6.9.2

Carbon-13 NMR (A2 Only)

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C13 NMR

The first type of NMR we shall look at is 13C NMR. This is slightly more simple than 1H NMR.

<sup>13</sup>C spectra

13C spectra

  • We can work out the different 13C environments from the 13C spectra.
    • In the spectra, different chemical shifts represent 13Cs in different environments.
  • Remember it is only the isotope 13C that this NMR works for, NOT the more common 12C.
    • 13C's abundance is only 1.1%.
Tetramethylsilane

Tetramethylsilane

  • Tetramethylsilane (TMS) is used during the 13C spectrum readings as a reference.
  • This is used because the chemical shifts along the x-axis are relative to the shift of TMS.
  • TMS is a good reference since it only produces one peak at 0ppm because each 13C is in the same environment.
    • For this reason, lots of spectra will have a single peak at 0ppm. Remember this is just your reference peak.
<sup>13</sup>C example

13C example

  • 13C NMR of ethanal. You need to look at a data table to determine the carbon environments represented by the peaks in the spectrum.
    • The peak at 200 ppm represents the carbon in the C=O bond.
    • The peak at 31 ppm represents the carbon in the C-C bond.
    • The peak at 0 ppm is the reference peak from TMS.
Diagram
Diagram
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1

Physical Chemistry

1.1

Atomic Structure

1.2

Amount of Substance

1.3

Bonding

1.4

Energetics

1.5

Kinetics

1.6

Equilibria

1.7

Redox

2

Physical Chemistry 2 (A2 Only)

3

Inorganic Chemistry

4

Inorganic Chemistry 2 (A2 Only)

5

Organic Chemistry 1

6

Organic Chemistry 2 (A2 Only)

6.1

Optical Isomerism (A2 Only)

6.2

Aldehydes & Ketones (A2 Only)

6.3

Carboxylic Acids & Esters (A2 Only)

6.4

Aromatic Chemistry (A2 Only)

6.5

Amines (A2 Only)

6.6

Polymers (A2 Only)

6.7

Biological Organic (A2 Only)

6.8

Organic Synthesis (A2 Only)

6.9

NMR Spectroscopy (A2 Only)

6.10

Chromatography (A2 Only)

6.11

A-A* (AO3/4) - Organic 2

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