and then compare its melt point to the two other possible substances. Theory Panacetin should be made up of about 50 percent of the unknown component that we previously separated out of Panacetin for testing. We suspect that this unknown compound is either acetanilide or phenacetin. From the solubility of acetaminophen and phenacetin, we could know both of them are relatively soluble in boiling water but insoluble in cold water so that we took the recrystallization as the method to purifying
Experiment 1: Recrystallization – Evaluation Summary Last Name: Xavier First Name: Jessica Date: October 1st 2013 Lab Day/TA/Group: Wednesday(1:35pm)/Group A Labs reports must be typed and chemical structures must be drawn with ChemDraw. Report must not exceed three pages (including this page). Page limit does not include any attached spectra or references. ** Deductions for hand written report/structures and exceeding page limit ** Report Breakdown Data/Results: _________________
This experiment introduces separation and purification methods used in research quite frequently. These methods include hot vacuum filtration and recrystallization to purify a crude sample of acetanilide containing two impurities. Recrystallization is a very common method that is used to purify solids. This process dissolves a crude solid with impurities in a mildly boiling solvent, and cooling down the mixture afterwards for crystals to reconstruct themselves in solution. This method allows impurities
acid. The purification of the isolated unknown acid was performed by recrystallization and its identity was established by analyzing the melting point range of the pure product and comparing it to the provided standards. In addition, a mixed melting point experimentation enhanced the fidelity of the unknown's identity when approximately equal amounts of the unknown and one of the standards (at a time) were mixed and the melting point range was recorded. Theory: Explain the theory behind acid base
distillation and recrystallization using a suitable solvent determined through a solubility test. The identification method used was through Melting Point Determination. By obtaining data of the melting points of the 2 purified compounds and cross-referencing from a list of possible organic compounds, the 2 organic compounds were identified to be Dibenzalacetone (Neutral) and o-Chlorobenzoic acid (Acidic). Results A solubility test was conducted to determine the recrystallization solvent to be used
order to make a proper identification of the acid, while learning proper techniques for scientific measurement and analysis of error. In order to ensure the most accurate data, a purification was performed by the process of recrystallization. To perform the recrystallization the powder was dissolved in a minimal amount of hot ethanol/H2O solvent that allowed the unknown powder to crystallize properly when cooled. This process allowed for the removal of soluble impurities when suction filtered. A
The Purity and Purification of Solids Recrystallization ABSTRACT In this experiment, impure adipic acid is purified though recrystallization. The impure adipic acid is dissolved in a solvent. After cooling it is ran through a vacuum filter to separate any moisture. The dry crystals are then weight for percent yield and the melting point range is taken to test the purity. There were two different trials ran in this experiment. The difference between the two was the addition of charcoal in
48% yield). The crude acetaminophen was then recrystallized in a solvent of water and methanol over heat resulting in 0.082 grams (39.61% yield) of pure acetaminophen. Melting points of both crude and pure acetaminophen were taken, and found to be 165.9 - 170.9°C and 168.2 - 171.5°C, respectively. The literature melting point of acetaminophen is 169.5 – 171.0°C, indicating that our final product was pure. Introduction The synthesis of acetaminophen involves the attraction
purpose of this experiment was to synthesize adipic acid from cyclohexanol via an oxidation reaction that was catalyzed by sulfuric acid. Purity of the product was assessed by measuring the melting point. Physical Properties/Structures: Name | Formula | Molecular Weight (g/mol) | Boiling Point (0C) | Melting Point(0C) | Density(g/mL) | Hazards | Sodium Dichromate Dihydrate | Na2Cr2O7 . 2H2O | 297.98 | 400.0 | 357.0 | 2.35 | -Eye/skin irritant-Affects Respiratory System | Water | H2O | 18.02
was to extract the Trimyristan from ground nutmeg using extraction, distillation and recrystallization procedures. This experiment involves extraction and separation techniques that yield a purified product. The product was extracted and a distillation process was used to remove any remaining solvent. The recrystallization of the sample in turn produced a pure sample, which was proven using the known melting points of the isolated product. Our outcome led us to a 28 percent recovery of the product