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Organic Functional Groups
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Equations, Electrochem, and Polymers
Organic Functional Groups
46 cards
Cards (92)
Alcohol Structure
R-OH
Aldehyde
Structure
A)
Hydrogen R Group
1
Alkene
Alkyne
Amide
Amine
Aromatics
Carboxylic Acid
Ester
(Note: R groups are not H)
Ether
Ketone
Note: H is not an R group
A)
R groups
1
Naphthalene
Nitrile
Thiol
Anthracene
Speed of light
3.0 x 10^8 m/s
Planck's Constant
6.63 x 10^-34 J*sec
Order the Electromagnetic Spectrum by Lowest Energy to Highest Energy
Radiowaves, Microwaves, Infrared, Visible, UV, X-ray, Gamma
Order the Electromagnetic Spectrum from Lowest Frequency (v) to Highest Frequency
Radio, Micro, IR, Visible, UV, X-ray, Gamma
Order the Electromagnetic Spectrum from Shortest Wavelength to Longest Wavelength
Gamma, X-ray, UV, Visible, IR, Micro, Radio
Molecules with large
dipole moments
are visible in a IR Spectroscopy graph.
A non-linear molecule with n atoms has
3n-6
vibration modes and
3
rotational modes
A linear molecule has
3n-5
vibrational modes and
2
rotational modes
Wave Number
(
v-
)
Units:
reciprocal centimeters
1/wavelength
v/c
Oscillation Potential Energy Expression
E = (1/2)kx^2
Relationship between frequency and wave number
v=c(v-)
Stretching frequency
(
v-
)
v- = (1/2pi(c))sqr(k/m)
Energy of Radiation
E=
hv
E=
hc/wavelength
E=
hc(v-)
Ethanol
A)
-OH
B)
CH2
C)
CH3
3
Phenol
A)
-OH
1
Relationship between frequency (v) and wavelength
v=
c/wavelength
What does the left side of the NMR graph indicate?
High
frequenc,
low
shielding,
low
magnetic field
What does the right side of the NMR graph indicate?
Low frequency
,
high shielding
, and
high magnetic field
High NMR peaks indicate…
more shielded
,
higher frequency
Low NMR peaks…
Less
molecular shielding and
lower
magnetic fields
IR Spect Wavenumber for isolated C double bonded to C
1640-1680
cm-1
IR Spect Wavenumber for conjugated C double bonded to C
1620-1640
cm-1
Wave number of aromatic C double bonded to C
~
1600
cm-1
Wave number O-H
3700-3100
Wave number double bond C, single to H
3100-3000
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