AQA GCSE Chemistry Chemistry Paper 2 (Foundation), June 2023: Question 2
12 marks · Low Demand difficulty · Short Answer
Evaluate properties of borosilicate glass and poly(propene) for beakers, identify the raw materials for glass, complete a table about propene's composition, identify its repeating unit, and name the stages of its production.
Practise this questionQuestion
Question text
02 This question is about glass and polymers.
Beakers can be made from borosilicate glass or poly(propene).
Table 1 shows information about materials used to make beakers.
Table 1
Material used to make beakers
borosilicate glass poly(propene)
Temperature at which
850 160
melting begins in °C
Flammability does not burn burns
Resistance to impact shatters tough
Cost of 100 cm3 beaker in £ 1.50 2.00
02.1 Suggest two reasons why a Bunsen burner should not be used to heat a liquid in a
poly(propene) beaker.
Use Table 1.
[2 marks]
02.2 Poly(propene) beakers are more expensive than borosilicate glass beakers.
Suggest one reason why using poly(propene) beakers instead of borosilicate glass
beakers could save money.
Use Table 1.
[1 mark]
02.3 Which is a raw material used to make borosilicate glass?
[1 mark]
Tick ( ) one box.
Boron trioxide
Clay
Limestone
Poly(propene) is produced from propene.
The displayed structural formula of propene is:
02.4 Table 2 shows some information about the elements in one molecule of propene.
Table 2
Symbol for Number of atoms of element
Name of element
element in one molecule of propene
C
H
Complete Table 2.
[2 marks]
02.5 Which structure is the repeating unit of poly(propene)?
[1 mark]
Tick ( ) one box.
02.6 Poly(propene) is produced in three stages:
• Stage 1: separating large alkane molecules from crude oil
• Stage 2: producing propene molecules from large alkane molecules
• Stage 3: joining many propene molecules together.
Name Stage 1, Stage 2 and Stage 3.
Choose answers from the box.
[3 marks]
cracking fermentation fractional distillation
polymerisation reverse osmosis
Stage 1 is .
Stage 2 is .
Stage 3 is .
02.7 A molecule of hexene contains a double carbon–carbon bond.
Many hexene molecules join together to form poly(hexene).
Which two words describe a hexene molecule in this process?
[2 marks]
*11* Tick ( ) two boxes.
Alkene
Catalyst
Composite
Element
Monomer
Mark scheme
Show the mark scheme
AO /
Question Answers Extra information Mark
Spec. Ref.
02.1 (the poly(propene) beaker will allow poly(propene) has a low 1 AO3
begin to) melt melting point
4.7.3.1
(the poly(propene) beaker will) allow poly(propene) is 1
burn / ignite flammable
AO /
Spec. Ref.
02.2 (poly(propene) beakers are) less allow (poly(propene) beakers 1 AO3
easily broken are) less likely to shatter 4.7.3.1
4.10.3.3
allow (poly(propene) beakers
are) tougher
allow (poly(propene) beakers
have a) higher resistance to
impact
AO /
Spec. Ref.
02.3 boron trioxide 1 AO1
4.10.3.3
AO /
Question Answers Mark
Spec. Ref.
02.4
Symbol for Name of Number of atoms of element
element element in one molecule of propene
C carbon 3 1 AO1
H hydrogen 6 1 AO2
if no other mark awarded allow 1 mark for a correct column 4.1.1.1
– HEMISTRY – – 4.7.2.1
AO /
Spec. Ref.
02.5 1 AO2 9
4.7.3.1
AO /
Spec. Ref.
02.6 (Stage 1 is) fractional distillation 1 AO1
(Stage 2 is) cracking 1 AO2
(Stage 3 is) polymerisation 1 AO2
4.7.1.2
4.7.1.4
4.7.3.1
AO /
Spec. Ref.
02.7 alkene 1 AO2
4.7.2.1
monomer 1 4.7.3.1
– – 8462/2F –
Total Question 2 12
Question 3
How to answer it
Materials, Glass, Alkenes & Polymerisation
This question assesses your ability to evaluate comparative material properties from a data table, recall raw materials for borosilicate glass, interpret molecular formulas and displayed structures of alkenes, identify polymer repeating units, and order the industrial stages from crude oil separation to addition polymerisation.
Parts 02.1 & 02.2: Evaluating Material Properties for Beakers
Data interpretation from Table 1
✅ Correct Answers
02.1 (2 marks - any two reasons):
- The poly(propene) beaker will melt (or has a low melting point / melts at 160 °C). [1 mark]
- The poly(propene) beaker will burn / ignite (or is flammable). [1 mark]
02.2 (1 mark - any one reason):
- Poly(propene) beakers are less easily broken / shatter-proof (tougher / do not shatter / have higher resistance to impact / last longer / do not need replacing as often). [1 mark]
🧠 Exam Technique: "Use Table 1"
- When the question says "Use Table 1", your answer must link directly to the table headings (Melting point, Flammability, Impact resistance).
- In 02.1, a Bunsen flame reaches over 1000 °C. State the consequence: poly(propene) melts at only 160 °C and burns.
- In 02.2, think about practical laboratory lifetime: even though one plastic beaker costs £2.00 vs £1.50 for glass, you save money over time because glass easily shatters and must be replaced repeatedly.
❌ Common Errors
- Vague answers like "it gets hot" or "it is dangerous" score zero. Name the exact property: melts or burns.
- For 02.2, simply quoting "it is tough" without linking it to why this saves money (e.g. fewer replacements needed because it won't shatter).
💡 Key Knowledge
- Thermosoftening polymers: Poly(propene) has weak intermolecular forces between polymer chains that are easily overcome with heat, leading to a low melting point (160 °C).
- Borosilicate glass: Has a high melting point (850 °C) and does not burn, making it ideal for direct heating.
Part 02.3: Raw Materials for Glass
Borosilicate vs. Soda-lime glass
✅ Correct Answer [1 mark]
Tick: Boron trioxide
💡 Key Knowledge: The Two Types of Glass
- Soda-lime glass: Made by heating a mixture of sand (silicon dioxide), sodium carbonate, and limestone (calcium carbonate). Used for window panes and jars.
- Borosilicate glass: Made by heating sand and boron trioxide. It melts at higher temperatures than soda-lime glass, making it ideal for laboratory glassware (e.g. Pyrex) and ovenware.
❌ Common Distractor Traps
- Clay: Used to make ceramics (bricks, pottery, china), not glass.
- Limestone: Used for soda-lime glass, not the key ingredient specific to borosilicate glass.
Part 02.4: Molecular Formula & Elements in Propene
Interpreting displayed structural formula
✅ Correct Answer [2 marks]
| Symbol for element | Name of element | Number of atoms of element in one molecule of propene |
|---|---|---|
| C | carbon [1 mark for both names] | 3 [1 mark for both numbers] |
| H | hydrogen | 6 |
🧠 Counting from Displayed Formulas
Propene is drawn as:
H CH₃
| |
C = C
| |
H H
- Carbons: 2 carbons in the C=C double bond + 1 carbon in the –CH₃ methyl group = 3 carbons.
- Hydrogens: 3 on the double bond carbons + 3 in the –CH₃ group = 6 hydrogens.
- Formula fits general alkene formula: CnH2n where n = 3 → C₃H₆.
❌ Common Miscount Trap
Students often forget to count the atoms packed into the attached functional group ( –CH₃ ). They see 2 carbons in the backbone and write 2 carbons and 3 hydrogens. Always count every single atom!
Part 02.5: Repeating Unit of Poly(propene)
Addition polymerisation structure
✅ Correct Answer [1 mark]
Tick the middle box:
( H CH₃ )
( | | )
——(—C — C——)——
( | | ) n
( H H )
🧠 3 Rules for Drawing / Identifying Repeating Units
- Open the double bond: The C=C double bond turns into a C–C single bond.
- Keep attached groups identical: The groups attached to each carbon atom do not change position (Carbon 1 has two H's; Carbon 2 has one H and one CH₃).
- Extend bonds & brackets: The extension bonds must poke through the brackets with an ' n ' subscript.
❌ Why the other options are wrong:
- Option 1 (all H's): This is poly(ethene), made from ethene ( C₂H₄ ). It is missing the methyl group ( –CH₃ ).
- Option 3 (two CH₃ groups): This is poly(but-2-ene), which has two methyl groups instead of one.
Part 02.6: Stages in Producing Poly(propene)
Ordering industrial organic processes
✅ Correct Answers [3 marks]
- Stage 1 (separating large alkane molecules from crude oil) is fractional distillation [1 mark]
- Stage 2 (producing propene molecules from large alkane molecules) is cracking [1 mark]
- Stage 3 (joining many propene molecules together) is polymerisation [1 mark]
💡 The Industrial Pathway
- 1. Fractional Distillation: Separates crude oil into fractions containing hydrocarbons of similar boiling points / chain lengths.
- 2. Cracking (Catalytic or Steam): Breaks down long-chain, less useful alkanes into shorter, more useful alkanes and alkenes (such as propene).
- 3. Addition Polymerisation: Uses high pressure and a catalyst to break double bonds and join thousands of small alkene monomers into long polymer chains.
❌ Irrelevant Options (Distractors)
- Fermentation: Biological production of ethanol using yeast and glucose.
- Reverse osmosis: Desalination method used to produce potable drinking water from sea water.
Part 02.7: Classification of Hexene in Polymerisation
Organic chemistry terminology
✅ Correct Answer [2 marks]
Tick two boxes:
- ☑️ Alkene [1 mark]
- ☑️ Monomer [1 mark]
🧠 Decoding the Clues in the Question
- "Contains a double carbon–carbon bond" → By definition, a hydrocarbon with a C=C double bond is an alkene (names ending in -ene).
- "Many hexene molecules join together to form poly(hexene)" → The individual small repeating starting molecules are called monomers (mono = one, mer = part).
❌ Why other boxes are incorrect:
- Catalyst: Hexene is a reactant consumed to form the product, not a catalyst that speeds up the reaction without being used up.
- Composite: A composite is a material made of a matrix and reinforcement fibres (e.g. fibreglass, reinforced concrete), not a pure hydrocarbon molecule.
- Element: Hexene consists of two different elements (carbon and hydrogen) chemically bonded, meaning it is a compound, not an element.
Topics
Chemistry · C1: Atomic Structure and the Periodic Table · C7: Organic Chemistry · C10: Using Resources
Question and mark scheme from the AQA GCSE Chemistry examination, Chemistry Paper 2 (Foundation), June 2023. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.