AQA A-Level Chemistry Paper 3, 2021: Question 35
1 mark · Easy difficulty · Multiple Choice
This question tests your understanding of zwitterions—molecules that have both a positive and a negative charge but are overall neutral. You're asked to identify which structure correctly shows a zwitterion form of an amino acid. Zwitterions typically form in aqueous solution where the amino group becomes protonated and the carboxylic acid group loses a proton.
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Question text
35 Which is the structure of a zwitterion of an amino acid?
[1 mark]
A
B
C
D
Mark scheme
Show the mark scheme
35 D 1
How to answer it
Multiple Choice Explained: Zwitterion of an Amino Acid
Correct Answer: D
This is the structure of a zwitterion: it contains a positively charged ammonium group (NH₃⁺) and a negatively charged carboxylate group (COO⁻). The R group here is –CH₂SH (from cysteine), but the presence of both charges on the main chain confirms it's a zwitterion.
Why A is incorrect:
This molecule has two positively charged NH₃⁺ groups and one COO⁻, resulting in an overall +1 charge. A zwitterion must be overall neutral.
Why B is incorrect:
This structure contains two COO⁻ groups and one NH₃⁺, making it overall negatively charged—not a zwitterion.
Why C is incorrect:
This contains a neutral –OH₂⁺ group instead of the correct zwitterionic structure. Additionally, the side chain seems unrealistic for an amino acid and doesn't represent a standard amino acid.
Topics
Organic Chemistry · 3.3.13 Amino Acids, Proteins and DNA
Question and mark scheme from the AQA A-Level Chemistry examination, Paper 3, 2021. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.