IR spectrometry\ Flashcards

1
Q

What happens in IR spectroscopy

A

IR radiation is shone through a sample and certain frequencies are absorbed as molecules move to higher vibrational energies

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2
Q

IR in diatomics

A

gain a IR photon

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3
Q

closely spaced absorption sets are known as

A

bands

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4
Q

what are the transitions called

A

fundermental, first and second overtone

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5
Q

why are there multiple peaks for the same vibration peak?

A

different transitions in the rotational energy

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6
Q

why is the fundamental overtone frequency is half the size of the first?

A

reflects the spacing of energy levels

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7
Q

as bond strength increases

A

the greater the vibrational frequency

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8
Q

what are overtones?

A

vigorous extremes of the same vibrations

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9
Q

how many modes can there be ?

A

assymetric - there are two but they are degenerate
symmetric
bending

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10
Q

how to calculate the number of modes

A

3n-6 for non linear
3n-5 for linear
n is the number of atoms in a molecule

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11
Q

why is assymetric stretching at a higher wave number than the other two modes?

A

while some of the bonds get shorter, some other bonds become longer resulting in a change in the dipole moment of the molecule. So, asymmetric stretching appears at a higher wavenumber and absorbs or needs more energy than symmetric stretching.

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12
Q

why is assymetric stretching at a higher wave number than the other two modes?

A

while some of the bonds get shorter, some other bonds become longer resulting in a change in the dipole moment of the molecule. So, asymmetric stretching appears at a higher wavenumber and absorbs or needs more energy than symmetric stretching.

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13
Q

what causes the IR absorption strength ?

A

the change in dipole moment during the vibration.

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14
Q

if the dipole moment does not change during the bond vibration

A

no IR activity will be detected

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15
Q

why in linear symmetrical molecules IR may not show

A

dipole changes may cancel out

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16
Q

why can IR show in symmetrical molecules during symmetrical stretch?

A

the dipole moment changes direction depending on which side it stretch.
A dipole is formed

17
Q

carbonyl attach to ring

A

the smaller the ring the greater the frequency of the c=o bond

18
Q

why does ring size effect the bond frequency?

A

it reflects how how it is to disort the ring. smaller rings have a greater force constant

19
Q

lone pairs can

A

conjuate pi bond. this is the alternating between double and single bonds

20
Q

resonance structures

A

As soon as we introduce some resonance structure, or conjugation, now those electrons can delocalise over 3-4 atoms or even more. This weakens the C=O
bond, moving the IR peak down to lower wavenumbers.

21
Q

ketone vs aldehyde

A

the sigma conjuation weakens the ketone carbonyl as alpha Hydrogen are sigma conjuated with carbonyl.

aldehyde have higher frequency

22
Q

acyl chloride

A

the 3p lone pair orbital on cl does not overlap well with pi system.
c-cl bonds strengthens the c=o bond . so it has a higher frequency.