1 — experimental techniques Flashcards

Density and solubility table to be memorise in the notes.

1
Q

Measurement of time

A

SI: seconds (s)
Apparatus: digital stopwatch is used to measure time.
Record seconds to a whole number.

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2
Q

Measurement of temperature

A

SI: Kelvin K
Commonly measured as degree Celsius in the lab.

Apparatus: alcohol or mercury thermometer

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3
Q

Measurement of length

A

SI:m
1m = 10dm =100cm = 1000nm
Apparatus: Metre rules, measuring tapes are used

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4
Q

Measurement of mass

A

SI: kg
Apparatus: electronic balance

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5
Q

Measurement of volume

A

SI: (m^3)
Apparatus: measures:

Pipette -> accurate fixed volumes(10.0, 25.0cm^3)
Volumetric flask -> accurate fixed volumes (100cm^3, 250cm^3)

Measuring cylinder -> a range of volumes to nearest 0.5cm^3
Burette -> range of volumes to nearest 0.05cm^3

Gas: gas syringe -> up to 100cm^3

1 volume: pipette < volumetric flask
Range of volumes: measuring cylinder > burette
Most accurate: burette

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6
Q

Collection of gases

A

1.gas syringe
2. Solubility
- water displacement (H2, O2, CO2, N2)
3. Density
- downward or upward delivery (other than H2, N2, NH3, all downward)

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7
Q

Drying of gases

A

Concentrated Sulfuric acid
- for acidic and neutral gases
- cannot be used to dry alkaline gases as they react w acid to form salt (NH3)

Quicklime (CaO)
- must be freshly heated b4 use as it absorbs moisture n CO2 from air
- suitable for alkaline n neutral gases
- cannot be used to dry acidic gases as they react w CaO to form salt

Fused calcium chloride
- must be freshly heated b4 use as it absorbs moisture from air
- suitable for all gases except NH3

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8
Q

Sublimation

A

Sublimation is the process a substance changes from solid to gaseous state directly.

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9
Q

Substances that undergo sublimation
(I Need AirCon)

A

Iodine, ammonium chloride, naphthalene (used in mothballs)

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10
Q

Process of sublimation

A
  1. The solid sublimes into a gas on heating and moves away from the mixture
  2. By providing a cool surface for the gas to deposit on, the gas will change state back into a solid
  3. The resulting solid deposit, known as the sublimate, can be collected by scraping them off the cool surface

Step 1: In an evaporating dish, heat gently to sublime ammonium chloride.
Step 2: Place an inverted filter funnel over the evaporating dish to provide a cool surface for the NH4Cl to cool and condense the gaseous ammonium chloride to form white solid.

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11
Q

evaporation to dryness

A

Evaporation to dryness is used to separate a dissolved solid from its solvent by heating the mixture until all the solvent has vaporised (gaseous state)

Procedure:
Heat the solution in an evaporating dish until all the solvent evaporates and only the solute is left.

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12
Q

Crystallisation

A

Crystallisation is used to obtain a pure solid from its saturated solution. A saturated solution is one in which no more solute can be dissolved in the solvent.

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13
Q

Process of crystallisation

A
  1. Gently heat the copper (II) surface solution in an evaporating dish to evaporate most of the liquid until a hot saturated solution is obtained, when mass of the solution becomes constant.
  2. Cool the solution gradually until all the solid copper (II) sulfate crystals appear within the solution
  3. Filter the mixture via filter funnel lined with filter paper to collect solid residue crystals.
  4. Wash copper (II) sulfate crystals with cold distilled water (to remove impurities) and dry the crystals between a few pieces of filter paper.
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14
Q

Process of simple distillation

A
  1. The saltwater is heated. Boiling chips are added for smooth boiling. At 100dgC, the water boils. The vapour rises and enters the condenser through the exit sidearm of the distillation flask
  2. The water vapour cools in the condenser and condenses water to liquid water. Pure water is collected in the conical flask as distillate
  3. As more water vapour condenses, the salt solution becomes more concentrated. Eventually, a solid residue of salt remains in the distillation flask.
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15
Q

What does the thermometer measure in simple distillation

A

The thermometer measures the tempt of the vapour entering the condenser and therefore tells you the boiling point of the liquid. The tempt remains constant until all the liquid has boiled off.

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16
Q

Purpose of condenser in simple distillation

A

Water enters from the bottom and exits from the top, ensuring an efficient cooling system as it prevents the condenser from heating up.

17
Q

Separating funnel

A

Separating funnel r used to separate immiscible liquids (forms a heterogenous mixture when mixed). When a heterogenous mixture of >/2 immiscible liquids r left undisturbed, they can separate into phases. Least dense liquid on top.

18
Q

Fractionating column in fractional distillation

A
  1. Contains glass beads which provide a larger sa for vapour to condense on
  2. Length determines its ability to separate substances
  3. Liquids w similar boiling points will require a longer fractionating column for better separation.
19
Q

Procedure of fractional distillation.

A
  1. As the solution is heated, both ethanol and water vapour rise up the column.
  2. Water has a higher boiling point than ethanol. The water vapour condenses on the cool surfaces within the fractionating column and the liquid water returns to the flask.
  3. Ethanol vapour continues to rise, at its boiling point of 78d.c., it exits the column thru the exit sidearm at the top.
  4. The hot ethanol vapour cools and condenses into a liquid as it travels thru the inner tube of the condenser.
  5. Liquid ethanol flows into the conical flask.

(Conical flask must be replaced once the thermometer reading rises bp of initial distillate)

20
Q

Applications of fractional distillation

A

Oil refineries, separating different substances from crude oil
Liquefied air separated to produce N2, O2, and Argon gas for industrial applications.
Ethanol produce by glucose fermentation is extracted in breweries.

21
Q

Chromatography

A

Is used to separate a mixture of substances which hv diff solubilities in a given solvent.

22
Q

What will happen if the start line is marked using ink soluble in solvent

A

The ink will dissolve in the solvent and interfere with the results obtained. Hence, start line has to be marked with insoluble in solvent substance such as graphite pencil.

23
Q

Identifying colourless substances

A
  1. Using locating agent
  2. Examine chromatogram under ultraviolet light
24
Q

Applications of chromatography

A
  1. Identify unauthorised substances like pesticides n poison in food.
  2. Detect small quantities of banned substances
  3. Separate components like DNA fragments in forensic investigation
25
Q

Determining method to use when separating 2 substances

A

Thru physical properties of the components such as particle size, solubility and melting and boiling points.

26
Q

How can components separated in paper chromatographs be identified against known substances

A

By comparing the Rf value of the components against Rf value of pure substances.

Step 1: On a chromatography paper, draw the starting line (approximately 0.5 – 1 cm from the
bottom) using a pencil.
Step 2: Apply the orange colouring, E110 and E129 to the chromatography paper.
Step 3: Place the chromatography paper into a solvent. Ensure that the start line is above the
solvent level.
Step 4: Remove the chromatography paper when the solvent front is near the top of the
chromatography paper. Draw in the solvent front using a pencil. Add a locating agent.
Step 5: Calculate the Rf values of the substances by taking distance travelled by substance divided by distance travelled by solvent.
Step 6: Compare the Rf values.

27
Q

Determining purity of substances

A
  1. Chromatography
    - pure: only 1 spot
    - impure: more than 1 spot
    - components do not match spots of chromatograms of x -> unidentified impurity
  2. Melting and or boiling point
    - pure: fixed
    - impure: over a range of tempt
    - greater amt of impurities, larger the change; increase bp, lowers mp
28
Q

A student comments that the ion chromatograms give more information about mixtures than the emission spectrum.

A

The ion chromatogram provides info about the relative concentrations of the components in the mixtures but the emission spectrum does not.

The ion chromatogram can be used to identify more types of mixtures as it works for all substances that are able to dissolve in water however the emission spectrum is only suitable for elements that produce a coloured flame when burned.

29
Q

Describe and explain the process of fractional distillation of liquid air separates liquid air into nitrogen and oxygen. [3]

A

Liquid air is heated and vapourised. [1]
Vapour cools and condenses at different temperatures as the temperature gets progressively cooler higher up the column. [1]
Nitrogen will be collected at the top of the fractionating column as it has a lower boiling point but oxygen will be collected lower down the fractionating column as it has a higher boiling point. [1]

30
Q

Describe fully the steps to obtain solid CaCl2 from its amours reaction mixture. [2]

A

Filter to collect the filtrate and heat to evaporate most of the of the water until a hot saturated solution is obtained.
COOL to room temperature TO FORM CRYSTALS.
Filter to obtain crystals as solid residue, wash with cold distilled water and dry between pieces of filter paper.
Note: COLD distilled water because CaCl2 is a soluble salt. Soluble salt can be obtained using crystallisation. FWD still applies but for soluble salts, COLD dw is very important so that it does not become aqueous. Also, if H2O is evolved along with other gases, such as collecting H2 gas or CO2 gas, use a DRYING AGENT.

31
Q

Which salts can be made by precipitation reactions?

A

X y and X. They are salts that are insoluble in water which can be prepared by 2 aqueous salts and collected as residue by filtration.

32
Q

Outline a method for process 1. [2]

A

Evaporation. [1]
Dilute aqueous ammonium sulfate will be heated in an evaporating dish until most of the water has vapourised. [1]