Quiz 4 Slides Flashcards

1
Q

Each mass will experience a restoring force that is proportional to its displacement from equilibrium

A

Hooke’s Law

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2
Q

Does harmonic oscillator obey hooke’s law?

A

yes

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3
Q

force constant of the bond is equivalent to the ___ of the potential energy function

A

curvature

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4
Q

masses m1 and m2 each have

A

displacements x1 x2 assuming simple harmonic motion oscillating as a cosine function of time

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5
Q

since both standard differential equations have to be true simultaneously, they also show

A

that each mass oscillates with the same frequency and phase constant; each mass goes through its equilibrium position simultaneously

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6
Q

transition spacings are all what frequency of oscillation

A

v0

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7
Q

resulting spectrum from harmonic oscillator has how many bands

A

1 abs band

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8
Q

fundamental vibrational frequency

A

transition v = 0 to v=1

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9
Q

harmonic oscillator approach is good for

A

very small displacements about equilibrium; first approximation to real spectra; not much else

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10
Q

a better approximation to physical reality from harmonic oscillator needs what

A

a more realistic potential function

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11
Q

morse potential

A

empirical function where Vx approaches infinity as x approaches 0, is asymptotically approaching a constant value De

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12
Q

correction factor that lowers each energy level relative to the harmonic energy levels

A

anharmonicity constant

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13
Q

result of anharmicity constant

A

energy levels of oscillatornot evenly spaced

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14
Q

transitions that appear with decreasing intensity at fundamental vibrational frequencies 2, 3, etc

A

overtones

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15
Q

transition that occurs more rapidly if temp is raised

A

hot bands

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16
Q

what causes hot bands

A

higher v states are more populated at higher temp

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17
Q

anharmonic oscillator equation overestimates De by 20% because…

A

it assumes a linear estimates – change in energy constant with v, which is not true, especially at higher v

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18
Q

energy levels equally spaced on the ladder

A

harmonic oscillator

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19
Q

energy levels get closer as energy increases; near dissociation, energy becomes continuous

A

real molecule

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20
Q

degrees of freedom also refers to

A

number of possible fundamental vibrations in a molecule

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21
Q

three of the possible fundamental vibrations are simply…

A

simultaneous, in phase translations of each atom together along one of the directional coordinates

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22
Q

do translations correspond to real molecular vibrations?

A

nope

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23
Q

three more possible fundamental vibrations exist that simply refer to…

A

rotation of each atom about 3 principle axes of rotation

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24
Q

does rotation correspond to real molecular vibration

A

no

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25
Q

to find translational movements for non-linear molecules

A

subtract 3 degrees freedom

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26
Q

for rotational movements of nonlinear molecules

A

subtract 3 degrees of freedom around its principle axes

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27
Q

for linear molecule’s translational movements

A

subtract three degrees of freedom

28
Q

for a linear molecules rotational movement

A

subtract 2 degrees of freedom

29
Q

do linear molecules have rotation around long axis?

A

no real discernable rotation along major axis

30
Q

linear polyatomic fundamental molecular vibration

A

3N-5

31
Q

nonlinear polyatomic fundamental molecular vibrations

A

3N-6

32
Q

of the possible fundamental molecular vibrations, how many are caused by bond stretching?

A

N-1

33
Q

of the possible fundamental molecular vibrations, how many will be caused by bond bending

A

2N-5 nonlinear, 2N-4 linear

34
Q

molecular motion in which all atoms move in phase and with the same frequency

A

normal modes of vibration

35
Q

types of normal mode molecular vibrations: stretching

A

symmetric and asymmetric

36
Q

types of normal mode molecular vibrations: bending

A

in plane rocking, in plane scissoring, out of plane wagging, out of plane twisting

37
Q

strength of polarity in chemical bond described by

A

the dipole moment

38
Q

chemical bonds and vibrations can be described on the basis of

A

molecular symmetry relative to a symmetry element in the molecule

39
Q

in order to absorb IR radiation, molecular vibration must

A

cause a change in the permanent dipole moment either parallel or perpendicular to a symmetry element in molecule

40
Q

is symmetric stretching vibration ir active

A

no

41
Q

IR activity requires

A

change in permanent dipole moment of the chemical bond

42
Q

very strong in IR spectrum

A

polar bonds with large dipole moments

43
Q

non polar bonds in IR spectrum

A

weak or absent

44
Q

when harmonic oscillator condition is relaxed

A

overtone vibrations become permissible

45
Q

also appear due to anharmonicity

A

combination and difference bands

46
Q

in addition to overtone vibrations, these bands also appear due to anharmonicity

A

combination and difference

47
Q

appear at the value due to the sum of 2+ fundamental molecular vibrations

A

combination bands

48
Q

arise from ground vibrational levels

A

combination bands

49
Q

binary combination level involves

A

2 different normal coordinates with nonzero quantum numbers

50
Q

1 photon excites 2 different vibrations simultaneously if

A

that photon has an energy approx. equal to the sum of energies needed to excite them separately

51
Q

do not arise from fundamental molecular vibrations

A

difference bands

52
Q

difference bands vs combination band strength

A

difference are weaker

53
Q

difference bands at low temps

A

disappear

54
Q

difference transition occurs from

A

excited level of one transition to that of another

55
Q

intensity of difference transition varies with

A

the population of the excited state

56
Q

when the energy of an overtone or combo band happens to have the same value as the energy of a fundamental vibration

A

accidental degeneracy

57
Q

Fermi resonance

A

accidental degeneracy results in sometimes 2 relatively strong bands where only one fundamental was expected; two observed occur at higher and lower energies than the expected

58
Q

two energy levels in fermi resonance interact

A

on quantum mechanical level due to anharmonic terms in potential energy

59
Q

does fermi resonance energy difference have to be big

A

no

60
Q

vibrations in fermi resonance should be

A

able to couple via anharmonic terms, with overtone and fundamental of same symmetry

61
Q

vibrations which involve large amplitudes of isotopically labelled atom should

A

shift by the greatest amount

62
Q

isotopic mass difference vs wavenumber shift

A

larger IMD greater WNS

63
Q

For H-D substitution new vibrational wavenumber of D substituted bond will always

A

be shifted to lower energy relative to H sub species by factor of 1/sqrt2

64
Q

certain sub molecular groups of atoms consistently produce vibrational bands in characteristic frequency regions of vibrational spectrum

A

group frequencies

65
Q

what causes group frequencies

A

coupling of oscillating dipole moments

66
Q

group frequencies can be very sensitive to

A

both config and conformation of local molecular groupings

67
Q

very sensitive probe for molecular structure

A

IR spectroscopy