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Ochem Ch14
| Absorption location | Functional group |
|---|---|
| IR absorption locations (Cm`1): 2850-2975 | Alkane (C-H) |
| IR absorption locations (Cm`1): 3200-3600 | Alcohol (O-H) |
| IR absorption locations (Cm`1): 1600-1700; 30-3100 | Alkene C=C) (C=C-H) |
| IR absorption locations (Cm`1): 2100-2200; 3300 | Alkyne (C-triple-C); (C-triple-C-H) |
| IR absorption locations (Cm`1): 2200-2300 | Nitrile (C-triple-N) |
| IR absorption locations (Cm`1): 3350-3500 | Amines (N-H) secondary |
| IR absorption locations (Cm`1): 1650-2000 | Aromatics, benzene |
| IR absorption locations (Cm`1): 1720-1740; 1715; 1735-1750; 1700-1725 | Carbonyls (C=O), Aldehyde (CHO), Ketone (RCOR), Ester (RCOOR), Acid (RCOOH) |
| (NMR) Nuclear Magnetic Resonance spectroscopy | uses radio wave frequencies to demonstrate specific arrangements of all carbon and hydrogens atoms in a compound |
| IR spectroscopy | uses infrared frequencies to demonstrate presence of functional groups in a compound |
| UV-vis | Uses visible to ultraviolet light to find any conjugated Pi systems present in the compound |
| Carboxylic acid | 2200-3600 |
| Anhydride | 2750-2850 |
| loss of methyl group in mass spectrometry? | -15 |
| loss of ethyl group in mass spectrometry? | -29 |
| loss of propyl group in mass spectrometry? | -43 |
| loss of Butyl mass spectrometry? | -57 |
| loss of water from an alcohol | -18 |
| m-x | Mclafferty rearrangement (x-1) (ketone or aldehyde (of x is even number |