C Unit 2.8 Instrumental Analysis Flashcards

1
Q

Advantage of instrumental anaylsis?

A
  • Require very small samples:
    less damaging or invasive
    Important if there is very little of the original to identify
  • They are quick to carry out
  • They give very accurate data
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2
Q

What are the 3 spectrometry’s you’ll be looking at?

A
  1. Mass spectrometry
  2. Infrared spectrometry (IR)
  3. Nuclear Magnetic Resonance spectroscopy (NMR)
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3
Q

What’s a mass spectrometer?
(3 things)

A
  • An analytical technique
  • Used to identify different isotopes
  • And find overall relative atomic mass of an element
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4
Q

Explain step 1: Ionisation in mass spectrometry?
(5 things)

A
  1. 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
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5
Q

Explain step 2: Acceleration in mass spectrometry?
(2 things)

A
  1. Positively charged ions are accelerated towards
    - Negatively charged detection plate
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6
Q

Explain step 3: Ion drift in mass spectrometry?
(4 things)

A
  1. Ions deflected by magnetic field
    - Into a curved path
    - Radius of their path dependent on
    - Charge & mass of ion
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7
Q

Explain step 4: Detection in mass spectrometry?
(4 things)

A
  1. When positive ions hit negatively charged detection plate,
    - They gain an electron
    - Producing flow of charge
    - Greater current produced = greater abundance
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8
Q

Explain step 5: Analysis in mass spectrometry?
(4 things)

A
  1. Current values used in combination
    - With flight times to produce
    - Spectra print-out
    - With relative abundance of each isotope displayed
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9
Q

In mass spectrum, why do we see a half traced version of the ion?
(5 things)

A
  • During ionisation process, 2+ charged ion may be produced
  • Will 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
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10
Q

In mass spectrum:
What m/z?
What relative abundance?

> _>

A
  1. Mass to charge ratio
  2. Relative atomic mass?

icl i haven’t seen where u had to put a number for a certain bar so i reckon u don’t get fucked up by this one

I changed it lol

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11
Q

For mass spectra graph, how u gain mass for the 2 isotopes

A

Formula for mass of 2 isotopes:

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

May seem a lil hard to remember but gl bro B)
^ past me said that

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12
Q

Define molecular ion (M+)

A

The positive ion formed in a mass spectrometer from the whole molecule

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13
Q

Define fragementation

A

Splitting of molecules in a mass spectrometer into smaller parts

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14
Q

How to identify molecular ions in a mass spectrum?
(4 steps)
(Major check-up)

A

Don’t take my word for it, for now
1. Assume there’s a fragment table?
2. U look at m/z (x-axis)
3. Check which bars correlate to what’s in the fragment table
4. Then it’s all about deduction based on what’s also not there

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15
Q

Describe infrared spectroscopy
(3 things)

A
  • Infrared radiation absorbed by organic molecules
  • Causes increased bending and vibrations
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16
Q

For Infrared spectroscopy, what does “different bonds absorb different energies” mean?
(3 things)

A
  • Said to be the characteristic of the bonds
  • The absorptions on the spectra can indicate
  • which groups of atoms are present
17
Q

What is energy absorbed in IR spectroscopy measured in?

A

wavenumbers (units cm-1)

18
Q

Which parts of a molecule absorb infrared energy?

A

The bonds

19
Q

Define wave number

A

A measure of energy absorbed used in IR spectra

20
Q

Define characteristic absorption

A

The wavenumber range at which a particular bond absorbs radiation

21
Q

How to identify chemical compounds in a IR spectrum?
(4 things)

A
  • U must use the data booklet for the wavenumber as it will guide u to identify bonds within the IR spectrum
  • Not based on peaks but based on troughs (the opposite of peaks)
  • Be aware of the wave number (must be within range)
    -. After gaining the bonds, gain mr and use ur brain to create the structural formula or molecular formula
22
Q

What typical troughs u should know for IR spectrum?
(2 things)

A

C=O bond - deep trough at 1700
O-H bond - usually within broad trough around 3000

23
Q

An example of an IR spectroscopy?

A

Breathalysers

24
Q

Issue with breathalysers against drunk ppl and ketosis?

A

Both have functional group carbonyl bond
However can spot the one who drank too much alcohol:
O-H = carboxylic acid = 2500 - 3550

25
Q

Describe Nuclear Magnetic Resonance (NMR) Spectroscopy
(5 things)

A
  • Corresponds to the energy required
  • to reverse the spin of the nucleus
  • of an atom within a magnetic field.
  • Causes resonance
  • Energy absorbed is shown by chemical shift, δ

Must know how to interpret the spectra of this

26
Q

An example of an NMR spectroscopy?

A

MRI scanner ig

27
Q

How to identify compounds in an NMR spectra?
(might need more work)
(5 steps)

A
  • It’s based on environments with n° of “protons”
  • U have data booklet for the chemical shifts
  • Number of peaks based on number of environments
  • Where they placed based on chemical shift
  • Height of peak (frequency) based on number of hydrogens (n° of protons)
28
Q

Propan-1-ol
How would u describe the environments of each of the hydrogens?

A
  • 4 environments
  • and so “8 protons”
  • Create graph:
    1. 4 bars based on n° of environments
    2. Height based on n° of protons of each environment
    3. But how do i figure out where it’s placed….
29
Q

Describe 13C (NMR) Spectroscopy

A

Based on the carbon atoms and it’s bonds

30
Q

If too unsure, still possible to go back

A

I need to do questions tho

31
Q

LET’S GO GAMBLING

A

99% of Gamblers…