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  • Lecture26 2 NMR AminoAcids

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    Emiliano Dal Molin
    4 views12 pages
    The document presents 1H and 13C NMR spectra of several amino acids: glycine, alanine, valine, phenylalanine, and tyrosine. All amino acids share common functional groups including an amino group (NH2), a carboxyl group (COOH or COO-), and a central alpha carbon (Cα) bonded to a hydrogen. The spectra show the characteristic peaks for these common structural features in the amino acids.

    Original Description:

    Description of how to identify aminoacids by means of NMR-1H

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    The document presents 1H and 13C NMR spectra of several amino acids: glycine, alanine, valine, phenylalanine, and tyrosine. All amino acids share common functional groups including an amino group (NH2), a carboxyl group (COOH or COO-), and a central alpha carbon (Cα) bonded to a hydrogen. The spectra show the characteristic peaks for these common structural features in the amino acids.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    4 views12 pages

    Lecture26 2 NMR AminoAcids

    Uploaded by

    Emiliano Dal Molin
    The document presents 1H and 13C NMR spectra of several amino acids: glycine, alanine, valine, phenylalanine, and tyrosine. All amino acids share common functional groups including an amino group (NH2), a carboxyl group (COOH or COO-), and a central alpha carbon (Cα) bonded to a hydrogen. The spectra show the characteristic peaks for these common structural features in the amino acids.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    of 12

    1H and 12C NMR spectra of some amino acids

    HO

    CH2

    NH2

    glycine

    O
    H2N

    HO

    OH

    NH2
    H

    phenylalanine

    CH3

    alanine
    HO

    NH2
    H

    OH
    O

    CH3
    H
    CH3
    NH2

    valine

    CH2

    What are the


    common groups
    of all amino
    acids?

    tyrosine

    OH

    HO

    NH2
    H

    1H NMR

    12

    10

    HO

    6
    PPM

    NH2

    HO

    CH2

    H
    O

    glycine

    NH2

    13 C NMR

    180

    160

    140

    120

    100
    PPM

    80

    60

    40

    20

    1H NMR

    12

    10

    HO

    6
    PPM

    HO

    NH2

    NH2
    H

    H
    O

    CH3

    alanine

    13 C NMR

    180

    160

    140

    120

    100
    PPM

    80

    60

    40

    20

    1H NMR

    12

    10

    HO

    6
    PPM

    NH2

    OH

    H
    O

    CH3
    H
    CH3

    valine

    NH2

    13 C NMR

    180

    160

    140

    120

    100
    PPM

    80

    60

    40

    20

    1H NMR

    12

    10

    HO

    6
    PPM

    NH2

    HO

    H
    O

    NH2

    phenylalanine

    H CH2

    13 C NMR

    180

    160

    140

    120

    100
    PPM

    80

    60

    40

    20

    1H NMR

    12

    10

    HO

    6
    PPM

    NH2

    HO

    NH2

    H
    O

    CH2

    OH

    tyrosine

    13C NMR

    180

    160

    140

    120

    100
    PPM

    80

    60

    40

    20

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