Chemistry- Analytical Techniques Flashcards

1
Q

What are the different analytical Techniques used in chemistry?

A
  • Mass Spectrometry
  • Combustion Analysis
  • Nuclear Magnetic Resonance
  • Infrared Spectroscopy
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2
Q

How does Infrared Spectroscopy work?

A

Molecules are not Rigid- The bonds within can move and vibrate.
Different functional groups and molecules can absorb IR radiation at different wavelengths, Which makes it possible to identify the functional group within a molecule.

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3
Q

How do you calculate the wavenumber?

A

Wavenumber = 1 / Wavelength (cm)

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4
Q

What are the different types of NMR?

A

Carbon NMR

Proton/Hydrogen NMR

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5
Q

What is the fingerprint Region in NMR?

A

The fingerprint region is to the right of the functional group bonds. It is specific to each molecule.

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6
Q

What do the O-H, C-O & C=O Peaks look like in NMR?

A

O-H: Strong and broad peak
C-O: Strong but narrow peak
C=O: Strong and narrow peak

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7
Q

What is NMR Spectroscopy?

A
  • Only interested in Carbon 13 Isotopes and Hydrogen atoms to work out Carbon and Hydrogen environments.
    Due to the Odd mass number in the atoms, each atom has a nuclear spin.
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8
Q

What is a carbon atom environment?

A
  • The environment around a C^13 Atom.
  • In non-polar bonds electrons in the bond shield the nucleus from the external magnetic field and you would have to increase the field to make the nucleus resonate again.
  • In polar (with an electronegative atom) the electrons are further away from the carbon^13’s nucleus and so do not affect the magnetic field around it so much.
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9
Q

In NMR what does the number of peaks mean?

A

The number of peaks is the same as the number of Carbon or hydrogen environments.

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10
Q

What is the standard comparison molecule used to C^13 NMR?

A

TMS (Tetramethylsilane)
- All carbons are in the same environment
- 4 Carbon nuclei in a similar environment
- C-Si bond is short so carbon nuclei are very well shielded.
Gives a Strong TMS peak at the right hand side of the NMR graph.
TMS is non toxic, inert, easy to removed from sample.

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11
Q

What is Chemical shift?

A

What type if environment/ bond the C atom is in.

  • Horizontal scale is shown as (ppm) is the chemical shift.
  • C^13 NMR peaks are less than (to the left) of TMS and are longer than (0-200ppm) the proton NMR (0-12)
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12
Q

What is HNMR or Proton NMR and why does hydrogen produce a peak?

A

Hydrogen (Proton) Nuclear Magnetic Resonance

Hydrogen atoms are uneven in mass (odd mass number) and therefore will resonate producing a peak.

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13
Q

What is the Integration Trace?

A

Gives the Number of Hydrogen atoms producing a peak.

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14
Q

Why is TMS used as a standard?

A

(Tetramethylsilane)
- Hydrogens are all in the same peak/environment
- 12 Hydrogens give a strong TMS peak.
TMS - Non toxic, Inert, Easy to remove from sample.

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15
Q

What is spin-spin splitting (spin-spin coupling)

A

The applied magnetic field felt by a hydrogen atom is affected by the magnetic field felt by any neighbouring H atoms. (attached to adjacent Carbon Atoms)
Peaks give characteristic splitting patterns which tell you about the neighbouring H atoms.

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16
Q

Why do you not get splitting on C^13 Peaks?

A

No splitting occurs in C^13 NMR as you do not get C^13 atoms adjacent to each other. The C^13 isotope is so uncommon in molecules that the chances of getting an molecule with to adjacent C^13 atoms is very rare.

17
Q

What is the spin-spin splitting rule?

A

Only happens in high resolution HNMR

Rule: Signal is split into the number of H atoms on the adjacent Carbon atoms + 1….. (n+1)

18
Q

What are the Common Solvents used in HNMR Spectroscopy?

A

Solvents not containing Hydrogen (unless Deuterium) so no peaks are present which may affect results.
- Deuterium has no peaks as the mass number is even (2 since 1 proton + 1 Neutron)
- Solvents used are usually Tetrachloromethane (CCl4)
CDCl3