EXAM PRACTICE

Exam practice: Chemistry for Biologists

1A review questions with worked reasoning, covering the section’s specification links.

Student Book 1 · p. 24

YOUR SPECIFICATION

What you need to know

  • 1.1–1.5Water, carbohydrates, lipids and food-test reasoning.
  • 2.6Protein structure and function.
Pearson specification · Issue 2, pp. 15–17

By the end, you should be able to…

  • Retrieve key mechanisms before checking the answers.
  • Apply ideas to unfamiliar numerical and experimental examples.
  • Identify and correct missing steps in an explanation.
SPECIFICATION-ALIGNED LEARNING

Build your understanding

Choose the relevant level

Start molecular explanations with the property asked about: for solubility, bond type for , branching for mobilisation or folding for protein function. Then explain the consequence.

Keep measurements defensible

Use units and dilution factors. A colour-standard result is an estimate or interval; describe the colour and precipitate consistently. Use Core Practical 1 for the full method.

EXAM TIPS & ADVICE

Make your reasoning visible

Answer the command word

Describe the pattern, explain the mechanism or evaluate the evidence as requested. A correct fact may still miss the question.

Show workings and units

Write a calculation before its result, and distinguish fractions, percentages and percentage-point changes.

Use answers diagnostically

Attempt the question first, then identify the missing step rather than only checking whether your final number matches.

Avoid this misconception

The claim: A longer answer automatically earns more credit.

The correction: Relevance, accuracy and the requested reasoning matter.

RETRIEVE · APPLY · CHECK

Check your understanding

Try each question before opening the suggested answer.

Check your understanding (continued)

  1. Practice question

    Retrieval and explanation · suggested answer

    Explain why glucose can be transported in plasma but a triglyceride is not freely soluble in its water.

    Show suggested answer

    Glucose has polar groups that interact with water, so it dissolves. A triglyceride has large non-polar hydrocarbon regions and does not interact sufficiently with water to dissolve readily; lipid transport needs other arrangements.

  2. Practice question

    Retrieval and explanation · suggested answer

    Compare amylose and amylopectin and explain one advantage of branching in a storage polysaccharide.

    Show suggested answer

    Amylose is unbranched with α-1,4 links and coils; amylopectin also has α-1,6 branch points. Branching provides more ends for enzymes involved in mobilisation, supporting rapid glucose release.

  3. Practice question

    Retrieval and explanation · suggested answer

    Describe formation of a triglyceride from its components.

    Show suggested answer

    One glycerol joins three fatty acids in condensation reactions, forming three ester bonds and releasing three water molecules.

  4. Practice question

    Retrieval and explanation · suggested answer

    An amino-acid substitution changes a globular enzyme’s active site. Explain how primary structure can affect activity.

    Show suggested answer

    A changed amino-acid sequence can alter interactions responsible for folding, changing the active site’s shape or chemical properties. Substrate binding or catalysis may be impaired.

  5. Practice question

    Retrieval and explanation · suggested answer

    A glucose test sample matches between the 0.4% and 0.6% Benedict’s colour standards. It was diluted fivefold before testing. Report a defensible original concentration estimate.

    Show suggested answer

    Approximately 2–3% in the original sample: multiply the estimated 0.4–0.6% range by five. A visual semi-quantitative comparison does not justify a precise value such as 2.437%.

STRETCH QUESTION

Take the idea further

Apply the same specification knowledge to an unfamiliar problem. Any extra assumptions are supplied in the question.

Stretch question

Two disaccharides have identical molecular formulae but only one is hydrolysed by an enzyme. Explain without assuming that one contains more energy.

Show a hint

Consider bonding arrangement and active-site specificity.

Explore the reasoning

Different arrangements of atoms or glycosidic links give different three-dimensional structures. Only one may form a productive enzyme–substrate complex; identical formulae do not imply identical enzyme recognition.

RECALL

Recall this lesson

Lesson recall questions

5 of 100 recall questions for 1.1, 1.2, 1.3, 1.4, 1.5, 2.60 of 5 rated0 secure

Question 1 of 5: Starch is a plant ________ made of ________ and ________.

011.2Complete

Saccharides and energy stores

Practice question

Retrieval and explanation · suggested answer

Starch is a plant ________ made of ________ and ________.

Try this from memory first.

Practise more of these specification points

Beyond the classroom

Put your biology to work

Explore where these ideas appear in the world. Enrichment, not extra required recall.

Research

A name is not a structure

1A · Thinking Bigger: TrehaloseFlyBase’s chemical entry identifies trehalose by its structure and links to chemical databases. Researchers need precise chemical identity when comparing experiments. For a food chemist, a familiar-sounding name…Specification 1.2(i) · 1.4Read & use the scienceClose article

Why this matters

FlyBase’s chemical entry identifies trehalose by its structure and links to chemical databases. Researchers need precise chemical identity when comparing experiments. For a food chemist, a familiar-sounding name is not enough to predict digestion. Two sugars can contain the same kinds of atom yet arrange their bonds differently. Whether a particular enzyme hydrolyses them depends on that arrangement and on its active site. Trehalose offers a useful unfamiliar case: apply the supplied structural evidence instead of guessing from an ending such as “-ose”. This is also why a claim about one sugar cannot automatically be transferred to every other sugar.

Back to the specification

Pearson Edexcel IAL Biology · Issue 2, February 2021 · Unit 1, pp. 15–18. The application extends beyond required recall.

  • 1.2(i) know the difference between monosaccharides, disaccharides and polysaccharides, including glycogen and starch (amylose and amylopectin)
  • 1.4 know how monosaccharides (glucose, fructose and galactose) join together to form disaccharides (maltose, sucrose and lactose) and polysaccharides (glycogen, amylose and amylopectin) through condensation reactions forming glycosidic bonds, and how these can be split through hydrolysis reactions
Read the Pearson specification

Use the science

Why is “a glucose-based sugar” too vague for a reproducible experiment?

Explore a possible response

It does not identify whether the sample is glucose, a particular disaccharide or a polymer, nor the linkages or concentration.

Explore the source

Pop CultureCareers

Can a blue test tube prove a drink has no sugar?

1A · Carbohydrates 1: Monosaccharides and DisaccharidesA food analyst and a drinks advertisement may use the word sugar in different ways. The FDA distinguishes total sugars from sugars added during manufacture: a drink can…Specification 1.2(i) · 1.3 · 1.4Read & use the scienceClose article

Why this matters

A food analyst and a drinks advertisement may use the word sugar in different ways. The FDA distinguishes total sugars from sugars added during manufacture: a drink can contain naturally occurring sugars without having sugar added. Your Benedict’s test asks another question, about reducing sugars. It is not a universal detector for every carbohydrate, nor can it tell whether a glucose molecule came from fruit or a factory. Comparing a chemical test with a label requires checking exactly what each measures, using appropriate standards and allowing for the colour of the drink itself.

Back to the specification

Pearson Edexcel IAL Biology · Issue 2, February 2021 · Unit 1, pp. 15–18. The application extends beyond required recall.

  • 1.2(i) know the difference between monosaccharides, disaccharides and polysaccharides, including glycogen and starch (amylose and amylopectin)
  • 1.3 CORE PRACTICAL 1 Use a semi-quantitative method with Benedict’s reagent to estimate the concentrations of reducing sugars and with iodine solution to estimate the concentrations of starch, using colour standards.
  • 1.4 know how monosaccharides (glucose, fructose and galactose) join together to form disaccharides (maltose, sucrose and lactose) and polysaccharides (glycogen, amylose and amylopectin) through condensation reactions forming glycosidic bonds, and how these can be split through hydrolysis reactions
Read the Pearson specification

Use the science

A sucrose-containing drink gives a negative Benedict’s test before hydrolysis. Explain why the claim “laboratory-proven sugar-free” does not follow.

Explore a possible response

Sucrose is non-reducing under the test conditions. Hydrolysis produces reducing monosaccharides. A negative reducing-sugar result cannot establish absence of all sugars; appropriate controls and sensitivity also matter.

Explore the source

Browse all Unit 1 connections →
END OF THE LESSON

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