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Proton (1H) NMR
For organic compounds the 1H isotope is 100% abundant, so 1H NMR is very sensitive and useful for a range of organic molecules. A small amount of sample (5-10 mg) is dissolved in 0.7-1 mL of deuterated solvent, such as CDCl3 or C6D6. This introduces two main questions:
Why must deuterated solvents be used for 1H NMR?
What is used to calibrate shifts in 1H (and 13C) NMR?
Common 1H NMR Shifts

Downfield = Deshielded; Upfield = Shielded
Multiplicity of signals (coupling) in 1H NMR is related to number of hydrogens on neighbouring atoms (3 bonds or less). The number of peaks per signal is counted and assigned an abbreviation: 1 = s (singlet); 2 = d (doublet); 3 = t (triplet); 4 = q (quartet); more = m (multiplet)
Multiplicity = 2nI + 1
Where n = number of atoms
I = atom spin (1/2 for 1H and 13C)

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- Grab a piece of paper and try this problem yourself.
- When you're done, check the "I have answered this question" box below.
- View the solution and report whether you got it right or wrong.

Mark Yourself Question
- Grab a piece of paper and try this problem yourself.
- When you're done, check the "I have answered this question" box below.
- View the solution and report whether you got it right or wrong.
