Practical common questions Flashcards

(64 cards)

1
Q

Increasing distillation yield (2 points) with products that will oxidise further

A

Keep the temperature of the reaction mixture below the boiling point of propan-1-ol/below 97 °C
Cool the distillate / collecting vessel

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2
Q

Irritant

A

dilute acid and alkalis- wear googles

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3
Q

Corrosive

A

stronger acids and alkalis wear goggles

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4
Q

Flammable

A

keep away from naked flames

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5
Q

Toxic

A

wear gloves- avoid skin contact- wash hands after use

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6
Q

Oxidising

A

Keep away from flammable / easily oxidised materials

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7
Q

when heating in a crucible why shouldnt large amounts of solid be used

A

Large amounts of hydrated calcium sulfate, such as 50g,
should not be used in this experiment as the decomposition is
likely to be incomplete.

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8
Q

why does the crucible need to be dry when heating

A

The crucible needs to be dry otherwise a wet crucible would
give an inaccurate result. It would cause mass loss to be too
large as the water would be lost when heating.

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9
Q

when heating in a crucible why shouldnt small amounts of solid be used

A

Small amounts of the solid , such as 0.100 g, should not be used in this experiment as the percentage uncertainties in weighing will be too high.

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10
Q

why use a lid when heating in a crucible

A

The lid improves the accuracy of the experiment as it prevents loss of solid from the crucible but should be loose fitting to allow gas to escape.

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11
Q

errors in gas syringe experiments

A

*gas escapes before bung inserted
*syringe sticks
* some gases like carbon dioxide or sulphur dioxide are
soluble in water so the true amount of gas is not
measured.

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12
Q

errors when drawing gas syringe

A

ALWAYS add markings to show measurement made
make sure everything is connected so gas cant escape

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13
Q

reason to invert in volumetric solution making

A

to ensure a uniform concentration.

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14
Q

why not heat volumetric flask

A

Do not heat or put hot
solutions in the volumetric flask because the heat would cause
the flask to expand and the volume would then be incorrect.

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15
Q

why volumetric pipette more accurate than cylinder

A

Using a volumetric pipette is more accurate than a measuring cylinder because it has a smaller uncertainty.

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16
Q

in standard phrase titrate a with b which in which container

A

However, the standard phrase: titrate solution A
with solution B means that A should be in the
conical flask and B should be in the burette.

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17
Q

why use conical flask

A

A conical flask is used in preference to a beaker because
it is easier to swirl the mixture in a conical flask without
spilling the contents.

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18
Q

common error when using burettte

A

make sure the jet space in the burette is filled with the
solution and air bubbles are removed.
If the jet space in the burette is not filled properly prior to commencing the
titration it will lead to errors if it then fills during the titration, leading to a
larger than expected titre reading.

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19
Q

degree of precision on burette

A

Even though a burette has marking reading to 0.1cm3
, the burette readings
should always be given to 2dp either ending in 0.00 or 0.05. 0.05cm3
is the
volume of 1 drop of solution delivered from a burette and so this is the
smallest difference in readings that can be measured. If the bottom of the
meniscus sits on a line it should end with a 0.00 as in the above example
9.00cm3. If the meniscus sits between two lines it should end 0.05. e.g. if the
bottom of the meniscus sits between the lines marked 9.1 and 9.2, you should
record 9.15

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20
Q

phenolphthalein colour change and when used

A

If acid is added from the burette the colour change would
be pink (alkali) to colourless (acid): end point pink colour
just disappears [use with titrations using strong alkalis e.g.
NaOH ]

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21
Q

Methyl orange colour change and when used

A

Methyl orange is a suitable indicator for neutralisation reactions where strong acids are used.
It is red in acid and yellow in alkali. It is orange at the end point.

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22
Q

concordent titration results

A

within 0.1cm3 of each other

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23
Q

titration between permanganate and iron (ii)

A

MnO4-(aq) + 8H+(aq) + 5Fe2+(aq)—-> Mn2(aq) + 4H2O(l) + 5Fe3+(aq)

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24
Q

acid used for permanganate titrations

A

dilute sulfuric acid needed to supply 8h+ ions - wont set up alternate redox reactions

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25
if not enough h+ ions added in permanganate titration what happens
mno2 formed which is brown masking the correct colour change and accurate endpoint wont be reached
26
why not hcl/ hno3 in permanganate titrations
Cl- ions would be oxidised to Cl2 by MnO4- as the Eo MnO4-/Mn2+ > EoCl2/Cl- This would lead to a greater volume of manganate being used and poisonous Cl2 being produced. It cannot be nitric acid as it is an oxidising agent. It oxidises Fe2+ to Fe3+ as Eo NO3-/HNO2 > Eo Fe3+/Fe2+ This would lead to a smaller volume of manganate being used.
27
permanganate with hydrogen peroxide equation titration
Overall 2MnO4 - (aq) + 6H+ (aq) + 5H2O2  5O2 + 2Mn2+ (aq) + 8H2O
28
permanganate with ethanedioate equation titration
Overall 2MnO4 - (aq) + 16H+ (aq) + 5C2O4 2-(aq) 10CO2 (g) + 2Mn2+(aq) + 8H2O(l)
29
why slow rxn between mno4- and c2o42-
The reaction between MnO4-and C2O42- is slow to begin with (as the reaction is between two negative ions). To do as a titration the conical flask can be heated to 60oC to speed up the initial reaction.
30
Readings def
the values found from a single judgement when using a piece of equipment
31
measurement def
the values taken as the difference between the judgements of two values (e.g. using a burette in a titration)
32
% uncertainty
% uncertainty = +_ uncertainty/ Measurement made on apparatus x 100
33
Reducing uncertainties in a titration
Replacing measuring cylinders with pipettes or burettes which have lower apparatus uncertainty will lower the % uncertainty To reduce the % uncertainty in a burette reading it is necessary to make the titre a larger volume. This could be done by: increasing the volume and concentration of the substance in the conical flask or by decreasing the concentration of the substance in the burette.
34
Reducing uncertainties in measuring mass
Using a balance that measures to more decimal places or using a larger mass will reduce the % uncertainty in weighing a solid. Weighing sample before and after addition and then calculating difference will ensure a more accurate measurement of the mass added.
35
slow reaction means what in calorimetry
If the reaction is slow then the exact temperature rise can be difficult to obtain as cooling occurs simultaneously with the reaction To counteract this we take readings at regular time intervals and extrapolate the temperature curve/line back to the time the reactants were added together.
36
errors in calorimetry experiment (5 of them)
* energy transfer from surroundings (usually loss) * approximation in specific heat capacity of solution. The method assumes all solutions have the heat capacity of water. * neglecting the specific heat capacity of the calorimeter- we ignore any energy absorbed by the apparatus. * reaction or dissolving may be incomplete or slow. * Density of solution is taken to be the same as water.
37
calorimetry questions remember
Remember in these questions: sign, unit exo or endo, increase or decrease in temp of surroundings?
38
reason enthalpy of hydration cant be done experimentally
This cannot be done experimentally because it is impossible to add the exact amount of water without the solid dissolving and it is not easy to measure the temperature change of a solid.
39
errors in flame calorimetry
energy losses from calorimeter * Incomplete combustion of fuel * Incomplete transfer of energy * Evaporation of fuel after weighing * Heat capacity of calorimeter not included * Measurements not carried out under standard conditions as H2O is gas, not liquid, in this experiment
40
in dissapreaing cross what is rate why works
1/t t= time taken for cross to dissappear (fixed mass of sulfur produced) assume same mass of sulfur each time
41
If titrating to find concentration of something as a reaction is happening what do you need to do?
Stop the reaction / quench By dilution / cooling / adding a reagent to react with H2O2/I-
42
What needs to be drawn in filtering diagram
filter paper
43
solid potassium dichromate danger what to do why
You must wear gloves when handling solid potassium dichromate(Vl) since it is highly toxic and a category 2 carcinogen; it is also an irritant. Avoid inhaling any dust.
44
Where is the thermometer placed in distilation
Bulb of the thermometer should be at the T junction connecting to the condenser to measure the correct boiling point
45
Where does water flow in condenser
Note the water goes in the bottom of the condenser to go against gravity. This allows more efficient cooling and prevents back flow of water.
46
IMPORTANT IN REFLUX DIAGRAM and why
Never seal the end of the condenser as the build up of gas pressure could cause the apparatus to explode. This is true of any apparatus where volatile liquids are heated including the distillation set up
47
anti bumping granules why
Anti-bumping granules are added to the flask in both distillation and reflux to prevent vigorous, uneven boiling by making small bubbles form instead of large bubbles
48
Watch out when drawing reflux diagram
It’s important to be able to draw and label this apparatus accurately. * Don’t draw lines between flask and condenser. * Don’t have top of condenser sealed * Condenser must have outer tube for water that is sealed at top and bottom * Condenser must have two openings for water in and out that are open
49
Hydrolysis def
the splitting of a molecule ( in this case a haloalkane) by a reaction with water
50
rate of reaction with hydrolysis of haloalkanes
The precipitate only forms when the halide ion has left the haloalkane and so the rate of formation of the precipitate can be used to compare the reactivity of the different haloalkanes. The quicker the precipitate is formed, the faster the substitution reaction and the more reactive the haloalkane The weaker the bond, the easier it is to break and the faster the reaction.
51
initial rate from conc time graph
The initial rate can be calculated from taking the gradient of a continuous monitoring conc vs time graph at time = zero
52
large excess of reactants rate of reaction
In reactions where there are several reactants, if the concentration of one of the reactant is kept in a large excess then that reactant will appear not to affect rate and will be pseudo-zero order . This is because its concentration stays virtually constant and does not affect rate.
53
ROR Technique measurement of the change in volume of a gas
change in the number of moles of gas in the reaction gas syringe
54
ROR Technique Measurement of change of mass
This works if there is a gas produced which is allowed to escape. Works better with heavy gases such as CO2
55
ROR Technique Titrating samples of reaction mixture with acid, alkali, sodium thiosulphate etc
Small samples are removed from the reaction mixture, quenched (which stops the reaction) and the titrated with a suitable reagent
56
ROR Technique Colorimetry.
If one of the reactants or products is coloured then colorimetry can be used to measure the change in colour of the reacting mixtures
57
ROR Technique Measuring change in electrical conductivity
Can be used if there is a change in the number of ions in the reaction mixture
58
ROR Technique Measurement of optical activity.
If there is a change in the optical activity through the reaction this could be followed in a polarimeter
59
salt bridge facts quick
The salt bridge is used to connect up the circuit. The free moving ions conduct the charge. A salt bridge is usually made from a piece of filter paper (or material) soaked in a salt solution, usually Potassium Nitrate. It can also be a glass U tube containing a salt solution plugged with cotton wool The salt should be unreactive with the electrodes and electrode solutions.. E.g. potassium chloride would not be suitable for copper systems because chloride ions can form complexes with copper ions. A wire is not used because the metal wire would set up its own electrode system with the solutions
60
Note: in the electrode system containing two solutions it is necessary to use a platinum electrode and both ion solutions must be of a 1M concentration so [Fe2+] = 1M and [Fe3+ ] = 1M .
61
calibration with pH curve
Calibrate meter first by measuring known pH of a buffer solution. This is necessary because pH meters can lose accuracy on storage. Most pH probes are calibrated by putting probe in a set buffer (often pH 4) and pressing a calibration button/setting for that pH. Sometimes this is repeated with a second buffer at a different pH
62
improving accuracy of titration curves
Can also improve accuracy by maintaining constant temperature
63
shape of pH curve at start and reason
At the start the pH rises quickly and then levels off. The flattened part is called the buffer region and is formed because a buffer solution is made
64