|
Hint
|
Answer
|
|
5. the first titration is the ____ titration to indicate roughly how much acid is required
|
rough
|
|
6. titrate again. run the acid solution to 1cm^3 below the rough titre then add acid ____
|
dropwise
|
|
swirl after each drop until the colour of the ____ just changes
|
indicator
|
|
7. repeat until you have three ____ results within 0.10cm^3 of each other and use the mean
|
concordant
|
|
____ ions are strong enough oxidising agents to oxidise iodide ions to iodine
|
chlorate
|
|
therefore, we can use iodine-thiosulfate titration to find the ____ of a solution of chlorate (I)
|
concentration
|
|
1. pour some chlorate (I) solution into a clean, dry beaker and transfer a 25cm^3 ____ into a conical flask
|
aliquot
|
|
2. add excess iodide ions, using a measuring cylinder to transfer e.g. 15cm^3 of 0.5 mol dm^3 potassium ____ to the conical flask
|
iodide
|
|
3. add excess hydrogen ions by adding 20cm^3 of 1 mol dm^3 ____ ____
|
sulfuric acid
|
|
at this stage, the contents will be ____ due to iodine being produced
|
brown
|
|
4. fill burette with a standard solution of 0.1mol dm^3 ____ ____
|
sodium thiosulfate
|
|
5. put the conical flask on a ____ ____ to make the end point easier to see
|
white tile
|
|
6. carry out titrations. near the end point, the contents of the flask will be a ____ ____ colour
|
pale straw
|
|
at this point, add a few drops of ____ solution
|
starch
|
|
the contents of the flask will turn ____ ____ due to iodine being present
|
blue-black
|
|
7. the end point is where the solution is ____
|
colourless
|
|
1. select the filter with the ____ colour to the test solution
|
complementary
|
|
this allows for the greatest values of ____
|
absorbance
|
|
2. make up a range of ____ ____ of the test solution, both above and below the concentration of the unknown solution
|
standard solutions
|
|
3. zero the colorimeter using a ____ of pure solvent
|
cuvette
|
|
4. measure the ____ of each of the standard solutions
|
absorbance
|
|
5. plot a ____ ____ of concentration against absorbance
|
calibration curve
|
|
6. measure the absorbance of the ____ sample and use the calibration curve to determine its concentration
|
unknown
|
|
1. pour a known volume of water into a copper ____ and record its temperature
|
calorimeter
|
|
2. weigh a ____ ____
|
spirit burner
|
|
keep the cap on to reduce fuel loss by ____
|
evaporation
|
|
3. support the calorimeter over a spirit burner containing the ____ to be tested
|
fuel
|
|
4. surround with a ____ ____ to help reduce energy losses
|
draught excluder
|
|
5. remove the cap of the spirit burner and light the ____
|
wick
|
|
6. carry on heating until the temperature has risen by about ____ to ____ K
|
15 20/1520/fifteentwenty/fifteen twenty
|
|
7. ____ the spirit burner and replace the cap
|
extinguish
|
|
8. keep stirring the water. make a note of the ____ temperature reached
|
highest
|
|
9. weigh the burner again. you can use this to determine ____ ____ __ ____
|
enthalpy change of combustion
|
|
1. use a measuring cylinder to add a known volume of a known concentration of acid to an ____ ____
|
insulated vessel
|
|
2. use a thermometer to take the initial ____
|
temperature
|
|
3. use a ____ ____ to add a known volume of a known concentration of alkali and stir to mix
|
measuring cylinder/volumetric pipette
|
|
4. top the vessel with a ____ with a hole in and place the thermometer through the hole in the ____
|
lid
|
|
5. record changes in ____ every 30 seconds until there is no further change
|
temperature
|
|
6. calculate the maximum temperature reached and use this to determine ____ ____ __ ____
|
enthalpy change of neutralisation
|
|
1. add a known volume of a known concentration of reactant solution to an ____ ____
|
insulated vessel
|
|
2. add a known mass of solid reactant in ____
|
excess
|
|
3. top the vessel with a ____ with a hole in
|
lid
|
|
4. record changes in temperature every 30 seconds until there is no ____ ____
|
further change
|
|
5. plot a graph of temperature against time and ____ to find the theoretical maximum temperature change
|
extrapolate
|
|
1. pass an electric current through the ____
|
electrolyte
|
|
you may need to collect ____ products
|
gaseous
|
|
if so, do this by filling test tubes with water as these will ____ the water
|
displace
|
|
if electrolysis to be carried out to ____ a metal:
|
purify
|
|
the ____ will need to be made of the impure metal
|
anode
|
|
the electrolyte must contain ____ of that metal
|
ions
|
|
the ____ should be made of the pure metal
|
cathode
|
|
1. set up apparatus, place several test tubes of water in the ____ ____
|
collection trough
|
|
2. strongly heat the ____
|
catalyst
|
|
this ensures that when the hydrocarbon vapour passes over it, the temperature is high enough for any ____ reactions to take place
|
cracking
|
|
3. heat the ____ gently, collecting any gases that pass into the collection tubes
|
hydrocarbon
|
|
4. change and cork any full tubes to prevent ____ ____ and continue to heat
|
suck back
|
|
5. discard the first tube of gas because this will just be ____ air
|
displaced
|
|
6. continue heating until no more ____ is produced
|
gas
|
|
7. remove the ____ ____ from the collection trough before stopping heating to prevent suck back
|
delivery tube
|
|
8. leave to ____, then dismantle
|
cool
|
|
9. test any liquid product with ____ ____. it should remain orange/brown
|
bromine water
|
|
10. test the gas by shaking with bromine water. it should ____
|
decolorise
|
|
add a few drops of ____ ____
|
bromine water
|
|
if an alkene is present, the bromine water will change from orange/brown to ____
|
colourless
|
|
similar to a ____ in that a light source is passed through a sample and absorbance or transmission is measured
|
colorimeter
|
|
in the case of a colorimeter, the coloured light used as a source can only be selected from a specific number of different ____
|
wavelengths
|
|
a visible spectrophotomer can give data for absorption or transmission for any given value of the ____ ____
|
visible spectrum
|
|
1. construct the ____ ____ whose electrode potential is to be measured
|
half cell
|
|
for a metal ion/metal half cell, the ____ will be made from the solid metal
|
electrode
|
|
if the reaction involves two ions of the same element in different oxidation states, the electron should be ____
|
platinum
|
|
in that case, the solution will contain a ____ of the two ions
|
mixture
|
|
in all cases, ensure ____ ____
|
standard conditions
|
|
2. connect the half-cell to a ____ ____ ____ ____
|
standard hydrogen half cell
|
|
3. connect the two electrodes to a ____ ____ ____
|
high resistance voltmeter
|
|
ensure the reading on the voltmeter is ____
|
positive
|
|
this ensures that the half-cell connected to the ____ ____ of the voltmeter is the positive electrode
|
positive terminal
|
|
if the reading is ____ switch the connections on the voltmeter
|
negative
|
|
4. take the voltmeter reading to find ____ ____ (or standard ____ ____ in this case
|
electrode potential
|
|
you need to ___ the pH electrode for temperature because pH is dependent on temperature
|
calibrate
|
|
1. wash the electrode with ____ ____
|
deionised water
|
|
2. transfer into a ____ ____ of pH 7.00
|
buffer solution
|
|
3. check the bulb of the electrode is completely immersed, then wait for the reading to ____
|
stabilise
|
|
ensure the ____ reads 7.00 and adjust to that value if necessary
|
meter
|
|
calibrate to pH ___ for acidic solutions
|
4.00
|
|
calibrate to pH ___ for alkaline solutions
|
10.00
|
|
to measure both acidic and alkaline solutions with a wide range of values, calibrate with acidic, alkaline and neutral ____
|
buffers
|
|
first, prepare a ____ ____ in deionised water
|
saturated salt
|
|
1. warm deionised water in a small conical flask and add the salt, ____ frequntly
|
shaking
|
|
2. keep adding ____ until no more dissolves
|
solute
|
|
3. leave the mixture to cool to ____ ____
|
room temperature
|
|
4. filter and discard the ____
|
residue
|
|
Ksp is ____ dependent, so take the ____ of the solutions you're working with
|
temperature
|
|
the second stage is determining ____ of one of the ions in solution
|
concentration
|
|
just one is sufficient because the concentration of one ion is ____ to the other
|
proportional
|
|
for a basic solution, concentration can be determined using acid-base titration with the ____ ions
|
hydroxide
|
|
for a coloured solution, it can be determined by ____
|
colorimetry
|
|
1. allow a mixture to reach ____
|
equilibrium
|
|
2. determine ____ of one of the components in the equilibrium mixture
|
concentration
|
|
3. use this to work out the other concentrations and calculate ____ using the equation
|
Kc
|
|
a measure of the closeness of agreement between an individual test result and the accepted reference value
|
accuracy
|
|
the closeness of agreement between independent measurements made under the same conditions
|
precision
|
|
the difference between an individual measurement and the true value or accepted reference value of the quantity being measured
|
error
|
|
an estimate attached to a measurement which characterises the range of values within which the true value is asserted to lie
|
uncertainty
|
|
the opposite of uncertainty (if uncertainty is great, the measurement is unreliable)
|
reliability
|
|
uncertainty is usually taken to be ____ a division on either side of the smallest scale on the scale you're using
|
half
|
|
percentage uncertainty = uncertainty x number of measurements x 100 divided by ____ ____
|
measured quantity
|
|
when you use a ____ measuring device, you should record all the figures shown on the instrument
|
digital
|
|
when using a non-digital device, you should record all the figures that are certain plus one that is ____
|
estimated
|