Required Practicals Flashcards
In the preparation of ethyl ethanoate, why must concentrated H2SO4 be added slowly and with cooling?
When sulfuric acid is dissolved it gives off a lot of heat which may act as a hazard
Why must the mixture in the preparation of ethyl ethanoate be homogenous?
So that the mixture can undergo reflux.
Why is concentrated sulfuric acid used in the preparation of ethyl ethanoate?
It acts as a catalyst.
What is the function of the solid calcium chloride in the preparation of ethyl ethanoate?
Soaks up any excess eater.
What is the nature and purpose of anti-bumping granules?
It prevents bumping (vigorous bubbles)
What is reflux?
Continuous boiling and condensing of a reaction mixture.
Why is reflux used?
This allows an organic reaction mixture to be heated without losing any reactants or products.
What is the purpose of a separating funnel?
To separate into two layers of
- A higher density liquid (typically aqueous) is the bottom layer
- Organic product is the layer above
Outline the method involved in using a separating funnel.
1) Place the distillate of impure product into a separating funnel
2) Wash product using either sodium hydrogencarbonate solution or saturated sodium chloride solution
3) Allow layers to separate in funnel, and then run and discard the aqueous layer
4) Run the organic liquid into a clean, dry conical flask and add drying agent (eg anhydrous calcium sulphate)
5) Decant the liquid into the distillation flask
6) Distil to collect pure product.
If a sample is pure or impure, what will the melting point be like?
If the sample is very pure the melting point will be sharp (the same value in data books), and if it contains impurities the melting point will be lowered.
How do you measure the boiling point of a liquid to determine the purity of it?
- This can be done in a distillation set up or by simply boiling a tube of the sample in a heating oil bath
- Pressure should be noted (as this can change boiling point)
- To get a correct measure the thermometer must be above the boiling liquid, not immersed so it measures the vapour.
Describe the method to recrystallisation.
1) Dissolve the impure compound in a minimum volume of (near boiling) solvent
2) filter hot solution through fluted filter paper quickly. (removes any insoluble impurities)
3) Cool the filtered solution by inserting beaker in ice
4) Suction filtrate with a Büchner flask to separate out crystals
5) Wash the crystals with distilled water (to remove soluble impurities)
6) Dry the crystals between absorbent paper (as water would affect yield)
Draw a Büchner flask set up.
What are some causes for a loss of yield in recrystallisation?
- Crystals lost when filtering or washing
- Some product stays in solution after recrystallisation
- Other side reactions occurring.
Draw the set up for gravitational filtration