1. Practice problems on the NMR of amino acids Test your ability to correlate NMR spectra with structure by trying the following problems. Use the correlation tables, the relative sizes of the signal, electronegativity and the number of signals and logic to connect the structures with the spectra.

2. These are the signals of protons (1H NMR). We think of the position (in ppm) of the NMR signals in the same way we viewed the frequency of IR signals. The 1H NMR signals are characteristic of certain types of protons in molecules NMR units are ppm (parts per million). We discuss where this ppm unit comes from in class.

3. These are the position of the signals of carbon atoms (13C) in ppm. We think of the position of a NMR signal in ppm in the same way we viewed the frequency of IR signals. The 13C NMR signals are characteristic of certain types of carbon atoms in molecules.

4. 024681012 PPM NH 2 CH 3 CH 3 O OH H H valine The 1H NMR of the amino acid valine is given below. Assign the protons of valine to the signals (a, b, c, d and e) in the NMR spectrum. a b c d d The answer is at the end of the ppt

5. Leucine and isoleucine are isomers. Two 13C NMR spectra A and B are shown below. One is leucine the other is isoleucine. Which is which? 020406080100120140160180 PPM 020406080100120140160180 PPM A B

6. The 13C NMR spectrum of valine and leucine are shown. Which is valine and which is leucine? 020406080100120140160180 PPM valine leucine 020406080100120140160180 PPM signal

7. 020406080100120140160180 PPM 020406080100120140160180 PPM Two signals Very close together tyrosine phenylalanine The 13C NMR spectrum of phenylalanine and tyrosine (both possess aromatic rings) are shown. Which is phenylalanine and which is tyrosine?

8. 024681012 PPM NH 2 CH 3 CH 3 O OH H H valine The 1H NMR of the amino acid valine is given below. Assign the protons of valine to the signals in the NMR spectrum. a b c d e a b a d e c

9. Leucine and isoleucine are isomers. Two 13C NMR spectra A and B are shown below. One is leucine the other is isoleucine. Which is which? 020406080100120140160180 PPM 020406080100120140160180 PPM A B Two equivalent carbon atoms (the two CH 3 groups) All the carbon atoms are unique

10. The 13C NMR spectrum of valine and leucine are shown. Which is valine and which is leucine? 020406080100120140160180 PPM valine leucine 020406080100120140160180 PPM signal An essential difference between valine and leucine is that leucine has one more carbon atom. In the bottom spectrum the CH 2 carbon atom of leucine is just to the left of the CH 3 carbon atom.

11. 020406080100120140160180 PPM tyrosine 020406080100120140160180 PPM Two signals Very close together phenylalanine The 13C NMR spectrum of phenylalanine and tyrosine (both possess aromatic rings) are shown. Which is phenylalanine and which is tyrosine? The most significant difference between the two structures is the OH on the benzene ring of the tyrosine. This substituent will cause the carbons of the benzene ring of tyrosine to be much more different chemically than those of phenylalanine. This difference will also be reflected in the differences in the separation of the carbon signal in the NMR