Amino acids can join together to form peptides and proteins. Describe how amino acids are structured and explain how they join together to form a dipeptide, including the type of bond formed and the small molecule released.
Written & reviewed by James Millett — Biology (Imperial College London), PGCE Science (University of Cambridge).
Model answer (5 marks)
An amino acid has a central ‘α’ carbon bonded to an amino group (–NH₂), a carboxyl group (–COOH), a hydrogen atom and a variable side chain (R group). When two amino acids join, the amino group of one reacts with the carboxyl group of the other, forming a peptide bond. This is a condensation reaction, so a molecule of water (H₂O) is released.
Examiner tips
- Use the exact terms – amino group, carboxyl group, peptide bond, condensation reaction, water released.
- Show the reaction as –NH₂ + –COOH → –NH–CO– + H₂O.
- Mention the central α‑carbon and the R side chain to demonstrate full structure.
- Keep the answer concise – 5 marks only.
Common mistakes
- Writing the bond as an ionic bond instead of a covalent peptide bond.
- Forgetting to mention that water is released (or incorrectly stating it is produced).
- Omitting the central α‑carbon or the R side chain in the description of the amino acid.
Mark scheme (5 marks)
- An amino acid contains an amino group (–NH₂)
- An amino acid contains a carboxyl (carboxylic acid) group (–COOH)
- The amino group of one amino acid reacts with the carboxyl group of another amino acid
- A peptide bond is formed between the two amino acids
- Water is released / produced during the reaction (condensation reaction)
Key terms in this question
Related
- All Eduqas A-Level Chemistry revision notes →
- How to answer a "Describe and Explain" question →
- Decode the mark scheme abbreviations →
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