Module 8 - Applying Chemical Ideas Flashcards

1
Q

Purpose of AAS

A

Atomic Absorption Spectroscopy is used to determine the concentration of metal ions in a substance at very low concentrations

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2
Q

Set up of AAS

A

A hollow cathode lamp with the metal to be analysed emits electrons at a certain wave length, a flame containing the vaporised sample absorbs some of the light, the monochromator selecting the wave length and the detector records the intensity

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3
Q

Using an AAS curve

A

Requires a calibration curve, using the absorbance to find the concentration

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4
Q

Units of concentration in AAS

A

ppm or mg/L

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5
Q

Purpose of mass spectrometry

A

Used to determine molar mass of element and the isotopes

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6
Q

Set up of mass spectrometry

A

Sample is vaporised and ionised, molecular ion breaks apart into smaller fragments, ions are accelerated through an electric field and deflected by the magnetic field with the amount depending on their mass-to-charge ratio (m/z), then detected

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7
Q

What is the base peak in mass spectrometry?

A

The highest peak is the most abundant peak (the highest)

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8
Q

What is the parent peak in mass spectrometry?

A

The peak with the highest m/z (furtherest to the right), usually the molar mass

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9
Q

Purpose of infrared spectroscopy

A

To determine the bonds/functional groups

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10
Q

How IR spectroscopy works

A

IR radiation causes molecules to stretch, bend and vibrate, each bond vibrating at a characteristic frequency

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11
Q

Set up of IR spectroscopy

A

IR is split into two beams so it is shot at sample and reference, the splitter and detector recording the results

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12
Q

The region below 1500cm in IR Spectroscopy

A

The fingerprint print - Can be compared with spectra of known compounds, but not as useful for functional groups

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13
Q

Purpose of NMR

A

To map the atomic structure - the presence and position of molecules

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14
Q

Set up of NMR

A

Matter is placed in a magnetic field, nuclei must have an odd number of nucleons, moving from low to high energy state allowing them to absorb energy (radiofrequency radiation)

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15
Q

Standardising chemical in NMR

A

TMS (very shielded)

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16
Q

Name of peaks in NMR and their number of peaks

A

Singlet - no split
Doublet - Two peaks
Triplet - Three peaks
Quartet - our peaks

17
Q

Number of peaks in H1 NMR

A

How many different chemical environments

18
Q

Location of the peaks in H1 NMR

A

The closer to the right is more shielded, left is less shielded

19
Q

Splitting in H1 NMR

A

n+1 peaks shows how n*H1 nuclei on neighbouring carbons

20
Q

Area under the curve in H1 NMR

A

Corresponds to the relative number of hydrogens present in the environment

21
Q

Differences in C13 vs H1 NMR

A

Height and splitting is not important

22
Q

Reading 13C NMR graphs

A

Use data sheet to determine functional groups

23
Q

What is colourimetry?

A

To determine the concentration of a coloured analyte in solution by absorption of a specific wavelength of visible light

24
Q

The Beer-Lambert Law

A

Concentration is proportional to the amount of light absorbed. A = e[molar absorptivity, depends on substance]l[path length]c[concentration] or A = log(Io[incident light]/I[transmitted light])

25
Q

Set up of colourimetry

A

Light source -> coloured filter -> sample solution -> detector -> recorder

26
Q

Colours absorbed in colourimetry

A

Solutions absorbs the complementary colour of the visible colour (e.g. a blue solution absorbs red) which must be chosen

27
Q

How to use colourimetry

A

Create a calibration curve using a series of standard solutions

28
Q

What is UV-Visible spectrophotometry?

A

Use of the absorption of UV, visible electromagnetic radiation (EMR) to deduce molecular structure. The substance must absorb UV and EMR to be useful. It is qualitative

29
Q

Set up of spectrophotometry

A

Light source -> monochromator -> sample solution -> detector -> recorder

30
Q

How to use spectrophotometry graph

A

Monochromator allows for the selection of specific wavelengths. Maximum absorbance (highest point on graph) + minimal interference with other substances

31
Q

How spectrophotometry operates

A

Measures absorbance at a range of wavelengths to plot absorbance vs wavelength, creating a spectrum

32
Q

Availability of reagents in chemical synthesis + design (example)

A

Haber process - take Nitrogen from the air and Hydrogen from natural gas (CH4)

33
Q

Reaction conditions in chemical synthesis + design (example)

A

Haber process - 500oC (exothermic but compromise which increases rate); 200atm (moderate as high risk + cost); magnetite (iron) catalyst; set up to remove ammonia so it favours the forward reaction

34
Q

Yield and purity in chemical synthesis + design (example)

A

Haber Process - Yield is maximised by using a moderate temperature (500oC which slows down yield but increases rate) & moderate pressure (200atm to increase yield but balance cost + risk); condenser used to liquefy NH3 while pumping back in N2 + H2 purifying the product; must also monitor the incoming gas so it’s pure as O2 at high temps can explode

35
Q

Industrial uses of chemical synthesis + design (example)

A

Ammonia from the Haber process used in fertilisers (ammonium nitrate), explosives, household cleaners/detergents, refrigerant gas

36
Q

Environmental, social and economic issues of chemical synthesis + design (example)

A

Solvay process for Na2CO3 (used in glass making)
Environmental - Mining CaCO3 can disrupt ecosystems; waste product of CaCl2 is discharged into the ocean (as already a lot of ions, but not in rivers)
Social - Site must not be too close to people due to noise and dust pollution, but close enough for workers
Economic - Site must be close to supply of raw materials and market to sell; accessible by transport

37
Q

What a precipitation titration involves + how to find equivalence point

A

Involves using Ag+ to detect halide ions (Group VII); Equivalence point determined by formation of a second coloured ppt, formation of a coloured complex ion, conductivity measurements