IR spectroscopy and mass spectroscopy

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17 Terms

1
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covalent bonds in molecules….

possess energy and vibrate naturally about a central point

2
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stretch (type of covalent bond vibration)

rhythmic movement along line between atoms so that distance betweeen 2 atomic centres increases and decreases

3
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bend (type of covalent bond vibration)

results in a change in bond angle

4
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how does mass of atoms in a bond affect strecthing and bending

heavier atoms vibrate more slowly than lighter atoms

5
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how does bond strength affect stretching and bending

stronger bonds vibrate faster than weaker bonds

6
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how does ir radiation affect covalent bonds

makes them bend and stretch more

7
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what type of radiation can bonds absorb

radiation with same frequency as natural bond frequency

8
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how IR spectroscopy happens

beam of IR in range 200-4000cm-1 passed through sample in spectrometer, molecule absorbs some IR frequencies, emerging beam analysed to identify frequencies absorbed by the sample

9
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fingerprint region (below 1500cm-1)

unique for every compound, can be used to check if compound is pure

10
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identifying pollutants with IR spectroscopy

uses IR spectral fingerprints which are analysed by remote sensors, measure co2, co and hc emissions, helps monitor localised pollution

11
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breathalysers using IR spectroscopy

pass IR beam through captured breath, characteristic ethanol bonds detected, more IR absorbed=higher reading=more alc in breath

12
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sequence when identifying unknown compound

elemental analysis with percentage composition, mass spectrometry, IR spectroscopy

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how does mass spectrometry work

sample vapourised, high energy fast moving es knock es out of sample to form +ve ions, electric field accelerates +ve ions to contant speed, magnetic field deflects charged ions (deflection depends on mass of ions)

14
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relative intensity in mass spectrometry

height of peaks in mass spectrum, shows abundance of ions of each mass

15
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meaning of m/z in mass spectrometry

mass/charge, assume it is same as mr because most ions have 1+ charge

16
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bease peak in mass spectrometry

tallest peak with relative intensity at 100%, usually most stable ion formed

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m+1 peak in mass spectrometry

molecular ion with mass 1 unit heavier than normal molecular ion, caused by presence of carbon-13 isotope with 1.1% abundance