chapter 29 - Polymerisation Flashcards

1
Q

What is condensation polymerisation and how is it formed

A

Condensation polymers are long chain molecules made from joining together many shorter molecules (monomers). These form long chains of molecules. Some smaller molecules are also formed (for example water).

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2
Q

Addition polymerisation what is it and how are they formed

A

Addition polymers are long chain molecules made from joining together many shorter molecules (monomers) together to form a long chain molecule. With no other products produced.

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3
Q

What are the types of monomers used in addition polymers

A

alkenes

molecules with C=C bonds

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4
Q

What type of monomers are used in condensation polymers

A

Dicarboxylic acid with diols

Dicarboxylic acid with diamines

Amino acids

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5
Q

What are some examples of addition polymers

A

poly(ethene)

PVC

poly(propene)

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6
Q

What are some examples of condensation polymers

A

Polyesters (Terylene)

polyamides (nylon, Kevlar)

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7
Q

Why are addition polymers nonbiodegradable

A

because they don’t have any polar bonds/the absence of polar bonds in the main chain (all bonds are carbon to carbon)

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8
Q

Why are condensation polymers biodegradable

A

because they have the presence of polar C-N or
C-O in the main chain

have polar bonds. therefore susceptible to nucleophillic attack (eg with H2O).

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9
Q

how is Terylene (PET) formed (polyester)

A

monomers:

benzene 1,4 di-carboxylic acid
ethane-1,2diol

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10
Q

How to draw one repeating unit when you have two of the same monomer and two different monomers. (Condensation polymerisation)

A

two of the same monomer: only draw one monomer with its trailing bonds

Two different monomers: draw the condensation reaction occurring between two different monomers. And draw the trailing bonds on either end, include both monomers.

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11
Q

How do you need to be careful when drawing a repeating unit for a condensation polymer

A

You need to make sure you include trailing bonds and only one water is removed

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12
Q

How is nylon 6,6 formed (Polyamide)

A

monomers:

hexanedioic acid
1,6 di-amino hexane

when drawing out CH2. only add 4 for hexanedioic acid and add 6 for 1,6 diamino hexane

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13
Q

How is Kevlar formed (polyamide)

A

monomers:

benzene-1,4-di-carboxylic acid

benzene-1,4-di-amine

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14
Q

Advantages and disadvantages of disposing polymers by landfill

A

advantages: cheap and easy

Disadvantages: Plastic decomposes to methane, takes up space

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15
Q

Disposing of polymers by burning Advantages and disadvantages

A

Advantages: heat can be used to generate electricity, gets rid of the polymers

Disadvantages: It’s can create toxic gases which have to be removed, carbon dioxide is released which is a greenhouse gas

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16
Q

Advantages and disadvantages of disposing of polymers by recycling

A

advantages: It saves on new material as oil is nonrenewable, Produces a lot less carbon dioxide than burning

Disadvantages: Plastic can become contaminated, it’s cost a lot more money than landfill.

17
Q

uses of poly(ethene)

A

packaging film, trash and grocery bags, agricultural mulch, wire and cable insulation, squeeze bottles, toys, and housewares.

18
Q

uses of PVC

A

window frames, drainage pipe, water service pipe, medical devices, blood storage bags, cable and wire insulation, resilient flooring, roofing membranes, stationary, automotive interiors and seat coverings.

19
Q

uses of poly(propene)

A

processed into film, for packaging and into fibres for carpets and clothing. It is also used for injection moulded articles ranging from car bumpers to washing up bowls, and can be extruded into pipe.

20
Q

uses of terylene

A

Terylene fibre is used as polyester tricot knit as a fashion garments fabric. It is mainly used in making plastic bottles, sheets, ropes, nets and sails. It is also used to make hard wear clothes like dresses, toestry, raincoat, fleece jackets and dress material.

21
Q

uses of nylon

A

clothing

22
Q

uses of kevlar

A

It is used in vast applications such as aerospace engineering (such as the body of the aircraft), body armor, bulletproof vests, car brakes, and boats.

TYRES

23
Q

What is aspirin used to treat

A

Fever, swelling, muscle pain, blood clot.

24
Q

what’s analgesic

A

painkiller

25
Q

what’s anti-pyretic

A

reduces temperatures (fever)

26
Q

what’s anti-inflammatory

A

reduces swelling

27
Q

what’s anti coagulant

A

Prevents blood clotting by thinning the blood

28
Q

What are the risks of taking aspirin

A

Gastrointestinal bleeding as aspirin thins the blood

29
Q

What two monomers are needed to make aspirin

A

Ethanoic anhydride

2-hydroxy benzene carboxylic acid / 2-hydroxy benzoic acid

30
Q

What are the advantages of using ethanoic anhydride

A
  • cheaper
  • less dangerous
  • safer to handle
  • easier to store
  • easier to control reactions
31
Q

why are acyl chlorides used on the small scale in labs?

A

as they react more quickly, use less energy and give higher yields.

32
Q

What is the structure of aspirin

A

benzoic acid remains. but O joins onto the benzene ring with C= and CH3

       O
      // CH3-C - O - benzoic acid 

other product is ethanoic acid

33
Q

what are the advantages of using ethanoyl chloride in a lab 

A

faster more vigorous reactions (therefore it requires a lower energy input)
don’t need to separate the products as HCl is a gas