We analysed every real Chemistry Paper 2 Higher Tier sitting AQA has made public since the pandemic disruption, including the actual questions students saw and the mark schemes examiners used. Below is what each recurring question type has asked, what the real data and diagrams showed, and a complete worked answer for each sitting we have. This is the closest you can get to seeing exactly what a full mark answer looks like without a real exam paper in front of you.
Questions © AQA, quoted for analysis. Diagrams and data described in our own words, not reproduced. Mark scheme content translated into plain English, not copied. PrepWise is independent and not endorsed by AQA.
Every sitting we checked asks you to name a flame test result or a chemical test result for a metal ion. The ions tested change, but the method (clean wire, blue Bunsen flame, observe colour) stays the same.
It wants the specific flame colour copper ions produce, not just 'coloured' or a vague description.
Copper sulfate solution produces a blue-green flame colour.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise flame tests and ion identificationIt wants both the method (flame test) and the specific result (lilac flame) for the Group 1 metal ion in potash alum, which is potassium.
The test is a flame test: dip a clean metal wire in a sample of the compound and hold it in a blue Bunsen burner flame. The result is a lilac flame colour, which shows the Group 1 metal ion present is potassium.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise flame tests and ion identificationIt wants a full planned method combining a flame test for potassium ions with a silver nitrate and nitric acid test for bromide ions, with both results stated.
To test for potassium ions, place a sample of the medicine on a clean metal wire and introduce it into a blue, non-luminous Bunsen burner flame. Observe a lilac flame colour, which shows potassium ions are present.
To test for bromide ions, dissolve a sample of the medicine in distilled water in a test tube, then add a few drops of dilute nitric acid followed by silver nitrate solution using a dropping pipette. Observe a cream precipitate forming, which shows bromide ions are present.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise flame tests and ion identificationThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
Which type of wire is used to carry out a flame test?
Flame test colours and ion tests come up almost every sitting. Learn the exact colour for each metal ion cold, since 'close' answers do not score.
Practise flame tests and ion identificationSulfate testing (add acidified barium chloride, look for a white precipitate) and halide testing (add acidified silver nitrate, check the precipitate colour) both come up as short, precisely worded point-marked questions.
It wants the specific reagent that confirms sulfate ions once dilute hydrochloric acid has already been added, which is barium chloride (or barium nitrate) solution.
Barium chloride solution would show the presence of sulfate ions, since it produces a white precipitate of barium sulfate with sulfate ions present.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise ion identification testsIt wants the full test method (acidify then add barium chloride) plus the precipitate colour, not just the reagent name.
Add dilute hydrochloric acid to the solution of potash alum, then add barium chloride solution. A white precipitate forms, which shows sulfate ions are present.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise ion identification testsIt wants sodium hydroxide solution added to the copper(II) sulfate solution, with the specific blue precipitate colour that identifies copper(II) ions.
Add sodium hydroxide solution to the copper(II) sulfate solution. A blue precipitate forms, which shows the presence of copper(II) ions.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise ion identification testsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
Which reagents are used to test for carbonate ions in a solution?
The sulfate test and the metal hydroxide precipitate tests are short, precisely worded questions. Learn each reagent and each exact precipitate colour so you never mix up copper, iron(II) and iron(III).
Practise ion identification testsBoth sittings we checked with a water question ask you to explain the standard fresh-water treatment steps (filter beds then sterilisation) as a logically linked account.
It wants the two-stage UK fresh-water treatment process explained as a logical account, not just a list of two words.
An appropriate source of fresh water is chosen, such as a river, stream, lake or borehole. The water is passed through filter beds, which removes undissolved solids from it. The filtered water is then sterilised, using chlorine, ozone or ultraviolet light, which destroys harmful microbes in the water so that it is safe to drink.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise water treatment questionsIt wants an explanation of why sterilisation (Process 2) is still needed even after ground water has already been filtered, because filtration alone does not remove harmful microbes.
A table comparing sea water and ground water treatment, showing filtration as Process 1 for ground water and UV light exposure as Process 2, alongside sodium and chloride ion concentrations before and after each process.
| Sea water | Ground water | |
|---|---|---|
| Concentration of Na+ and Cl- ions before Process 1 | Na+: 0.5 mol/dm3, Cl-: 0.5 mol/dm3 | Na+: 0.001 mol/dm3, Cl-: 0.001 mol/dm3 |
| Process 1 | Reverse osmosis | Filtration |
| Concentration of Na+ and Cl- ions after Process 1 | X | Na+: 0.001 mol/dm3, Cl-: 0.001 mol/dm3 |
| Process 2 | Add ozone | Expose to ultraviolet light |
The ground water contains microbes which are harmful to health. Process 2, exposure to ultraviolet light, sterilises the water so that the harmful microbes are destroyed.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise water treatment questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What does the term 'potable water' mean?
Water treatment questions reward the two-stage process explained as a logical account: filtration removes solids, sterilisation destroys microbes. Practise linking each step to its purpose.
Practise water treatment questionsThis short suggest question rewards naming a desalination process (distillation or reverse osmosis) when a country cannot rely on fresh water sources.
It wants a named desalination process appropriate for a coastal country with plentiful energy but little fresh water, since desalination is energy-intensive.
This country could use distillation, or reverse osmosis, to desalinate sea water and obtain potable water.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise water resource questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What does the term 'potable water' mean?
When a country lacks fresh water but has sea water and energy, desalination (distillation or reverse osmosis) is the answer. Keep this distinction from ordinary water treatment clear.
Practise water resource questionsThis extended question always gives you a data table comparing two or three materials for the same product (food plates, milk bottles) and asks for a judgement built from raw materials, manufacturing, use and disposal stages.
It wants a judgement comparing paper, polymer and ceramic food plates across every LCA stage, using the actual figures given for raw materials, packaging, reuse and disposal.
A table comparing paper, polymer and ceramic food plates of equal diameter, showing raw material (wood, crude oil, mined clay), number packaged in a fixed box volume, average number of times used, and whether each is biodegradable and recyclable.
| Material | Raw material | Plates fitting in a 10 dm3 box | Average number of times used | Biodegradable | Recyclable |
|---|---|---|---|---|---|
| Paper | Wood | 500 | 1 | Yes | Yes |
| Polymer | Crude oil | 100 | 400 | No | Yes |
| Ceramic | Mined clay | 50 | 1000 | No | No |
Looking at raw materials, wood used for paper plates is a renewable resource, while crude oil for polymer plates and mined clay for ceramic plates are both finite resources that will eventually run out, so paper plates score better here.
For manufacturing and packaging, 500 paper plates fit in the same 10 dm cubed box as only 100 polymer plates or 50 ceramic plates, so paper plates need the least packaging per plate and less transport energy overall, conserving raw materials used in packaging and fuel used in transport.
For use and operation, paper plates are used only once on average, while polymer plates are used 400 times and ceramic plates 1000 times, meaning far fewer polymer and ceramic plates need to be manufactured over their working lives, which reduces raw material and energy use overall despite each plate individually requiring more resources to make.
For disposal, paper plates are biodegradable and recyclable, so they do not build up in landfill, while ceramic plates are neither biodegradable nor recyclable and will sit in landfill permanently, and polymer plates, though not biodegradable, can at least be recycled into different polymer products.
Overall I judge paper plates are the most sustainable for single or occasional use because they use the least packaging, are biodegradable and are recyclable, even though each individual plate is used only once; but for a setting where plates are reused many times, such as a canteen, ceramic plates become more sustainable overall because their very high reuse figure of 1000 outweighs the fact that clay is a finite raw material and that ceramic cannot be recycled.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise life cycle assessment questionsIt wants a judgement comparing glass and polymer milk bottles across raw materials, manufacturing energy, mass, reuse and disposal, using the exact energy and reuse figures given.
A table comparing glass and polymer milk bottles of equal volume, showing raw materials, energy needed to process raw materials in kilojoules, energy needed to manufacture the bottle in kilojoules, mass of the bottle, mean number of times used, and one disposal method for each.
| Material | Raw materials | Energy to process raw materials (kJ) | Energy to manufacture bottle (kJ) | Mean number of times used | Disposal method |
|---|---|---|---|---|---|
| Glass | Limestone, sand, sodium carbonate | 6750 | 750 | 25 | Recycled into different products of the same type |
| Polymer | Crude oil | 1710 | 90 | 1 | Recycled into different products of the same type |
Glass is made from limestone, sand and sodium carbonate, while the polymer is made from crude oil. Since crude oil is finite, relying on it for single bottles is less sustainable in raw material terms than glass, though glass's raw materials still require quarrying, which has its own environmental impact.
The energy figures make the biggest difference at the processing and manufacturing stages: processing raw materials for glass takes 6750 kJ against only 1710 kJ for the polymer, and manufacturing the bottle itself takes 750 kJ for glass against 90 kJ for the polymer, so producing one glass bottle from scratch uses roughly four times more total energy than one polymer bottle.
However, glass bottles are reused on average 25 times each, while polymer bottles are used only once, and the glass bottle has ten times the mass of the polymer bottle, meaning the huge one-off energy cost of making a glass bottle is spread across 25 uses rather than one, which changes the overall energy picture in glass's favour once reuse is accounted for.
At disposal, both materials can be recycled into different products of the same type, so this stage does not distinguish them strongly, though the polymer's lower mass means less material enters the recycling or landfill stream per bottle even before accounting for reuse.
Overall I judge glass is the more sustainable choice for milk bottles specifically because of its high reuse figure of 25, which offsets its much higher raw material and manufacturing energy demand; if the polymer bottle were also reused many times rather than once, this judgement would likely reverse, since the polymer's much lower energy cost per bottle would then dominate.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise life cycle assessment questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What does LCA stand for in the context of environmental science?
LCA evaluation questions always give you a data table. The top band comes from quoting the actual figures and weighing conflicting factors (like high energy cost against high reuse), not from generic LCA theory.
Practise life cycle assessment questionsThis extended comparison question always gives you two displayed structural formulae and asks for both structural differences and reaction differences.
It wants a structured comparison of ethane and ethene covering bonding differences and reaction differences, since the two compounds have almost identical formulae but very different chemical behaviour.
The displayed structural formulae of ethane and ethene, showing ethane with a single carbon-carbon bond and six hydrogen atoms, and ethene with a double carbon-carbon bond and four hydrogen atoms.
Both ethane and ethene are hydrocarbons containing two carbon atoms per molecule and small molecules held together by covalent bonds, but ethane contains six hydrogen atoms per molecule while ethene contains only four, because ethane's carbon atoms are joined by a single C-C bond, whereas ethene's carbon atoms are joined by a double C=C bond, which uses up bonding positions that would otherwise hold two more hydrogen atoms.
In terms of reactions, both undergo complete combustion in oxygen to produce carbon dioxide and water, and both can undergo incomplete combustion to produce carbon monoxide and water if oxygen is limited, though incomplete combustion is more likely with ethene because of its higher carbon to hydrogen ratio.
The biggest reaction difference is that ethene decolourises bromine water, turning it from orange to colourless, while ethane does not decolourise bromine water at all, because ethene's C=C double bond can open up to add the bromine atoms across it in an addition reaction, a reaction ethane cannot do since it has no double bond to react across.
Because of its reactive double bond, ethene is more reactive overall than ethane and can also react with hydrogen to produce ethane, with water to produce ethanol, with halogens, and can polymerise to form poly(ethene), none of which ethane can do since its single bonds are much less reactive.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise alkane and alkene comparison questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What is the general formula for alkenes?
Comparison questions reward specific numbers (atom counts, bond types) linked to specific reaction outcomes, not two separate lists. Practise linking structure to reactivity.
Practise alkane and alkene comparison questionsThis question type either asks you to plan the full chromatography method from scratch, or gives you a diagram of an already-set-up experiment and asks you to spot what is wrong with it.
It wants the complete, correctly sequenced chromatography method, from drawing the start line to calculating the Rf value using both distance measurements.
Draw a pencil start line near the bottom of a piece of chromatography paper, then place a small spot of the food colouring on the start line and allow it to dry. Place the paper into a beaker containing a suitable solvent, making sure the solvent level is below the start line so the spot of dye does not dissolve straight into the solvent.
Wait for the solvent to travel up the paper, near to the top, then remove the paper and immediately mark the position of the solvent front in pencil before it evaporates and dries.
Once the paper has dried, measure the distance from the start line to the centre of the dye spot, and separately measure the distance from the start line to the solvent front. Then calculate the Rf value by dividing the distance moved by the dye by the distance moved by the solvent.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise chromatography planning and analysisIt wants two specific, correctly identified errors from the diagram shown: comparing what the student did against the standard correct method.
A diagram showing a student's chromatography set-up with a beaker, a lid, chromatography paper, and a start line marked in ink positioned below the level of water in the beaker.
The first mistake is that the start line was drawn in ink rather than in pencil, which risks the ink itself dissolving and mixing with the food colouring being tested, making the results unreliable.
The second mistake is that the start line was drawn below the level of the water in the beaker, meaning the orange food colouring spot would dissolve directly into the water rather than being carried up the paper by it, ruining the separation.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise chromatography planning and analysisThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What is the purpose of chromatography?
Chromatography questions test the full standard method: pencil start line above the solvent, correct measurements, correct Rf formula. Learn the standard errors examiners plant in diagrams too.
Practise chromatography planning and analysisThis calculation always rearranges the Rf formula (Rf = distance moved by substance / distance moved by solvent) to find a missing value.
It wants the Rf formula rearranged to find the distance moved by the solvent, given the Rf value and the distance moved by the dye.
A diagram of a chromatogram showing a start line, two dye spots (yellow and blue) close together, and a solvent front, with the diagram marked as not to scale.
Rf = distance moved by substance divided by distance moved by solvent, so 0.60 = 5.7 divided by the distance moved by the solvent. Rearranging gives distance moved by solvent = 5.7 divided by 0.60, which equals 9.5 cm.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise Rf value calculationsIt wants the Rf formula rearranged to find the missing distance moved by the yellow dye, using the given Rf value of 0.60 and the given solvent distance of 12.0 cm.
A table comparing type A and type B chromatography paper for red and yellow dye, showing distance moved by dye, distance moved by water, and Rf value for each combination, with one distance value missing and marked X.
| Type A: Red dye | Type A: Yellow dye | Type B: Red dye | Type B: Yellow dye | |
|---|---|---|---|---|
| Distance moved by dye in cm | 4.8 | 6.6 | 5.4 | X |
| Distance moved by water in cm | 12 | 12 | 12 | 12 |
| Rf value | 0.4 | 0.55 | 0.45 | 0.6 |
0.60 = distance moved by dye divided by 12.0, so distance moved by dye = 0.60 multiplied by 12.0, which equals 7.2 cm. This is the value of X.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise Rf value calculationsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What is the purpose of chromatography?
Rf calculations are simple rearrangement practice, but the direction of rearrangement changes depending on which value is missing. Practise both directions.
Practise Rf value calculationsEvery sitting we checked includes a tangent-to-curve rate calculation, always following the same method: draw the tangent, find the gradient, then convert using a given conversion factor if the y-axis is not already in moles.
It wants a tangent drawn at 80 seconds on the given curve, then the gradient calculated and rounded to 2 significant figures, using cm3 of gas per second as the unit.
A graph of volume of gas produced (cm3) against time (seconds) for the reaction of zinc powder with two different concentrations of sulfuric acid, showing two curves that both level off, with the 0.05 mol/dm3 curve reaching a lower final volume than the 0.10 mol/dm3 curve.
Draw a tangent to the 0.05 mol/dm3 curve at 80 seconds. Reading from the tangent, take a convenient x-step, for example from 60 to 100 seconds (an x-step of 40 seconds), and read the corresponding y-step over that range, for example from about 50 cm3 to about 60 cm3 (a y-step of 10 cm3).
Rate = y-step divided by x-step = 10 divided by 40 = 0.25 cm3 per second.
To 2 significant figures, the rate of reaction at 80 seconds is 0.25 cm3/s.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise rate of reaction graph questionsIt wants a tangent drawn at 30 seconds, the gradient read as a percentage-per-second rate, then converted into mol/s using the given conversion factor.
A graph of the percentage of light from a light source reaching a light sensor, plotted against time in seconds, for the reaction of sodium thiosulfate solution with hydrochloric acid, showing a decreasing curve that levels off at around 24%.
Draw a tangent to the curve at 30 seconds. Reading from the tangent, take an x-step of 20 seconds, for example from 20 to 40 seconds, and the corresponding y-step, for example a decrease of about 24% in that time.
The ratio of y-step to x-step is 24 divided by 20, which equals 1.2 (percent per second).
Since a 1% decrease corresponds to 7.1 x 10 to the power minus 5 moles of sulfur produced, the rate in mol/s is 1.2 multiplied by 7.1 x 10 to the power minus 5, which equals about 8.5 x 10 to the power minus 5 mol/s.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise rate of reaction graph questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
According to collision theory, which of the following must happen for a chemical reaction to take place?
Tangent-to-curve rate questions are pure technique: an accurate tangent, a clean x-step and y-step, and the correct conversion factor if one is given. Practise drawing tangents on real exam graphs.
Practise rate of reaction graph questionsThis short question always asks you to link a changing or different rate directly to a changing or different concentration, referencing the graph given.
It wants the rate change (fastest at the start, slowing down) explained specifically in terms of the falling concentration of a reactant as the reaction proceeds.
A graph of the percentage of light reaching a light sensor plotted against time, showing a curve that falls steeply at first and then levels off as the reaction between sodium thiosulfate and hydrochloric acid proceeds.
The rate of reaction is greatest at the start because the concentration of the reactants is at its highest. As the reaction proceeds, the concentration of the reactants decreases, so the rate of reaction decreases too, which is why the curve becomes less steep over time.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise rate and concentration questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
Which of the following factors does NOT affect the rate of a chemical reaction?
Rate-concentration explanation questions want a direct cause-and-effect link: concentration falls, so collisions become less frequent, so rate falls. Practise stating this chain precisely.
Practise rate and concentration questionsThis extended question always covers the same reasoning pattern: the chosen conditions balance a faster rate of reaction against a better position of equilibrium (yield), while also considering cost.
It wants an explanation of why 450 degrees Celsius and 200 atmospheres are a compromise for the Haber process, covering both rate and yield effects and the cost of using more extreme conditions.
A table showing the percentage yield of ammonia at 450 degrees Celsius across a range of pressures from 60 to 420 atmospheres, with yield increasing with pressure but by a smaller amount at higher pressures.
| Pressure in atmospheres | Percentage (%) yield of ammonia |
|---|---|
| 60 | 9 |
| 120 | 18 |
| 180 | 25 |
| 240 | 31 |
| 300 | 36 |
| 360 | 40 |
| 420 | 43 |
A higher temperature gives a higher rate of reaction because particles collide more frequently and more particles have the activation energy needed to react, so ammonia is produced faster at 450 degrees Celsius than at a lower temperature.
However, since the forward reaction is exothermic, a higher temperature shifts the position of equilibrium to the left, towards the reactants, reducing the percentage yield of ammonia. This means 450 degrees Celsius is a compromise: high enough to give a reasonably fast rate, but not so high that the equilibrium yield of ammonia becomes too low.
A higher pressure also gives a higher rate of reaction because particles collide more frequently when they are more concentrated in a smaller space, and higher pressure shifts the position of equilibrium to the right, towards ammonia, because there are fewer gas molecules on the right-hand side of the equation (two moles of ammonia compared to four moles of nitrogen and hydrogen combined), increasing the yield.
Even though a higher pressure than 200 atmospheres would increase the yield further, as shown by the data continuing to rise beyond 420 atmospheres, higher pressures need more energy to generate and stronger, more expensive reaction vessels to contain safely, so 200 atmospheres is chosen as a compromise between yield and cost, in the same way 450 degrees Celsius is chosen as a compromise between rate and yield.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise Haber process and equilibrium conditions questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
Industrial equilibrium questions always reward the same structure: rate effect, equilibrium effect, then a cost-based compromise. Learn this template and apply it to any reversible industrial reaction.
Practise Haber process and equilibrium conditions questionsThis question gives you a coloured reversible reaction and asks you to explain a specific colour change caused by adding a reagent, changing temperature, or changing pressure.
It wants the colour change (towards red) explained as the equilibrium position shifting right because more thiocyanate ions were added, in line with Le Chatelier's principle.
The ionic equation for the reversible reaction between iron(III) ions (yellow) and thiocyanate ions (colourless) forming FeSCN2+ ions (red), with the equilibrium mixture described as orange at room temperature.
The mixture becomes more red because the position of equilibrium moves to the right. Adding more thiocyanate ions increases the concentration of thiocyanate ions in the mixture, so the equilibrium shifts to counteract this increase, favouring the forward reaction that uses up thiocyanate ions to produce more of the red FeSCN2+ ion.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise equilibrium and Le Chatelier's principle questionsIt wants the correct colour outcome identified from increasing pressure on the NO2/N2O4 equilibrium, based on which side of the equation has fewer gas molecules.
A diagram of a sealed gas syringe containing a brown-coloured mixture of nitrogen dioxide (brown) and dinitrogen tetroxide (colourless), with the balanced equation 2NO2(g) reversible reaction N2O4(g) shown, and the forward reaction stated as exothermic.
The mixture becomes a lighter shade of brown. Increasing the pressure shifts the position of equilibrium towards the side with fewer gas molecules, which is the N2O4 side (one mole of gas, compared to two moles of NO2 on the other side), and since N2O4 is colourless while NO2 is brown, more N2O4 forming makes the mixture a lighter shade of brown overall.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise equilibrium and Le Chatelier's principle questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
At dynamic equilibrium, which of the following is true?
Le Chatelier colour-change questions always want you to name the shift direction and the specific reason (concentration, temperature or pressure change), not just describe the colour.
Practise equilibrium and Le Chatelier's principle questionsBoth fractional distillation questions we checked test the same underlying model: crude oil is heated to vaporise, then fractions condense at different heights in a temperature gradient depending on their boiling point.
It wants the fractional distillation process explained, linking the different boiling point ranges given in the table to where each fraction condenses in the column.
A table showing three fractions obtained from crude oil (lubricating oil, naphtha, petroleum gases) alongside their boiling point range in degrees Celsius, with lubricating oil having the highest range and petroleum gases the lowest.
| Fraction | Boiling point range (degrees Celsius) |
|---|---|
| Lubricating oil | 300 to 350 |
| Naphtha | 90 to 200 |
| Petroleum gases | below 25 |
Crude oil is heated to vaporise the hydrocarbons it contains. There is a temperature gradient in the fractionating column, cooler at the top than at the bottom, so the vaporised hydrocarbons condense at different levels depending on their boiling point.
Lubricating oil, with the highest boiling point range of 300 to 350 degrees Celsius, condenses lower down the column where it is still hot, naphtha, with a boiling point range of 90 to 200 degrees Celsius, condenses higher up where it is cooler, and petroleum gases, with a boiling point below 25 degrees Celsius, do not condense at all inside the column and are collected as a gas at the very top, all because of their different boiling points.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise crude oil and fractional distillation questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
A hydrocarbon is a compound that contains only:
Fractional distillation questions want the temperature gradient explicitly linked to the specific boiling point data given, not a generic textbook description.
Practise crude oil and fractional distillation questionsThis is the same rate-versus-yield-versus-cost reasoning template as the Haber process question, applied to the industrial production of ethanol from ethene and steam.
It wants the same rate-yield-cost compromise reasoning as the Haber process, applied to the reversible reaction between ethene and steam that produces ethanol.
The equation C2H4(g) + H2O(g) reversible reaction C2H5OH(g), with the forward reaction stated as exothermic.
A higher temperature gives a higher rate of reaction because particles collide more frequently and more particles have enough energy to react. However, since the forward reaction is exothermic, a higher temperature shifts the position of equilibrium to the left, away from ethanol, reducing the yield.
A higher pressure gives a higher rate of reaction because particles collide more frequently, and higher pressure also shifts the position of equilibrium to the right, towards ethanol, because there are fewer gas molecules on the product side (one mole of ethanol) than on the reactant side (two moles combined, ethene and steam), increasing the yield of ethanol.
Because higher temperatures and higher pressures both use more energy and require stronger, more expensive equipment, the chosen temperature is a compromise between a fast enough rate and a high enough yield, and the chosen pressure is a compromise between yield and the cost of generating and containing that pressure.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise industrial equilibrium reaction questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What is the functional group present in all alcohols?
This is the exact same rate-yield-cost template as the Haber process, just applied to ethanol production. Learn the template once and it applies to any industrial reversible reaction question.
Practise industrial equilibrium reaction questionsEvery sitting we checked with a polymers question asks you to move between a monomer's structure and its polymer's structure, or to circle the functional group responsible for addition polymerisation.
It wants the monomer's structure derived by reversing the polymer's repeat unit: replacing the C-C single bond between the two repeat-unit carbons with a C=C double bond.
Figure 1 shows the displayed structural formula of poly(butene) as a repeating unit in brackets with a methyl group on each of the two backbone carbons. Figure 2 shows a partially completed monomer diagram with the same methyl and hydrogen groups but the bond between the two carbons left unlabelled.
The bond between the two carbon atoms shown in Figure 2 should be a double bond (C=C), since a polymer's repeating unit always has a single C-C bond where the monomer originally had a C=C double bond. The remaining bonds to the methyl group and hydrogen atom on each carbon stay as single bonds, unchanged from the polymer diagram.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise addition polymer structure questionsIt wants the C=C double bond specifically circled, since this is the functional group that opens up to allow addition polymerisation, not any other part of the molecule.
The displayed structural formula of chloroethene, showing two carbon atoms joined by a double bond, with one carbon bonded to two hydrogen atoms and the other bonded to one hydrogen atom and one chlorine atom.
The circle should be drawn around the C=C double bond between the two carbon atoms, since this double bond is the functional group that opens up during addition polymerisation to link monomer units together.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise addition polymer structure questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What type of monomers are needed for addition polymerisation?
Polymer structure questions reward knowing exactly which bond changes (the C=C double bond becomes a single bond) and which stays the same. Practise moving between monomer and polymer diagrams in both directions.
Practise addition polymer structure questionsCarboxylic acid weak-acid reasoning always comes back to the reversible arrow in the ionisation equation, and to comparing pH or reaction rate as evidence of relative acid strength.
It wants the reversible arrow in the given equation identified as evidence of incomplete ionisation, which is the defining feature of a weak acid.
The equation CH3COOH(aq) reversible reaction CH3COO-(aq) + H+(aq), showing a reversible arrow rather than a single forward arrow.
The reversible arrow in the equation shows that ionisation is incomplete or partial, because the reaction is reversible, meaning not all of the ethanoic acid molecules split up into ions; some remain as CH3COOH molecules while others ionise. This partial ionisation is what defines a weak acid, unlike a strong acid which ionises completely, shown with a single forward arrow.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise carboxylic acids and weak acid questionsIt wants the faster reaction rate of methanoic acid explained using its lower pH (from the given table) as evidence of a higher concentration of hydrogen ions, leading to more frequent collisions.
A table showing methanoic, ethanoic and propanoic acid, their formulae, and the pH of a 0.01 mol/dm3 solution of each, with methanoic acid having the lowest pH of 2.91.
| Name | Formula | pH of a 0.01 mol/dm3 solution |
|---|---|---|
| Methanoic acid | ? | 2.91 |
| Ethanoic acid | CH3COOH | 3.39 |
| ? | CH3CH2COOH | 3.44 |
Table 3 shows that 0.01 mol/dm3 methanoic acid has a lower pH than 0.01 mol/dm3 ethanoic acid, so methanoic acid has a higher concentration of hydrogen ions in solution at the same overall concentration. This means methanoic acid ionises to a greater extent than ethanoic acid, making it a (relatively) stronger weak acid.
Because there is a higher concentration of hydrogen ions in the methanoic acid solution, there are more frequent collisions between hydrogen ions and the zinc carbonate per unit time, which is why the rate of reaction with methanoic acid is greater than with ethanoic acid at the same overall concentration.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise carboxylic acids and weak acid questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
What is the functional group present in all carboxylic acids?
Weak acid questions want the reversible arrow linked explicitly to incomplete ionisation, and rate comparisons linked through pH to ion concentration to collision frequency. Practise the full reasoning chain.
Practise carboxylic acids and weak acid questionsThis shorter Haber process question asks about where the nitrogen and hydrogen come from, and how ammonia is separated from the unreacted gases that get recycled.
It wants the two named raw material sources: air for nitrogen and natural gas for hydrogen.
Nitrogen is obtained from the air. Hydrogen is obtained from natural gas.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise Haber process raw materials and separation questionsIt wants the cooling and condensing step explained, showing that ammonia liquefies while nitrogen and hydrogen remain as gases and are recycled back to the reactor.
A flow diagram of the Haber process showing nitrogen and hydrogen entering a reactor, the mixture of nitrogen, hydrogen and ammonia passing to a box labelled X, unreacted nitrogen and hydrogen being recycled back to the reactor, and ammonia leaving as the final product.
The mixture is cooled, so that only the ammonia liquefies. The unreacted nitrogen and hydrogen remain as gases and are recycled back into the reactor to react again.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise Haber process raw materials and separation questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
The Haber process raw materials and separation steps are short, precise recall questions. Learn the sources (air, natural gas) and the separation method (cooling to liquefy only ammonia) exactly.
Practise Haber process raw materials and separation questionsBoth alternative copper extraction methods come up as description questions: phytomining (grow plants, burn them, dissolve the ash) and bioleaching (using bacteria to produce a leachate solution).
It wants the full phytomining sequence described: growing plants, burning them, dissolving the ash, then extracting the copper from solution.
Plants are grown on land containing copper ore, and they absorb copper compounds from the soil as they grow. The plants are then burnt, which produces ash containing copper compounds. This ash is dissolved in acid to produce a solution containing a copper compound. Finally, copper is extracted from this solution either by electrolysis, or by displacement using scrap iron added to the solution.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise copper extraction and resource questionsIt wants bioleaching defined as the use of bacteria to produce a leachate solution containing copper compounds extracted from a low-grade ore.
Bioleaching is the use of bacteria to produce a leachate solution that contains metal compounds, such as copper compounds, extracted from a low-grade ore.
Could you have written this? Every fact in this answer is drilled in our quizzes — the writing is the easy part once the evidence is automatic.
Practise copper extraction and resource questionsThe topic changes by sitting — the mark scheme never does. Learn this once, then open your question above for that sitting’s sources and a full worked answer.
Which of the following best describes a finite resource?
Phytomining and bioleaching are both alternative copper extraction methods for low-grade ores. Keep the sequence of steps for phytomining and the bacteria-based definition of bioleaching clearly separate.
Practise copper extraction and resource questionsAcross the 4 sittings we have full papers for, these are the topics with the most exam appearances and marks at stake on Paper 2.
Greenhouse effect and climate change as a standalone extended question (it appeared as short factual recall questions in one sitting rather than a full extended question) · Instrumental methods of analysis as a full standalone question (it has appeared only as short 1-mark recall questions) · Recycling as a standalone extended question separate from life cycle assessment
These topics have not been the main focus of a question in the papers we analysed, but can still support your revision, so do not skip them entirely.
The diagrams and data are described in our own words, not reproduced, and the worked answers are written entirely by us, aimed at the top level descriptors of the real AQA mark schemes for each sitting. They are not copied from AQA's own exemplar materials, since that would breach copyright, but they are built to hit exactly what the real mark scheme rewarded that year. PrepWise is independent of AQA and not endorsed by them.
Sometimes stems repeat closely, but you cannot rely on repeats alone, since the actual data, diagrams and numbers change every time even when the topic and question style repeat. Use this page to see which TOPICS and question TYPES keep returning (like tangent-to-curve rate calculations, or the rate-versus-yield-versus-cost equilibrium template) and make sure you know the method cold, whatever the exact numbers turn out to be.
Extended questions like the LCA evaluation or the equilibrium conditions question are worth up to 6 marks each and are marked using levels, not individual points. If you are short on time, still write a short concluding judgement, even a brief one, rather than leaving the answer unfinished, since a partial answer with a clear structure usually scores better than an unfinished list of facts.
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