common 1 h nmr patterns 1. triplet (3h) + quartet (2h) -ch 2 ch 3 2. doublet (1h) + doublet (1h)...
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![Page 1: Common 1 H NMR Patterns 1. triplet (3H) + quartet (2H) -CH 2 CH 3 2. doublet (1H) + doublet (1H) -CH-CH- 3. large singlet (9H) t-butyl group 4. singlet](https://reader035.vdocuments.us/reader035/viewer/2022081415/56649e8e5503460f94b9132a/html5/thumbnails/1.jpg)
Common 1H NMR Patterns 1. triplet (3H) + quartet (2H) -CH2CH3
2. doublet (1H) + doublet (1H) -CH-CH-
3. large singlet (9H) t-butyl group
4. singlet 3.5 ppm (3H) -OCH3 group
5. large double (6H) + muliplet (1H) isopropyl
6. singlet 2.1 ppm (3H) methyl ketone
O
CH3
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Common 1H NMR Patterns
7. multiplet ~7.2 ppm (5H) aromatic ring, monosubstituted
8. multiplet ~7.2 ppm (4H) aromatic ring, disubstituted
9. broad singlet, variable -OH or –NH chemical shift (H on heteratom)
![Page 3: Common 1 H NMR Patterns 1. triplet (3H) + quartet (2H) -CH 2 CH 3 2. doublet (1H) + doublet (1H) -CH-CH- 3. large singlet (9H) t-butyl group 4. singlet](https://reader035.vdocuments.us/reader035/viewer/2022081415/56649e8e5503460f94b9132a/html5/thumbnails/3.jpg)
Solving NMR Problems
1. Check the molecular formula and degree of unsaturation. How many rings/double bonds?
2. Make sure that the integration adds up to the total number of H’s in the formula.
3. Are there any signals in the double bond region?
4. Check each signal and write down a possible sub-structure for each one.
5. Try to put the sub-structures together to find the structure of the compound.
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Proton NMR Spectrum: C9H12
D. of Unsat = 4aromatic,disubst.
H
HH
H
CH3
CH3-CH2-
CH3-CH2-
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1H NMR Spectrum: C4H7O2Br
Br O
O
t2H
t2H
s3H
O CH3
5.0 4.0 3.0 2.0 1.0 0
H H
HH
CC
O
C Br
![Page 6: Common 1 H NMR Patterns 1. triplet (3H) + quartet (2H) -CH 2 CH 3 2. doublet (1H) + doublet (1H) -CH-CH- 3. large singlet (9H) t-butyl group 4. singlet](https://reader035.vdocuments.us/reader035/viewer/2022081415/56649e8e5503460f94b9132a/html5/thumbnails/6.jpg)
Electronegative Substituents: Shift Left
HH33C—CHC—CH22—CH—CH33 OO22N—CHN—CH22—CH—CH22—CH—CH33
0.90.9 0.90.9 1.31.3 1.01.0 4.3 2.02.0
– CHCH33ClCl 3.1 3.1 (one Cl) (one Cl)
– CHCH22ClCl22 5.3 5.3 (two (two
Cl’s)Cl’s)
– CHClCHCl33 7.3 7.3 (three Cl’s) (three Cl’s)
Effect is cumulativeEffect is cumulative
Propane:Propane: heteroatomregion
smalleffect
~noeffect
![Page 7: Common 1 H NMR Patterns 1. triplet (3H) + quartet (2H) -CH 2 CH 3 2. doublet (1H) + doublet (1H) -CH-CH- 3. large singlet (9H) t-butyl group 4. singlet](https://reader035.vdocuments.us/reader035/viewer/2022081415/56649e8e5503460f94b9132a/html5/thumbnails/7.jpg)
Hydrogens on Heteroatoms
Type of protonType of protonChemical shift (ppm)Chemical shift (ppm)
1-31-3 HH NRNR
0.5-50.5-5 HH OROR
6-86-8 HH OArOAr
10-1310-13 CC
OO
HOHO
Chemical shifts for protons on heteroatoms are variable, Chemical shifts for protons on heteroatoms are variable, and signals are often and signals are often broadbroad (not generally useful). (not generally useful).
may beuseful
farleft
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13C NMR Spectroscopy
• Carbon-13: only carbon isotope with a nuclear spin
natural abundance of 13C is only 1.1%
(99% of carbon atoms are 12C, with no NMR signal)
• All signals are obtained simultaneously using a broad pulse of energy. The resulting “mass signal” changed into an NMR spectrum mathematically using the operation of Fourier transform (FT-NMR)
• Frequent repeated pulses give many data sets that are averaged to eliminate noise
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13C signals go from 0 to 240 ppm. 13C signals: always sharp singlets.
(wider range than in 1H NMR) (1H signals: broad multiplets)
These two facts mean that in carbon-13 NMR, each separate signal is usually visible, and you can accurately count the number of different carbons in the molecule.
Chemical shift affected by electronegativity of nearby atoms:
alkane-like range: 0 – 40 ppm (R-CH2-R)
heteroatom range: 50 – 100 ppm (O-CH2-R)
double bond range: 100 – 220 ppm (sp2 carbons)
No signal overlap!No signal overlap!
13C NMR Spectroscopy
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NMR: Scanning for All Nuclei
An instrument can only examine one area at a time.
To see both proton and C-13 nuclei, a very wide region would have to be scanned.
1H area is small
13C area is much wider
![Page 11: Common 1 H NMR Patterns 1. triplet (3H) + quartet (2H) -CH 2 CH 3 2. doublet (1H) + doublet (1H) -CH-CH- 3. large singlet (9H) t-butyl group 4. singlet](https://reader035.vdocuments.us/reader035/viewer/2022081415/56649e8e5503460f94b9132a/html5/thumbnails/11.jpg)
Why does 13C NMR give singlets?13C is only 1.1% natural abundant, so most carbons are 12C,
and give no NMR signal.
No splitting seen with carbon, because carbons next to the 13C are likely to be carbon-12:
Sample of 1-Propanol:
12CH3-12CH2-12CH2-OH 12CH3-12CH2-12CH2-OH
12CH3-13CH2-12CH2-OH 13CH3-12CH2-12CH2-OH
12CH3-12CH2-12CH2-OH 12CH3-12CH2-12CH2-OH
12CH3-13CH2-13CH2-OH 12CH3-12CH2-12CH2-OH
![Page 12: Common 1 H NMR Patterns 1. triplet (3H) + quartet (2H) -CH 2 CH 3 2. doublet (1H) + doublet (1H) -CH-CH- 3. large singlet (9H) t-butyl group 4. singlet](https://reader035.vdocuments.us/reader035/viewer/2022081415/56649e8e5503460f94b9132a/html5/thumbnails/12.jpg)
NMR: Number of Signals for 13C NMR
How many signals should appear in the carbon-13 NMR spectrum for these compounds?
In theory: 10 4
Signals actually resolved: 10 4
O
octane
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13C NMR ExampleNote the wide spectral width and the sharp singlets in the
spectrum below.
Also note that there is no integration with 13C NMR.
![Page 14: Common 1 H NMR Patterns 1. triplet (3H) + quartet (2H) -CH 2 CH 3 2. doublet (1H) + doublet (1H) -CH-CH- 3. large singlet (9H) t-butyl group 4. singlet](https://reader035.vdocuments.us/reader035/viewer/2022081415/56649e8e5503460f94b9132a/html5/thumbnails/14.jpg)
13C NMR: smaller signal to noise ratio
Noise
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13C NMR Spectrum: C5H11Cl
Cl
Cl
Cl
5 signals
5 signals
3 signals
D. of Unsat = 0
five 13Csignals
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O
C
13C NMR Spectrum: C4H7O2Br
200 150 100 50 0
CDCl3
double bond region
D. of Unsat = 1