Interpreting Organic Spectra

Chapter 9: 1H Nuclear Magnetic Resonance Spectroscopy

Overview

1H nuclear magnetic resonance spectroscopy tells us about the environment of the hydrogen atoms in a molecule. The technique is based on exactly the same principles as 13C NMR spectroscopy: the 1H nucleus has nuclear spin 1/2, so when placed in a strong magnetic field it can exist in higher or lower energy states. When the nucleus is irradiated, it absorbs radiofrequency radiation, and nucleii in lower energy spin states are promoted to higher energy spin states.

There are important differences between 1H and 13C NMR spectroscopy. The main one is that the 1H atom, which has nuclear spin, comprises 99.98% of naturally occurring hydrogen. Consequently, most 1H NMR spectra can be measured by a single scan, and Fourier transform methods are used only in exceptional circumstances. This means that peak areas are proportional to the number of hydrogen atoms that the peak represents, and this is very valuable when analysing spectra.

Another important difference is that since 12C, the main carbon isotope, does not possess nuclear spin, most hydrogen atom spectra do not have any splitting from the carbon atom to which the hydrogen is attached. The few hydrogen atoms which are attached to 13C atoms and hence are split produce tiny peaks which are usually lost in the background electronic noise on the spectrum. Consequently, we need consider only 1H to 1H coupling, unless we have present other atoms with nuclear spin such as fluorine or...

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