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high frequency of vibration =
high energy
strong bonds =
high frequency
high atomic mass =
low frequency
highest frequency =
highest bond strength, lowest mass
IR spec > 3000 cm^-1
unsaturated C-H bonds, sp and sp2 hydridized
IR spec < 3000 cm^-1
saturated C-H bonds, sp3
alcohols appear as a
smooth absobance peak, and have NO carbonyl absorbance ~1760-1670 cm^-1
carboxylic acids appear as
a “jagged peak” due to more interferance and has a carbonyl peak
an NMR singlet
has no “neighbors”
an NMR singlet that integrates at 3 is
usually an isolated methyl group
exchangeable protons frrom solvent
protons directly attached to EN atoms (usually N or O) cause broadened or disappearing peaks with inaccurate integrations
aromatic protons and solvents
cause unexplected NMR splits
C13 Chemical shifts tell us
how many types of C
what type of chemical environment
confirms NMR