C1 Reactivity Trend
What happens if a metal reacts with a dilute acid?
You see bubbles of hydrogen leaving the surface od the metal.
C1 Reactivity Trend
The faster the bubbling…?
The more reactive the metal is (being reacted w/ acid).
C1 Reactivity Trend
True or False?: very reactive metals are safe to used with an acid, as long as the acid is dilute.
False; it isn’t safe to react v. reactive metals (like calcium & lithium) with dilute acid.
C1 Reactivity Trend
Which metals can you react with a dilute acid?
Small pieces of metals like magnesium, aluminium, zinc, iron & copper.
C1 Reactivity Trend
What dilute acid should you use (to react with metals)?
Typically:
1) 1.0 mol/dm^3 HCl
2) or 0.5 mol/dm^3 H2SO4
C1 Reactivity Trend
What is the general idea for the reactivity trend practical?
1) test each metal in acid at room T & record observations
2) for any metals that show no reaction or v. slow reaction, can warm mixture & record any further observations
C1 Reactivity Trend
How do you warm something safely?
Ensure you wear eye protec..
Don’t overfill test tubes - should be no more than 1/4 full.
Can warm reaction mixture by placing test tube in beaker of hot water.
Have test tube rack ready to put test tube into post-warming.
How do you warm something safely (specifically for using a Bunsen Burner)?
1) half-open air hole
2) hold test tube securely w/ test-tube holder
3) tilt test tube so it pts away from you & other people
4) hold test tube few cm above flame w/ liquid’s surface over flame
5) move test tube in & out of flame & take it away pre-boiling begins
6) have test tube rack ready to put test tube into post-warming
C1 Reactivity Trend
How do you collect and test hydrogen?
Hydrogen is less dense than air so can collect it by upward delivery.
Hold empty test tube upside down over reaction mixture. Hydrogen will rise & fill test tube. Allow time to collect enough gas, then hold lighted splint to mouth of test tube & observe if there is a pop.
How can you show reactivity trends?
Displacement reactions:
1) start by measuring out small amt halide salt solution in test tube
2) + few drops of halogen solution to it & shake tube gently
3) if colour change seen, then reaction has happened
-> halide has displaced halide ion from the salt
-> if no reaction occurs, won’t be colour change
4) repeat process w/ diff. combos of halide salt & hydrogen
5) table for diff. combos
6) chlorine displaces both bromine & iodine from salt solutions
7) bromine can’t displace chlorine, but does displace iodine
8) iodine can’t displace chlorine or bromine
9) -> shows reactivity trends
10) -> halogens get less reactive as you go down group (to do w/ how easily they gain e^-s)
How do you show reactivity trends (table)?
start w/ / KCL(aq) - colourless / KBr(aq) - colourless / KI(aq) - colourless
add Cl2(aq) - colourless / no reaction / orange solution (Br2) formed / brown solution (I2) formed
add Br2(aq) - orange / no reaction / no reaction / brown solution (I2) formed
add I2(aq) - brown / no reaction / no reaction / no reaction
How do you set up an electrochemical cell? (electrolysis of copper sulfate)
1) get 2 electrodes (should use inert electrodes - platinum or carbon); clean surfaces of electrodes w/ piece of emery paper (or sandpaper)
2) from -> pt on, be careful not to touch the surfaces of the metals w/ hands -> could transfer grease back onto strips
3) place both electrodes into beaker filled w/ ur electrolyte
4) connect electrodes to power supply using crocodile clips & wires
How do you set up an experiment with non-inert electrodes?
1) non-inert electrodes can decompose into the electrolyte
2) e.g. could use copper electrodes in solution of copper sulfate
3) get 2 copper electrodes (not inert carbon or platinum 1s); clean surfaces of the electrodes w/ piece of emery paper (or sandpaper)
4) from -> pt on, be careful not to touch surfaces of metals w/ ur hands -> could transfer grease back onto strips
5) place both electrodes into beaker filled w/ ur electrolyte
6) connect electrodes to power supply using crocodile clips & wires
7) as reaction cont.s, mass of anode will decrease & mass of cathode will increase
-> bc copper is transferred from anode to cathode
8) reaction takes bit of time to happen, so will need to leave cell running for 30 mins or so to get decent change in mass
9) if want to measure how mass of electrodes has changes in experiment like this one, should dry electrodes before weighing them
-> any copper sulfate solution on electrodes may mean they appear to have higher mass than they rlly do
What are the results for the electrolysis practical with inert electrodes and copper sulfate solution?
Solution of copper sulfate (CuSO4) contains 4 diff. ions: Cu^2+, SO4^2-, H^+ & OH^-.
1) copper metal is less reactive than hydrogen so at cathode, copper metal prod.d & you’d see coating of copper forming on cathode:
Cu^2+ + 2e^- -> Cu
2) aren’t any halide ions present so at anode, oxygen & water prod.d; ud see bubbles of gas forming:
4OH^- -> O2 + 2H2O + 4e^-
What are the results for the electrolysis of copper sulfate solution using non-inert electrodes?
Non-inert electrodes can take part in electrolysis reactions.
Electrical supply acts by:
1) pulling electrons off copper atoms at anode, causing them to go into solution as Cu^2+ ions:
anode: Cu(s) -> Cu^2+(aq) + 2e^0
2) then offering electrons at cathode to nearby Cu^2+ ions to turn them back into copper atoms:
cathode: Cu^2+(aq) + 2e^- -> u(s)
How do you conduct the thin-layer chromatography (TLC) practical?
1) draw line neat bottom of plate w/ pencil bc pencil marks are insoluble & won’t move w/ solvent as ink might
-> put spot of mixture to be separated on line
2) put ~ of solvent into beaker; dip bottom of plate (not spot) into solvent
3) put watch glass over beaker to stop any solvent from evaporating away
4) solvent will start to move up plate; when chemicals in mixture dissolve in solvent, they will move up plate too
5) will see diff. chem.s in sample separate out, forming spots at diff. places on plate
6) remove plate from beaker before solvent reaches top; mark distance solvent has moved (the solvent front) in pencil
-> can use -> technique to separate the diff. components of a dye
Outline the set-up for the TLC practical.
1) watch glass
2) solvent front
3) plate
4) spot of unknown substance
5) point of origin
6) solvent
How do you conduct the simple distillation practical?
Used for separating out liquid from solution:
1) pour sample of seawater into distillation flask
2) set up apparatus (diagram for this); connect bottom end of condenser to cold tap using rubber tubing; run cold water thru condenser to keep it cool
3) grad.ly heat distillation flask; part of solution w/ lowest bpt will evap, in this case, the water
4) water vapour passes into condenser where it cools & condenses (turns back into liquid), then flows into beaker where it’s collected
5) event.ly end up w/ salt left in flask
Outline the set-up for the simple distillation practical.
1) thermometer
2) water out
3) condenser
4) water in
5) pure distilled water
6) seawater
7) heat
How do you conduct the fractional distillation practical?
If mixtr of liquids, can separate it w/ fractional distillation; lab demo that can be used to model fractional distillation of crude oil at refinery:
1) put mixture in flask; attach fractionating column & condenser above flask (diagram for this)
2) grad.ly heat flask; diff. liquids will all have diff, bpts
-> so will evap at diff. Ts
3) liquid w/ lowest bpt evap.s 1st; when T on thermometer matches bpt of liquid, will reach top of column
4) liquids w/ higher bpts might also start to evap.
-> but column cooler towards top so will only get part of way up before condensing & running back down to flask
5) when 1st liquid has been collected, raise temperature until next 1 reaches top
Outline the set-up for the fractional distillation practical.
1) thermometer
2) coldest bit of column
3) fractionating column filled w/ glass rods
4) hottest bit of column
5) crude oil substitute
6) heat
7) condenser
8) water out
9) water in
10) fractions collected at lower temperatures
How do you test for anions? (halide ions)
To test for chloride ions (Cl^-), bromide ions (Br^-) or iodide ions (I^-):
1) add some dilute nitric acid (HNO3)
-> to 1st get rid of any carbonate ions which prod. pale ppt w/ silver nitrate too
-> can’t use HCl, bc that would add chloride ions
2) followed by few drops of silver nitrate solution (AgNO3)
a) chloride ions give white ppt of silver chloride:
Ag^+(aq) + Cl^-(aq) -> AgCl(s)
b) bromide ions give cream ppt of silver bromide:
Ag^+(aq) + Br^-(aq) -> AgBr(s)
c) iodide ions give yellow ppt of silver iodide:
Ag^+(aq) + I^-(aq) -> AgI(s)
How do you test for anions? (carbonates)
1) to test for carbonate ions in solution, 1st add ~ barium chloride solution
-> if carbonate ions present, will prod. white ppt of barium carbonate
2) then + ~ dilute HCl
3) if carbonate ions present, mxtr will fizz
-> this bc carbonate will react w/ acid to prod. CO2 gas:
-> barium carbonate + acid -> barium ions + carbon dioxide + water
BaCO3(s) + 2H^+(aq) -> Ba^2+(aq) + CO2(g) + H2O(l)
4) if gas collected and passed thru limewater, limewater should turn cloudy
5) once all of barium carbonate has reacted, will end up w/ colourless solution containing Ba^2+ ions
How do you test for anions? (sulfate ions)
1) test for sulfate ions in solution is similar to test for carbonate ions
2) add some barium chloride solution
-> if sulfate ions in solution, white ppt of barium sulfate will form:
barium ions + sulfate ions -> barium sulfate
Ba^2+(aq) + SO4^2-(aq) -> BaSO4(s)
3) then add some dilute hydrochloric acid to the test sample
4) barium sulfate will not react with dilute hydrochloric acid, so white ppt will not dissolve
-> that’s how u know you’ve got sulfate ions & not carbonate ions