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  • 13C NMR Correlations

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    Дьего Фернандо
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    This document lists common 1H NMR chemical shift ranges for various structural types of carbon atoms. It provides the typical chemical shift ranges in parts per million (ppm) for saturated hydrocarbons like CH3, CH2, and CH groups, as well as carbon atoms bonded to heteroatoms such as oxygen, nitrogen, halogens, and aromatic groups. The chemical shifts can be used to determine the type of carbon atom environment present in organic compounds analyzed by 1H NMR spectroscopy.

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    NMR

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    13C Nmr Correlations

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    This document lists common 1H NMR chemical shift ranges for various structural types of carbon atoms. It provides the typical chemical shift ranges in parts per million (ppm) for saturated hydrocarbons like CH3, CH2, and CH groups, as well as carbon atoms bonded to heteroatoms such as oxygen, nitrogen, halogens, and aromatic groups. The chemical shifts can be used to determine the type of carbon atom environment present in organic compounds analyzed by 1H NMR spectroscopy.

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    15 views1 page

    13C NMR Correlations

    Uploaded by

    Дьего Фернандо
    This document lists common 1H NMR chemical shift ranges for various structural types of carbon atoms. It provides the typical chemical shift ranges in parts per million (ppm) for saturated hydrocarbons like CH3, CH2, and CH groups, as well as carbon atoms bonded to heteroatoms such as oxygen, nitrogen, halogens, and aromatic groups. The chemical shifts can be used to determine the type of carbon atom environment present in organic compounds analyzed by 1H NMR spectroscopy.

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    SELECTED 1 3C NMR CORRELATIONS

    structural type

    chemical shift range (ppm)

    cyclopropyl

    - 10 - 10

    CH3 (saturated)

    10 - 30

    CH2 (saturated)

    10 - 55

    CH (saturated)

    25 - 55

    (saturated)

    30 - 55

    C I

    - 10 - 45

    C Br

    25 - 65

    C Cl

    35 - 80

    O
    C

    20 - 50

    C N

    30 - 70

    C O

    40 - 80

    C C

    65 - 85
    100 - 150

    C C

    110 - 125

    C N

    110 - 160

    ArH
    O
    C
    O
    C

    OH

    O
    C
    O
    C

    155 - 185

    190 - 210

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