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Polymers

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Total cards: 17•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

What are the two types of polymers

Back (Answer)

Addition and condensation

#2
Front (Question)

When does an addition polymer form

Back (Answer)

When unsaturated monomers react to form a polymer

#3
Front (Question)

Why are polyalkanes non biodegradable

Back (Answer)

Strong C-C and C-H bonds

#4
Front (Question)

A tip for drawing repeat unitsor whatevrr

Back (Answer)

It is best to first draw out the monomer with groups of atoms arranged around the double bond basically lay them out as e-z isomers

#5
Front (Question)

What are the two types of linkages in polymers

Back (Answer)

Ester link- when making polyesters Amide links when making polyamids

#6
Front (Question)

What are the by products of condensation polymerisation

Back (Answer)

H2O or HCl

#7
Front (Question)

Equations for the formation of Amides and Esters

Back (Answer)

Carboxylic acid + alcohol –> ester + water Acyl chloride + alcohol –> ester + HCl Carboxylic acid + amine –> amide + water Acyl chloride +amine –>amide + HCl If it is the di versionof any of them they form polys so like dicarbolxylic acids + diol forms poly esters plus water

#8
Front (Question)

Note on classification for condensation polymers If asked for type of polymer:

Back (Answer)

It is polyamide or polyester Whereas type of polymerisation is condensation

#9
Front (Question)

Chemical reactivity of condensation polymers

Back (Answer)

polyesters and polyamides can be broken down by hydrolysis and are, therefore, biodegradable The reactivity can be explained by the presence of polar bonds

#10
Front (Question)

Hydrolysis

Back (Answer)

Polyesters and polyamides can be hydrolysed by acid and alkali The hydrolysis will result in the original monomers forming-although the carboxylic acid or amine group will be in salt form depending on whether the conditions are alkaline or acidic

#11
Front (Question)

Intermolecular bonding between condensation polymers chains

Back (Answer)

Polyesters have permanent dipole forces between the Cδ+=Oδ-groups in the different chains in addition to the Van der Waals forces between the chains. Polyamides (and proteins) have hydrogen bonding between the oxygen in Cδ+=Oδ-groups and the H in the Nδ-—Hδ+groups in the different chains in addition to the Van der Waals forces between the chains. Polyamides will therefore have higher melting points than polyesters.

#12
Front (Question)

Disposal of Polymers Landfill

Back (Answer)

Landfill The most common method of disposal of waste in UK Many are now reaching capacity. Most polymers (polyalkenes) are non-biodegradable and take many years to break down. Could use more biodegradable plastics, e.g. Polyamides and cellulose and starch based polymers to improve rates of decomposition

#13
Front (Question)

Disposal of Polymers Incineration

Back (Answer)

Rubbish is burnt and energy produced is used to generate electricity. Some toxins can be released on incineration. Modern incinerators can burn more efficiently and most toxins and pollutants can be removed. Greenhouse gases will still be emitted though. Volume of rubbish is greatly reduced.

#14
Front (Question)

Disposal of Polymers Recycling

Back (Answer)

Saves raw materials-nearly all polymers are formed from compounds sourced/produced from crude oil. Saves precious resources. Polymers need collecting/ sorting-expensive process in terms of energy and manpower. Polymers can only be recycled into the same type –so careful separation needs to be done. Thermoplastic polymers can be melted down and reshaped

#15
Front (Question)

Kevlar

Back (Answer)

Benzene 1,4 dicarboxylic acid and 1,4 diaminobenzene react to form kevlar Takes away OH from COOH and H from NH2 When drawing the repeat unit you need both Benzene 1,4 dicarboxylic acid and 1,4 diaminobenzene in it

#16
Front (Question)

Nylon

Back (Answer)

Hexanedioic acidCOOH(CH2)4COOH +1,6 diaminohexane

#17
Front (Question)

Use of terylene

Back (Answer)

Used in plastic bottles