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    Synthesis of Methyl Salicylate from Aspirin Esters are a class of organic compounds. An ester compromises an organic or inorganic acid in which one or more hydroxy (OH) groups have been replaced by and alkoxy (O-alkyl) group. For example‚ the simplest ester‚ methyl formate (CHOOCH3)‚ is made up of formic acid (CHO-OH) in which the hydroxyl group has been replaced by a methoxy group (-OCH3). Similarly‚ ethyl acetate (CH3CO-OCH2CH3) is made up of acetic acid (CH3CO-OH) in which the hydroxy group

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    the ester. The reaction is a nucleophillic acylsubstitution carried out under acidic conditions of acetic acid and Dowex was also used for supplying protons. The alcohol used was 1-butanol which limits the ester to a side butyl chain. After completing the esterification‚ it was found that 0.734 grams of n-butyl acetate was formed with a percent yield of 61%. The product was confirmed using IR spectroscopy and boiling point confirmation. The IR spectroscopy graph showed the characteristic Ester--1735

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    Esterification Lab

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    Esterification Lab Introduction Esters are classified as organic compounds commonly derived from carboxylic acids. They are compounded from the reaction of a carboxylic acid with an alcohol in the presence of a strong acid to be used as a catalyst. The formula that represents an ester is R-COO-R where both Rs’ are alkyl groups‚ one which is bonded to an oxygen‚ and the other to a carbon which is double bonded to 1 oxygen and single bonded to the other. Esters are named in almost a reverse fashion

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    Yoyoma

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    The Preparation of Methyl Salicylate Introduction: Esters have various smells that differ due to the types of carboxylic acids and alcohols one mixes together. This is called esterfication. The reaction is catalyzed by an inorganic acid usually H2SO4 Purpose: In this lab Methanol alcohol and Salicylic acid were reacted together to form Methyl Salicylate. This was done to determine the characteristic odour of the Methyl Salicylate. Safety: Safety goggles must be worn at all times. Methanol: Toxic

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    acetic acid to produce an ester (ethyl laurate). THEORY Esters are among the most widespread of all naturally occurring compounds. Many simple esters are pleasant-smelling liquids that are responsible for the fragrant odors of fruits and flowers. Examples are methyl butanoate‚ which is find in pineapple oil‚ and isopentyl acetate‚ which is a constituent of banana oil. The ester linkage is also present in animal fats and in many biologically important molecules. Esters can be formed from both

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    dispersion of liquid into another immiscible liquid. In this manner‚ oil does not mix with water whereby able to induce dirt. 2. Raw materials and soap making Soap making requires two major raw materials: * Fats and oils Fats and oils are esters of fatty acids and glycerol. These are obtained from natural substances which are classified into three: a. Nut oils Cold process soap making is the most suitable for this type of oil which is also characterized by large proportion of fatty

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    Isopentyl Acetate

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    acetate by direct esterification of acetic acid with isopentyl alcohol. After refluxing there is an isolation procedure where excess acetic acid and remaining isopentyl alcohol are easily removed by extraction with sodium bicarbonate and water. The ester is then purified by simple distillation and the IR is then obtained. Techniques and equipment used throughout the experiment include a reflux apparatus‚ separatory funnel for isolation‚ vacuum filtration‚ and simple distillation. The reflux condenser

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    How Carboxylic Acids and Alcohols React to Produce Esters: Esters and Ester Production: Esters are abundant and ever present‚ and are the chemical basis of almost all fatty acids and oils. Small esters are responsible for the aroma of fruits‚ perfumes and‚ by extension‚ wines and other alcohols. Esters are formed when a carboxylic acid and an alcohol chemically combine‚ losing a molecule of water in the process. Carboxylic acids are organic molecular compounds that form a homologous series

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    carboxylic acids

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    Benzoic acid + NH3 - red litmus paper turned blue  Benzoic acid + NH3+ FeCl3 - orange precipitate/ flesh-colored precipitate formed  Formation of Esters a. From Carboxylic acids  Acetic acid + ethanol + H2SO4 - produced a sweet smell b. From Acyl Halides  Ethanol + H2O + H2SO4 - produced a sweet smell  Hydroxamic acid test for the Ester group  Ethyl acetate in ether + NH2OH.HCl + KOH heat effervescence + alcoholic HCl + FeCl3 – red colored solution  Hydrolysis of acid derivatives

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    Aspirin Lab

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    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

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