ANALYSIS OF ASPIRIN TABLETS The aim of this investigation is to determine the percentage by mass of aspirin aspirin present in different commercial preparations and to find out‚ which the best value is‚ using a neutralization reaction followed by a direct titration with NaOH. Chemicals Used: 100 ml of distilled water in a wash bottle 50 ml of 0.100 M NaOH 40 mL of 96% ethanol phenolphthalein as an indicator (3 drops per titration) 325 mg non buffered aspirin tablets Materials Used: One
Premium Titration Erlenmeyer flask
synthesize and purify aspirin. The theoretical yield was calculated to 3.766g. The actual yield of pure aspirin was 2.863g with a yield of 76%. The percent yield indicates that our synthesis was a success but the yield is low and indicates that some of the aspirin was lost during synthesis. Some reasons for loss can result from human error such as loosing product from sticking on the spatula and the Buchner funnel and several weighings. Also‚ when transferring the crude aspirin into the vacuum filtration
Premium Chemistry Aspirin Acid
Jennie K. Daniels Organic Chemistry 2121 11 February 2014 Synthesis of Aspirin Salicylic acid derivatives‚ or salicin‚ are found in the bark of the willow tree. In the 5th century B.C.‚ Hippocrates ground the bark into a powder‚ and later‚ the Natives Americans chewed on the bark to alleviate fever and pain1. In the 19th century‚ a German chemist by the name of Felix Hoffman wanted to find a medication that would ease
Premium Aspirin
in the first part of the lab; when we have to produce crystals of aspirin. Analysis is the separation‚ identification‚ and quantification of the chemical components of natural and artificial materials. This concept is used throughout the lab when we are analyzing different reactions that are happing during the duration of the lab. The goal of this lab is to synthesize a sample of acetylsalicylic acid‚ otherwise known as aspirin. This is the most important goal of the lab. This‚ however‚ has side
Free Aspirin Acetic acid Acetic anhydride
EXERCISE 11 SYNTHESIS OF ASPIRIN MARAVILLA‚ Ana Mikaela B Group 4 CHEM 40.1 1L Date performed: September 30‚ 2013 Date submitted: October 7‚ 2013 VI. RESULTS AND DISCUSSION Aspirin is prepared by the esterification of salicylic acid with acetic anhydride under acidic conditions. The phenol group in salicylic acid is replaced by a carboxyl group through electrophilic substitution. The mechanism for the reaction can be summarized
Free Aspirin Carboxylic acid Acetic acid
Table of Contents Introduction Materials Chemicals Equipment Safety Containers Measuring Devices Other Equipment Procedure Synthesis of Aspirin Crystalizing the Aspirin Recrystallizing the Crude Aspirin Finding the Melting Point Range Safety Precautions Acetic Anhydride Sulphuric and Salicylic Acid Heating Observations Mass of Aspirin Synthesized Melting Point Calculations Percentage Yield Maximum Yield Crude Product Final Product Melting Range Percentage Error Crude
Free Aspirin Acetic acid Sulfuric acid
Formal Lab Report 1 Chemistry 100-03 March 19‚ 2012 Abstract: • Introduction/Objective: Prepare and analyze aspirin from salicylic acid and acetic anhydride‚ and calculate the percent yield of the synthesized aspirin. • Materials and Methods: This experiment called for the synthesis of acetylsalicylic acid‚ or aspirin‚ by using salicylic acid‚ acetic anhydride‚ sulfuric acid‚ and vacuum filtration. The salicylic acid and the acetic anhydride were mixed in a flask. Sulfuric
Premium Aspirin Acetic anhydride Acetic acid
Synthesis of Aspirin and Oil of Wintergreen INTRODUCTION: Synthesis and use of organic compounds is an extremely important area of modern chemistry. Approximately half of all chemists work with organic chemicals. In everyday life‚ many if not most of the chemicals you come in contact with are organic chemicals. Examples include drugs‚ synthetic fabrics‚ paints‚ plastics‚ etc. Synthesis of Aspirin and Methyl Salicylate. The two compounds we will be preparing‚ aspirin (acetylsalicylic acid) and oil
Premium Aspirin Salicylic acid Carboxylic acid
Preparation of an Ester Acetylsalicylic Acid (Aspirin) OBJECTIVE: To become familiar with the techniques and principle of esterification. DISCUSSION: Aspirin is a drug widely used as an antipyretic agent (to reduce fever)‚ as an analgesic agent (to reduce pain)‚ and/or as an anti-inflammatory agent (to reduce redness‚ heat or swelling in tissues). Chemically‚ aspirin is an ester. Esters are the products of reaction of acids with alcohols‚ as shown in the following equation using
Premium Acetic acid Carboxylic acid Ester
Synthesis of Aspirin Name: Xuanyi Li Teaching assistant: Deirdre Zwilling November 15‚ 2009 Purpose: To synthesize aspirin‚ a common analgesic drug‚ via nucleophilic acid-catalyzed substitution reaction of salicyclic acid with acetic anhydride. The whole reaction is catalyzed by phosphoric acid. (The experiment involved three parts: The synthesis of aspirin‚ the isolation and purification of aspirin‚ and the estimation of the purity of the final product.) [pic] Procedure[1]: A mixture
Free Aspirin Carboxylic acid Salicylic acid