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Organic Chemistry 2273A Laboratory, Section 043Liquid-Liquid Extraction and Recrystallization

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Liquid-Liquid Extraction and Recrystallization Lucas D’Onofrio Organic Chemistry 2273A Laboratory, Section 043 Monday, November 7th 2016 Objective In experiment two liquid-liquid extraction was done on an organic acid, base and neutral components. Recrystallization was done to purify the organic solids and then the melting points were compared from before and after the recrystallization. Introduction In this lab the organic acid, neutral and base were extracted from a mixture containing benzoic acid, azobenzene and 3-nitroaniline. These were then crystallized and filtered using Buchner filtration. The melting points were observed of the acid, neutral and base. The crystals were recrystallized and then filtered again using Buchner filtration. The melting points were then observed of the purified crystals and IR spectra was taken from the purified crystals. Procedure The lab was performed following the procedures outlined in the Chem 2273a Laboratory manual 2016.There were no changes made in the lab procedure. Some errors in this lab could be from the transferring of crystals. The crystals were transferred back and forth from scale to beakers, to plastic bags which could have resulted in loss of some crystals. Dich

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28 september 2025
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2025/2026
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Liquid-Liquid Extraction and Recrystallization


Lucas D’Onofrio


Organic Chemistry 2273A Laboratory, Section 043
Monday, November 7th 2016


Objective
In experiment two liquid-liquid extraction was done on an organic acid, base and neutral
components. Recrystallization was done to purify the organic solids and then the melting points
were compared from before and after the recrystallization.
Introduction
In this lab the organic acid, neutral and base were extracted from a mixture containing benzoic
acid, azobenzene and 3-nitroaniline. These were then crystallized and filtered using Buchner
filtration. The melting points were observed of the acid, neutral and base. The crystals were
recrystallized and then filtered again using Buchner filtration. The melting points were then
observed of the purified crystals and IR spectra was taken from the purified crystals.
Procedure
The lab was performed following the procedures outlined in the Chem 2273a Laboratory manual
2016. There were no changes made in the lab procedure. Some errors in this lab could be from
the transferring of crystals. The crystals were transferred back and forth from scale to beakers, to
plastic bags which could have resulted in loss of some crystals.




Dichloromethane Solution




3-nitroaniline Benzoic Acid Azobenzene


3 M HCl




This study source was downloaded by 100000899606070 from CourseHero.com on 09-27-2025 21:57:10 GMT -05:00


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, Upper Aqueous Layer Lower Organic Layer




6 M NaOH 3 M NaOH




Upper Aqueous Layer Lower Organic Layer




6M
HCl




Results
Mass of Unknown = 1.14g
Since there is a 1:1:1 ratio with acid, base and neutral each have a mass of 0.38g.




This study source was downloaded by 100000899606070 from CourseHero.com on 09-27-2025 21:57:10 GMT -05:00


https://www.coursehero.com/file/18157315/Liquid-liquid-Extraction-and-Recrystallization/

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