A-level Chemistry: 3.3.12 Polymers
This set of flashcards covers condensation polymers, focusing on polyamides—their monomer components, the type of bond formed (amide link), examples such as Nylon 6,6 and Kevlar, and their common uses. It highlights the chemical basis and practical applications of these polymers.
Name 3 examples of condensation polymers
polyamides
polyesters
polypeptides
Key Terms
Name 3 examples of condensation polymers
polyamides
polyesters
polypeptides
What are polyamides made out of?
Dicarboxylic acids + diamines
Polyamides
State the name of the bond that forms between the carboxyl
groups and amino groups
Amide link
Name 2 examples of polyamides
Nylon 6,6
Kevlar
State what nylon 6,6 is made from
1,6-diaminohexane + hexanedioic acid
Name some uses of nylon 6,6
Used to make clothing, carpet, rope, airbags and parachutes
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| Term | Definition |
|---|---|
Name 3 examples of condensation polymers |
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What are polyamides made out of? | Dicarboxylic acids + diamines |
Polyamides State the name of the bond that forms between the carboxyl | Amide link |
Name 2 examples of polyamides |
|
State what nylon 6,6 is made from | 1,6-diaminohexane + hexanedioic acid |
Name some uses of nylon 6,6 | Used to make clothing, carpet, rope, airbags and parachutes |
Draw an equation showing how nylon 6,6 is formed | |
State what kevlar is made from | 1,4-diaminobenzene and benzene-1,4-dicarboxylic acid |
Name some uses of kevlar | Used in bulletproof vests, boat construction, car tyres and lightweight spots equipment |
Draw an equation showing how kevlar is formed | |
What are polyesters made out of? | Dicarboxylic acids + diols |
Polyesters State the name of the bond that forms between the carboxyl | Ester link |
Name an example of polyester | Terylene (PET) |
State what terylene (PET) is made from | Benzene-1,4-dicarboxylic acid and ethane-1,2diol |
Name some uses of terylene (PET) | Used in plastic bottles, clothing, sheets and sails |
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Why are condensation polymers stronger & more rigid than addition polymers? |
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Why are polyalkenes (addition polymers) non-biodegradable and won’t react when being used? | Have non-polar C-C bonds = unreactive and chemically inert |
Why are condensation polymers biodegradable? |
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Name 3 ways of disposing waste plastics |
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When are plastics placed in landfills? | When plastic is:
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Name an advantage of using landfills to dispose plastics | Landfill is cheap and easy method of waste disposal |
Name 3 disadvantages of using landfills to dispose plastics |
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What is an advantage of burning plastics (excluding its cost and ease)? | Heat can be used to generate electricity |
Why when burning waste plastics, does the process need to be carefully controlled? | To reduce release of toxic gases e.g. polymers that contain chlorine (PVC) produce HCl when burned = has to be removed |
Burning Waste Plastics How is the release of toxic gases reduced? | Waste gases from combustion as passed through scrubbers which neutralise gases like HCl by allowing them to react with a base |
What is a disadvantage of burning waste plastics? | Waste gases e.g. CO2 will still contributed to greenhouse effect |
Name 2 ways to recycle plastics |
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Name 4 advantages of recycling waste plastics |
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Name 4 disadvantages of recycling waste plastics |
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1,4-butanedioic acid |