydrogen groups attached to each carbon.
cis
non-hydrogen groups / atoms on the
SAME SIDE of C=C bond
trans
non-hydrogen groups / atoms on
OPPOSITE SIDES of C=C bond
GEOMETRICAL ISOMERISM IN ALKENES
E/Z or CIS-TRANS
CIS /
TRANS
Should only be used when there are two H’s and two nonhydrogen groups attached to each carbon.
cis
non-hydrogen groups / atoms on the
SAME SIDE of C=C bond
trans
non-hydrogen groups / atoms on
OPPOSITE SIDES of C=C bond
cis
trans
cis
trans
GEOMETRICAL ISOMERISM IN ALKENES
E/Z or CIS-TRANS
E/Z
Z (zusammen)
higher priority groups / atoms on
the SAME SIDE of C=C bond
E (entgegen)
higher priority groups / atoms on
OPPOSITE SIDES of C=C bond
Side 1
Side 2
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
E/Z
Priority
Z (zusammen)
higher priority groups / atoms on
the SAME SIDE of C=C bond
E (entgegen)
higher priority groups / atoms on
OPPOSITE SIDES of C=C bond
use the CAHN, INGOLD and PRELOG (CIP) convention
C2H5 > CH3 > H
greater
priority
lower
priority
I > Br > Cl > F > H
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
Priority
use the CAHN, INGOLD and PRELOG (CIP) convention
C2H5 > CH3 > H
greater
priority
lower
priority
I > Br > Cl > F > H
Example
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
Priority
use the CAHN, INGOLD and PRELOG (CIP) convention
C2H5 > CH3 > H
greater
priority
lower
priority
I > Br > Cl > F > H
Example
Calculate the relative masses of the
atoms/groups attached to the C=C
15
1
29
15
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
Priority
use the CAHN, INGOLD and PRELOG (CIP) convention
C2H5 > CH3 > H
greater
priority
lower
priority
I > Br > Cl > F > H
Example
Calculate the relative masses of the
atoms/groups attached to the C=C
15
29
Work out the higher priority group at
either end
1
15
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
Priority
use the CAHN, INGOLD and PRELOG (CIP) convention
C2H5 > CH3 > H
greater
priority
lower
priority
I > Br > Cl > F > H
Example
Calculate the relative masses of the
atoms/groups attached to the C=C
15
29
Work out the higher priority group at
either end
Work out if the higher priority groups
are on the same (Z) or different (E)
side of the C=C
1
15
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
Priority
use the CAHN, INGOLD and PRELOG (CIP) convention
C2H5 > CH3 > H
greater
priority
lower
priority
I > Br > Cl > F > H
Example
Calculate the relative masses of the
atoms/groups attached to the C=C
15
29
Work out the higher priority group at
either end
Work out if the higher priority groups
are on the same side (Z) or different
side (E) of the C=C
1
15
Z
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
Priority
use the CAHN, INGOLD and PRELOG (CIP) convention
C2H5 > CH3 > H
greater
priority
lower
priority
I > Br > Cl > F > H
29
15
15
29
1
E
15
Z
CAHN, INGOLD & PRELOG CONVENTION
Determines the priority of atoms/groups around a double bond
E/Z
Z (zusammen)
higher priority groups / atoms on
the SAME SIDE of C=C bond
E (entgegen)
higher priority groups / atoms on
OPPOSITE SIDES of C=C bond
Examples
GEOMETRICAL ISOMERISM IN ALKENES
E/Z or CIS-TRANS
E/Z
Z (zusammen)
higher priority groups / atoms on
the SAME SIDE of C=C bond
E (entgegen)
higher priority groups / atoms on
OPPOSITE SIDES of C=C bond
Examples
E
Z
Z
E
GEOMETRICAL ISOMERISM IN ALKENES
Isomerism in butene
There are 3 structural isomers of C4H8 that are alkenes*. Of these ONLY
ONE exhibits geometrical isomerism.
but-1-ene
cis but-2-ene
(Z) but-2-ene
trans but-2-ene
(E) but-2-ene
2-methylpropene
* YOU CAN GET ALKANES WITH FORMULA C4H8 IF THE CARBON ATOMS ARE IN A RING
OPTICAL ISOMERISM
Occurrence
another form of stereoisomerism
occurs when compounds have non-superimposable mirror images
Isomers
the two different forms are known as optical isomers or enantiomers
they occur when molecules have a chiral centre
a chiral centre contains an asymmetric carbon atom
an asymmetric carbon has four different atoms (or groups)
arranged tetrahedrally around it.
OPTICAL ISOMERISM
Occurrence
another form of stereoisomerism
occurs when compounds have non-superimposable mirror images
Isomers
the two different forms are known as optical isomers or enantiomers
they occur when molecules have a chiral centre
a chiral centre contains an asymmetric carbon atom
an asymmetric carbon has four different atoms (or groups)
arranged tetrahedrally around it.
CHIRAL CENTRES
There are four different colours
arranged tetrahedrally about
the carbon atom
2-chlorobutane exhibits optical isomerism
because the second carbon atom has four
different atoms/groups attached
OPTICAL ISOMERISM
SPOTTING CHIRAL CENTRES
Look at each carbon atom in the chain and see what is attached to it. For a chiral centre
you need an asymmetric carbon with four different atoms/groups) arranged tetrahedrally around it.
IF A CARBON HAS MORE THAN ONE OF ANY ATOM/GROUP ATTACHED, IT CAN’T BE CHIRAL
CH3CH2CH2CH2Cl
1-chlorobutane
C
C
C
C
3 H’s around it
2 H’s around it
2 H’s around it
2 H’s around it
NOT chiral
NOT chiral
NOT chiral
NOT chiral

OPTICAL ISOMERISM
SPOTTING CHIRAL CENTRES
Look at each carbon atom in the chain and see what is attached to it. For a chiral centre
you need an asymmetric carbon with four different atoms/groups) arranged tetrahedrally around it.
IF A CARBON HAS MORE THAN ONE OF ANY ATOM/GROUP ATTACHED, IT CAN’T BE CHIRAL
CH3CH2CH2CH2Cl
1-chlorobutane
CH3CH2CHClCH3
2-chlorobutane
C
C
C
C
3 H’s around it
2 H’s around it
2 H’s around it
2 H’s around it
NOT chiral
NOT chiral
NOT chiral
NOT chiral

C
C
C
C
3 H’s around it
2 H’s around it
H, CH3, Cl,C2H5 around it
3 H’s around it
NOT chiral
NOT chiral
CHIRAL
NOT chiral

OPTICAL ISOMERISM
SPOTTING CHIRAL CENTRES
Look at each carbon atom in the chain and see what is attached to it. For a chiral centre
you need an asymmetric carbon with four different atoms/groups) arranged tetrahedrally around it.
IF A CARBON HAS MORE THAN ONE OF ANY ATOM/GROUP ATTACHED, IT CAN’T BE CHIRAL
CH3CH2CH2CH2Cl
1-chlorobutane
CH3CH2CHClCH3
2-chlorobutane
(CH3)2CHCH2Cl
1-chloro-2-methylpropanane
(CH3)3CCl
2-chloro-2-methylpropanane
C
C
C
C
3 H’s around it
2 H’s around it
2 H’s around it
2 H’s around it
NOT chiral
NOT chiral
NOT chiral
NOT chiral

C
C
C
C
3 H’s around it
2 H’s around it
H, CH3, Cl,C2H5 around it
3 H’s around it
NOT chiral
NOT chiral
CHIRAL
NOT chiral

C 3 H’s around it
C 2 CH3’s around it
C 2 H’s around it
NOT chiral
NOT chiral
NOT chiral

C 3 H’s around it
C 3 CH3’s around it
NOT chiral
NOT chiral

OPTICAL ISOMERISM
Spatial differences between isomers
• two forms exist which are NON-SUPERIMPOSABLE MIRROR IMAGES of each other
• non-superimposable means you you can’t stack one form exactly on top of the other
OPTICAL ISOMERISM
Spatial differences between isomers
• two forms exist which are NON-SUPERIMPOSABLE MIRROR IMAGES of each other
• non-superimposable means you you can’t stack one form exactly on top of the other
Some common objects are mirror images and superimposable
superimposable but not mirror images
non-superimposable mirror images
spoons
books
hands
OPTICAL ISOMERISM
Spatial differences between isomers
• two forms exist which are NON-SUPERIMPOSABLE MIRROR IMAGES of each other
• non-superimposable means you you can’t stack one form exactly on top of the other
Some common objects are mirror images and superimposable
superimposable but not mirror images
non-superimposable mirror images
NB
For optical isomerism in molecules, both conditions must apply...
they must be mirror images AND be non-superimposable
spoons
books
hands
OPTICAL ISOMERISM
What is a non-superimposable mirror image?
Animation doesn’t
work in old
versions of
Powerpoint
OPTICAL ISOMERS - DIFFERENCE
•
•
•
•
•
isomers differ in their reaction to plane-polarised light
plane polarised light vibrates in one direction only
one isomer rotates light to the right, the other to the left
rotation of light is measured using a polarimeter
rotation is measured by observing the polarised light coming out towards the observer
OPTICAL ISOMERS - DIFFERENCE
•
•
•
•
•
isomers differ in their reaction to plane-polarised light
plane polarised light vibrates in one direction only
one isomer rotates light to the right, the other to the left
rotation of light is measured using a polarimeter
rotation is measured by observing the polarised light coming out towards the observer
• If the light appears to have
turned to the right
DEXTROROTATORY
d or + form
turned to the left
LAEVOROTATORY
l or - form
OPTICAL ISOMERS - DIFFERENCE
•
•
•
•
•
isomers differ in their reaction to plane-polarised light
plane polarised light vibrates in one direction only
one isomer rotates light to the right, the other to the left
rotation of light is measured using a polarimeter
rotation is measured by observing the polarised light coming out towards the observer
• If the light appears to have
turned to the right
DEXTROROTATORY
d or + form
turned to the left
LAEVOROTATORY
l or - form
Racemate
a 50-50 mixture of the two enantiomers (dl) or (±) is a racemic mixture.
The opposite optical effects of each isomer cancel each other out
Examples
Optical activity is common in biochemistry and pharmaceuticals
• Most amino acids exhibit optical activity
• many drugs must be made of one optical isomer to be effective
- need smaller doses (safer and cost effective)
- get reduced side effects
- improved pharmacological activity
OPTICAL ISOMERISM
The polarimeter
A
B
C
D
E
F
A
B
C
D
E
F
Light source produces light vibrating in all directions
Polarising filter only allows through light vibrating in one direction
Plane polarised light passes through sample
If substance is optically active it rotates the plane polarised light
Analysing filter is turned so that light reaches a maximum
Direction of rotation is measured coming towards the observer
If the light appears to have
turned to the right
DEXTROROTATORY
turned to the left
LAEVOROTATORY
OPTICAL ISOMERISM
How optical isomers can be formed
Carbonyl compounds undergo nucleophilic addition. If there are two different
groups attached to the C=O bond, the possibility of forming optical isomers arises.
THE NUCLEOPHILIC ADDITION OF HCN TO ETHANAL
If the nucleophilic cyanide ion
attacks from above one
optical isomer is formed
OPTICAL ISOMERISM
How optical isomers can be formed
Carbonyl compounds undergo nucleophilic addition. If there are two different
groups attached to the C=O bond, the possibility of forming optical isomers arises.
THE NUCLEOPHILIC ADDITION OF HCN TO ETHANAL
If the nucleophilic cyanide ion
attacks from above one
optical isomer is formed
However, attack from below,
gives the non-superimposable
mirror image of the first
OPTICAL ISOMERISM
How optical isomers can be formed
Carbonyl compounds undergo nucleophilic addition. If there are two different
groups attached to the C=O bond, the possibility of forming optical isomers arises.
THE NUCLEOPHILIC ADDITION OF HCN TO ETHANAL
If the nucleophilic cyanide ion
attacks from above one
optical isomer is formed
However, attack from below,
gives the non-superimposable
mirror image of the first
The reaction produces a mixture of the two optical
isomers because both modes of attack are possible
OPTICAL ISOMERISM
How optical isomers can be formed
Carbonyl compounds undergo nucleophilic addition. If there are two different
groups attached to the C=O bond, the possibility of forming optical isomers arises.
THE NUCLEOPHILIC ADDITION OF HCN TO ETHANAL
ANIMATION
The reaction produces a mixture of the two optical
isomers because both modes of attack are possible
OPTICAL ISOMERISM
Synthesis of 2-hydroxypropanoic acid (lactic acid)
LACTIC ACID can be formed from ethanal in a two stage process.
1. Nucleophilic addition of hydrogen cyanide to ethanal
2 Hydrolysis of the nitrile group
HCN
H+ / H2O
OPTICAL ISOMERISM
Synthesis of 2-hydroxypropanoic acid (lactic acid)
LACTIC ACID can be formed from ethanal in a two stage process.
1. Nucleophilic addition of hydrogen cyanide to ethanal
2 Hydrolysis of the nitrile group
HCN
During the first stage, the nucleophilic CN- ion
can attack from below, or above, the aldehyde.
A mixture of the two enantiomers is formed.
H+ / H2O
OPTICAL ISOMERISM
Synthesis of 2-hydroxypropanoic acid (lactic acid)
LACTIC ACID can be formed from ethanal in a two stage process.
1. Nucleophilic addition of hydrogen cyanide to ethanal
2 Hydrolysis of the nitrile group
HCN
During the first stage, the nucleophilic CN- ion
can attack from below, or above, the aldehyde.
A mixture of the two enantiomers is formed.
Acid hydrolysis of the mixture provides a
mixture of the two lactic acid forms.
H+ / H2O
OPTICAL ISOMERISM - THALIDOMIDE
The one obvious difference between optical isomers is their response to plane
polarised light. However, some naturally occurring molecules or specifically
synthesised pharmaceuticals show different chemical reactivity.
The drug, THALIDOMIDE is a chiral molecule and can exist as two enantiomers. In the
1960’s it was used to treat anxiety and morning sickness in pregnant women.
Tragically, many gave birth to children with deformities and missing limbs.
It turned out that only one of the enantiomers (the structure on the right) was effective
and safe; its optically active counterpart was not. The major problem was that during
manufacture a mixture of the isomers was produced. The drug was banned worldwide, but not after tens of thousands of babies had been affected.
OPTICAL ISOMERISM – Other points
The following points are useful when discussing reactions producing optical isomers.
The formation of racemic mixtures is more likely in a laboratory reaction
than in a chemical process occurring naturally in the body.
If a compound can exist in more than one form, only one of the optical
isomers is usually effective.
The separation of isomers will make manufacture more expensive.
A drug made up of both isomers will require a larger dose and may cause
problems if the other isomer is ‘poisonous’ like thalidomide.
REVISION CHECK
What should you be able to do?
Recall the definitions of structural isomerism and stereoisomerism
Explain and understand how structural, geometrical and optical isomerism arise
Work out all the possible isomers for a given formula
Recall and understand the importance of optical activity in natural product chemistry
CAN YOU DO ALL OF THESE?
YES
NO
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relevant topic(s) again
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ISOMERISM
The End
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