spectroscopy nuclear magnetic resonance. the nmr spectra included in this presentation have been...
TRANSCRIPT
![Page 1: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/1.jpg)
Spectroscopy
nuclear magnetic resonance
![Page 2: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/2.jpg)
The nmr spectra included in this presentation have been taken from the SDBS database with permission.
National Institute of Advanced Industrial Science and Technology
(http://www.aist.go.jp/RIODB/SDBS/menu-e.html)
![Page 3: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/3.jpg)
Nuclear Magnetic Resonance (nmr)
-the nuclei of some atoms spin: 1H, 13C, 19F, …
-the nuclei of many atoms do not spin: 2H, 12C, 16O, …
-moving charged particles generate a magnetic field ()
-when placed between the poles of a powerful magnet, spinning nuclei will align with or against the applied field creating an energy difference. Using a fixed radio frequency, the magnetic field is changed until the ΔE = EEM. When the energies match, the nuclei can change spin states (resonate) and give off a magnetic signal.
ΔE
![Page 4: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/4.jpg)
magnetic field = 14,092 gauss
for 1H v = 60,000,000 Hz (60 MHz)
nmr spectrum
inte
nsit
y
10 9 8 7 6 5 4 3 2 1 0
chemical shift (ppm)
magnetic field
![Page 5: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/5.jpg)
1H nuclei are shielded by the magnetic field produced by the surrounding electrons. The higher the electron density around the nucleus, the higher the magnetic field required to cause resonance.
CH3Cl versus CH4
lower electron higher electrondensity densityresonate at lower resonate at higherapplied field applied field
CHCCl3 ??
![Page 6: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/6.jpg)
Information from 1H-nmr spectra:
1. Number of signals: How many different types of hydrogens in the molecule.
2. Position of signals (chemical shift): What types of hydrogens.
3. Relative areas under signals (integration): How many hydrogens of each type.
4. Splitting pattern: How many neighboring hydrogens.
![Page 7: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/7.jpg)
1. Number of signals: How many different types of hydrogens in the molecule.
Magnetically equivalent hydrogens resonate at the same applied field.
Magnetically equivalent hydrogens are also chemically equivalent.
# of signals? CH4 CH3CH3
![Page 8: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/8.jpg)
CCH3H3C
CH3C CH3
CH3
CH3
oneone
one
two
number of signals?
![Page 9: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/9.jpg)
H3C C
CH3
Br
CH3 CH3CH2-Br
CH3CH2CH2-Br CH3CHCH3
Cl
onetwo
threetwo
![Page 10: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/10.jpg)
CH3
CH2Cl
CH3CHCH2CH3
BrCl-CH2CH2CH2-Cl
four two
three
![Page 11: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/11.jpg)
2. Position of signals (chemical shift): what types of hydrogens.
primary 0.9 ppmsecondary 1.3tertiary1.5aromatic 6-8.5allyl 1.7benzyl 2.2-3chlorides 3-4 H-C-Clbromides 2.5-4 H-C-Briodides2-4 H-C-Ialcohols 3.4-4 H-C-Oalcohols 1-5.5 H-O- (variable)
Note: combinations may greatly influence chemical shifts. For example, the benzyl hydrogens in benzyl chloride are shifted to lower field by the chlorine and resonate at 4.5 ppm.
![Page 12: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/12.jpg)
reference compound = tetramethylsilane (CH3)4Si @ 0.0 ppm
remember: magnetic field
chemical shift
convention: let most upfield signal = a, next most upfield = b, etc.
… c b a tms
![Page 13: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/13.jpg)
toluene
ab
CH3
ab
![Page 14: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/14.jpg)
CCH3H3C
CH3C CH3
CH3
CH3
a a
a b
a
a
chemical shifts
![Page 15: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/15.jpg)
H3C C
CH3
Br
CH3 CH3CH2-Br
CH3CH2CH2-Br CH3CHCH3
Cl
a a
a a b
a b c a b a
![Page 16: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/16.jpg)
CH3
CH2Cl
CH3CHCH2CH3
BrCl-CH2CH2CH2-Cl
b d c a b a b
a
b
c
![Page 17: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/17.jpg)
3. Integration (relative areas under each signal): how many hydrogens of each type.
a b cCH3CH2CH2Br a 3H a : b : c = 3 : 2 : 2
b 2Hc 2H
a b aCH3CHCH3 a 6H a : b = 6 : 1
Cl b 1H
![Page 18: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/18.jpg)
CCH3H3C
CH3C CH3
CH3
CH3
a a
a b
a
a
a 12 H a 12 H
a 6 H
a 6 Hb 4 H
integration
![Page 19: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/19.jpg)
H3C C
CH3
Br
CH3 CH3CH2-Br
CH3CH2CH2-Br CH3CHCH3
Cl
a a
a a b
a b c a b a
a 9 H
a 3 Hb 2 H
a 3 Hb 2 Hc 2 H
a 6 Hb 1 H
![Page 20: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/20.jpg)
CH3
CH2Cl
CH3CHCH2CH3
BrCl-CH2CH2CH2-Cl
b d c a b a b
a
b
c
a 3 Hb 3 Hc 2 Hd 1 H
a 2 Hb 4 H
a 3 Hb 2 Hc 4 H
![Page 21: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/21.jpg)
Integration: measure the height of each “step” in the integration and then calculate the lowest whole number ratio: a:b:c = 24 mm : 16 mm : 32 mm = 1.5 : 1.0 : 2.0 3H : 2H : 4H
abc
![Page 22: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/22.jpg)
If the formula is known ( C8H9OF ), add up all of the “steps” and divide by the number of hydrogens = (24 + 16 + 32 mm) / 9H = 8.0 mm / Hydrogen. a = 24 mm / 8.0 mm/H 3 H; b = 16 mm/8.0 mm/H 2H; c = 32 mm/8.0 mm/H 4H.
![Page 23: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/23.jpg)
4. Splitting pattern: how many neighboring hydrogens.
In general, n-equivalent neighboring hydrogens will split a 1H signal into an ( n + 1 ) Pascal pattern.
“neighboring” – no more than three bonds away
n n + 1 Pascal pattern:
0 1 1singlet
1 2 1 1doublet
2 3 1 2 1triplet
3 4 1 3 3 1quartet
4 5 1 4 6 4 1quintet
![Page 24: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/24.jpg)
note: n must be equivalent neighboring hydrogens to give rise to a Pascal splitting pattern. If the neighbors are not equivalent, then you will see a complex pattern (aka complex multiplet).
note: the alcohol hydrogen –OH usually does not split neighboring hydrogen signals nor is it split. Normally a singlet of integration 1 between 1 – 5.5 ppm (variable).
![Page 25: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/25.jpg)
CCH3H3C
CH3C CH3
CH3
CH3
a a
a b
a
a
a 12 H singlet a 12 H singlet
a 6 H singlet
a 6 H singletb 4 H singlet
splitting pattern?
![Page 26: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/26.jpg)
H3C C
CH3
Br
CH3 CH3CH2-Br
CH3CH2CH2-Br CH3CHCH3
Cl
a a
a a b
a b c a b a
a 9 H singlet
a 3 H tripletb 2 H quartet
a 3 H tripletb 2 H complexc 2 H triplet
a 6 H doubletb 1 H septet
![Page 27: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/27.jpg)
CH3
CH2Cl
CH3CHCH2CH3
BrCl-CH2CH2CH2-Cl
b d c a b a b
a
b
c
a 3 H tripletb 3 H doubletc 2 H complexd 1 H complex
a 2 H quintetb 4 H triplet
a 3 H singletb 2 H singletc 4 H ~singlet
CH3CH2-OH
a b c
a 3 H tripletb 2 H quartetc 1 H singlet
![Page 28: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/28.jpg)
Information from 1H-nmr spectra:
1. Number of signals: How many different types of hydrogens in the molecule.
2. Position of signals (chemical shift): What types of hydrogens.
3. Relative areas under signals (integration): How many hydrogens of each type.
4. Splitting pattern: How many neighboring hydrogens.
![Page 29: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/29.jpg)
cyclohexane
a singlet 12H
![Page 30: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/30.jpg)
2,3-dimethyl-2-butene
CCH3
CH3C
H3C
CH3
a singlet 12H
![Page 31: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/31.jpg)
benzene
a singlet 6H
![Page 32: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/32.jpg)
p-xyleneH3C CH3
a ab
a singlet 6H
b singlet 4H
![Page 33: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/33.jpg)
tert-butyl bromide
C CH3H3C
Br
CH3 a singlet 9H
![Page 34: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/34.jpg)
ethyl bromide
a bCH3CH2-Br
a triplet 3Hb quartet 2H
![Page 35: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/35.jpg)
1-bromopropane
a b c
CH3CH2CH2-Br
a triplet 3Hb complex 2Hc triplet 3H
![Page 36: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/36.jpg)
isopropyl chloride
a b aCH3CHCH3
Cl
a doublet 6Hb septet 1H
![Page 37: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/37.jpg)
2-bromobutane b d c aCH3CHCH2CH3
Br
a triplet 3Hb doublet 3Hc complex 2H d complex 1H
![Page 38: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/38.jpg)
o-methylbenzyl chloride
CH3
CH2Cl
ab
c a singlet 3Hb singlet 2Hc ~ singlet 4H
![Page 39: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/39.jpg)
ethanol
a c b
CH3CH2-OH
a triplet 3Hb singlet 1Hc quartet 2H
![Page 40: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/40.jpg)
ethylbenzeneCH2CH3
c b a
a triplet 3Hb quartet 2Hc ~singlet 5H
![Page 41: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/41.jpg)
p-diethylbenzenea b c b a
a triplet 6Hb quartet 4Hc singlet 4H
CH3CH2 CH2CH3
![Page 42: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/42.jpg)
m-diethylbenzene
![Page 43: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/43.jpg)
o-diethylbenzene
![Page 44: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/44.jpg)
2-bromo-2-methylbutane
b CH3
b CH3CCH2CH3 a Br c
a triplet 3Hb singlet 6Hc quartet 2H b & c overlap
![Page 45: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/45.jpg)
di-n-propylether
a b c c b aCH3CH2CH2-O-CH2CH2CH3
a triplet 6Hb complex 4Hc triplet 4H
![Page 46: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/46.jpg)
1-propanol
a b d cCH3CH2CH2-OH
a triplet 3Hb complex 2Hc singlet 1Hd triplet 2H
![Page 47: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/47.jpg)
C11H16
5H2H
9Ha 9H = 3CH3, no neighbors
c 5H = monosubstituted benzene
b 2H, no neighbors
CH2
CH3
C
CH3
CH3
c b a
neopentylbenzene
![Page 48: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/48.jpg)
C4H8Br2
6H
2H
a = 6H, two CH3 with no neighbors
(CH3)2C—
b = CH2, no neighbors & shifted downfield due to Br
Br
C CH2H3C
CH3
Br
![Page 49: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/49.jpg)
C7H8O
5H
2H
1H
c = monosubst. benzene
b = CH2
c = OHH2COH
![Page 50: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/50.jpg)
C4H9Br
a doublet 1.04 ppm 6Hb complex 1.95 ppm 1Hc doublet 3.33 ppm 2H
a = two equivalent CH3’s with one neighboring H (b?)
c = CH2 with one neighbor H (also b)
a CH3 a 6H doubletCH3CHCH2Br b 1H complex a b c c 2H doublet
![Page 51: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/51.jpg)
C10H13Cl
a singlet 1.57 ppm 6Hb singlet 3.07 ppm 2Hc singlet 7.27 ppm 5H
a = two-equilalent CH3’s with no neighbors
c = monosubstituted benzene ring
b = CH2
CH2 C CH3
Cl
CH3
abc
a singlet 6Hb singlet 2Hc singlet 5H
![Page 52: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/52.jpg)
13C – nmr 13C ~ 1.1% of carbons
1) number of signals: how many different types of carbons
2) splitting: number of hydrogens on the carbon
3) chemical shift: hybridization of carbon sp, sp2, sp3
4) chemical shift: evironment
![Page 53: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/53.jpg)
2-bromobutane
a c d b CH3CH2CHCH3
Br
13C-nmr
![Page 54: Spectroscopy nuclear magnetic resonance. The nmr spectra included in this presentation have been taken from the SDBS database with permission. National](https://reader035.vdocuments.mx/reader035/viewer/2022062407/56649dce5503460f94ac2940/html5/thumbnails/54.jpg)
mri
magnetic resonance imaging
This image is copyrighted, and used by kind permission of Joseph Hornak for use in Chem-312.
http://www.cis.rit.edu/htbooks/mri/