Title: The Recipe for the Highest Bouncing Super Ball Name: Date: November 14‚ 2013 Question: How much borax is needed from 1g to 5g to produce a super ball with the highest bounce from the height of 1.5m? Hypothesis: If 2 g of borax is used to make the super ball then it will produce the highest bounce because 2 g will make the appropriate number of bonds without producing a ball that is too soft or too hard to bounce. Materials: Paper cup Beaker Graduated cylinder Stir stick Pencil
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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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Synthesis of Isopentyl Acetate (Banana Oil) Using A Fischer Esterification Reaction Purpose: The purpose of this experiment is to synthesize Isopentyl Acetate using a Fischer esterification reaction. Fischer esterification is an acid-catalyzed condensation of an alcohol and a carboxylic acid‚ yielding an ester and water. Isopentyl Acetate has the scent of banana oil‚ once synthesized it will be purified by distillation. Then the analysis of the sample using H NMR and IR will determine purity
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Abstract Isopentyl acetate was synthesized in 44.9% yield through a reaction between isopentyl alcohol and acetic acid‚ with sulfuric acid as a catalyst. Identify and purity of the product was confirmed by infrared spectrum analysis of the product and the boiling point (141-142˚C) to the published value of (lit1142.5 ˚C). Procedure: Isopentyl alcohol (.893g)‚ acetic acid (2ml)‚ and concentrated sulfuric acid (4 drops) was added to a 5ml conical vial‚ and then attached to a reflux apparatus.
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Synthesis of Isopentyl Acetate Abstract Isopentyl acetate was synthesized via a Fischer Esterification and purified via simple distillation. The yield was determined to be 25%. The identity and purity of the product was confirmed by comparison of the measured ultra-micro boiling point (140°C) to the published value (142°C).1 Chemical Equation Procedure Isopentyl alcohol (0.787 g‚ 1.2 mL‚ 8.93 mmol)‚ acetic acid (1.574 g‚ 1.5 mL‚ 26.20 mmol)‚ and sulfuric acid (0.368
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Ethyl Acetate – NaOH Reaction Kinetics Experiment Martin Novick Group 14‚ Chemical Engineering Laboratory Submitted to Prof. David B. Henthorn September 25‚ 2012 Summary The goal of this project was to determine the pre-exponential factor‚ k o ‚ the activation energy‚ E‚ and the reaction rate constants‚ k‚ of the saponification process of ethyl acetate using sodium hydroxide (NaOH) at 5 temperature between 15 and 25 degrees Celsius. Two trails were performed at temperatures 16‚ 18‚ 20‚ 22‚ and 24
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INTRODUCTION Isopentyl acetate‚ "banana oil"‚ is a naturally occurring compound that possesses a distinctive odor. It is found in bananas‚ as well as many other organisms. This experiment attempts to produce isopentyl acetate by heating under reflux‚ which involves heating the mixture in a flask with a condenser placed vertically in the neck since any escaping vapours condense and run back into the flask‚ by combining isopentyl alcohol with acetic acid and an acid catalyst. The product was isolated
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The objective of this experiment was the synthesis of Isopentyl Acetate using an esterification reaction between acetic acid and Isopentyl Alcohol‚ using a strong acid as a catalyst. The product was washed‚ and distilled. This approach is called Fisher esterification‚ whereby esters are produced by the esterification of a Carboxylic acid where it is heated with an alcohol in the presence of a strong acid which acts as a catalyst. The ester produced had a banana flavor. The extraction of the
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PRE LAB REPORT Reynaldo Riboul TLC and Column Chromatography October 6‚ 2013 Table of Chemicals: Chemical Hazards Mol. Wt. Density Grams Moles Acetone Flammable‚ Irritant 58.08 g mol−1 0.791 g cm−3 2.0 g 0.0344 Hexane Flammable‚ Irritant‚ Dangerous to Environment 86.18 g mol−1 .6548 g mL−1 9.0 g 0.1044 Fluorene Very toxic to aquatic life with long lasting effects 166.223 g/mol 1.202 g/mL 0.3 g 0.00180 Fluorenone Irritant 180.20 g mol−1 1.13 g/cm3 0.3 g 0.00166
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Experiment 1: Bromination of Acetanilide1 Precautions: Ethanol is flammable Sodium hypochlorite is an oxidizing agent and releases toxic fumes (handle in fume hood) Acetic acid is corrosive‚ harmful if inhaled‚ flammable and can cause burns (handle in fume hood) Gloves are recommended to avoid chemical contact with skin Reaction Scheme: Conversion of acetanilide to p-bromoacetanilide Procedure: To a 125 mL Erlenmeyer flask containing a mixture of 95% ethanol (6 mL) and acetic acid (5 mL)‚ dissolve
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