3.15 NMR spectroscopy Flashcards
What are the 2 main types of NMR?
- C13 NMR
- H (proton) NMR
In C13 NMR spectrum, how many signals (peaks) are there for each set of equivalent C atoms?
In C13 NMR spectrum, there is one signal (peak) for each set of equivalent C atoms
How many signals (peaks) does propanal have in the C13 NMR spectrum?
3 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does ethyl ethanoate have in the C13 NMR spectrum?
4 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does 2-methylbutane have in the C13 NMR spectrum?
4 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does ethnoic anhydride have in the C13 NMR spectrum?
2 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does 2-chloro-2-methylpropane have in the C13 NMR spectrum?
2 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does 4-nitro-1-methylbenzene have in the C13 NMR spectrum?
5 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does 1,2-dinitrobenzene have in the C13 NMR spectrum?
3 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does 1,3-dinitrobenzene have in the C13 NMR spectrum?
4 peaks
see page 1 in the chemrevise revision guide
How many signals (peaks) does 1,4-dinitrobenzene have in the C13 NMR spectrum?
2 peaks
see page 1 in the chemrevise revision guide
How many signals does ethanol have in the H (proton) NMR spectrum?
3 signals
Ethanol has 3 groups of different hydrogen atoms.
(see page 1 in the chemrevise revision guide)
What is the intensity (integration value) of each signal proportional to in the H (proton) NMR spectrum?
The intensity (integration value) of each signal is proportional to the number of equivalent H atoms it represents.
(see page 1 in the chemrevise revision guide)
What is the ratio of the equivalent H’s in 2-methylbutane in H (proton) NMR?
4 sets of equivalent H’s
6:1:2:3
(see page 1 in the chemrevise revision guide)
What is the ratio of the equivalent H’s in propanone in H (proton) NMR?
1 signal
see page 1 in the chemrevise revision guide
What is the ratio of the equivalent H’s in methyl propanoate in H (proton) NMR?
3 set of equivalent H’s
3:2:3
(see page 1 in the chemrevise revision guide)
What is the ratio of the equivalent H’s in 2-bromobutane in H (proton) NMR?
4 sets of equivalent H;s
3:1:2:3
(see page 1 in the chemrevise revision guide)
What is the ratio of the equivalent H’s in 1,1-dimethylethyl propanoate in H (proton) NMR?
3 sets of equivalent H’s
3:2:9
(see page 1 in the chemrevise revision guide)
What is the ratio of the equivalent H’s in prop-1-ene in H (proton) NMR?
3 sets of equivalent H’s
3:1:2
(see page 1 in the chemrevise revision guide)
Why are samples dissolved in solvents without any 1H atoms for the H NMR? Give two examples of these solvents.
This means that in the H NMR the solvent will not give any peaks.
CCL4
CDCl3
Why is a small amount of TMS (tetramethylsilane) added to the sample in both C13 and H NMR spectroscopy?
To calibrate the sprectrum.
TMS is used because:
- its signal is away from all the others
- it only gives one signal
- it is non-toxic
- it is inert
- it has a low boiling point and so can be removed from sample easily
What does the squiggle (that kinda looks like partial charge symbol but I can write it on here) mean? (see page 2 in the chemrevise revision guide for the symbol)
It is a measure in parts per million (ppm) is a relative scale of how far the frequency of the proton signal has shifted away from that for TMS.
Draw the displayed formula for tetramethylsilane.
(see page 2 in the chemrevise revision guide)
Read bottom half of page 2 in the chemrevise revision guide.
Understand?
Read bottom half of page 3 in the chemrevise revision guide.
Understand?
For a singlet signal:
- What does it look like on the spectra?
- How many split number of peaks?
- The number of neighbouring inequivalent H atoms?
- The relative size?
(see page 4 in the chemrevise revision guide)
For a doublet signal:
- What does it look like on the spectra?
- How many split number of peaks?
- The number of neighbouring inequivalent H atoms?
- The relative size?
(see page 4 in the chemrevise revision guide)
For a triplet signal:
- What does it look like on the spectra?
- How many split number of peaks?
- The number of neighbouring inequivalent H atoms?
- The relative size?
(see page 4 in the chemrevise revision guide)
For a quartet signal:
- What does it look like on the spectra?
- How many split number of peaks?
- The number of neighbouring inequivalent H atoms?
- The relative size?
(see page 4 in the chemrevise revision guide)
Decide the signal peaks in ethyl ethanoate
(see page 4 in the chemrevise revision guide)
Decide the signal peaks in methyl propanoate
(see page 4 in the chemrevise revision guide)
Decide the signal peaks in ethanol
(see page 4 in the chemrevise revision guide)
Read all of page 5 in the chemrevise revision guide
Understand? Make some flashcards on it.
If you see a triplet + triplet in proton NMR, what does this tell you?
(see my own drawing on page 3 in the chemrevise revision guide)
If you see a triplet + quartet in proton NMR, what does this tell you?
(see my own drawing on page 3 in the chemrevise revision guide)