INTEGRATION

1. INTEGRATION

2. NMR Spectrum of Phenylacetone RECALL Each different type of proton comes at a different place . You can tell how many different types of hydrogen there are in the molecule. from last time

3. INTEGRATION OF A PEAK Not only does each different type of hydrogen give a distinct peak in the NMR spectrum, but we can also tell the relative numbers of each type of hydrogen by a process called integration. Integration = determination of the area under a peak The area under a peak is proportional to the number of hydrogens that generate the peak.

4. Benzyl Acetate The integral line rises an amount proportional to the number of H in each peak METHOD 1 integral line integral line simplest ratio of the heights 55 : 22 : 33 = 5 : 2 : 3

5. Benzyl Acetate (FT-NMR) Actually : 5 2 3 21.215 / 11.3 = 1.90 33.929 / 11.3 = 3.00 58.117 / 11.3 = 5.14 METHOD 2 assume CH3 33.929 / 3 = 11.3 digital integration Integrals are good to about 10% accuracy. Modern instruments report the integral as a number.

6. DIAMAGNETIC ANISOTROPY SHIELDING BY VALENCE ELECTRONS

7. Bo applied Diamagnetic Anisotropy The applied field induces circulation of the valence electrons - this generates a magnetic field that opposes the applied field. valence electrons shield the nucleus from the full effect of the applied field magnetic field lines B induced (opposes Bo) fields subtract at nucleus

8. SPECTRUM DOWNFIELD UPFIELD Less shielded protons appear here. Highly shielded protons appear here. It takes a higher field to cause resonance. PROTONS DIFFER IN THEIR SHIELDING All different types of protons in a molecule have a different amounts of shielding. They all respond differently to the applied magnetic field and appear at different places in the spectrum. This is why an NMR spectrum contains useful information (different types of protons appear in predictable places).

9. CHEMICAL SHIFT

10. PEAKS ARE MEASURED RELATIVE TO TMS Rather than measure the exact resonance position of a peak, we measure how far downfield it is shifted from TMS. reference compound tetramethylsilane “TMS” Highly shielded protons appear way upfield. TMS Chemists originally thought no other compound would come at a higher field than TMS. shift in Hz downfield n 0

11. g 2p REMEMBER FROM OUR EARLIER DISCUSSION Stronger magnetic fields (Bo) cause the instrument to operate at higher frequencies (n). field strength frequency hn = Bo NMR Field Strength 1H Operating Frequency constants 60 Mhz 1.41 T 2.35 T 100 MHz n = ( K) Bo 7.05 T 300 MHz

12. HIGHER FREQUENCIES GIVE LARGER SHIFTS The shift observed for a given proton in Hz also depends on the frequency of the instrument used. Higher frequencies = larger shifts in Hz. TMS shift in Hz downfield n 0

13. THE CHEMICAL SHIFT The shifts from TMS in Hz are bigger in higher field instruments (300 MHz, 500 MHz) than they are in the lower field instruments (100 MHz, 60 MHz). We can adjust the shift to a field-independent value, the “chemical shift” in the following way: parts per million shift in Hz chemical shift = d = = ppm spectrometer frequency in MHz This division gives a number independent of the instrument used. A particular proton in a given molecule will always come at the same chemical shift (constant value).

14. HERZ EQUIVALENCE OF 1 PPM What does a ppm represent? 1 part per million of n MHz is n Hz 1H Operating Frequency Hz Equivalent of 1 ppm 1 ( ) n MHz = n Hz 60 Mhz 60 Hz 106 100 MHz 100 Hz 300 MHz 300 Hz ppm 3 2 1 0 7 6 5 4 Each ppm unit represents either a 1 ppm change in Bo (magnetic field strength, Tesla) or a 1 ppm change in the precessional frequency (MHz).

15. NMR Correlation Chart -OH -NH DOWNFIELD UPFIELD DESHIELDED SHIELDED CHCl3 , TMS d (ppm) 12 11 10 9 8 7 6 5 4 3 2 1 0 H CH2Ar CH2NR2 CH2S C C-H C=C-CH2 CH2-C- CH2F CH2Cl CH2Br CH2I CH2O CH2NO2 C-CH-C RCOOH RCHO C=C C C-CH2-C C-CH3 O Ranges can be defined for different general types of protons. This chart is general, the next slide is more definite.

16. O O O O O O O APPROXIMATE CHEMICAL SHIFT RANGES (ppm) FOR SELECTED TYPES OF PROTONS R-CH3 0.7 - 1.3 R-N-C-H 2.2 - 2.9 R-C=C-H R-CH2-R 1.2 - 1.4 4.5 - 6.5 R-S-C-H 2.0 - 3.0 R3CH 1.4 - 1.7 I-C-H 2.0 - 4.0 H R-C=C-C-H 1.6 - 2.6 Br-C-H 2.7 - 4.1 6.5 - 8.0 Cl-C-H 3.1 - 4.1 R-C-C-H 2.1 - 2.4 R-C-N-H RO-C-H 3.2 - 3.8 5.0 - 9.0 RO-C-C-H 2.1 - 2.5 HO-C-H 3.2 - 3.8 R-C-H HO-C-C-H 2.1 - 2.5 9.0 - 10.0 R-C-O-C-H 3.5 - 4.8 N C-C-H 2.1 - 3.0 O2N-C-H 4.1 - 4.3 R-C-O-H R-C C-C-H 2.1 - 3.0 11.0 - 12.0 F-C-H 4.2 - 4.8 C-H 2.3 - 2.7 R-N-H 0.5 - 4.0 Ar-N-H 3.0 - 5.0 R-S-H R-O-H 0.5 - 5.0 Ar-O-H 4.0 - 7.0 1.0 - 4.0 R-C C-H 1.7 - 2.7

17. YOU DO NOT NEED TO MEMORIZE THE PREVIOUS CHART IT IS USUALLY SUFFICIENT TO KNOW WHAT TYPES OF HYDROGENS COME IN SELECTED AREAS OF THE NMR CHART C-H where C is attached to an electronega-tive atom CH on C next to pi bonds aliphatic C-H acid COOH aldehyde CHO benzene CH alkene =C-H X=C-C-H X-C-H 12 10 9 7 6 4 3 2 0 MOST SPECTRA CAN BE INTERPRETED WITH A KNOWLEDGE OF WHAT IS SHOWN HERE

18. DESHIELDING AND ANISOTROPY Three major factors account for the resonance positions (on the ppm scale) of most protons. 1. Deshielding by electronegative elements. 2. Anisotropic fields usually due to pi-bonded electrons in the molecule. 3. Deshielding due to hydrogen bonding. We will discuss these factors in the sections that follow.

19. DESHIELDING BY ELECTRONEGATIVE ELEMENTS

20. DESHIELDING BY AN ELECTRONEGATIVE ELEMENT d- d+ Chlorine “deshields” the proton, that is, it takes valence electron density away from carbon, which in turn takes more density from hydrogen deshielding the proton. Cl C H d- d+ electronegative element NMR CHART “deshielded“ protons appear at low field highly shielded protons appear at high field deshielding moves proton resonance to lower field

21. Electronegativity Dependence of Chemical Shift Dependence of the Chemical Shift of CH3X on the Element X Compound CH3X CH3F CH3OH CH3Cl CH3Br CH3I CH4 (CH3)4Si Element X F O Cl Br I H Si Electronegativity of X 4.0 3.5 3.1 2.8 2.5 2.1 1.8 Chemical shift d 4.26 3.40 3.05 2.68 2.16 0.23 0 most deshielded TMS deshielding increases with the electronegativity of atom X

22. Substitution Effects on Chemical Shift most deshielded The effect increases with greater numbers of electronegative atoms. CHCl3 CH2Cl2 CH3Cl 7.27 5.30 3.05 ppm most deshielded -CH2-Br -CH2-CH2Br -CH2-CH2CH2Br 3.30 1.69 1.25 ppm The effect decreases with incresing distance.

23. ANISOTROPIC FIELDS DUE TO THE PRESENCE OF PI BONDS The presence of a nearby pi bond or pi system greatly affects the chemical shift. Benzene rings have the greatest effect.

24. fields add together

25. ANISOTROPIC FIELD IN AN ALKENE protons are deshielded H H Deshielded shifted downfield fields add C=C H H secondary magnetic (anisotropic) field lines Bo

26. ANISOTROPIC FIELD FOR AN ALKYNE H C C H secondary magnetic (anisotropic) field Shielded hydrogens are shielded Bo fields subtract

27. HYDROGEN BONDING

28. HYDROGEN BONDING DESHIELDS PROTONS The chemical shift depends on how much hydrogen bonding is taking place. Alcohols vary in chemical shift from 0.5 ppm (free OH) to about 5.0 ppm (lots of H bonding). Hydrogen bonding lengthens the O-H bond and reduces the valence electron density around the proton - it is deshielded and shifted downfield in the NMR spectrum.

29. SOME MORE EXTREME EXAMPLES Carboxylic acids have strong hydrogen bonding - they form dimers. With carboxylic acids the O-H absorptions are found between 10 and 12 ppm very far downfield. In methyl salicylate, which has strong internal hydrogen bonding, the NMR absortion for O-H is at about 14 ppm, way, way downfield. Notice that a 6-membered ring is formed.