Preview

Preparation of Fruit Flavors

Good Essays
Open Document
Open Document
711 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Preparation of Fruit Flavors
Abstract Fisher Reaction is a special type of esterification that uses an acid catalyst to reflux Carboxylic acid and Alcohol. The product Ester is in equilibrium to the reactants acid and alcohol. Ester is responsible for the smell and aroma of different fruits. After using the Fisher reaction, a combination of techniques is used to separate the product.

Introduction

Esters are naturally occurring compounds that possess a distinctive odor. It is responsible for the smell of different fruits such as bananas and strawberries. Esters are most commonly from Carboxylic acids, and Alcohols. They have a pleasant and fruity odor. Esters may be produced in the laboratory via the Fischer reaction. The objective of this experiment is to be able to prepare the assigned ester by using the Fischer Reaction and to calculate the percent yield.

Methodology

Materials:
Isoamyl Alcohol
Acetic Anhydride
Concentrated H2SO4
Saturated NaHCO3
NaCl solution

Reflux Setup:

The reflux setup contains a condensing system at a 90-degree angle with the flasks that prevents the solvent from evaporating but at the same time maintaining the temperature of the solvent. The 90-degree angle allows condensed solvent to go back to the reaction pot.

PROCEDURE Two dry test tubes labelled A and B containing the required 2.5 mL isoamyl alcohol and 2.6 mL acetic anhydride respectively were placed in an ice water bath. Concentrated H2SO4 was cautiously added in test tube B. The solution was mixed well using a dropper. While keeping both tubes in an ice bath, the contents of test tube B was slowly added to test tube A. The tube was swirled constantly. The resulting mixture was transferred in a reflux setup. Boiling chips were added in the setup and was heated in a water bath at 80 degrees Celsius for 30 minutes. After 30 minutes, the hot bath was removed from the setup. It was cooled for a minute and the contents were poured in a small beaker containing a cube of crushed



References: McMurry, J. (2007). Organic Chemistry: A Biological Approach. Belmont, Ca: Thomson Higher Education Solomons, T. W. Graham. (2011). Organic chemistry. Hoboken, NJ : Wiley. Smith, Janice G. (2011). Organic chemistry. New York, NY : McGraw-Hill, c2011.

You May Also Find These Documents Helpful

  • Good Essays

    Experiment 13B

    • 972 Words
    • 4 Pages

    To prepare isopentyl acetate (banana oil), an ester, from isopentyl alcohol and acetic acid through the Fischer Esterification reaction.…

    • 972 Words
    • 4 Pages
    Good Essays
  • Good Essays

    The main purpose of this experiment was to synthesize banana oil (isopentyl acetate.) Ester are often prepared by the Fischer esterification method, which involves heating a carboxylic acid with an alcohol in the presence of an acid catalyst.…

    • 1073 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    Experiment D

    • 502 Words
    • 3 Pages

    3. Refluxing is when the reactants are boiled and the vapor that is produced is cooled. When the vapor is cooled it changes back to its liquid state and returns to the flask.…

    • 502 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    Competing Nucleophiles Lab

    • 2607 Words
    • 11 Pages

    Assemble a reflux apparatus including the 25 mL round bottom flask and a heating mantle as a heat source. 5 mL of n-butyl alcohol is added to the flask by detaching the flask and adding the alcohol via a Pasteur pipet. Allow the mixture to boil at a temperature sustainable for a gentle boil for approximately 75 minutes. After this process has been completed, turn the heat off and allow the mixture to cool for approximately 10 minutes. Once ten minutes has elapsed, carefully place the flask into a cool water bath (without ice) until the mixture cools to room temperature. At this point, an organic layer should be visible. Transfer this solution into a separatory funnel. Drain most of the bottom aqueous layer into a beaker.…

    • 2607 Words
    • 11 Pages
    Good Essays
  • Good Essays

    The objective of this lab was to prepare n-butyl bromide or n-bromobutane, which is derived from an alcohol and an acid. In this case, n-butyl alcohol and sulfuric acid were the reagents. There were two methods of distillation that was involved in this experiment. The first was by reflux distillation, which is used to speed up a chemical reaction without having the reactants/ products evaporate or explode. Data Table 1 indicates the amount of each reagents that was prepared for the reflux apparatus. However, the reagents, sodium bromide, water, and butanol, were combined and cooled in an ice bath previously before transferred to the apparatus. Sulfuric acid was then slowly added to the cooled mixture, causing the solution to turn a dark yellow.…

    • 768 Words
    • 4 Pages
    Good Essays
  • Better Essays

    Isoborneol With Bleach

    • 1188 Words
    • 5 Pages

    Procedure: Using a 50-mL Erlenmeyer flask, 1.316 g (8.5 mmol) isoborneol and 1.0 mL (17 mmol) glacial acetic acid were stirred vigorously with a magnetic stir plate. A volume of 1.7 mL NaOCl was added to solution, and it was then heated to 50° C. Drop-wise, 15 mL of NaOCL were added to the solution over the following 10 minutes. The solution was heated at 70° C to maintain a temperature of 50° C. When it momentarily reached 55 ° C it was placed in an ice bath until it was 50° C again. The solution was then heated at 65 ° C for the remainder of the reaction. Over the next 20 minutes, the presence of NaOCl in the reaction mixture was ascertained every 5 minutes using a starch-iodide test. If the test was negative, additional NaOCl was added to achieve a positive test (0.5 – 1 ml fractions). After 20 minutes, the reaction mixture tested positive for NaOCl, and NaHSO3 was…

    • 1188 Words
    • 5 Pages
    Better Essays
  • Better Essays

    Mechanism: Fischer esterification is the acid catalyzed condensation of an alcohol and a carboxylic acid, where it is protonated at the carbonyl oxygen, then the nucleophillic attack of the alcohol. The proton…

    • 1537 Words
    • 7 Pages
    Better Essays
  • Good Essays

    1. Assemble an apparatus for heating under reflux using a 50-mL round-bottomed flask, a water cooled reflux condenser, and a gas trap containing 1 M NaOH. The gas trap can be omitted if you under a fume hood.…

    • 512 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Competitive Nucleophiles

    • 628 Words
    • 3 Pages

    To begin the experiment, we assembled a reflux apparatus in the fume hood with a 100 mL round bottom flask and a condenser. Next we added 44 mL of sulfuric acid to a 125 mL Erlenmeyer flask. We also measured 4.75g ammonium chloride and 8.75g ammonium bromide into a 125 mL beaker, crushed the lumps, and placed in a 250 mL Erlenmeyer flask along with the sulfuric acid. We used heat to help the solutes dissolve. When they had dissolved, we allowed the flask to cool and then poured 17 mL of the solution into a separatory funnel and the rest of the solution into the reflux apparatus. 2.5 mL of 1-butanol was added to the reflux apparatus along with a boiling stone. We then started the circulation of water and brought the mixture to a gentle boil for 75 minutes. After that time we allowed it to cool in an ice bath. We then transferred the solution to a 125 mL separatory funnel and allowed the phases to separate. The lower layer was drained and the halide solution was decanted into a ground-glass stoppered flask. We then analyzed the sample using refractometry.…

    • 628 Words
    • 3 Pages
    Powerful Essays
  • Satisfactory Essays

    Esters Lab Report

    • 148 Words
    • 1 Page

    The purpose of this lab, to form various esters by combining various carboxylic acids and alcohols, was successful. The process of esterification are when a carboxylic acid reacts with an alcohol and produces an ester, or an organic compound, and water. Esters produce a certain scent which is usually fruity. In the first reaction, glacial acetic acid, or ethanoic acid, reacted with isoamyl alcohol and produced isoamyl ethanoate and water. The resulting ester scent was banana.…

    • 148 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Lab: Synthesis Of Esters

    • 573 Words
    • 3 Pages

    Purpose- the Purpose of this lab is to synthesize Esters by combining Carboxylic Acid and Alcohols. In this lab we will synthesize and then detect the odour of Esters formed.…

    • 573 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Lab 8 Isopentyl acetate 1

    • 599 Words
    • 3 Pages

    Esters are carboxylic acid derivatives in which the acyl carbon bears an ether group instead of the hydroxy group. Esters are synthesized by different methods such as an Sn2 process where a carboxylic acid is treated with a strong base followed by an alkyl halide. Fischer Esterification is a nucleophilic acyl substitution reaction that converts a carboxylic acid into an ester when the carboxyl group of an acid and the hydroxyl group of an alcohol are condensed with the expulsion of a water molecule. The by product is removed to exploit Le Chatelier’s principle in order to favor the formation of the ester over the starting material.…

    • 599 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    Purpose: In this experiment we are to take a cold solution of an aromatic ester that is first dissolved in sulfuric acid and is then reacted with nitric acid. This is a highly exothermic reaction and is kept under control by means of cooling; after which the mixture is poured onto ice. The solid product will then be isolated by filtration and recrystallized from methanol, in which it is very soluable.…

    • 491 Words
    • 2 Pages
    Good Essays
  • Satisfactory Essays

    Esters are a chemical functional group that usually forms by loosing a hydroxyl group and having it replaced with an alkoxy group with the loss of hydrogen. Esters are most commonly produced by taking a carboxylic acid, and reacting it with an alcohol with a acid catalyst in a process known as Fischer esterfication. Esters can be used in many ways including perfumes and artificial flavorings, and can be used alone or in a cocktail of different esters working together. Isopentyl acetate is the ester being synthesized in this lab. Isopentyl acetate has a strong banana odor when undiluted, and a pear odor when diluted. It is also used as an artificial flavor of butterscotch, honey, coffee, banana, and pear.…

    • 552 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    Experimental: Sodium metal was patted dry to remove any oil and was cat into small pieces. A dry 100cm3 round bottom flask was placed on a cork ring, on a balance and tarred sodium metal (0.6g) was placed into the flask. The flask was then attached to the dry reflux condenser and industrial methylated spirits (IMS, 15cm3) was added. Once all of the sodium has dissolved the solution was cooled to room temperature and the para-acetamidophenol (3.5g) was added. Ethyl iodine (3.0cm3) was slowly introduced to the mixture through the top of the condenser and the resulting in the mixture was boiled at reflux temperature for 20 minutes and was placed in a rotary evaporator to remove any excess solvent. Distilled water (40cm3) was added to the mixture and the flask was placed in ice until crystals were formed. The crude product was filtered using vacuum filtration the filtrates were washed with very little cold water and were left dry as much as possible.…

    • 652 Words
    • 3 Pages
    Good Essays