Table of Contents
- 1 Why is a hot gravity filtration not always necessary during a recrystallization?
- 2 Why do you need to reheat the solution after hot gravity filtration?
- 3 What is the purpose of doing the gravity filtration hot?
- 4 Why is it important to Minimise evaporation during the filtration of the hot solution?
- 5 What will happen if the hot solution is not saturated enough?
- 6 Why can slow filtration lead to disaster with hot filtration?
- 7 Why is it necessary to cool hot supersaturated solution slowly during recrystallization?
- 8 Is temperature change important in recrystallization?
- 9 What is a hot gravity filtration?
- 10 What are the disadvantages of vacuum filtration in organic chemistry?
Why is a hot gravity filtration not always necessary during a recrystallization?
Hot filtration is necessary for recrystallization when impurities exist in solution. Firstly, recrystallization requires a hot solution because the solution needs to be super saturation in order for crystals to form upon cooling. The impurity is then filtered out during the hot gravity filtration process.
Why do you need to reheat the solution after hot gravity filtration?
Heating the solvents decreases the kinetic energy necessary to dissolve the compound. This also means that less solvent is needed to dissolve the compound, which makes the solution more saturated.
What is the purpose of doing the gravity filtration hot?
A filtration procedure called “hot gravity filtration” is used to separate insoluble impurities from a hot solution. Hot filtrations require fluted filter paper and careful attention to the procedure to keep the apparatus warm but covered so that solvent does not evaporate.
Why must students perform the gravity filtration when the solution is hot and after all the benzoic acid has dissolved?
The solid compound (solute) must be only slightly soluble in the solvent at room temperature, while being virtually completely soluble in the solvent at higher temperatures. This “hot filtration” technique removes those insoluble impurities all the while keeping your solute in solution.
How does recrystallization affect melting point?
Impurities found in the solid will tend to change the melting point by causing it to “spread” out into larger range. Observing a small quantity of the solid as it is heated carries out the measurement of melting point….
alcohol | formula | Solubility (g/100 ml H2O) |
---|---|---|
n-pentanol | CH3CH2CH2CH2CH2CH2CH2OH | 0.1 |
Why is it important to Minimise evaporation during the filtration of the hot solution?
A hot filtration is used for filtering solutions that will crystallize when allowed to cool. It is therefore important that the funnel is kept hot during filtration through contact with hot solvent vapors, or crystals may prematurely form on the filter paper or in the stem of the funnel (Figure 1.82).
What will happen if the hot solution is not saturated enough?
Dissolve the solute. Remember that the solute should dissolve only when the solvent is heated. If too much solvent is added, the solution will not be saturated upon cooling and no crystals will form.
Why can slow filtration lead to disaster with hot filtration?
Slow filtration can lead to disaster in hot filtration during recrystallization. Since filter funnels and filter papers come in different sizes, choose a filter paper of diameter just less than twice the diameter of the funnel. When fluted, the filter paper will be just below the rim of the funnel.
Why it is necessary to remove all the solvent before the melting point of the pure compound can be determined?
Regardless of crystallization method, the purity of the solid can be verified by taking the melting point. The solvent should not react with the compound being purified and it should have the boiling point below the melting point of the compound being purified because solid melts before dissolves (oiling out).
Why do you need to heat the sample slowly to record its melting point?
It is important to heat the sample slowly using this method so that a thermal equilibrium can be established. Generally, you will heat the capillary tube to near melting point and then decrease the speed of the temperature increase so that you can observe when the sample melts.
Why is it necessary to cool hot supersaturated solution slowly during recrystallization?
Crystallize the solute. This involves allowing the hot solution with the solute dissolved to return to room temperature slowly. The slower the cooling process, the less chance of trapping impurities in the developing crystal lattice.
Is temperature change important in recrystallization?
The rate of cooling is also important in recrystallization. Rapid cooling favors the formation of many nucleation sites and the growth of smaller crystals, whereas cooling slowly induces the formation of fewer nucleation sites and the growth of fewer, larger but purer crystals. So, slower cooling is preferred.
What is a hot gravity filtration?
A filtration procedure called “hot gravity filtration” is used to separate insoluble impurities from a hot solution. Hot filtrations require fluted filter paper and careful attention to the procedure to keep the apparatus warm but covered so that solvent does not evaporate.
What is the difference between gravity and vacuum filtration?
Vacuum filtration is faster than gravity filtration, because the solvent or solution and air is forced through the filter paper by the application of reduced pressure. Do not use vacuum filtration to filter a solid from a liquid if it is the liquid that you want, and if the liquid is low boiling.
What precautions should be taken when performing a vacuum filtration?
However, there are several points that have to be considered when performing a vacuum filtration. Due to the fact that reduced pressure is used in this procedure, special attention has to be paid to the equipment used in this procedure. The glassware (i.e. filter flask) should not have any cracks on the sides or the bottom.
What are the disadvantages of vacuum filtration in organic chemistry?
The low pressure in the filter flask sucks the water back into the mother liquor, and if this is the part of interest, the experimenter is in big trouble. Also, a vacuum filtration is not suitable for solvents with low boiling points e.g. diethyl ether, dichloromethane or other low boiling solvents.