EMPA Flashcards

1
Q

How can percentage errors be reduced?

A

Use larger quantites (volumes, masses etc)

Use more precise equipment

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2
Q

How can procedural errors be reduced when making a standard solution?

A
  • Rinse out weighing bottle with distilled water and add this to the volumetric flask
  • Ensure the bottom of the meniscus is level with the graduated mark
  • Invert the flask many times to ensure complete mixing of the solution
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3
Q

How can procedural error be reduced when carrying out a titration?

A
  • Rinse out pipette and burette with the solutions that are going in them.
  • Swirl the flask during the titration
  • Rinse the side of the flask with distilled water
  • Add the solution in the burette dropwise near the end point
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4
Q

What is the setup for collecting a gas?

A
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5
Q

What are the issues with the methods of collection gases?

A

Gas syringe:

  • Syringe can stick due to the damp gas

Collection over water:

  • Some gas dissolves in the water

Both:

  • Some of the gas escapes before the bung is inserted
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6
Q

How can insoluble impurities be removed from a sample?

A
  1. Dissolve the sample in a suitable solvent
  2. Filter the mixture (rinse the residue on the filter paper with a little solvent)
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7
Q

How can dry crystals of x be produced from the solution?

A
  1. Put the solution in an evaporating basin and heat gently
  2. Evaporate half and then allow the rest to evaporate at room temperature
  3. Transfer the crystals on filter paper and wash with ice cold water
  4. Place the filter paper in an oven to dry out the crystals
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8
Q

What precautions should be taken if chemical x is an irritant/corrosive/toxic?

A

Wear gloves/goggles

Avoid contact with the skin

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9
Q

What precautions should be taken if x is flammable/volatile?

A

Avoid naked flames

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10
Q

Why is recrystallisation necessary?

A
  • Chemicals may be impure
  • Chemicals may decompose over time to form other compounds
  • The reaction may not go to completion
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11
Q

How is a chemical purified by recrystallisation?

A
  1. Dissolve in a minimum volume of hot water
  2. Filter solution hot
  3. Cool filtrate in ice
  4. Collect crystals and wash with cold water
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12
Q

When carrying out a recrystallisation, why is a minimum volume of hot water used?

A
  • To obtain a saturated solution
  • To increase yield (reduce amount left in solution)
  • Enable crystallisation on cooling
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13
Q

When carrying out a recrystallisation, why is the solution filtered hot?

A
  • To remove insoluble impurities
  • To prevent crystals forming during filtration
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14
Q

When carrying out a recrystallisation, why is the filtrate cooled in ice?

A

To increase the amount of crystals that are formed

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15
Q

When carrying out a recrystallisation, why are the crystals washed with cold water?

A

To remove soluble impurities

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16
Q

How can the purity of a product be tested?

A

Melting point determination

17
Q

Why do pH meters have to be calibrated before use?

A

Over time the meters gives inaccurate readings

18
Q

Before recording the pH with a meter, how would you ensure the reading was accurate?

A

Calibrate using a buffer solution of know pH

Adjust the meter accordingly

19
Q

How does the purity of a sample affect its melting point?

A

Impure samples with melt of a wide range

Pure samples will melt “sharply”

20
Q

Why might the melting point of a sample be lower than the data book value?

A
  • Temperature in thermometer lower than in capillary tube
  • Sample too small
  • Heating too quickly
21
Q

What is the setup for filtration under reduced pressure?

A
22
Q

What is the setup for reflux?

A
23
Q

What is the setup for distillation?

A
24
Q

Why might a reaction have a low percentage yield?

A
  • Incomplete reaction
  • Transfer losses
  • Gas escaping
  • Product dissolving (either gas or a salt)