polymers Flashcards

1
Q

polymer

A

long chain molecules made of lots of small molecules joined together by covalent bonds

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2
Q

monomer

A

small molecules that join together to form polymers

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3
Q

addition polymerisation

A

the formation of longchain molecules from lots of small molecules joining together with no other products formed. unsaturated monomers of the same type (?) (have C=C; alkenes) react to form a polymer

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4
Q

condensation polymerisation

A

formation of longchain molecules by the condensation reactions between many monomers. two different types of molecule(?) join together and release a small molecule

(if reaction not polymerisation then modulate answer)

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5
Q

polyalkenes have the following characteristics

A

chemically inert and non biodegradable

this is because they are nonpolar so unreactive and not susceptible to attack by nucleophiles

many strong and nonpolar CC and CH bonds

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6
Q

examples of polyalkenes

A

polyethene

PVC - rigid used for guttering, window frames; plasticised used for clothing and wire insulation

polypropene

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7
Q

repeat unit

polymer structure

A

without the n and brackets

with the n AND brackets

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8
Q

what are the forces between polymer chains in addition polymers/polyalkenes

A

because they have non-polar bonds (so non biodegradable) they have VdW forces between molecules

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9
Q

what are the forces between polymer chains in condensation polymers

?

A

they have polar bonds in their chains so they could have permanent D-D interactions unless polar bonds cancel out i supporse

could have H bonding eg polyamides because H bonded to very electronegative atom of N (,O, or F). h bonding due to polarity of NH bonds within molecules. so polyamide bp > polyester bp because h bonding > dd

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10
Q

the __ bonds in polyalkenes means what 2 things

A

STRONG NONPOLAR non biodegradable; unreactive

no D-D interactions, have VdW as strongest IMF between molecules

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11
Q

the __ bonds in condensation polymers means what 2 things

A

POLAR bonds in their chains

so they can be attacked by nucleophiles ad broken down by hydrolysis reactions. they are biodegradable (but is slow)

have dd or h bonding as strongest imfs

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12
Q

hydrolysis

how can polyester and polyamides be hydrolysed

A

type of decomposition reaction where a molecule is broken down into components by adding water.

polyesters and polyamides can be hydrolysed by acid and alkali.
- the acid hydrolysis reforms the monomers, but because it’s acidic conditions the diamines forming a polyamide will be protonated (so nh3+ instead of nh2)
- the alkali hydrolysis ?

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13
Q

where else have we seen acid or alkali hydrolysis?

A

hydrolysis of esters or triglycerides

ACID HYDROLYSIS
- of esters is just the backwards reaction of the eqm. ester and water react to frm c acids and alcohol
- of triglycerides ?

ALKALINE HYDROLYSIS
- of esters makes carboxylate salt and alcohol
- of triglycerides is saponification. forms salts of fatty acids and glycerol. forms soap because hydrophilic and hydrophobic regions. must be boiled with excess metal hydroxide

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14
Q

condensation polymers are…

they are formed in the reactions between…

A

they are organic molecules formed from c. reactions.

reactions
- dioic acids and diols (polyesters)
- dioic acids and diamines (synthetic polyamides)
- amino acids (polypeptides - biological polyamides)

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15
Q

what are two examples of types of c polymers

A

polyesters or polyamides.

polyesters have an ester linkage

polyamides are polymers with -CONH- repeating bonds; an amide linkage. includes polypeptides (biological, cellular), or aliphatic polyamides (man made) or aromatic polyamides (man made)

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16
Q

how can you form an ester

A

c acid and alcohol. also forms water

acyl chloride and alcohol. also forms HCl

so for forming polyesters you have dioic acids with diols, or diacyl chlorides with diols

17
Q

why is making an ester (or polyester) using acyl chloride and alcohol better than c acid and alcohol

(the di’s for the polyester formation)

A

goes to completion

esterification remember requires acid catalyst and is an equilibrium.

18
Q

how can you form amides

A

c acid and amine. also forms water

acyl chloride and amine. also forms HCl

so for making a polyamide you react a dioic acid with diamine, or diacyl chloride with diamine.

19
Q

examples of polyamides

A

nylon. this is an aliphatic polyamide

kevlar. this is an aromatic polyamide.

20
Q

about nylon 6,6

A

hexanedioic acid and 1,6 diaminoethane

react to form nylon polymer and H2O

6,6 is the C chain length. Different length carbon chains produce different polyamides

21
Q

about kevlar

A

polyamide made from 1,4-benzenedicarboxylic acid and
1,4-benzenediamine.

Bullet proof vests, bc the strong h bonding due to polar bonds of N-H hold separate polymer chains in strong structure

22
Q

example of polyester. monomers and useage

A

terylene.
monomers: made from ethanediol and 1,4-benzenedicarboxylic
acid.

t fabric is used in clothing and tire cords

23
Q

general equation for c polymerisation

A

n monomer + n different monomer —> polymer structure + 2n-1 water

24
Q

shortcut for finding the repeating unit/polymer structure of given monomers

condensation

A

identify f groups reacting

have them react so have the middle linkage there and ready

then on either side, whatever reacts, remove and leave dangling bond

25
in what three ways are polymers disposed of
(buried in) landfill burned; incineration recycled
26
what are the pros and cons of burying polymers in landfill to dispose of them 2,4
PROS - cheap - easy CONS - limited space, many reaching capacity - CH4 released when decompose which is a GHG - leaks contaminate water bodies - decomp is very slow
27
what are the pros and cons of burning polymers to dispose of them 2,1
PROS - heat produced can generate electricity - volume of rubbish is greatly reduced CONS - when some plastics are burned they release toxic gases eg HCl or GHGs
28
what are the pros and cons of recycling polymers 2,1
PROS - saves raw materials because less crude oil used - uses less energy bc not making from scratch CONS - careful separation and sorting needs to be done. expensive