C Unit 2.8 Instrumental Analysis Revamp Flashcards

1
Q

The 3 spectrometry to of our concerns?

A
  • Mass spectrometry
  • IR spectrometry
  • NMR spectrometry
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What’s mass spectrometry?
(3-way)

A
  • An analytical technique
  • used to identify different isotopes
  • and find overall relative atomic mass of an element
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the 5 stages within mass spectrometry?

A

Stage 1: Ionisation
Stage 2: Acceleration
Stage 3: Ion drift
Stage 4: Detection
Stage 5: Analysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Explain stage 1: Ionisation?
(2-way + 3-way)

A
  • A sample of an element is vapourised and injected
  • into mass spectrometer
  • Where high voltage passed over chamber
  • causes electrons to be removed from atoms (ionised)
  • leaving 1+ charged ions in chamber
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Explain stage 2: Acceleration?
(2-way)

A
  • Positively charged ions are accelerated towards
  • negatively charged detection plate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Explain stage 3: Ion drift?
(2-way + 2-way)

A
  • Ions deflected by magnetic field
  • into a curved path
  • Radius of their path dependent on
  • charge & mass of ion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Explain stage 4: Detection?
(3-way + 1… way)

A
  • When positive ions hit negatively charged detection plate,
  • they gain an electron
  • , producing flow of charge
  • Greater current produced = greater abundance
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Explain stage 5: Analysis?
(3-way + one. way)

A
  • Current values used in combination
  • with flight times to produce
  • a spectra print-out
  • With relative abundance of each isotope displayed
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

In mass spectrum (probably the graph?), why do we see a half traced version of the ion?
(3-way + 2 things)

A
  • During ionisation process, 2+ charged ion may be produced
  • which’ll be affected more by magnetic field
  • producing curved path of a smaller radius
  • As a result, mass to charge ratio (m/z) is halved
  • Can be seen on spectra as a trace at half the expected m/z value
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What’s m/z?
What’s relative abundance? (<_<)
(Mass spectrometry)

A
  • Mass to charge ratio
  • …. Ig it’s how much of the ion there is? Consider the fact that u gain their isotopes in the spectra sooo…. yea….
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How to calculate RelativeAtomicMass of elements from mass spectra?

A

The formula:
1(relative abundance x m/z)+2(relative abundance x m/z)/ra1 + ra2

1 & 2 meaning the isotopes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

There’s 2 isotopes with relative isotopic masses of 35 & 37.
One with 35 has RA of 3
One with 37 has RA of 1
Calculate the RAM of the element?

A

((35x3) + (37x1))/3+1
= 35.5

(There’s a different method in the actual booklet, I took the one from 1.3 O_o)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Define molecular ion (M+)
(2-way)

A
  • The positive ion formed in a mass spectrometer
  • from the whole molecule
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How is a molecular ion gained from within mass spectrometry?
(2-way + 1-way)
(Could it be optional…?)

A
  • Molecules introduced into mass spectrometer
  • bombarded by high energy electrons
  • Knocks off electrons leaving M+
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Define fragmentation?
(2-way)
(Ig it speaks for itself anyway)

A
  • Splitting of molecules in a mass spectrometer
  • into smaller parts
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

In mass spectra, how to find out the molecules Mr?
(2 points)

A
  • The highest m/z
  • That’s also its molecular ion
17
Q

Hence, in mass spectra, how to identify the structure?
(5, thought provoking, must observe,-way)

A
  • First know Mr
  • Given fragment table otherwise:
  • OH = 17
  • CH3 = 15, CH3CH2 = 29
  • All about ur judgement
18
Q

In mass spectra, do we care about the height of the bars for the molecule?

19
Q

How to truly tell if the molecule in mass spectra is an alcohol?

A

If there’s a peat at 17

20
Q

Concluding… what are the 4 things we can gain from mass spectrometry?
(2 of em with () )

A
  • Molecular mass (M+)
  • Molecular formula
  • Structural features (fragmentation)
  • Presence of halogens
21
Q

What’s infrared spectroscopy?
(4-way)

A
  • An analytical technique (<_<… again)
  • to identify & analyse substances
  • by measuring how they absorb IR light
  • which causes molecular vibrations
22
Q

Meaning of “different bonds absorb different energies” in IR spectroscopy?
(1 + 2-way)

A
  • Said to be the characteristic of the bonds
  • The absorptions on the spectra can indicate
  • which groups of atoms are present
23
Q

Measurement of energy absorbed in IR spectroscopy?

A

Wavenumbers
(cm-1)

24
Q

Which parts of a molecule absorb infrared energy?

A

The bonds…

25
Q

Define characteristic absorption?
(2-way)

A
  • The wave number range at which
  • a particular bond absorbs radiation
26
Q

Within infra-red spectrum of a molecule, what’s the right hand side area called?
(3 things…. bro u’ll probably only need to know it’s name…)

A
  • The fingerprint region
  • Specific to the molecule
  • Whole spectrum can be compared with known samples using a database….?
27
Q

Within infra-red spectrum of a molecule, how to tell if a certain bond is rlly in there?

A

…. based on the trough being there… broadness also showing like wavenumber range….

28
Q

But, what can we mostly gain from analysing an infra-red spectrum of a molecule?
(3 things)

A
  • Functional groups present
  • Possible type of compound
  • Certain structural features
29
Q

2 examples of infrared spectroscopy being used?

A
  1. Breathalysers
  2. Global warming
30
Q

Issue with breathalysers against drunk people and people suffering from ketosis?
Solution perhaps?
(3-way)

A
  • Both have function group -C=O
  • But can spot one who drank too much alcohol:
  • O-H carboxylic, definitely not ketones
31
Q

NMR spectroscopy…. NMR means what?

A

Nuclear Magnetic Resonance

32
Q

Explain NMR spectroscopy?
(3-way + 2-way)

A
  • Corresponds to the energy required
  • to reverse spin of nucleus
  • of an atom within magnetic field
  • Causes resonance
  • E absorbed shown by chemical shift (δ)
33
Q

What’s an example of NMR spectroscopy?

A

MRI scanner :b

34
Q

What are 2 types of NMR spectroscopy to of our concern?
(Each provide their own table in data sheet ,’:0)

A
  • 13C NMR spectroscopy
  • 1H NMR spectroscopy (low resolution… no singlet n stuff das A2)
35
Q

Explain 13C NMR spectroscopy?
(2 things + 2-way)

A
  • Focuses on carbon environments in a molecule
  • C-13 = naturally abundant ∴ weaker signals than 1H NMR spectroscopy
  • The chemical shift tells us the type of carbon present
  • ;different functional groups give different peaks
36
Q

What can the peak height be based on in 13C NMR spectroscopy?
Can there be the same bond with different δ?

A

Number of same molecules (n° of the same environment).
… Yes, remember when i said different functional groups give different peaks?

37
Q

Explain 1H NMR spectroscopy (low resolution)?
(4 points)

A
  • Focuses on hydrogen (proton) environments in a molecule
  • n° of peaks = n° of environments
  • Height of peak = n° of H in environment
  • Be aware whether it’s 1 whole environment or actually just 2 (Any example?)
38
Q

Tell me about the δ values in 1H NMR spectroscopy (low resolution)?
(2 things)

A
  • Values vary within the ranges stated in data sheet
  • E.g. -O-H has quite a big range (1.0 - 5.5)
39
Q

This one is mostly a big heads up on questions, the true applying knowledge. Ig I have my book but still.