Exp8 - Potassium Bitartrate
Exp8 - Potassium Bitartrate
8
POTASSIUM BITARTRATE
OBJECTIVE:
At the end of the experiment, Student should know how to:
1. Synthesize Potassium bitartrate and to test for its identity
2. And identify its medicinal uses
MATERIALS:
Laboratory set of apparatus
REAGENTS
Potassium sodium tartrate Resorcinol
Diluted Acetic acid Conc. Hydrochloric acid
50% alcohol Conc. Sulfuric acid
Sodium hydroxide T.S. Conc. Acetic acid
Silver nitrate T.S. Ferrous sulfate T.S.
Ammonia T.S. Hydrogen peroxide T.S.
PROCEDURE:
1. Dissolve 5 grams of Potassium sodium tartrate in 5 ml of water.
2. Add diluted Acetic acid until precipitation ceases.
3. Filter off the white crystalline precipitate of Potassium bitartrate, wash it with a small
quantity of cold 50% alcohol and dry.
Actual yield:
Theoretical yield:
Percentage yield:
IDENTIFICATION TESTS:
1. Heat the crystals at high temperature.
Result: _____________________________________________
2. Dissolve the residue in water and perform Beilstein's test.
Result: _____________________________________________
3. Prepare a saturated aqueous solution of Potassium bitartrate, neutralized with Sodium
hydroxide, add Silver Nitrate T.S to the precipitate formed, dissolved it with Ammonia T.S.
and the solution warmed.
Result: _____________________________________________
Chemical reaction:
4. Prepare a 1% Resorcinol solution in Hydrochloric acid. Add a few drops of this solution to a
dry salt of Potassium bitartrate. Then add 3 ml of Sulfuric acid and slowly heat the solution.
Result: _____________________________________________
5. Acidify a tartrate solution with Acetic acid. Add a drop of Ferrous sulfate T.S. and Hydrogen
peroxide T.S., then add an excess of Sodium Hydroxide T. S.
Result: _____________________________________________
2. Why is the precipitate washed with alcohol and not with water?
Most precipitates are insoluble in alcohol, mainly because of the "like dissolves like"
rule. Moreover, Alcohols are nonpolar solvents, and most precipices are polar, thus being
insoluble in nonpolar solvents. Therefore, for the precipitates to not dissolve again by
washing, we use alcohols; because if we use water, the precipitates are more likely to
dissolve again in an aqueous solution
References:
https://go.drugbank.com/drugs/DB11107
https://pubchem.ncbi.nlm.nih.gov/compound/Sodium-potassium-tartrate
Rogers, C., Soine, T., & Wilson, C. (1949). A text-book of inorganic pharmaceutical chemistry.
Lea&Febiger. USA
https://study-assistantph.com/chemistry/question1940788#otvet