Sunday, May 26, 2019

Lab 5 Acid/Base Extractions Essay

The purpose of this experiment is to separate either the organic base (amine) or organic acid (carboxylic acid) from a mixture that contains inorganic impurities (salt) by performing a liquid-liquid extraction and then taking a melting point.Key Experimental Details and ObservationsOur starting material, Compound B, was a amercement white powder and weighed 0.535g. The final product was a shiny white sheet that resembled acrylic paint and weighed 0.109g.ResultsOur percent yield was 0.109g/0.535g x 100 = 20.4%. backchat and ConclusionsThe melting point ranges we got for commingle B ranged from 110.8-114.0 C, while the melting point range for benzoic acid is 121.0-123.0C and 103.0-107.0C for 4-amino acetophenone. Since the ranges we acquired for compound B ar directly in between both acid and base melting points, we can conclude that the purity for compound B is relatively high due to the compound being made up of equal parts of benzoic acid and 4-amino acetophenone. Thus saying th at our melting point ranges are fairly accurate because they exemplify an equal percentage of both compounds, which is exactly what compound B is made up of. The purity can also be concluded done the melting points depression because depression arises from impurities within the lattice of a crystalized sample.We acquired a percent yield of 20.4%, which is relatively low. This result could be from part of the compound B solution being left behind in the Erlenmeyer flask when pouring the solution into the vacuum filtrate. The efficiency of a liquid-liquid extraction is high because it did entrust us to gain some of our starting product back.We were able to isolate the acid from the base by deprotonating the solution with 10mL of NaOH. This caused the benzoic acid to settle at the bottom of the separatory flask because the NaOH broke it into ions, which made the acid polar. We then protonated the solution by adding HCl, which cause the acid to separate from the solution.

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