Chemistry Practical Techniques
This page summarises the practical techniques required for the exams (i.e. the last chapter in the official textbook). I am not currently planning on further developing this page or adding flashcards since the content is covered within the other Chemistry pages on my site.
Measurements:
I didn't do notes on these since they're quite simple- Weighing a solid
- Pipette
- Burette
- Gas volumes (gas syringe or inverted burette/measuring cylinder)
Organic:
- Heating under reflux
- Water in bottom, out top of condenser
- Anti-bumping granules burst bubbles, reducing chance of boiling over
- Purifying an organic liquid product
- Separating funnel
- Add sodium hydrogen carbonate or dilute acid
- Dry by adding anhydrous sodium sulfate
- Then use distillation
Inorganic:
- Making water-soluble inorganic salts
- Acid + alkali
- Titration to find how much acid needed for neutralisation
- Repeat but without indicator
- Evaporating basin and Bunsen until crystals appear
- Leave to cool
- Heat in watch glass and oven, until constant mass
- Acid + insoluble base
- Heat mixture until neutral (indicator paper), adding base as needed
- Filter, evaporating basin until crystals appear
- Leave to cool
- Filter, wash, heat in watch glass in oven until constant mass
- Making water insoluble inorganic salts
- Mix equal volumes in beaker, forming precipitate
- Filter, wash
- Watch glass in oven until constant mass
Purification:
- Distillation
- Water goes in furthest from the pear shaped flask
- Thin layer (silica plate), paper chromatography
- Recrystallisation
- Solvent: desired compound dissolves at high temperatures only, impurities all dissolve at all temperatures
- Dissolve in the minimum amount of hot solvent
- Preheat the filter funnel and conical flask
- Filter (to remove insoluble impurities), keep filtrate. Cool. Filter, keep crystals
- Dry
- Vacuum filtration
- Vacuum pump through side arm of conical flask
- Damp filter paper in Buchner funnel
- Disconnect flask from vacuum pump before turning it off (prevent suck-back)
Analysis:
- Melting point determination
- Fill Thiele tube with a liquid/oil
- Solid sample in capillary tube alongside mercury thermometer
- Heat, recording the temperature when the sample starts/ends melting
- Range between two readings is the melting range
- The higher the melting range, the more impure the sample is
- Colorimetry
- Filter (complementary colour to solution colour)
- Zero with cuvette of solvent (usually water)
Making standard solutions:
- From a solid
- Mix with deionised water in a beaker before pouring into volumetric flask
- From higher concentration solution
- Calculations: use
Titration:
- Acid-base
- Iodine-thiosulfate
- Redox
Energy transfer:
- Burning fuel
- Use spirit burner (keep cap on when not in use to prevent evaporation)
- Use copper calorimeter, draught excluder
- Reaction
- Insulated polystyrene cup
- Extrapolate backwards if readings were taken every 30 s/60 s etc
Electro:
- Electrolysis
- Use inverted test tubes (filled with water) to collect gases
- Purification: pure metal cathode, impure anode, (aq) solution
- Finding standard electrode potentials
- H+(aq) and platinum wire electrode surrounded by H2(g)
- Other electrode is the metal to be measured in its solution
- Salt bridge, voltmeter
Measuring pH:
- Calibrate in a neutral solution (pH is temperature dependent)
- Also calibrate in pH 4.00 for acid measurement, or pH 10.00 for alkali measurement
- Then rinse electrode and use for testing
Alkenes:
- Cracking
- Porcelain chips to be heated in centre of boiling tube
- Mineral wool soaked in alkene [e.g. paraffin (l)] at end
- Discard first tube
- Heat whilst changing tubes to prevent suck-back
- Testing for unsaturation
- Br2(aq) (yellow/orange → colourless if an alkene)