Chemistry · A-Level · AQA · AQA A-level Chemistry - (7405) · Specification point · 3.3.15 · Organic chemistry
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3.3.15 Nuclear magnetic resonance spectroscopy (A-level only)
Chemists use a variety of techniques to deduce the structure of compounds. In this section, nuclear magnetic resonance spectroscopy is added to mass spectrometry and infrared spectroscopy as an analytical technique. The emphasis is on the use of analytical data to solve problems rather than on spectroscopic theory.
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Appreciation that scientists have developed a range of analytical techniques which together enable the structures of new compounds to be confirmed. Nuclear magnetic resonance (NMR) gives information about the position of ¹³C or ¹H atoms in a molecule. ¹³C NMR gives simpler spectra than ¹H NMR. The use of the δ scale for recording chemical shift. Chemical shift depends on the molecular environment. Integrated spectra indicate the relative numbers of ¹H atoms in different environments. ¹H NMR spectra are obtained using samples dissolved in deuterated solvents or CCl₄ The use of tetramethylsilane (TMS) as a standard. Students should be able to:
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use the n+1 rule to deduce the spin–spin splitting patterns of adjacent, non-equivalent protons, limited to doublet, triplet and quartet formation in aliphatic compounds.
Students should be able to use data in the Chemistry Data Booklet to suggest possible structures for molecules. |