Methods Flashcards
Method of a reaction using colorimeter
- Samples of diff concentrations
- Calibrate colorimeter - blank solution
- Absorbance of each solution of known conc
- Calibration curve of absorbance against conc
- Reaction mixture in colorimeter and record absorbance at diff times
- Use calibration curve to convert absorbance to concentration and plot graph of concentration against time
- Gradient of tangent at any concentration equals rate
Rate using quenching and titrating
- Mix solutions - remove samples by pipette at various times
- Quench - stop reaction - rapid cooling/large vol of water/add chemical to remove reactant that is not being monitored
- Titrate - find conc of reactant/product
- Graph conc against tine - grad of tangent at any concentration equals rate
Measuring rate through pH
- Start reaction
- Record pH at diff times - pH meter
- H ion conc using pH = -log(H+)
- Graph H+ against time - grad of tangent equals rate
Rate using volume of gaseous product over time
- Attach gas syringe to reaction vessel or collect gas over water in inverted measuring cylinder
- Start reaction
- Vol of gas at different time intervals
- Vol of gas against time
Calculate rate by measuring the mass if a gaseous product over time
- Place a flask containing one reactant on a balance and record mass
- Add second reactant and start clock
- Mass at different time intervals
- Graph of mass against time
How do you make a buffer solution
- Use burette to measure out calculated volumes of solutions containing equimolar amounts of weak acid and its salt and add to beaker
- Mix using magnetic stirrer
- Record pH using pH meter
Determine the shape of a titration curve by measuring the pH
- Record pH os solution - pH paper
- Fill burette - known conc
- Add in 5cm^3 from burette and mix w magnetic stirrer
- Record pH after each addition
- Add in 0.5cm^3 near end point
- Add two 5cm^3 portions after end point
- Graph of pH against volume of solution added
What is the method for preparing, recrystallising and determining the melting point of 2,4-dinitrophenylhydrazones
See notes
Use Fehling’s solution and Tollens’ reagent to distinguish between aldehydes and ketones
- Add a few drops of unknown compound to 1cm^3 of freshly prepared Tollens’ reagent in clean test tube
- Warm in hot water bath
- Freshly prepare Fehling’s solution - mix 1cm^3 of Fehling’s solution A with 1cm^3 of Fehling’s solution B
- Add few drops of unknown compound - warm in water bath
What is the method for preparing carboxylic acid from an alcohol
See notes
How do you prepare a liquid Ester from a carboxylic acid and an alcohol
See notes
How do you prepare methyl 3-nitrobenzoate
See notes
Titrating iodine with sodium thiosulfate solution using starch and hence estimate oxidising agents by their reaction with excess acidified potassium iodide
- Rinse pipette with sodium iodate(V) solution, using pipette filler, pipette 25cm^3 of standard potassium iodate(V) solution into conical flask
- Add approximately 1.5g of potassium iodide (excess) and excess sulfuric acid
- Rinse burette with standard sodium thiosulfate, fill burette w it
- Add standard sodium thiosulfate from burette until solution is straw coloured, add 3 drops of starch indicator
- Titration until blue-black to colourless
- Repeat until results are concordant
Titrating acidified potassium manganate(VII) solution with reducing agents
- Rinse pipette with solution of reducing agent and use pipette to transfer 25cm^3 to conical flask
- Rinse burette w standard solution of potassium manganate(VII) and then fill burette
- Add excess sulfuric acid using measuring cylinder to conical flask
- Add potassium manganate(VII) solution from burette into conical flask and swirl until colourless to pink
- Repeat until results are concordant
Determine purity of a group II metal oxide or carbonate by back titration
- Weigh out mass of the solid
- Add excess HCl
- Add to 250 volumetric flask - make up w deionised water until meniscus on mark
- Rinse pipette with solution from volumetric flask and pipette 25cm^3 to conical flask
- 3 drops phenolphthalein
- Rinse burette with alkali and fill
- Add alkali until indicator changes colour
- Repeat until concordant
Carrying out paper and thin-layer chromatography and measure the Rf values of the components and interpret the chromatogram
- Base line in pencil close to bottom
- Spot samples on line using capillary tube - dry - repeat till spot concentrated
- Place paper in tank with shallow amount of solvent - cover with lid - allow solvent to run up over spots until solvent almost reaches top - mark solvent front - allow to dry
- If substances are colourless then spray with locating agent eg ninhydrin
- Measure dist travelled by the solvent front and each spot - calculate the Rf
Two-way chromatography
Chromatography method then
- Rotate through 90°
- Run in second solvent
- Locating agent if colourless
- Rf
Carrying out the reduction of acidified ammonium vanadate(V) with zinc and observing the sequence of colours
- Dissolve some ammonium vanadate(V) in HCl in conical flask
- Add two spatulas of zinc as reducing agent
- Stopper with cotton wool, allow H to escape and slow entry of air
- Observe sequence of colours
Determining the electrode potentials of a series of cells and predicting their values using standard electrode potentials
- Set up a half cell - a metal dipping in 1M solution of its ions in a beaker
- Attach via wires, and a voltmeter to a second half-cell using a different metal and a 1M solution of its ions
- Use salt bridge to connect two beakers
- Record the voltage
Preparing aspirin using salicylic acid and ethanoic anhydride
- Place 1g of 2-hydroxybenzoic acid in a dry pear shaped flask and add 2cm^3 of ethanoic anhydride
- Safely add 8 drops of concentrated phosphoric(V) acid
- Heat under reflux for 30 mins
- Add water to hydrolyse any unreacted ethanoic anhydride to ethanoic acid
- Pour the mixture onto 400g of crushed ice in a beaker
- Remove product by suction filtration
- Recrystallise from water
- Dry in low temp oven
- Determine melting point
Using chromatography to compare the purity of laboratory-made aspirin with commercial tablets
- Base line with pencil close to bottom and draw two pencil crosses on it
- Place some laboratory-made aspirin solid on watch glass and dissolve in a few drops of solvent such as ethanol - spot solvent on pencil cross using capillary tube, dry and repeat until conc - repeat for commercial solid
- Place in solvent, cover with lid, run up until near top - mark solvent front and allow to dry
- Spots visible by placing in beaker containing iodine crystals
- Rf
How do you determine something’s melting point
- Place solid in capillary tube/melting point tube sealed at one end
- Heat slowly
- Record temp at which solid starts and finishes melting
- Repeat and average the temperatures
- Compare temp with known values in data book