NMR spectroscopy

Cards (25)

  • What is NMR spectroscopy used for?
    It is used to determine the structure of a molecule.
  • How does NMR spectroscopy analyze bond environments?
    It analyzes the energy absorbed by different bond environments.
  • What does each peak in an NMR spectrum represent?
    Each peak represents a different bond environment within the molecule.
  • What is the standard molecule used in NMR spectroscopy?
    Tetramethylsilane (TMS) is the standard molecule.
  • Why is TMS considered a standard molecule in NMR?
    It contains four identical carbon and hydrogen environments.
  • At what value does TMS appear on the NMR spectrum?
    TMS appears at ∂=0 ppm on the x-axis.
  • What does C<sup>13</sup> NMR analyze?
    C<sup>13</sup> NMR analyzes the different carbon environments in a molecule.
  • How do carbon environments near oxygen behave in C<sup>13</sup> NMR?
    They have ∂ values that are shifted to the right.
  • Why might a molecule with symmetry display fewer ∂ peaks than carbon atoms?
    Symmetry can cause multiple carbon atoms to have the same environment.
  • How many carbon atoms does 1,2-cyclohexanediol contain?
    It contains six carbon atoms.
  • How many peaks does the NMR spectrum of 1,2-cyclohexanediol show?
    It shows three peaks due to the symmetry of the molecule.
  • What does H<sup>1</sup> NMR analyze?
    H<sup>1</sup> NMR analyzes the different hydrogen environments in a molecule.
  • What must samples be dissolved in for H<sup>1</sup> NMR analysis?
    They must be dissolved in a non-hydrogen-containing solvent.
  • What is a common solvent used in H<sup>1</sup> NMR?
    CCl<sub>4</sub> is a common solvent used.
  • Why are H<sup>1</sup> NMR spectra more complex than C<sup>13</sup> spectra?
    Because the heights of the peaks show the relative intensity of each ∂ value.
  • What do the heights of the peaks in H<sup>1</sup> NMR correspond to?
    They correspond to the number of hydrogens in that certain environment.
  • What does the splitting pattern in H<sup>1</sup> NMR indicate?
    It indicates how many hydrogens are on the adjacent carbon atom.
  • What is the 'n+1' rule in NMR spectroscopy?
    The 'n+1' rule states that n is the number of hydrogens on the adjacent carbon.
  • What does a singlet indicate in H<sup>1</sup> NMR?
    A singlet indicates no hydrogens on the adjacent carbon.
  • What does a doublet indicate in H<sup>1</sup> NMR?
    A doublet indicates one hydrogen on the adjacent carbon.
  • What does a triplet indicate in H<sup>1</sup> NMR?
    A triplet indicates two hydrogens on the adjacent carbon.
  • What does a quartet indicate in H<sup>1</sup> NMR?
    A quartet indicates three hydrogens on the adjacent carbon.
  • What is a common splitting pattern in H<sup>1</sup> NMR?
    A triplet-quartet splitting pattern is a common combination.
  • What does the triplet-quartet splitting pattern represent?
    It represents a -CH<sub>2</sub>-CH<sub>3</sub> fragment.
  • How can multiple fragments be used in NMR spectroscopy?
    • They can be pieced together to determine the full molecule structure.
    • Each fragment corresponds to a specific splitting pattern.