13C NMR
Shows distinct carbon environments in a molecule.
Practise Analytical, Lab & Spectroscopy All Analytical, Lab & Spectroscopy topics
Shows distinct carbon environments in a molecule.
Practise Analytical, Lab & Spectroscopy All Analytical, Lab & Spectroscopy topics
Carbon-13 NMR spectroscopy observes the carbon atoms of a molecule, and most spectra are recorded with proton decoupling, which removes C-H splitting so that each distinct carbon environment appears as a single sharp line. Because the natural abundance of 13C is only about 1.1 percent, the technique is less sensitive than proton NMR and spectra take longer to acquire. Carbon shifts span roughly 0 to 220 ppm, with carbonyl carbons at about 160 to 220 ppm, aromatic carbons at 110 to 160 ppm and alkyl carbons at 0 to 60 ppm. The number of signals reveals the number of distinct carbon environments and therefore the symmetry of the molecule. Peak heights in standard decoupled spectra are not normally proportional to the number of carbons.
Key ideas: Typical ranges: alkyl 0 to 50, C-O or C-N 50 to 90, alkyne 65 to 90, alkene and aromatic 100 to 150, carbonyl 160 to 220 (aldehydes and ketones above 190). Count lines to deduce symmetry. DEPT experiments distinguish CH3, CH2, CH and quaternary carbons. The solvent triplet of CDCl3 appears at 77 ppm, from deuterium coupling.
Common mistakes and connections: Students expect integration to match carbon counts, but decoupled spectra give unreliable peak heights, and quaternary carbons give weak lines. They also forget that equivalent carbons by symmetry give one line, so counting lines undercounts carbons. Splitting is absent in standard spectra. Related to symmetry, proton NMR, DEPT and structure determination.
Toluene gives five 13C lines for its five distinct carbons (CH3 at 21 ppm and four aromatic), whereas symmetric benzene would give only one. The interactive lesson shows this as a live animation or chart.
Benzene gives a single 13C peak because all six carbons are equivalent, while toluene gives five.
Shows distinct carbon environments in a molecule.
13C NMR is a advanced topic in Analytical, Lab & Spectroscopy. It builds on beginner and intermediate topics, so review those first if needed.
Study these earlier topics in Analytical, Lab & Spectroscopy first: Chemical Shift, Spin-Spin Splitting, Integration in NMR.
The next topics in Analytical, Lab & Spectroscopy are MRI and Atomic Absorption Spectroscopy.
Yes. The interactive lesson includes a self-check question on 13C NMR, and the Analytical, Lab & Spectroscopy quiz draws on every topic in this area.
13C NMR is topic 49 of 99 in Analytical, Lab & Spectroscopy.