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AQA GCSE Chemistry Smart practice A mixed round aimed at your weak spots
Unit 1
Atomic structure and the periodic table
Unit 2
Bonding, structure, and the properties of matter
Unit 3
Quantitative chemistry
Unit 4
Chemical changes
Unit 5
Energy changes
Unit 6
The rate and extent of chemical change
Unit 7
Organic chemistry
Unit 8
Chemical analysis
Unit 9
Chemistry of the atmosphere
Unit 10
Using resources
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Formulations

Practise 20 exam-style questions on Formulations for AQA GCSE Chemistry. Write your answer as you would in the exam and get it marked in seconds against the mark scheme, point by point, with an AI tutor on hand if you get stuck.

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20 questions, marked as you go

Sample questions with model answers

Here are 4 of the questions in this topic, each with a model answer, an explanation of why it earns the marks and the mark scheme an examiner would use.

Question 1

2 marks

Explain why the components of a formulation must be mixed in carefully measured quantities.

Model answer

The quantities are carefully measured so that the product has exactly the properties it was designed to have. If there were too much or too little of one component, the product might not work, could be unsafe, or might be different from one batch to the next.

Explanation

The properties of a formulation depend on its exact composition. For example, a medicine with too much active ingredient could be dangerous, and one with too little would not work.

Mark scheme
  1. 1 mark

    so that the product has the required properties / works as intended

  2. 1 mark

    too much or too little of a component could make the product ineffective / unsafe / different each time

    allow 'so that every batch is the same'

Question 2

2 marks

Toothpaste is a formulation. It contains a fluoride compound to help prevent tooth decay.

Suggest why the amount of fluoride compound in toothpaste must be carefully controlled.

Model answer

If there is too little fluoride compound, the toothpaste will not protect the teeth from decay. If there is too much, it could be harmful to the person using it. So the amount must be carefully measured.

Explanation

Each component of a formulation is there for a reason, and its quantity is chosen to give the right effect safely. 'Too little does not work, too much is harmful' applies to many formulations, especially medicines and products used on the body.

Mark scheme
  1. 1 mark

    too little would not protect the teeth / would be ineffective

  2. 1 mark

    too much could be harmful

    allow 'toxic' or 'could damage teeth'

Question 3

3 marks

A paracetamol tablet contains paracetamol (the active ingredient), starch, a binder and a coating. Each tablet contains exactly 500 mg of paracetamol.

Explain why the tablet is described as a formulation.

Model answer

The tablet is a mixture of several components that has been designed as a useful product. Each component has a purpose: the paracetamol relieves pain, the binder holds the tablet together and the coating makes it easier to swallow. The components are mixed in carefully measured quantities, so that every tablet contains exactly 500 mg of paracetamol and gives the correct dose.

Explanation

To identify a formulation from information, look for three features: a mixture, designed for a use, with measured quantities of each component. A medicine tablet shows all three.

Mark scheme
  1. 1 mark

    it is a mixture of several components

  2. 1 mark

    it is designed as a useful product, with each component having a particular purpose

    allow an example of a purpose, e.g. the binder holds the tablet together / the coating makes it easier to swallow

  3. 1 mark

    the components are in carefully measured quantities (e.g. exactly 500 mg of paracetamol so the dose is correct)

Question 4

4 marks

A company makes tablets that should each contain 500 mg of active ingredient. A tablet is acceptable if it contains between 475 mg and 525 mg. The table shows the mass of active ingredient in five tablets from each of two batches, A and B.

Calculate the mean mass of active ingredient for each batch. Explain which batch should be rejected.

Table with columns "Tablet", "Batch A: mass in mg", "Batch B: mass in mg". Tablet: 1; Batch A: mass in mg: 498; Batch B: mass in mg: 470 | Tablet: 2; Batch A: mass in mg: 502; Batch B: mass in mg: 520 | Tablet: 3; Batch A: mass in mg: 501; Batch B: mass in mg: 455 | Tablet: 4; Batch A: mass in mg: 499; Batch B: mass in mg: 530 | Tablet: 5; Batch A: mass in mg: 500; Batch B: mass in mg: 525.

Model answer

Batch A: mean = (498 + 502 + 501 + 499 + 500) ÷ 5 = 2500 ÷ 5 = 500 mg
Batch B: mean = (470 + 520 + 455 + 530 + 525) ÷ 5 = 2500 ÷ 5 = 500 mg
Both batches have the correct mean, but batch B contains tablets with 455 mg, 470 mg and 530 mg, which are outside the acceptable range of 475-525 mg. Batch B should be rejected, because a patient taking one of these tablets would get the wrong dose. In batch A every tablet is within the range.

Explanation

A mean can hide large variation. In a medicine every single tablet must contain the right amount, which is why the components of a formulation must be measured and mixed carefully. Always look at the spread of the data as well as the mean.

Mark scheme
  1. 1 mark

    mean for batch A = 2500 ÷ 5 = 500 mg

  2. 1 mark

    mean for batch B = 2500 ÷ 5 = 500 mg

  3. 1 mark

    batch B has tablets outside the acceptable range (455 mg, 470 mg and 530 mg)

    at least one value outside the range identified

  4. 1 mark

    so batch B should be rejected, even though its mean is correct, because each tablet must give the correct dose

    allow 'the components are not mixed in carefully controlled quantities in batch B'

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