Back to marketplace

Unit 3: Section 7 - Polymers

No description yet. This curated deck is ready for daily study.

Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

What is condensation?

Back (Answer)

Small molecule eliminated (usually H2O) to form a larger molecule

#2
Front (Question)

How many monomers are condensation polymers usually formed from?

Back (Answer)

2

#3
Front (Question)

What properties do the monomers forming condensation polymers have?

Back (Answer)

Each has 2 functional groups

#4
Front (Question)

What are 3 examples of condensation polymers?

Back (Answer)

• Polyesters • Polyamides • Polypeptides

#5
Front (Question)

What are the 2 monomers which form a polyester?

Back (Answer)

• Diol and carboxylic acid or a molecule with both alcohol and a carboxylic acid functional groups

#6
Front (Question)

What monomers is Terylene made from?

Back (Answer)

Benzene-1,4-dicarboxylic acid and ethane-1,2-diol

#7
Front (Question)

What is Terylene used for?

Back (Answer)

As a fibre for making clothes

#8
Front (Question)

What are the 2 monomers used to form a polyamide?

Back (Answer)

Diamine and dicarboxylic acid

#9
Front (Question)

What are 2 examples of polyamides?

Back (Answer)

Nylon and Kevlar

#10
Front (Question)

Which monomers is Nylon-6,6 made from?

Back (Answer)

1,6-diaminohexane and hexane-1,6-dioic acid H2N-(CH2)6-NH2 and HOOC-(CH2)4-COOH

#11
Front (Question)

If you are making Nylon in the lab, what monomers would you use and why? What molecule is eliminated?

Back (Answer)

Use hexane-1,6-diacyl chloride and 1,6-diaminohexane as the rate of reaction is must faster than using hexane-1,6-dioic acid HCl is elimated

#12
Front (Question)

What is Kevlar used for?

Back (Answer)

In body armour (bullet proof vests, stab vests), helmets (F1 drivers), oven gloves

#13
Front (Question)

Which monomers is Kevlar made from?

Back (Answer)

1,4-diaminobenzene and benzene-1,4-dicarboxylic acid

#14
Front (Question)

Why is Kevlar so strong?

Back (Answer)

Rigid chains and close packing of flat aromatic rings

#15
Front (Question)

Why are poly(alkanes) not biodegradable?

Back (Answer)

Non-polar C-H and C-C bonds

#16
Front (Question)

Why is it bad to burn poly(alkanes)?

Back (Answer)

Released CO2, CO, C (soot) and other toxic chemicals from monomers

#17
Front (Question)

Where do most poly(alkenes) end up?

Back (Answer)

Landfill sites

#18
Front (Question)

Why can condesation polymers be broken down?

Back (Answer)

They have polar bonds

#19
Front (Question)

How are condensation polymers broken down?

Back (Answer)

Hydrolysis

#20
Front (Question)

Why does hydrolysis not happen in normal conditions?

Back (Answer)

Very slow rate in standard conditions

#21
Front (Question)

What are the 4 stages needed when recycling polymers?

Back (Answer)

• Collected • Sorted • Melted • Reformed

#22
Front (Question)

What are the advantages of recycling polymers?

Back (Answer)

• Saves expense of crude oil and preserves a non-renewable resource • Reduces landfill

#23
Front (Question)

What are the disadvantages of recycling polymers?

Back (Answer)

• Energy and manpower is needed for collecting, sorting and melting the polymers, making it expensive • Can only be done a limited number of times

#24
Front (Question)

What does draw the polymer mean?

Back (Answer)

Draw with square brackets, n, and trailing bonds