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Polymers

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

Card preview (24)

#1
Front (Question)

How to draw a repeating unit for a polyester

Back (Answer)

Take an H2O from the middle and from the ends

#2
Front (Question)

2 ways to form a polyester

Back (Answer)

Di-acid and Di-ol Or Di- acyl chloride and Di-ol

#3
Front (Question)

Polymerisation with a di-acyl chloride and a Di-ol produces what?

Back (Answer)

HCl and a polyester

#4
Front (Question)

How to form a polyamide

Back (Answer)

Di-acid + Di-amine

#5
Front (Question)

2 polymers used to form nylon-6,6

Back (Answer)

Hexanedioic acid Hexane-1,6-diamine

#6
Front (Question)

How do polyamides differ when formed from amino acids or from diacid - diamine

Back (Answer)

Amino acid: alternating n-h and C=O

#7
Front (Question)

What does Kevlar make?

Back (Answer)

Bullet proof vests

#8
Front (Question)

What are the monomers that produce Kevlar?

Back (Answer)

Diamino benzene Benzene-1,4-Di carboxylic acid

#9
Front (Question)

When making Kevlar what monomer can be used instead of benzene-1,4-di carboxylic acid?

Back (Answer)

Acyl chloride equivalent

#10
Front (Question)

Why can condensation polymers be broken down?

Back (Answer)

Delta positive C on C=O can be attacked by nucleophiles

#11
Front (Question)

Technical term for condensation polymers being broken down?

Back (Answer)

Hydrolysis

#12
Front (Question)

What can condensation polymers be broken down by?

Back (Answer)

An acid (eg HCl) or base (eg NaOH)

#13
Front (Question)

Why are condensation polymers environmentally friendly?

Back (Answer)

Can be hydrolysed by an acid or base due to delta positive C on C=O which can be attacked by nucleophiles (Therefore biodegrades)

#14
Front (Question)

What must always be included in a diagram of lab fractional distillation?

Back (Answer)

Fractionating column Ice bath Heat

#15
Front (Question)

Can bifunctional molecules form condensation polymers?

Back (Answer)

Yep

#16
Front (Question)

For bifunctional molecules, how do you arrange to molecule to draw the repeating unit?

Back (Answer)

Put functional groups on each end

#17
Front (Question)

Name 2 uses for condensation polymers Why are they a good basis for these materials?

Back (Answer)

Preparation of plastic bottles for fizzy drinks and fabrics Biodegradable (susceptible to hydrolysis)

#18
Front (Question)

Why are alkanes un reactive

Back (Answer)

They have only strong, non-polar C-H and C-C Not naturally broken down

#19
Front (Question)

How are addition polymers disposed of?

Back (Answer)

Landfill Melted down and remoulded

#20
Front (Question)

3 problems with burning poly(alkenes)

Back (Answer)

Produces CO2 (greenhouse gas) CO (toxic gas) Carbon (exacerbates asthma)

#21
Front (Question)

What are the advantages of recycling polymers?

Back (Answer)

All plastic derived from crude oil so recycling saves using this non-renewable resource and the energy needed to refine it If not recycled usually ends up in landfills

#22
Front (Question)

What are the disadvantages of recycling?

Back (Answer)

Plastics needed to be collected, transported and sorted which uses energy (CO2 produced) and man power (expensive)

#23
Front (Question)

Why are condensation polymers biodegradable?

Back (Answer)

The delta positive C of C=O can be attacked by nucleophiles

#24
Front (Question)

Poly(alkenes) are made from additional polymerisation. True or false?

Back (Answer)

False It is “addition” polymerisation not “additional”