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Mass spectrometry in organic analysisAQA A-Level Chemistry: Mind map

Molecular ion
Resolution

Mass spectrometry

Organic analysis

M⁺m/zPrecise Mᵣ
Precise masses
Finding the formula
Limits

Exam questions on Mass spectrometry in organic analysis

  1. A pure organic compound is analysed by mass spectrometry. In the mass spectrum, the peak with the highest mass-to-charge ratio (ignoring any very small peaks above it) is at m/z = 74.
    The compound is known to contain only carbon, hydrogen and oxygen. Explain why the m/z value of 74 alone cannot be used to find its molecular formula.2 marks
  2. High-resolution mass spectrometry measures relative molecular masses to four decimal places. Precise relative atomic masses: H = 1.0078, C = 12.0000, N = 14.0031, O = 15.9949.
    A compound has a precise relative molecular mass of 46.0054. Calculate the precise relative molecular masses of C₂H₆O and CH₂O₂ and decide which is the molecular formula of the compound.2 marks
  3. A pharmaceutical analyst finds that a compound containing only carbon, hydrogen and oxygen has a precise relative molecular mass of 88.0524 by high-resolution mass spectrometry. Precise relative atomic masses: H = 1.0078, C = 12.0000, O = 15.9949.
    The compound has a nominal mass of 88. Calculate the precise relative molecular masses of C₄H₈O₂ and C₅H₁₂O and deduce the molecular formula of the compound.3 marks
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Written by the Exaim team, led by Shaun Daswani (Head of Upper Secondary, Improve ME Institute; MSc Financial Mathematics, Imperial College London; BSc, UCL) and Jason Daswani (operational lead, Improve ME Institute; LSE).