IB Chemistry SL Topic 2 — From Models to Materials Paper 1 & 2 Materials ~11 min read

Polymers

A polymer is not a complicated idea. It is one molecule, made by joining thousands of identical small ones end to end, like beads threaded on a string. Everything odd about plastics — why they are light, why they float, why they last for centuries in a landfill — comes from that single fact about their size.

📘 What you need to know

What makes a molecule a polymer

Ethene, C2H4, is a gas you could hold in a syringe. Join ten thousand ethene units together and you get poly(ethene): a waxy solid you can make a shopping bag from. Nothing new was added and nothing was taken away — the atoms simply became part of one enormous molecule instead of ten thousand tiny ones.

That change in size is what changes the properties. Small molecules are easy to pull apart from each other, so they are gases or runny liquids. A chain thousands of atoms long tangles with its neighbours and has a huge surface in contact with them, so the forces between chains add up to something substantial. The result is a solid.

Monomers becoming a polymer Same atoms, same bonds. One molecule instead of thousands. many separate monomer molecules polymerisation one very long molecule: the polymerThe links between the beads are strong covalent bonds. Real chains are not straight — they coil and tangle around each other.
The chain is drawn with open ends on purpose. A polymer sample contains chains of many different lengths, which is why a polymer has no single fixed relative molecular mass.

Monomer, repeat unit, and that little n

Three words get confused constantly, so pin them down now.

How a polymer is written n × monomer  →  [ repeat unit ]n

The monomer and the repeat unit are usually made of the same atoms but joined slightly differently. Getting from one to the other is a standard exam skill, and it is covered properly on the next two pages.

One monomer or several

If every monomer in the chain is the same, the polymer is a homopolymer. Poly(ethene) and PVC are homopolymers — one ingredient, repeated.

If two or more different monomers alternate along the chain, it is a copolymer. Nylon is the classic synthetic example, and proteins are the natural one: your body strings together twenty different amino acid monomers in whatever order the gene specifies.

Proteins are the reason copolymers matter. Change the order of the monomers and you change the whole molecule’s shape and job. Same trick, wildly different outcome — which is worth remembering when biology comes up in a chemistry paper.

Natural and synthetic polymers

PolymerNatural or syntheticMonomerWhere you meet it
Starch and celluloseNaturalGlucoseFood storage in plants; plant cell walls
ProteinsNaturalAmino acidsEnzymes, muscle, hair, antibodies
DNANaturalNucleotidesGenetic information in every cell
Poly(ethene)SyntheticEtheneBags, bottles, packaging film
NylonSyntheticA diamine and a dicarboxylic acidRopes, clothing, engineering parts

Where the properties come from

Every property in the list below comes from the same two facts: the bonds along the chain are strong covalent bonds, and the forces between chains are weak.

Two kinds of force in a plastic Strong one way, weak the other. That is the whole explanation.strong covalent bonds run along each chain only weak intermolecular forces act between the chainsMelt a plastic and you separate the chains — you do not break them. Loose packing is also why plastics have such a low density.
The dashed lines are the weak forces. There are a lot of them along a chain thousands of atoms long, which is how something held together by weak forces can still make a solid object.
PropertyReason
Low densityLong tangled chains cannot pack tightly, so a lot of the volume is empty space
UnreactiveThe chain is mostly strong C–C and C–H bonds with no polar sites for reagents to attack
WaterproofNon-polar chains do not attract water molecules, so water is not absorbed
Strong and flexibleStrong covalent bonds along the chain, plus chains that can slide and uncoil past each other
Electrical insulatorNo delocalised electrons and no free ions anywhere in the structure

The problem with lasting forever

Being unreactive is exactly what makes a plastic useful and exactly what makes it a problem. Most addition polymers have no bonds that water, air or enzymes can attack, so they are non-biodegradable: they break into smaller and smaller pieces without ever chemically breaking down. A bag made this year can still be recognisable in a century.

A hint of what is coming: polymers that contain ester or amide links in the chain can be attacked by water, so some of them do break down. That is one of the big practical differences between addition and condensation polymers.

Worked examples

WORKED EXAMPLE

A poly(ethene) chain contains 10 000 repeat units. Estimate its relative molecular mass.

The repeat unit is C2H4. Use Ar(C) = 12.01 and Ar(H) = 1.01.

Step 1: mass of one repeat unit (2 × 12.01) + (4 × 1.01) = 24.02 + 4.04 = 28.06 Step 2: multiply by the number of units 28.06 × 10 000 = 280 600 Mr ≈ 2.81 × 105 the two end groups add a couple of extra atoms, which is nothing next to 280 000 — ignore them
WORKED EXAMPLE

A sample of poly(propene) has an average Mr of 1.40 × 105. How many repeat units are in an average chain?

The repeat unit is C3H6.

Step 1: mass of one repeat unit (3 × 12.01) + (6 × 1.01) = 36.03 + 6.06 = 42.09 Step 2: divide n = 140 000 ÷ 42.09 = 3326 about 3.3 × 103 repeat units the word “average” matters — a real sample has chains of many different lengths
WORKED EXAMPLE

Classify each of these as natural or synthetic, and as a homopolymer or a copolymer: PVC, silk, poly(propene).

PVC Made in industry from chloroethene only. synthetic homopolymer Silk A protein, made by an organism from a mixture of different amino acids. natural copolymer Poly(propene) Made in industry from propene only. synthetic homopolymer Count the different monomers, then ask who made it

💡 Exam tip

⚠ Common mix-up

Up next: Addition Polymerisation — the simplest way of making a polymer, where a double bond opens up, the monomers link, and absolutely nothing is left over.

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