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empirical formula calculation
# of element = (percentage)/(molecular mass)
for ratio divide all elements by lowest #
*always assume oxygen unless stated otherwise
IR spectroscopy
gives information about what functional groups are present in a molecule
NMR Spectroscopy
gives information about structure and bonding in a molecule
H NMR signals
- chemical shifts = location of peaks (connectivity of H to elements)
- determine the # of different types of H atoms
H NMR splitting
- N+1, where N is the # of protons on the adjacent carbon
shorter
higher frequencies have a ______ wavelength
stretching frequencies
- bonds to H have higher stretching than those to heavier atoms
- double bonds lower stretching frequency
degrees of unsaturation
(2C+2-H-hal+N)/2
C-H
around 3000cm^-1
O-H
- broad rounded tip, around 3300cm^-1
N-H
- broad sharp tip, around 3300cm^-1
R2-NH
- broad w/ one sharp tip, around 3300cm^-1
N-H2
- broad w/ two sharp tip, around 3300cm^-1
C=O
- around 1710cm^-1
Aldehyde
two C-H signals around 2700cm^-1