- Shuffle
Toggle OnToggle Off
- Alphabetize
Toggle OnToggle Off
- Front First
Toggle OnToggle Off
- Both Sides
Toggle OnToggle Off
Front
How to study your flashcards.
Right/Left arrow keys: Navigate between flashcards.right arrow keyleft arrow key
Up/Down arrow keys: Flip the card between the front and back.down keyup key
H key: Show hint (3rd side).h key
![]()
PLAY BUTTON
![]()
PLAY BUTTON
![]()
15 Cards in this Set
- Front
- Back
|
why is it pointless to perform carbon decoupled 1H NMR
|
b/c the C13 has little efect on signal of the protons due to low nautural abundance
|
|
List 3 advantages of porton decoupled 13 C NMR
|
increases sensitivity (NOE)
faster T2 decrease relaxation time simplified spectra increases resolution incease S/n ratio |
|
2 disadvatnages to proton decoupled 13 C nmr
|
no conectivity data
no quantative data |
|
how does noe affect an nmr signal?
|
in spin decoupling
1)it incraeases # of spin states on low energy side by cross polarization & increases intensity 2) it decreases T1 time |
|
assuming a simple harmonicoscillation what happens to the maximum vibrational amplitude, vibrational frequ, & average interatomic distnace of a simple diatomic mcule when it absorbs IR light?
|
amplitude increaes
vib frequency & interatomic distance staty the same |
|
based on this diatomic harmonic oscillator mode, whichof the 2 stretching vibrations (c-h or c-cl) would vibrate at a higher frequency? why?
|
C-h would have a higher frequ b/c cl is a heavier mcule and therfoe would not vibrate as much
|
|
how do vibrationally excited mucles usually return back to their lowest energy state (v=o)?
|
give off thermal energy as heat
|
|
in ir what are we probing?
|
molecular vibrations
|
|
what kind of vibrations in ir?
|
stretching & bending
asy symmetric twisting wag rocking |
|
whats important about dipole w/ir w/distance
|
w/distance b/t charge seperation creates dipole & magnitude dependant on seperation
|
|
why is anharmonic model more realistic than harmonic?
|
the anharmonci takes into acount the distance of the bond & that the bond may break
also when energy levels get higher, the levels get closer together so you get overtones |
|
why are observed vibrational freq of funct groups often observed to be diff from that predicted w/harmonic oscillator mode?
|
the harmoci oscilator is ideal model & not all funct groups adhere to it. Some mcules may have high high repulsion for 1 antoher & want to break a bond. Also b/c of vibrational coupling
|
|
vibrational coupling adds to complexty but helps w/fingerprinting of materials by 3 ways
|
1.b/t stretching vib have to have an atome in common
2.b/t bending vib must have to have a comon bond to be coupled 3.b/t stretching & bending vib the stretch bond form 1 side of angle in bend bond |
|
what is uniform periodic motion explotied in ir spectroscopy? in raman spectroscopy?
|
vibrational motion for both
|
|
what conditoin must be met to observe the interacion f the electromagnet radiation w/uniform eriodic moition in ir spect? in raman spect?
|
ir-change in dipole moment
raman-change in polarizabiltiy |