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IGCSE Chemistry: Polymers Overview

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0% found this document useful (0 votes)
26 views14 pages

IGCSE Chemistry: Polymers Overview

Uploaded by

Mahmoud AbuSrea
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

Cambridge (CIE) IGCSE Your notes

Chemistry
Polymers
Contents
Polymers
Addition & Condensation Polymers
Plastics & their Disposal
Proteins

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Polymers
Your notes

Polymers: the basics


Polymers are large molecules built by linking 50 or more smaller molecules called
monomers
Each repeat unit is connected to the adjacent units via covalent bonds
Examples of polymers include PVC and nylon

Many monomers join together to form a polymer


Poly(ethene) is formed by the addition polymerisation of ethene monomers
Addition polymerisation involves the addition of many monomers to make a long
chained polymer
In this case, many ethene monomers join together due to the carbon carbon double
bond breaking

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Your notes

Poly(ethene) is formed by addition polymerisation using ethene monomers

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Addition & Condensation Polymers
Your notes

Addition polymers
Extended tier only
Addition polymers are formed by the joining up of many monomers and only occur in
monomers that contain C=C bonds
One of the bonds in each C=C bond breaks and forms a bond with the adjacent
monomer
The polymer formed will only contain single bonds
Many polymers can be made by the addition of alkene monomers
Others are made from alkene monomers with different atoms attached to the monomer
such as chlorine or a hydroxyl group
The name of the polymer is deduced by putting the name of the monomer in brackets
and adding poly- as the prefix
For example if propene is the alkene monomer used, then the name is poly(propene)
Poly(ethene) is formed by the addition polymerisation of ethene monomers

Deducing the polymer from the monomer


Polymer molecules are very large compared with most other molecule
Repeat units are used when displaying the formula
To draw a repeat unit:
Change the double bond in the monomer to a single bond in the repeat unit
Add a continuation bond to each end of the repeat unit
The bonds on either side of the polymer must extend outside the brackets
(these are called extension or continuation bonds)
A small subscript n is written on the bottom right hand side to indicate a large
number of repeat units
Add on the rest of the groups in the same order that they surrounded the double
bond in the monomer

Examples of some addition polymers

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Your notes

The repeat unit for the polymer should have an n in the bottom right hand corner

Deducing the monomer from the polymer


To deduce the monomer from the polymer:
Identify the repeating unit in the polymer
Change the single bond in the repeat unit to a double bond in the monomer
Remove the bond from each end of the repeat unit

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Th monomer has been identified, a double bond added and the atoms drawn in
Your notes

Examiner Tips and Tricks


You could be asked to draw the repeat unit for any given monomer and vice versa.
You would only need to draw the structure of one monomer if you have been given the
polymer.

Condensation polymers
Extended tier only
Condensation polymers are formed when two different monomers are linked together
with the removal of a small molecule, usually water
This is a key difference between condensation polymers and addition polymers:
Addition polymerisation forms the polymer molecule only
Condensation polymerisation forms the polymer molecule and
one water molecule per linkage
The monomers have two functional groups present, one on each end
The functional groups at the ends of one monomer react with the functional group on
the end of the other monomer, in so doing creating long chains of alternating
monomers, forming the polymer

Forming nylon
Nylon is a polyamide made from dicarboxylic acid monomers (a carboxylic with a -
COOH group at either end) and diamines (an amine with an -NH2 group at either end)
Each -COOH group reacts with another -NH2 group on another monomer
An amide linkage is formed with the subsequent loss of one water molecule per link

Forming nylon

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Your notes

Nylon is a polyamide formed from a dicarboxylic acid and a diamine


The structure of nylon can be represented by drawing out the polymer using boxes to
represent the carbon chains

Diagram showing a section of nylon

Forming polyesters
PET or polyethylene terephthalate to give its full name, is a polyester made from
dicarboxylic acid monomers (a carboxylic with a -COOH group at either end) and diols
(alcohol with an -OH group at either end)
Each -COOH group reacts with another -OH group on another monomer
An ester linkage is formed with the subsequent loss of one water molecule per link

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For every ester linkage formed in condensation polymerisation, one molecule of water is
formed from the combination of a proton (H+) and a hydroxyl ion (OH–)
Your notes
PET is also used in synthetic fibres as is sold under the trade name of terylene
Forming PET

PET is a polyester formed from a dicarboxylic acid and a diol


The structure of PET can be represented by drawing out the polymer using boxes to
represent the carbon chains
This can be done for all polyesters

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Diagram showing a section of PET
Your notes

Examiner Tips and Tricks


You don't need to know the detailed chemical structure of PET, just the symbolic
drawing showing the alternating blocks and the linking ester group. Be careful not to
exactly repeat the linking group in nylon or PET; the link alternates by reversing the
order of the atoms, rather like a mirror image.

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Plastics & their Disposal
Your notes

Plastics & their disposal


Plastics are made from polymers
Many polymers are chemically unreactive, which means that they are non-
biodegradable
This means that the disposal of plastics can cause environmental issues

Incineration
Polymers release a lot of heat energy when they burn and produce carbon dioxide,
which is a greenhouse gas that contributes to climate change
Some polymers release toxic fumes when they burn
An example of this is poly(vinylchloride), which releases toxic hydrogen chloride gas
when burned
If incinerated by incomplete combustion, carbon monoxide will be produced which is a
toxic gas

Polluting oceans
Plastic waste is accumulating in oceans and causing huge disruptions to marine life

Landfills
Waste polymers are disposed of in landfill sites
But, this takes up valuable land
Most polymers are non-biodegradable
This means that micro-organisms, such as decomposers, cannot break them down
This causes sites to quickly fill up

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Your notes

Disposal of polymers is an environmental problem

PET re-polymerisation
Extended tier only
PET stands for polyethylene terephthalate
This is a common polymer used to make things like plastic bottles
It is a condensation polymer consisting of repeating ester units
So, PET is a type of polyester, like terylene
One of the problems with recycling polymers is that the conditions needed to break
them down, which are usually high temperatures and pressures, can degrade the
monomers making them unusable for re-polymerisation
PET is relatively easy to convert back into the monomers
It can be depolymerised either using enzymes or by chemical methods
Enzymes present in microbes breakdown the PET into the original monomers
The same can be achieved using solvents a catalyst and mild heating
The monomers are recovered and be re-polymerised into new PET
This saves on resources and energy, reducing the carbon footprint of the production
process

The re-polymerisation of PET

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Your notes

The breakdown of PET into its two monomers takes place using enzymes or chemical
catalysts and mild conditions

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Proteins
Your notes

Proteins
Extended tier only
Proteins are an example of condensation polymers
They are formed from amino acid monomers joined together by amide links
Amino acids are small molecules containing NH2 and COOH functional groups
Due to containing amide links and being found in biological systems, proteins are known
as natural polyamides
In proteins, the amide links are known as peptide links
There are twenty common amino acids, each differing by their side chain, represented
by R

General structure of an amino acid


Proteins can contain between 60 and 600 of these amino acids in different orders
These are the monomers which polymerise to form the protein

The formation of a protein

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Your notes

A protein is produced by a condensation polymerisation reaction


The structure of proteins can be represented using the following diagram whereby the
boxes represent the carbon chains

Diagram showing a section of protein

Examiner Tips and Tricks


For your exam, you are only required to draw proteins using the boxes representing
the carbon chains.

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Common questions

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In condensation polymerisation, functional groups play a crucial role in forming polyamides and polyesters. Polyamides are formed from a reaction between dicarboxylic acids (with -COOH groups) and diamines (with -NH groups), creating amide linkages with the release of water . In the formation of polyesters, dicarboxylic acids react with diols (with -OH groups), resulting in ester linkages accompanied by the removal of water .

Addition polymers differ from condensation polymers in that they are formed from monomers with C=C bonds that simply join together without losing any atoms, resulting in chains of single-bonded carbon atoms . Condensation polymers, on the other hand, are formed by joining monomers and eliminating small molecules like water, resulting in alternating structures of monomers linked by the formation of new functional groups such as esters or amides. This fundamental structural difference influences properties such as degradability and reactivity .

Environmental issues from the disposal of polymers like PET include non-biodegradability, which leads to accumulation in landfills, pollution of oceans, and release of toxic fumes when incinerated . To mitigate these issues, PET can be depolymerised using chemical or enzymatic methods into its monomers, allowing for re-polymerisation into new PET. This process saves resources and energy, reducing the carbon footprint of polymer production .

The arrangement of functional groups in the polymerisation of PET, which is chemically similar to terylene, is significant as it affects the polymer's physical properties and potential uses. PET is formed from dicarboxylic acid and diol monomers with COOH and OH groups, respectively, leading to the formation of ester linkages . The precise orientation and sequence of these functional groups influence the polymer's flexibility, melting point, and mechanical strength, allowing for its widespread use in fibers and packaging materials .

The primary distinction between addition polymerisation and condensation polymerisation lies in their chemical processes and by-products. In addition polymerisation, monomers containing C=C bonds join together without the loss of any small molecules, resulting in polymers that contain only single bonds . Conversely, condensation polymerisation involves the joining of monomers with the elimination of small molecules, typically water. This reaction requires monomers with two different functional groups, and each linkage in the polymer is accompanied by the formation of a water molecule .

Identifying repeating units of a polymer involves analyzing the polymer's structure and reversing the polymerisation process. By recognizing repeating units and converting single bonds within these units back to double bonds, chemists can deduce the structure of the original monomer . This deduction is significant in polymer chemistry as it enables the understanding of polymer properties and facilitates the design and synthesis of new polymers with desirable characteristics .

Re-polymerisation of PET has environmental advantages over traditional recycling methods. It involves breaking down PET into its original monomers using enzymes or chemical catalysts under mild conditions. This process avoids the degradation of monomers that can occur with high temperatures and pressure in traditional recycling, thus allowing for efficient reuse. Additionally, it reduces resource and energy consumption, lowering the carbon footprint of the production process .

Proteins are classified as natural polyamides because they are formed from amino acid monomers joined by peptide links (amide bonds), similar to synthetic polyamides like nylon . However, proteins consist of up to 20 different amino acids in various sequences, which contributes to their complex and diverse structures compared to the repetitive sequences in synthetic polyamides .

Ecological concerns associated with incinerating polymers include the release of carbon dioxide, a greenhouse gas, and potentially toxic fumes like hydrogen chloride from burning poly(vinylchloride) and carbon monoxide from incomplete combustion . These emissions contribute to air pollution and climate change, impacting policies on waste management by encouraging the development of more sustainable practices such as recycling and reducing landfill usage .

Nylon's chemical structure facilitates its formation through condensation polymerisation because it consists of dicarboxylic acid monomers with -COOH groups and diamine monomers with -NH groups. These groups react to form amide linkages, each accompanied by the loss of a water molecule, allowing nylon chains to form between alternating monomers .

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