WJEC A-Level Chemistry 1410QS
Formulae and Equations
Basic Ideas About Atoms
Chemical Calculations
Bonding
Solid Structures
The Periodic Table
Simple Equilibria and Acid-Base Reactions
Thermochemistry
Rates of Reaction
The Wider Impact of Chemistry
Organic Compounds
Hydrocarbons
Halogenoalkanes
Alcohols and Carboxylic Acids
Instrumental Analysis
Redox and Standard Electrode Potential
Redox Reactions
Chemistry of the P-Block
Chemistry of the D-Block Transition Metals
Chemical Kinetics
Enthalpy Changes for Solids and Solutions
Entropy and Feasibility of Reactions
Equilibrium Constants
Acid-Base Equilibria
Stereoisomerism
Aromaticity
Alcohols and Phenols
Aldehydes and Ketones
Carboxylic Acids and Their Derivatives
Amines
Amino Acids, Peptides and Proteins
Organic Synthesis and Analysis
Practical Skills and Techniques
Planning, Analysis and Evaluation
Core Experiments and Their Chemistry
Mathematical Skills in Chemistry
Organic Synthesis and Analysis
Addition and condensation polymerisation: polyesters and polyamides
- 3 things to know
- A2 Unit 4
Overview
Recall questions on polyesters and polyamides.
What you need to know
Answer each one before you reveal it.
Exactly which two functional groups condense together to form an amide link?
When a carboxylic acid condenses with an alcohol or with an amine, what small molecule is eliminated, and which atoms make it up?
Questions from this subtopic
Each one with the model answer underneath.
- 1
Why can a polyester be hydrolysed back towards its monomers while poly(ethene) cannot?
Model answer
The ester links in a polyester are polar and can be attacked by water or hydroxide ions, whereas poly(ethene) has only strong non-polar carbon–carbon bonds with no group for a nucleophile to attack.
- 2
What is condensation polymerisation?
Model answer
It is the joining together of a large number of monomer molecules in which a small molecule, usually water or hydrogen chloride, is eliminated every time two monomers link. The link formed contains the atoms left behind by the two functional groups that reacted.
- 3
What feature must a monomer have in order to undergo addition polymerisation?
Model answer
It must contain a carbon–carbon double bond. The π bond is what breaks to provide the electrons for the new bonds to the units on either side, so a saturated molecule cannot polymerise by addition.
- 4
What feature must monomers have in order to undergo condensation polymerisation?
Model answer
Each monomer must carry two reactive functional groups, so that after reacting at one end it still has a group free to react at the other and the chain can keep growing. This can be two monomers each with two identical groups, such as a diol with a dicarboxylic acid, or a single monomer carrying one group of each kind, such as an amino acid.
- 5
Set out three differences between addition and condensation polymerisation.
Model answer
First, addition polymerisation gives only the polymer, whereas condensation polymerisation also eliminates a small molecule such as water at every link. Second, addition monomers contain a C=C double bond, whereas condensation monomers contain two functional groups such as −COOH, −OH or −NH₂. Third, the backbone of an addition polymer is a continuous chain of carbon atoms with no polar links, whereas the backbone of a condensation polymer contains ester or amide links that can be hydrolysed.
- 6
Give the repeat unit of poly(propene) and explain how it relates to the monomer.
Model answer
The repeat unit is −CH₂−CH(CH₃)− written between extension bonds. It contains exactly the same atoms as the propene monomer, C₃H₆, because nothing is lost in addition polymerisation; the C=C has simply become a C−C single bond, with the two spare bonds joining to neighbouring units.
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