SINGAPORE POLYTECHNIC SCHOOL OF CHEMICAL AND LIFE SCIENCES Diploma in Applied Chemistry with Pharmaceutical Science Organic Chemistry (CP4120/CP4502) Project Preparation and Recrystallisation of Aspirin. AY2010/2011 Name: XXXX Class: DACP 1B/02 Admin no.: P1234567 Table of Contents Page List of illustration
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diabetes but no other major risk factors for heart disease probably should not be on low-dose aspirin therapy‚ new research suggests. The new recommendations are based on close examination of nine studies that found the risks of some aspirin side effects‚ such as stomach bleeding‚ should be better balanced against the possible benefits of using aspirin. The larger theme here is that use of low-dose aspirin to prevent heart attacks in people who have not already experienced one is probably not as efficacious
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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 reactant of the equation
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Chewable aspirin can be chewed‚ crushed or swallowed whole but after being consumed the consumer should drink full glass of water. There are many uses for Aspirin. Prescription Aspirin is used to relieve symptoms of rheumatoid arthritis‚ arthritis caused by the swelling of the lining of joints‚ osteoarthritis‚ arthritis caused by breakdown of lining of joints‚ systemic lupus erythematosus‚ the immune system attacks joints and organs‚ and can cause pain/swelling. Nonprescription Aspirin is commonly
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Preparation of Sodium Chloride through titration Abstract: acid-base titration is a technique commonly used to determine the moles of acid in a sample by adding a known volume of strong base of a known concentration. The strong base provides the hydroxide ion‚ to react quantitatively with the acid. The point at which the acid is completely and exactly consumed the known quantity of base is called the equivalence end point and is signalled by a colour change in the solution (end point). This colour
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Exp 23 B Synthesis of t-Pentyl Chloride 11-8-12 Purpose: The sysnthesis of t-Pentyl Chloride from alcohol. Procedure: Preparation of t-Pentyl Chloride. In a 125-mL separatory funnel‚ place 10.0 mL of t-pentyl alcohol (2-methyl-2-butanol‚ MW _ 88.2‚ d _ 0.805 g/mL) and 25 mL of concentrated hydrochloric acid (d _ 1.18 g/mL). Do not stopper the funnel. Gently swirl the mixture in the separatory funnel for about 1 minute. After this period of swirling‚ stopper the separatory funnel and
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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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ISE: The Determination of Chloride Unknown: #34 I. Purpose: In experiment V‚ “ISE: The Determination of Chloride”‚ the concentration of an Unknown Chloride solution‚ and the Wt% of NaCl in a sample of celery salt‚ were both determined. To determine the concentration of an Unknown Chloride solution‚ a Calibration plot is first prepared. The Calibration plot is made by first measuring a series of known concentrations of Cl- (with the same activity of the unknown solution) and obtaining
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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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CHEM%2315%Fall%2014% Creating useful and beautiful molecules using synthetic organic chemistry – Synthesis of Aspirin and Indigo INTRODUCTION Aspirin Salicylic acid occurs naturally in the bark of willow trees. Prior to the 1800’s‚ willow bark was often brewed into a tea‚ or chewed to relieve pain. While the salicylic acid is effective at reducing pain it was found to irritate the lining of the stomach. It was mostly by chance that on August 10‚ 1897 Felix Hoffmann‚ a German chemist who obtained
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