Liquid Chromatography Analysis of Aspirin Problem: Was aspirin (acetylsalicylic acid) successfully synthesized? Are there impurities or by-products present in the synthesized aspirin? How pure is the synthesized aspirin? Introduction: In the last experiment‚ aspirin was synthesized followed by characterization of the product using several different techniques. Melting point was a test that provided information about the identity and purity of the aspirin product. The iron(III)chloride test
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purpose of this lab is to synthesise acetylsalicylic acid (aspirin) by creating a reaction between acetic anhydride and salicylic acid. This was be accomplished through the use of recrystallization. Acetic anhydride and salicylic acid are mixed together‚ and then acidified by the addition of a few drops of concentrated sulfuric acid‚ which catalyzed the reaction. The percent yield is calculated to determine the effectiveness of the reaction in preparing the desired product (aspirin). The limiting
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Aspirin Synthesis Introduction Out of all the pharmaceutical drugs in the worlds‚ aspirin is made the most. Any potential pharmacist must be familiar with synthesizing the drug. The goal of this lab is to synthesize as much pure aspirin as possible. The reactants‚ acetyl anhydride and salicylic acid‚ must react in phosphoric acid. With phosphoric acid as a catalyst‚ the reaction yields aspirin and acetic acid. The equation for the reaction is as follows: “(CH3CO)2O + HOC6H4COOH □(→┴yields ) CH3CO2C6H4CO2H
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acidity of the catalyst‚ the production of aspirin will increase. Our hypothesis was proven correct. In our data‚ we calculated the percent yield and percent error of each trial. We also calculated the average of the percent yields and the percent errors of each catalyst. In the end‚ we saw that for the sulphuric acid catalyzed aspirin‚ we saw an average of 69.7% percent yield and an average 30.3% percent error. As for the phosphoric acid catalyzed aspirin‚ we saw an average of 55.0% percent yield
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Synthesis of Aspirin (Acetylsalicylic Acid) Abstract: This experiment is about the synthesis of aspirin under laboratory conditions. Aspirin is prepared by reacting salicylic acid and acetic anhydride; in the presence of sulfuric acid. After fully dissolving the salicylic acid with acetic anhydride‚ the solution is cooled and cold water is then added. Once the crystals form they are then filtered and left to dry out. There mass is measured and recorded then the yield is calculated. Introduction:
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Abstract: The goal of this experiment was to synthesize aspirin. In this experiment aspirin‚ also known as acetylsalicylic acid‚ was synthesized from salicylic acid and acetic anhydride. In the reaction the hydroxyl group on the benzene ring in salicylic acid reacted with acetic anhydride to form an ester functional group. This method of forming acetylsalicylic acid is an esterification reaction. Since this esterification reaction is not spontaneous‚ sulfuric acid was used as a catalyst to initiate
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Rebecca Boreham 7/1/14 Chem 2423 Experiment #5 Synthesis of Aspirin Elizabeth Ajasa Kaylee Seymour Lauren Hatfield Suveda Perikala Introduction/ Purpose Aspirin is the most commonly used drug in the United States. Forty million pounds are produced each year. The chemical name for aspirin is Acetylsalicylic acid. Aspirin is a pain reliever and a fever reducer. Aspirin originated from the bark of a White Willow Tree. Chewing the bark however is extremely acidicand irritates the mucous membranes
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EXP. NUMBER EXPERIMENT/SUBJECT DATE 1 NAME Organic Chem 2 Lab LOCKER NO. 2/29/00 COURSE & SECTION NO. 1 John Doe (TA: Gregg N. Yard) 55 chem 3341-111 The Preparation of Aspirin The purpose of this experiment is to synthesize aspirin (acetyl salicylic acid) from salicylic acid and acetic anhydride. CO2H OH salicylic acid 2g 0.014 mole O O O CH3 H2SO4 ethyl acetate CO2H O O acetyl salicylic acid acetic acid CH3 O + H3C + H3C OH acetic anhydride 5
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effects for some people‚ yet it is safe enough to be sold without a prescription. Because it is easy to prepare‚ aspirin is one of the most inexpensive drugs available. It is produced in vast amounts. In fact‚ industry makes 43‚000‚000 pounds of the drug every year. This microscale experiment will permit you to make an amount of aspirin equivalent to about 1/2 of that found in an aspirin tablet. Purpose: To synthesize acetylsalicylic acid on a microscale basis. Equipment / Materials: |salicylic
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What is the more formal chemical name for aspirin? Acetylsalicylic acid 2. Using your data from Experiment 2‚ how can you be sure you synthesized aspirin? By using the colors as a guide‚ we can compare the Acetylsalicylic acid + 8 mL FeCl3 to the Aspirin Crystals from Experiment 1 + 8 mL FeCl3 in order to see if it synthesized. 3. Would you say that your synthesized aspirin is relatively pure? How can you tell? One way that the purity of aspirin can be judged is by it’s color as pure acetylsalicylic
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