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Flashcards · 9701 · A Level Topic 35
Polymerisation (A Level) flashcards
12 cards on A Level Topic 35, subtopics 35.1 to 35.3. Pick a subtopic or study them all.
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35.1 Condensation polymerisation
- Condensation polymerisation
- Monomers, each with two functional groups, join with the elimination of a small molecule (usually H₂O, or HCl from an acyl chloride) at every linkage.
- Polyester and polyamide: monomers and linkage
- Polyester: diol + dicarboxylic acid (or diacyl chloride); ester link –COO–. Polyamide: diamine + dicarboxylic acid (or diacyl chloride); amide link –CONH–. Or one monomer with both groups (hydroxy acid, amino acid).
- Repeat unit from ethane-1,2-diol and benzene-1,4-dicarboxylic acid
- –OCH₂CH₂OOCC₆H₄CO– (a polyester); one H₂O lost per ester link.
- Why are polyamides generally stronger than polyesters?
- Amide groups form hydrogen bonds between chains; ester groups only give permanent dipole–dipole attractions.
- How do you deduce the monomers from a section of a condensation polymer?
- Find the repeating ester or amide links, break each one and add back H₂O (–OH to the C=O side, –H to the O or N side) to regenerate the diacid and the diol or diamine.
35.2 Predicting the type of polymerisation
- Which monomers give addition and which give condensation polymers?
- A C=C double bond: addition, no small molecule lost. Two reactive groups per monomer (–OH, –NH₂ with –COOH or –COCl): condensation, losing H₂O or HCl.
- How can you tell from a polymer section how it was made?
- A continuous saturated carbon backbone: addition polymer. Repeating ester or amide links in the chain: condensation polymer.
- Addition vs condensation polymerisation: by-product and atom economy
- Addition: nothing eliminated, 100% atom economy. Condensation: H₂O or HCl eliminated, atom economy below 100%.
35.3 Degradable polymers
- Why are poly(alkenes) difficult to biodegrade?
- They are chemically inert: the non-polar C–C backbone has no bonds that water or enzymes can attack.
- Why are polyesters and polyamides biodegradable?
- Their polar ester or amide links can be hydrolysed by acid or alkali (and by enzymes), breaking the chain into monomers.
- Products of acid and alkaline hydrolysis of polyesters and polyamides
- Polyester: acid → carboxylic acid + alcohol; alkali → carboxylate salt + alcohol. Polyamide: acid → carboxylic acid + ammonium salt; alkali → carboxylate salt + amine.
- Photodegradable polymer
- A polymer with bonds or additives that absorb UV light and break, fragmenting the material. This is a different process from biodegradation by hydrolysis.