Synthesis of Isopentyl Acetate Abstract The purpose of this experiment was to produce isopentyl acetate‚ banana oil. Acetic acid and isoamyl alcohol were used to synthesize isopentyl acetate. The techniques used for the separation and purification of isopentyl acetate were reflux‚ liquid-liquid extraction‚ neutralization and distillation. The identification of isopentyl acetate was based on boiling points and an infrared spectrum. This experiment resulted in a 11.68% yield. The reactants
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Isopentyl Acetate Synthesis Results: Crude % Yield Calculation Reaction: H2SO4 C2H4O2(aq) + C5H12O(aq) ----> C7H14O2(aq) + H2O(l) (1 mole of acetic acid reacts with 1 mole of isopentyl alcohol to make 1 mole of isopentyl acetate and 1 mold of water) Volume of isopentyl alcohol (d=0.809g/mL; MW=88.15g/mol): 2.5mL Moles of isopentyl alcohol: (2.5mL)(0.809g/1mL)(1mol/88.15g) = 0.02294mol Volume of glacial acetic acid (d=1.06g/mL; MW=60g/mol): 3.5mL Moles of glacial
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Eastman solvents—Technical tip Using Eastman methyl acetate in cleaning applications Introduction Considerations Eastman Chemical Company‚ the world’s leading producer of methyl acetate‚ offers this solvent in two grades to suit a variety of application needs: Wide formulation latitude • Regular (industrial) grade offers a minimum assay of 96%‚ a maximum methanol content of 2.5%‚ and a maximum water content of 1.5%. • High purity grade offers a minimum assay of 99.5%‚ a maximum
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Preparation of an Acetic Acid Ester Abstract: 14.1 g of octyl acetate were synthesized from the esterification process using 20.0 ml of acetic acid and 17.9 g of n-octanol. The theoretical yield was 23.8 g of octyl acetate. The percent yield was 59.2%. The purification of the final ester was confirmed by boiling point (186-199°C) and infrared index (nD=1.419). It was a colorless liquid that had a slight fragrance of orange and indescribable chemicals. The Infrared spectra confirmed ester
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In this experiment‚ the objective is to successfully perform an SN1 reaction to determine the reactivity of tert-butyl chloride‚ through the usage of sodium iodide/silver nitrate reagents and to synthesize tert-butyl chloride. The tert-butyl chloride was synthesized through the use of separation (aqueous and organic layers) and distillation. Tert-butyl chloride is the alkyl halide which is being synthesized throughout the course of the experiment. Alkyl halides are derived from alkanes. Once an alkane
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The percent yield of the isopentyl acetate was 74.3% and this low percent yield could have occurred due to some amount of gas escaping from reflux apparatus’ top or apparatus was not fully closed so that some of the heat escaped and did not proceed the reaction well‚ leaving reagents. Another source of error could be that some of the organic layer could have been transferred along with the aqueous layer when the aqueous layer was getting separated from the organic layer by a pipette. One of the
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250 ppm‚ 200 ppm‚ 100 ppm‚ and 25 ppm of 12C solution was prepared from a caffeine stock solution using ethyl acetate as the solvent. 250 µL of each dilution was added to a respective 0.6 mL vials with 50 µL of 13C and mixed. Next‚ three 15 mL centrifuge tubes were labeled as “Unknown A‚” three were labeled as “Unknown B” and one was labeled “Control.” To each tube‚ 4 mL of ethyl acetate and 1 mL of the respective unknown or control (100 ppm 12C solution) was added to the respective flasks. Each
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Synthesis The old acetate department located in an old four storey building follows a workflow that is heavily based on shifts/rotations because production is based on a per batch basis. A typical shift‚ the group leader and his crew would complete two or three batches. The night shift usually has lesser work because no deliveries were made. In the new system‚ the management wants to improve productivity. The department was redesigned from batches to continuous processing. Technical changes
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Undoped and Ce doped ZnO thin films were prepared by the sol-gel process. Zinc acetate dehydrate was dissolved in a mixture of absolute ethanol and monoethanolamine (MEA) yielding to a precursor concentration of 0.4 M .The MEA to zinc acetate molar ratio was set to 1. For doped films‚ cerium nitrate was added to the mixture with an atomic percentage fixed at 0.1‚ 0.3‚ 0.5‚ 0.7‚ and 0.9 at.% Ce‚ respectively. The resulting sols were magnetically stirred at 60°C for 1 hour and then aged at room temperature
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Lab 8: Isopentyl Acetate CHM 2211L October 22‚ 2014 Abstract Many esters are naturally occurring compounds that are responsible for the fragrance of fruits and flowers. Isopentyl Acetate is the compound responsible for the smell of bananas. However‚ when Isopentyl acetate is treated with H3O+ it will hydrolyze back into the carboxylic acid‚ which will change the fragrance. In this experiment 3.11g of Isopentyl Acetate were produced with a 51.92 percent yield. Introduction Esters are carboxylic
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