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Understanding Proton NMR and Signal Splitting

Feb 13, 2025

Lecture 9-5: Proton NMR and Signal Splitting

Introduction to Signal Splitting

  • Signal splitting is unique to NMR.
  • Helps deduce molecular structure by organizing parts of a molecule like a jigsaw puzzle.
  • Observed through interaction between magnetic fields of hydrogen nuclei.

Concept of Signal Splitting

  • Magnetic fields from adjacent hydrogen nuclei influence the observed magnetic field of a hydrogen signal.
  • This influence results in splitting of the signal into multiple lines (doublets, triplets, etc.).
  • N + 1 Rule: Helps predict the number of lines in the splitting:
    • Adjacent hydrogens (n) + 1 = Number of lines in the signal

Example of Signal Splitting

  • Observing a signal for a red hydrogen adjacent to a methyl group:
    • Methyl group has 3 hydrogens.
    • Signal for red hydrogen is split into four lines (quartet) following the N + 1 rule (3+1=4).
  • Methyl hydrogens give a signal that appears as a doublet (1 adjacent hydrogen, 1+1=2).

Overview of Signal Splitting Patterns

  • Table of Adjacent Hydrogens and Resulting Signal
    • 0 adjacent hydrogens โ†’ Singlet
    • 1 adjacent hydrogen โ†’ Doublet
    • 2 adjacent hydrogens โ†’ Triplet
    • 3 adjacent hydrogens โ†’ Quartet
    • 4+ adjacent hydrogens โ†’ Multiplet (lines may be difficult to distinguish, call it a multiplet)

Application: Isopropyl Methyl Ether

  • Predicting NMR spectrum signals:
    • Equivalents: Identify equivalent hydrogens.
      • Two methyl groups on the right labeled as A.
      • Unique CH labeled as B.
      • CH3 on the left labeled as C.
    • Signals and Splitting:
      • A: Adjacent to 1 hydrogen โ†’ Doublet (1+1=2)
      • B: Adjacent to 6 hydrogens โ†’ Multiplet (6+1=7, hard to resolve)
      • C: No adjacent hydrogens โ†’ Singlet (0+1=1)

Observation in NMR Spectrum

  • Signal A: Appears as a doublet around 1 ppm.
  • Signal B: Appears as a multiplet around 4 ppm (can resolve 7 lines here).
  • Signal C: Appears as a singlet due to no adjacent hydrogens.
  • Area under the signals is proportional to the number of protons.

Conclusion

  • Signal splitting provides a way to analyze and predict molecular structures using NMR.
  • Upcoming videos will continue to explore examples and applications.

End of Recording

  • A question is posed for understanding check; answer to be determined by the student.