Nucleophilic Acyl Substitution the Synthesis of Esters

Nucleophilic Acyl Substitution: The Synthesis of Esters Razon, Valjean Paulo Mella Rico, Fatima Sarah Rogel Institute of Chemistry, University of the Philippines, Diliman, Quezon City 1101 Philippines Department of Food and Nutrition, College of Home Economics, University of the Philippines, Diliman, Quezon City 1101 Philippines Abstract ------------------------------------------------- ------------------------------------------------- The purpose of this experiment is to observe the synthesis of esters (also known as esterification), to understand the chemical processes that ester synthesis undergoes, and to know the optimum conditions needed for high yields. Esterification is a Nucleophilic Acyl Substitution Reaction†¦show more content†¦However, the proton that left replenishes that acid catalyst to help repeat the mechanism for other molecules. The general mechanism of Nucleophilic Acyl Substitution could be simplified and shown by Figure 3 and the specific mechanism of the Fischer Esterification reaction that ensues in the experiment is portrayed by figure 4. (John McMurry, 2007) Figure 3 Nucleophylic Acyl Substitution Reaction Mechanism Figure 4 Fischer Esterification Mechanism (Gunawardena, 2009) Practically, the procedure involves the heating a mixture of an alcohol and a carboxylic acid in the presence of an acid catalyst to yield an ester and water as end product. The reaction is reversible and the position of equilibrium depends on the reaction conditions. An excess of the alcohol favor the formation of the ester. While the presence of water drives the reaction backwards. (John McMurry, 2007) This concept of driving thereaction forward makes use of Le Chatelier’s principle states that â€Å"When an equilibrium system is subjected to change in temperature, pressure, or concentration of reacting species, the system responds by attaining a new equilibrium that partially offsets the impact of change.† (Petrucci, 2010) The structure of the reagents greatly affects the rate of Esterification. Presence of bulk groups on the alpha carbon or the site of the reaction causes esterification to slowShow MoreR elatedClassification Tests for Carboxylic Acid and Derivatives1580 Words   |  7 Pagesacid halides,acid anhydrides, esters and amides.Carboxylic acids and their derivatives areusually seen in industrial processes and mostbiological pathways. Esters can be seen as fatsand within the cell membrane. Esters are alsopresent in pleasant smelling liquids that areresponsible with the fragrant odor of fruits andflowers. Amides are also present in animalprotein and also in industrial products such asnylon. Acid chlorides and acid anhydrides areused in the synthesis of carboxylic derivatives.TheseRead MoreEsters And The Process Of Esterification709 Words   |  3 PagesEsterification Esters are the carboxylic acid derivatives most commonly produced by the reactions esterification. The most famous esterification is also called Fischer esterification, which is actually an acid-catalyzed reaction of alcohol and carboxylic acid. In addition to acid, alcohols can react with acyl chlorides, anhydrides, and esters are also formed. U with the reaction of alcohol and acyl chloride, with the ester there is HCl, so in such esterification reactions should be added to the baseRead MoreSynthesis of Salicylic Acid and Potentiometric Determination of Its Purity and Dissociation Constant4209 Words   |  17 PagesSynthesis of Salicylic Acid and Potentiometric Determination of its Purity and Dissociation Constant ------------------------------------------------- Abstract The purpose of the study is to synthesize salicylic acid from the ester, methyl salicylate, and determine the acid’s dissociation constant and purity. The ester was converted to salicylic acid by base hydrolysis. The products were refluxed and recrystallized, to ensure maximum purity, and filtered, dried, and weighed. 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