3 techniques to provide evidence of the organic molecue you have made
IR, MS, and NMR
IR
tells you what functional groups are present
MS
tells you molecular weight, components of a mxture, isotopic distributions, and select functional groups
NMR
tells you skeletal structure and select functional groups
IR uses this type of radiation
electromagnetic (light)
changes in vibrational motions of a molecule are caused by?
absorption of IR light
bonds can ?
stretch or vibrate
types of stretching (motion)
symetric and asymetric
types of vibration
scissor, rock, twist, and wag
bond strength and atom mass affect?
bond absorption
Transmittance
when wavelength goes through and finds a bond to absorb, it will be low or high depending on the strength
low transmittance
high absorption, strong peak
high transmittance
low absorption, weak peak
Sharp Peaks (represent?)
specific bond vibration (pure sample) (ex: carbonyls, nitriles, alkynes) (shown by?)
broad peaks (represent?)
H-bonds or mixtures of secondary structures due to distribution of bond strength
Group frequencies or Diagnostic region
(1500/cm<) include H-C/O/N, x triple bound to x, x=x=, and x=x (x= c/n/o),
Fingerprint region
(1500/cm>) include C-X (X=C/N/O)
Strong peaks
low, close to 0%
Weak peaks
high, close to 100%
saturated
only single bonds (no pi bonds), absorbs higher wave numbers, higher frequencies
conjugated
alternating, long chain of bonds (x2, x1, x2, x1), absorbs lower wave numbers, lower frequencies (due to resonance)
Functional groups of interest
OH, COOH, carbonyls, CC and CN x3 bonds, C-H bonds and their hybridization
wording for IR report
disappearance/appearance of [strength] peaks at [wavenumber range] of [functional group]
wavenumber is proportional to
frequency