References only, not question text. Open Official paper ↗ where Cambridge publishes the paper,
or see the official Cambridge past-papers page; for other papers, ask your
school. “Paper 42” means Paper 4, variant 2.
Practice questions
Original questions written by HomiLabs in the style of the exam, with answers and mark schemes. They are not
Cambridge past paper questions and have not been reviewed by Cambridge. Try each one before opening the answer.
Q1Naming, formulae, homologous series & isomers · Core · Paper 2 style · 1 mark
(a)Which compound is an alkane?[1]
Show answer
(a) B C₅H₁₂
Alkanes have the general formula CₙH₂ₙ₊₂: n = 5 gives C₅H₁₂. A fits CₙH₂ₙ, the alkenes.
Q2Naming, formulae, homologous series & isomers · Core · Paper 4 style · 4 marks
(a)State three characteristics of a homologous series.[3]
(b)Give the name of the homologous series with the functional group –OH.[1]
Show answer
(a) Any three of: same general formula; same functional group; similar chemical properties; trend in physical properties; each member differs from the next by CH₂.
1 mark each.
(b) alcohols
Q3Naming, formulae, homologous series & isomers · Standard · Paper 4 style · 5 marks
(a)Explain what is meant by structural isomers.[2]
(b)Give the structural formulae of the two structural isomers with molecular formula C₄H₁₀.[2]
(c)Name the unbranched isomer.[1]
Show answer
(a) Compounds with the same molecular formula but different structural formulae.
B1 same molecular formula; B1 different structural formula.
(b) CH₃CH₂CH₂CH₃ and CH₃CH(CH₃)CH₃
1 mark each.
(c) butane
Q4Naming, formulae, homologous series & isomers · Standard · Paper 4 style · 6 marks
(a)Name the functional group present in each compound: (i) propanoic acid, (ii) but-1-ene, (iii) propan-1-ol.[3]
(b)But-1-ene and but-2-ene have the formula C₄H₈. Give the structural formula of each and state how they are related.[3]
Show answer
(a) (i) carboxylic acid, –COOH; (ii) C=C double bond (alkene); (iii) hydroxyl, –OH (alcohol)
1 mark each.
(b) but-1-ene CH₂=CHCH₂CH₃; but-2-ene CH₃CH=CHCH₃; they are structural isomers
1 mark each.
Q5Naming, formulae, homologous series & isomers · Challenge · Paper 4 style · 6 marks
(a)Name the compounds: (i) CH₃CH₂OH, (ii) CH₃COOH, (iii) CH₃CH=CH₂, (iv) CH₃COOCH₃.[4]
(b)Give the molecular formula of the alkene with six carbon atoms and calculate its relative molecular mass. [Ar: C = 12, H = 1][2]
Q6Polymers (addition, condensation, proteins, plastics) · Core · Paper 4 style · 4 marks
(a)Name the type of polymerisation used to make poly(ethene) from ethene.[1]
(b)Give the repeat unit of poly(ethene) as a structural formula.[1]
(c)Give two problems caused by the disposal of poly(ethene) shopping bags.[2]
Show answer
(a) addition polymerisation
(b) –CH₂–CH₂–
Accept a written description: two carbon atoms joined by a single bond, each with two H atoms, with continuation bonds at both ends.
(c) Any two of: non-biodegradable, so they stay in landfill for a long time; litter and harm to animals (e.g. in rivers and seas); burning releases toxic gases / greenhouse gases.
1 mark each.
Q7Polymers (addition, condensation, proteins, plastics) · Core · Paper 4 style · 3 marks
(a)Suggest why plastic bottles found on a beach in Karachi can stay there for hundreds of years.[1]
(b)Give one disadvantage of burning waste plastics.[1]
(c)Suggest one way of reducing the amount of plastic waste.[1]
Show answer
(a) Plastics are non-biodegradable (not broken down by microorganisms).
(b) It releases toxic gases / carbon dioxide (greenhouse gas).
(c) Recycling (e.g. PET bottles) / reusing / using less plastic packaging.
Q8Polymers (addition, condensation, proteins, plastics) · Standard · Paper 2 style · 1 mark
(a)Poly(chloroethene) is used to make water pipes. What is its monomer?[1]
Show answer
(a) B CH₂=CHCl
An addition polymer is made from an alkene; chloroethene is CH₂=CHCl. A has no C=C double bond, so it cannot undergo addition polymerisation.
Q9Polymers (addition, condensation, proteins, plastics) · Standard · Paper 4 style · 3 marks
Poly(propene) is used to make ropes for fishing boats in Gwadar. It is made from propene, CH₃CH=CH₂.
(a)Give the structural formula of the repeat unit of poly(propene).[1]
(b)Calculate the relative formula mass of one repeat unit. [Ar: C = 12, H = 1][1]
(c)A molecule of poly(propene) has a relative molecular mass of 84 000. Calculate the number of repeat units in the molecule.[1]
Show answer
(a) –CH₂–CH(CH₃)–
(b) 42
C₃H₆: 3 × 12 + 6 = 42.
(c) 2000
84 000 ÷ 42.
Q10Polymers (addition, condensation, proteins, plastics) · Standard · Paper 4 style · 4 marks
Lentils (daal) are a good source of protein.
(a)Name the monomers from which proteins are made.[1]
(b)Proteins are natural polyamides. Name the type of polymerisation that forms them.[1]
(c)Give the name of the small molecule released each time two monomers join.[1]
(d)State the name of the synthetic polymer that has the same linkage as proteins.[1]
Show answer
(a) amino acids
(b) condensation polymerisation
(c) water
(d) nylon
Q11Polymers (addition, condensation, proteins, plastics) · Challenge · Paper 4 style · 7 marks
(a)Nylon is made from a dicarboxylic acid and a diamine. Name the type of polymerisation and the small molecule formed.[2]
(b)Name the linkage in nylon and give its structure.[2]
(c)PET is made from a dicarboxylic acid and a diol. Name the type of linkage in PET.[1]
(d)State two differences between addition polymerisation and condensation polymerisation.[2]
Show answer
(a) condensation polymerisation; water
1 mark each.
(b) amide linkage; –CONH– (–CO–NH–)
1 mark each.
(c) ester linkage (–COO–)
(d) Addition: only one product (the polymer) and monomers have C=C bonds; condensation: a small molecule (e.g. water) is also formed and monomers have two functional groups.
1 mark each difference.
Q12Polymers (addition, condensation, proteins, plastics) · Challenge · Paper 2 style · 1 mark
(a)PET is used to make drinks bottles. Which linkage joins the monomer units in PET?[1]
Show answer
(a) B –COO–
PET is a polyester; its linkage is the ester group –COO–. A is the amide linkage found in nylon and proteins.
Q13Fuels, petroleum & cracking · Core · Paper 4 style · 6 marks
(a)Name the process used to separate petroleum into fractions.[1]
(b)Give one use of each fraction: (i) refinery gas, (ii) kerosene, (iii) bitumen, (iv) naphtha.[4]
(c)Describe how chain length changes from the top to the bottom of the fractionating column.[1]
Show answer
(a) fractional distillation
(b) (i) heating and cooking; (ii) jet fuel; (iii) surfacing roads (and roofs); (iv) feedstock for making chemicals
1 mark each.
(c) Chain length increases (molecules get larger) towards the bottom.
Q14Fuels, petroleum & cracking · Standard · Paper 4 style · 5 marks
(a)State two conditions used to crack long-chain alkanes.[2]
(b)Complete the equation: C₁₀H₂₂ → C₈H₁₈ + ______[1]
(c)Give two reasons why cracking is carried out.[2]
Show answer
(a) high temperature; catalyst
1 mark each.
(b) C₂H₄
C: 10 − 8 = 2; H: 22 − 18 = 4.
(c) To meet the demand for shorter-chain alkanes such as petrol; to produce alkenes for making polymers (and hydrogen).
1 mark each.
Q15Fuels, petroleum & cracking · Challenge · Paper 4 style · 5 marks
(a)Hexadecane, C₁₆H₃₄, is cracked to form octane, C₈H₁₈, two molecules of propene and one molecule of compound Z. Deduce the molecular formula of Z.[2]
(b)Name compound Z and state the homologous series to which it belongs.[2]
(c)Explain why the supply of long-chain fractions from fractional distillation is greater than the demand for them.[1]
(c) Petroleum naturally contains a large proportion of long-chain hydrocarbons, but they have few uses (e.g. fuel oil, bitumen), so less is needed than is produced.
Accept: more long chains in crude oil than are needed / demand is mainly for short chains such as petrol.
Q16Alcohols · Core · Paper 2 style · 1 mark
(a)What are the products of the complete combustion of ethanol?[1]
Show answer
(a) C carbon dioxide and water
Complete combustion in plenty of oxygen gives CO₂ and H₂O. A and D are products of incomplete combustion.
Q17Alcohols · Core · Paper 4 style · 4 marks
(a)Give two uses of ethanol.[2]
(b)Write the balanced equation for the complete combustion of ethanol.[2]
Show answer
(a) solvent; fuel
1 mark each. Accept: in hand sanitisers (as a solvent / antiseptic).
(b) C₂H₅OH + 3O₂ → 2CO₂ + 3H₂O
B1 formulae; B1 balanced.
Q18Alcohols · Standard · Paper 4 style · 8 marks
Pakistan makes ethanol from sugar-cane molasses. Ethanol can also be made from ethene.
(a)Give the conditions for making ethanol by fermentation.[3]
(b)Give the conditions for making ethanol from ethene and steam.[3]
(c)Give one advantage of fermentation and one advantage of the hydration of ethene.[2]
Show answer
(a) Yeast; about 25–35 °C; absence of oxygen (anaerobic); aqueous sugar (glucose).
Any three, 1 mark each.
(b) about 300 °C; about 6000 kPa (60 atm); phosphoric acid catalyst
1 mark each.
(c) Fermentation: uses a renewable raw material (sugar cane) / low temperature; hydration: faster / continuous / produces pure ethanol.
1 mark each.
Q19Alcohols · Challenge · Paper 4 style · 6 marks
C₆H₁₂O₆ → 2C₂H₅OH + 2CO₂
(a)Calculate the maximum mass of ethanol formed from 45 g of glucose. [Mr: glucose = 180, ethanol = 46][3]
(b)Calculate the volume of carbon dioxide formed at room temperature and pressure, in dm³. [1 mol of gas occupies 24 dm³ at r.t.p.][2]
(c)Suggest why the fermentation stops when the ethanol concentration reaches about 15 %.[1]
(c) It is only partially dissociated (ionised) in water.
Q21Carboxylic acids & esters · Standard · Paper 2 style · 1 mark
(a)Which ester is formed when ethanol reacts with propanoic acid?[1]
Show answer
(a) B ethyl propanoate
The alcohol gives the first part of the name (ethyl) and the acid gives the second part (propanoate). A reverses the two parts.
Q22Carboxylic acids & esters · Standard · Paper 4 style · 5 marks
(a)State the conditions needed to make an ester from an alcohol and a carboxylic acid.[2]
(b)Write the word equation for the reaction between methanol and ethanoic acid.[2]
(c)Give one use of esters.[1]
Show answer
(a) Heat (warm); concentrated sulfuric acid as a catalyst.
1 mark each.
(b) methanol + ethanoic acid ⇌ methyl ethanoate + water
B1 methyl ethanoate; B1 water. Accept → arrow.
(c) flavourings / perfumes / solvents
Q23Carboxylic acids & esters · Challenge · Paper 4 style · 5 marks
(a)Ethanoic acid can be made by heating ethanol with acidified potassium manganate(VII). State the colour change and the type of reaction.[2]
(b)Name another method of making ethanoic acid from ethanol.[1]
(c)Calculate the maximum mass of ethanoic acid that can be made from 9.2 g of ethanol. [Mr: ethanol = 46, ethanoic acid = 60][2]
Show answer
(a) Purple to colourless; oxidation.
1 mark each.
(b) Bacterial oxidation / fermentation by bacteria (in air), as in making vinegar.
(c) 12.0 g
M1 9.2 ÷ 46 = 0.20 mol; A1 0.20 × 60 = 12.0 g.
Q24Carboxylic acids & esters · Challenge · Paper 4 style · 5 marks
(a)Propyl ethanoate smells of pears. Name the alcohol and the carboxylic acid used to make it.[2]
(b)Give the structural formula of propyl ethanoate.[1]
(c)Give the molecular formula of propyl ethanoate and calculate its relative molecular mass. [Ar: C = 12, H = 1, O = 16][2]
Show answer
(a) propan-1-ol (propanol); ethanoic acid
1 mark each.
(b) CH₃COOCH₂CH₂CH₃
(c) C₅H₁₀O₂; 102
B1 C₅H₁₀O₂; B1 102.
Q25Alkenes · Core · Paper 4 style · 3 marks
Two unlabelled bottles contain hexane and hexene.
(a)Describe a chemical test to show which liquid is hexene.[2]
(b)Explain why hexene is described as unsaturated.[1]
Show answer
(a) Add bromine water; hexene turns it from orange to colourless, hexane leaves it orange.
B1 bromine water; B1 orange to colourless with hexene.
(b) It contains a C=C double bond.
Q26Alkenes · Standard · Paper 4 style · 5 marks
(a)Name the product when ethene reacts with hydrogen, and state the catalyst.[2]
(b)Name the product when ethene reacts with steam.[1]
(c)Name the product when ethene reacts with bromine.[1]
(d)State the type of reaction in (a), (b) and (c).[1]
Show answer
(a) ethane; nickel
1 mark each.
(b) ethanol
(c) 1,2-dibromoethane
(d) addition
Q27Alkenes · Challenge · Paper 2 style · 1 mark
(a)Propene reacts with bromine. What is the molecular formula of the product?[1]
Show answer
(a) B C₃H₆Br₂
Addition across the C=C bond adds both bromine atoms and keeps all six H atoms: C₃H₆ + Br₂ → C₃H₆Br₂. A would be a substitution product.
Q28Alkanes · Core · Paper 4 style · 4 marks
LPG cylinders used for cooking in many Pakistani homes contain propane.
(a)Write the balanced equation for the complete combustion of propane.[2]
(b)Name the toxic gas produced if the supply of air to the cooker is limited.[1]
(c)Apart from combustion, alkanes are generally unreactive. Explain why, in terms of bonding.[1]
Show answer
(a) C₃H₈ + 5O₂ → 3CO₂ + 4H₂O
B1 formulae; B1 balanced.
(b) carbon monoxide
(c) They contain only single C–C and C–H bonds (saturated).
Q29Alkanes · Standard · Paper 4 style · 5 marks
(a)Name the type of reaction between methane and chlorine.[1]
(b)State the condition needed.[1]
(c)Write the equation for the reaction that forms chloromethane.[2]
(d)Explain the role of the UV light.[1]
Show answer
(a) substitution (photochemical)
(b) ultraviolet (UV) light
(c) CH₄ + Cl₂ → CH₃Cl + HCl
B1 products; B1 balanced.
(d) It provides the energy to break the Cl–Cl bond (start the reaction).
Q30Alkanes · Challenge · Paper 2 style · 1 mark
(a)50 cm³ of butane, C₄H₁₀, is burned completely in oxygen. All volumes are measured at the same temperature and pressure. What volume of oxygen is needed?[1]
Show answer
(a) C 325 cm³
2C₄H₁₀ + 13O₂ → 8CO₂ + 10H₂O, so 1 volume of butane needs 6.5 volumes of O₂: 50 × 6.5 = 325 cm³. A is the volume of CO₂ formed.
Similar questions
Questions that test the same subtopic in different years, grouped so you can work on one skill at a time.
References only: find each question in its paper (official link where available, otherwise through your school).
Naming, formulae, homologous series & isomersBanker127 questions · 9/9 sessions