A guide for A level students KNOCKHARDY PUBLISHING

A guide for A level students KNOCKHARDY PUBLISHING
ISOMERISM A guide for A level students 2015 SPECIFICATIONS KNOCKHARDY PUBLISHING

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... Navigation is achieved by... either clicking on the grey arrows at the foot of each page or 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

Before you start it would be helpful to…
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 STRUCTURAL ISOMERISM
CHAIN ISOMERISM STRUCTURAL ISOMERISM POSITION ISOMERISM Same molecular formula but different structural formulae FUNCTIONAL GROUP ISOMERISM GEOMETRICAL ISOMERISM Occurs due to the restricted rotation of C=C double bonds... two forms… E and Z (CIS and TRANS) STEREOISOMERISM Same molecular formula but atoms occupy different positions in space. OPTICAL ISOMERISM Occurs when molecules have a chiral centre. Get two non- superimposable 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

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

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 2 3 PENT-1-ENE double bond between carbons 1 and 2 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.

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 BUT 1 2 2 1-CHLOROBUTANE halogen on carbon 1 2-CHLOROBUTANE halogen on carbon 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

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

ALCOHOLS and ETHERS Name ETHANOL METHOXYMETHANE Classification ALCOHOL ETHER Functional Group R-OH R-O-R Physical properties polar O-H bond gives rise No hydrogen bonding to hydrogen bonding low boiling point get higher boiling point insoluble in water and solubility in water Chemical properties Lewis base Inert Wide range of reactions

ALDEHYDES and KETONES Name PROPANAL PROPANONE Classification ALDEHYDE KETONE Functional Group R-CHO R-CO-R Physical properties polar C=O bond gives polar C=O bond gives dipole-dipole interaction dipole-dipole interaction Chemical properties easily oxidised to acids of undergo oxidation under same number of carbons extreme conditions only reduced to 1° alcohols reduced to 2° alcohols

STRUCTURAL ISOMERISM – FUNCTIONAL GROUP CARBOXYLIC ACIDS and ESTERS
Name PROPANOIC ACID METHYL ETHANOATE Classification CARBOXYLIC ACID ESTER Functional Group R-COOH R-COOR Physical properties O-H bond gives rise No hydrogen bonding to hydrogen bonding insoluble in water get higher boiling point and solubility in water Chemical properties acidic fairly unreactive react with alcohols hydrolysed to acids

• GEOMETRICAL ISOMERISM • OPTICAL ISOMERISM
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  GEOMETRICAL ISOMERISM Two similar atoms/groups attached Two similar atoms/groups attached  Once you get two similar atoms/groups attached to one end of a C=C, you cannot have geometrical isomerism Two similar atoms/groups attached Two different atoms/groups attached  Two different atoms/groups attached Two different atoms/groups attached  GEOMETRICAL ISOMERISM

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.

E/Z or CIS-TRANS CIS / TRANS Should only be used when there are two H’s and two non-hydrogen 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

E/Z or CIS-TRANS CIS / TRANS Should only be used when there are two H’s and two non-hydrogen 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

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 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 Priority use the CAHN, INGOLD and PRELOG (CIP) convention C2H5 > CH3 > H greater lower priority priority I > Br > Cl > F > H

Determines the priority of atoms/groups around a double bond Priority use the CAHN, INGOLD and PRELOG (CIP) convention C2H5 > CH3 > H greater lower priority priority I > Br > Cl > F > H Example

Determines the priority of atoms/groups around a double bond Priority use the CAHN, INGOLD and PRELOG (CIP) convention C2H5 > CH3 > H greater lower priority priority I > Br > Cl > F > H Example 15 29 Calculate the relative masses of the atoms/groups attached to the C=C 1 15

Determines the priority of atoms/groups around a double bond Priority use the CAHN, INGOLD and PRELOG (CIP) convention C2H5 > CH3 > H greater lower priority priority I > Br > Cl > F > H Example 15 29 Calculate the relative masses of the atoms/groups attached to the C=C Work out the higher priority group at either end 1 15

Determines the priority of atoms/groups around a double bond Priority use the CAHN, INGOLD and PRELOG (CIP) convention C2H5 > CH3 > H greater lower priority priority I > Br > Cl > F > H Example 15 29 Calculate the relative masses of the atoms/groups attached to the C=C 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

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 lower priority priority I > Br > Cl > F > H Example 15 29 Calculate the relative masses of the atoms/groups attached to the C=C 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

E 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 lower priority priority I > Br > Cl > F > H 29 15 29 15 1 15 E Z

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

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

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 CHIRAL CENTRES
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

SPOTTING CHIRAL CENTRES
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 C 3 H’s around it NOT chiral C 2 H’s around it NOT chiral  1-chlorobutane

SPOTTING CHIRAL CENTRES
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 C 3 H’s around it NOT chiral C 2 H’s around it NOT chiral  1-chlorobutane CH3CH2CHClCH3 C 3 H’s around it NOT chiral C 2 H’s around it NOT chiral C H, CH3, Cl,C2H5 around it CHIRAL  2-chlorobutane

OPTICAL ISOMERISM     SPOTTING CHIRAL CENTRES CH3CH2CH2CH2Cl
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 C 3 H’s around it NOT chiral C 2 H’s around it NOT chiral  1-chlorobutane CH3CH2CHClCH3 C 3 H’s around it NOT chiral C 2 H’s around it NOT chiral C H, CH3, Cl,C2H5 around it CHIRAL  2-chlorobutane (CH3)2CHCH2Cl C 3 H’s around it NOT chiral C 2 CH3’s around it NOT chiral C 2 H’s around it NOT chiral  1-chloro-2-methylpropanane (CH3)3CCl C 3 H’s around it NOT chiral C 3 CH3’s around it NOT chiral  2-chloro-2-methylpropanane

Spatial differences between isomers
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 spoons superimposable but not mirror images books non-superimposable mirror images 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 spoons superimposable but not mirror images books non-superimposable mirror images hands NB For optical isomerism in molecules, both conditions must apply... they must be mirror images AND be non-superimposable

What is a non-superimposable mirror image?
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

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 turned to the left DEXTROROTATORY LAEVOROTATORY d or + form l or - form

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 turned to the left DEXTROROTATORY LAEVOROTATORY d or + form l or - form Racemate a 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 Light source produces light vibrating in all directions B Polarising filter only allows through light vibrating in one direction C Plane polarised light passes through sample D If substance is optically active it rotates the plane polarised light E Analysing filter is turned so that light reaches a maximum F Direction of rotation is measured coming towards the observer If the light appears to have turned to the right turned to the left DEXTROROTATORY 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

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

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 ANIMATION 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

Synthesis of 2-hydroxypropanoic acid (lactic acid)
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 H+ / H2O During the first stage, the nucleophilic CN- ion can attack from below, or above, the aldehyde. A mixture of the two enantiomers is formed.

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 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.

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 world- wide, 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.

What should you be able to do?
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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A guide for A level students KNOCKHARDY PUBLISHING

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