Edexcel A-Level Chemistry A2 15.19 Data From 13c Nmr Spectroscopy to I Predict the Different Environments for Carbon Atoms Present in a Molecule Given Values Questions

Count distinct carbon environments, use symmetry to identify equivalent atoms, and combine chemical-shift evidence with the molecular formula to deduce structures.

Syllabus
First assessment 2019
Course
Chemistry YCH11
Level
A2

Exam points

  • Predict the number of carbon-13 NMR peaks by identifying equivalent carbon environments and molecular symmetry.
  • Match a carbon-13 chemical shift or range to a carbon environment and use it as evidence for a functional group.
  • Draw an isomer that fits the molecular formula, functional groups and peak count, then label the distinct carbon environments.
  • Compare peak counts and shift ranges to distinguish two structures or explain why their carbon-13 spectra cannot distinguish them.

Edexcel A-Level Chemistry A2 15.19 Data From 13c Nmr Spectroscopy to I Predict the Different Environments for Carbon Atoms Present in a Molecule Given Values Questions question 1

[Maximum number: 1]

This question concerns six isomers each with the molecular formula C5H10O2\mathrm{C}_{5} \mathrm{H}_{10} \mathrm{O}_{2}.

State the number of peaks in the carbon-13 (13C)\left({ }^{13} \mathrm{C}\right) NMR spectrum of E.

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