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13.8 \(^1H\) NMR Spectroscopy and Proton Equivalence

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  • Page ID
    67294
  • Objectives

    After completing this section, you should be able to

    1. identify those protons which are equivalent in a given chemical structure.
    2. use the 1H NMR spectrum of a simple organic compound to determine the number of equivalent sets of protons present.

    Key Terms

    Make certain that you can define, and use in context, the key terms below.

    • diastereotopic
    • enantiotopic
    • homotopic

    Study Notes

    It is important at this stage to be able to identify equivalent protons in any organic compound given the structure of that compound. Once you know the number of different groups of equivalent protons in a compound, you can predict the number (before coupling) and relative strength of signals. Look at the following examples and make sure you understand how the number and intensity ratio of signals are derived from the structure shown.

    Structure Number of Signals Ratio of Signals
    $\ce{\sf{CH3OCH2CH2Br}}$ 3 A : B : C 3 : 2 : 2
    cyclopentane 1    
    2,2-dimethyloxetane 3 A : B : C 2 : 2 : 6 (or 1 : 1 : 3)
    1,3-cyclohexadiene 3 A : B : C 2 : 4 : 2 (or 1 : 2 : 1)
    1-methoxy-2-butanone 4 A : B : C : D 3 : 2 : 2 : 3
    3-methylpyridine 5 A : B : C : D : E 3 : 1 : 1 : 1 : 1

    If all protons in all organic molecules had the same resonance frequency in an external magnetic field of a given strength, the information in the previous paragraph would be interesting from a theoretical standpoint, but would not be terribly useful to organic chemists. Fortunately for us, however, resonance frequencies are not uniform for all protons in a molecule. In an external magnetic field of a given strength, protons in different locations in a molecule have different resonance frequencies, because they are in non-identical electronic environments.  In methyl acetate, for example, there are two ‘sets’ of protons. The three protons labeled Ha have a different - and easily distinguishable – resonance frequency than the three Hb protons, because the two sets of protons are in non-identical environments: they are, in other words, chemically nonequivalent. 

    image006.png

    On the other hand, the three Ha protons are all in the same electronic environment, and are chemically equivalent to one another.  They have identical resonance frequencies. The same can be said for the three Hb protons.

    The ability to recognize chemical equivalancy and nonequivalency among atoms in a molecule will be central to understanding NMR.  In each of the molecules below, all protons are chemically equivalent, and therefore will have the same resonance frequency in an NMR experiment. 

    image008.png

    You might expect that the equitorial and axial hydrogens in cyclohexane would be non-equivalent, and would have different resonance frequencies.  In fact, an axial hydrogen is in a different electronic environment than an equitorial hydrogen.  Remember, though, that the molecule rotates rapidly between its two chair conformations, meaning that any given hydrogen is rapidly moving back and forth between equitorial and axial positions.  It turns out that, except at extremely low temperatures, this rotational motion occurs on a time scale that is much faster than the time scale of an NMR experiment. 

    image010.png

    In this sense, NMR is like a camera that takes photographs of a rapidly moving object with a slow shutter speed - the result is a blurred image.  In NMR terms, this means that all 12 protons in cyclohexane are equivalent.

    Each the molecules in the next figure contains two sets of protons, just like our previous example of methyl acetate, and again in each case the resonance frequency of the Ha protons will be different from that of the Hb protons. 

    image012.png

    Notice how the symmetry of para-xylene results in there being only two different sets of protons.

    Most organic molecules have several sets of protons in different chemical environments, and each set, in theory, will have a different resonance frequency in 1H-NMR spectroscopy.

    image014.png

     

    image016.png

    When stereochemistry is taken into account, the issue of  equivalence vs nonequivalence in NMR starts to get a little more complicated.  It should be fairly intuitive that hydrogens on different sides of asymmetric ring structures and double bonds are in different electronic environments, and thus are non-equivalent and have different resonance frequencies. In the alkene and cyclohexene structures below, for example, Ha is trans to the chlorine substituent, while Hb is cis to chlorine.

    image018.png

    What is not so intuitive is that diastereotopic hydrogens (section 3.10) on chiral molecules are also non-equivalent:

    image020.png

    However, enantiotopic and homotopic hydrogens are chemically equivalent.

    image022.png

    Example 13.8.1

    How many different sets of protons do the following molecules contain? (count diastereotopic protons as non-equivalent).

    image024.png

    Solution

    Exercise

    Questions

    Q13.8.1

    How many non-equivalent hydrogen are in the following molecules; how many different signals will you see in a H1 NMR spectrum.

    A. CH3CH2CH2Br

    B. CH3OCH2C(CH3)3

    C. Ethyl Benzene

    D. 2-methyl-1-hexene

    Solutions

    S13.8.1

    A. 3; B. 3; C. 5; D. 7

    Contributors