NMR Flashcards
2 types of NMR
- 13C NMR
- 1H (proton) NMR
number of signals = methylpropene
2
number of signals in methylamine
2
number of signals in propene
CH2=CH-CH3
3
calibration
-small quantity of TMS (tetramethylsilane) is added to samples as it produces a single providing internal standard to which other peaks are compared
-only givies one single, non-toxic, inert, low boiling point
NMR
-number of peaks in an NMR spectrum refers to Hydrogen atoms
-area under the peak = proportional to the number of hydrogen atoms
Chemical shift = closer the hydrogen is to an electronegative atom the greater the shift
why compounds absorb radiowaves
-the nucleus of some atoms have a nuclear spins e.g 1H, 13C, 19F etc)
-a nucleus with spin generates a small magnetic field
-there is a small difference in energy ebtween these 2 alignments that corresponds to the energy of radiowaves
how NMR is done
-the sample is usually dissolved in a solvent in a long thin tube and placed inside the machine where it is bombarded with radiowaves in a strong magnetic field
-the stronger the magnetic field the better the resolution of the signals
solvents
-if the solvent contains any 1H atoms then these will appear in the spectrum
-common solvents used = CCl4
chemical shifts
-the chemical shift depends on what other atoms/groups are near the H. The closer the H to electronegative atoms the greater the shift.
scales
-horizontal scale = chemical shift
-vertical axis = intensity of the absorption
signals
-same distance of CH3 = 1 signal. Difference = multiple signals
-in 1 H NMR the area of the signal is proportional to the number of hydrogen atoms is represents
-the height of the signal doesn’t matter but rather the area which the signal covers.
At A-level to indicate the relative intensity of the signals from which the simplest whole number ratio can be calculated:
e.g 1.2 : 1.2 : 1.8 = 2:2: 3
calculating signals
1) Divide all values with the smallest number
2) Find whole number
splitting patterns
-the number of lines in a signal is split into and gives information about neighbouring H atoms
-usually only H atoms on the neighbouring C atom cause splitting
-number of lines = 1 + number of H atoms on adjacent carbon atoms (n+1)
-H atom on OH group in alcohols rarely causes splitting or is split itself.
Doublet = 1:1
Triplet = 1:2:1
Quartllet = 1: 3: 3: 1