EXPERIMENT 5 - Preparation of Acetanilide Preparation and purification of Acetanilide [pic] Purpose: a) To synthesis acetanilide by reaction of aniline and acetic anhydride. b) To purify acetanilide by crystallization method from water c) Purity check by melting range Equipment / Materials and Hazars: hot plate beakers(150‚250mL) ice stirring rod spatula Büchner
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must be discovered. Panacetin tablets are known to contain aspirin‚ acetaminophen‚ and sucrose; therefore‚ the tablets tested‚ containing aspirin and sucrose‚ are thought to contain an unknown of something similar to that of acetaminophen such as acetanilide or phenacetin. Another problem trying to be sought out in the experiments is whether or not the composition of Panacetin as stated on the label is accurate. The experiment involved the separation of the unknown from the Panacetin by first isolating
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Organic Chemistry Laboratory ABSTRACT In this experiment‚ acetanilide was used as the pure organic compound. Acetylation of aniline and acetic anhydride yields the crude product or crude acetanilide. The crude acetanilide was purified by dissolving it in hot water and then the solution was cooled slowly by placing in an ice bath. The yielded crystals were pure acetanilide since molecules of other compounds present in the crude acetanilide were excluded from the growing crystal lattice. Lattice is
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crystals of pure compound. Impurities are excluded from the growing crystals and the pure solid crystals can be separated from the dissolved impurities by filtration. Chemical requirement. Solvent: Distilled water‚ Ethanol‚ and Acetone. Solute: Acetanilide. Result: Data and Report Sheet. 1.1 Choosing a suitable solvent. Solvents | solubility | Appearances and quantity of the crystal at room temperature | | Room temperature
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Title: Acetanilide Synthesis Objective: To synthesize Acetanilide by recrystallization. To check its purity by calculating its percent yield. Introduction: Aniline is a primary aromatic amine and weak base which forms salts with mineral acids. In acidic solution‚ nitrous acid converts aniline into a diazonium salt that is an intermediate in the preparation of a great number of dyes and other organic compounds of commercial interest. When aniline is heated
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Name: Date: Lab Section: Selected Known Compounds Name Structural Formula Literature Melting Point Acetanilide C8H9NO 114.3°C Fluorene C13H10 116.5°C Experimental Data Sample Composition 1. 100% Acetanilide 2. 10% Acetanilide 3. 25% Acetanilide 4. 50% Acetanilide Fluorene 5. 75% Acetanilide 6. 90% Acetanilide 7. 100% Fluorene Melting Range 108-116°C 108-112°C 105-112°C 102-109°C 105-112°C 109-115°C 108-114.5°C Graph of Data Discussion
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EXP-10 CHEM 233L SYNTHESIS OF p-BROMOANILINE Introduction: In this experiment‚ p-bromoaniline was synthesized in three steps starting from aniline. Since the amino group of aniline is a strong activator of aromatic ring‚ direct bromination is impractical (equation 1). In order to make a desired product‚ amino group needed to be protected as the acetamide which also maintained ortho and para position but slowed down the rate of reaction (equation 2). Slow reaction rate would increase
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RECRYSTALLIZATION OF ACETANILIDE De Ocampo‚ Yves Aaron Julian Q.‚ Dela Vega‚ Roderick B. Jr.‚ Elguira‚ Cedric Tristan D. Enriquez‚ Joanne B.‚ Gabat‚ John Elliot N. Group 5 2D-Medical Technology Faculty of Pharmacy‚ University of Santo Tomas ABSTRACT The experiment was executed in order to purify compounds through recrystallization. Recrystallization is the primary used operation for purifying solid organic compounds that differ in solubility at different temperature. It is a process of dissolving
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how to dry them and how to obtain a melting point. PRECAUTION: ACETANILIDE AND PHENACETIN ARE EYE AND SKIN IRRITANTS. Minimize contact with your unknown compound. THEORY: In this experiment‚ Panacetin‚ a pharmaceutical preparation will be separated from its components by making use of their solubilities and acid-base properties. Panacetin contains aspirin‚ sucrose and an unknown component that may be either acetanilide or phenacetin. Of the three components‚ only sucrose is insoluble
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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 the unknown component
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