1H NMR

#Chemistry 

Integration

  • The area under the curve for a signal corresponds proportionally to the number of hydrogens that emit that signal

Peaks vs Signals

  • Each group of equivalent hydrogens produce exactly one signal
  • These signals can be composed of 1, 2, 3, 4, or multiple peaks. We then may say a signal is split into/has a multiplicity of a singlet, doublet, triplet, quartet, or multiplet

Chemical Shifting

  • A greater chemical shift in NMR means a lower $\displaystyle \nu$ relative to that of TMS
  • Downfield (deshielded or more polar) molecules have greater chemical shift
  • Upfield (shielded or more nonpolar) molecules have less chemical shift
    600
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    500

Signal Splitting

  • $\displaystyle (n+1)$ rule
    • $\displaystyle \ce{^{1}H}$ NMR signal is split into $\displaystyle n+1$ peaks, where $\displaystyle n$ is the number of non-equivalent hydrogen neighbors
    • Only applicable if the hydrogen neighbors are the same or similar in coupling to each other
  • Coupling Constant $\displaystyle (J)$
    • Describes the separation between two peaks in a signal
  • Vicinal Splitting
  • Geminal Splitting
    • Caused by hydrogens geminal to each other
    • Splitting is much smaller than that caused by vicinal splitting
  • Benzene Protons
    • Can couple only with each other to produce multiplets
  • $\displaystyle \ce{-OH}$ and $\displaystyle \ce{-NH}$ show up only as singlets
  • Complex Splitting
    • Honestly, just check out Notability notes in CHEM 30B