Preparation of Fruit Flavors

Embed Size (px)

Citation preview

  • 7/25/2019 Preparation of Fruit Flavors

    1/12

    Preparation ofFruit Flavors

  • 7/25/2019 Preparation of Fruit Flavors

    2/12

    Abstract

    The experiment was conducted to synthesize the Isoacetate through the sher esterication mechanism isoamyl alcohol and acetic anhydride. It was reuxe!" mins at a constant temperature of #"o$ and was

    extracted to remove the unneeded a%ueous layer. Ththeoretical yield that was calculated was &.'( grams)hile* the Actual yield that was obtained was + to &grams. Around (' to #&, percent yield was determ

  • 7/25/2019 Preparation of Fruit Flavors

    3/12

    Introduction

    -ne of the most important avor compounds used food industries is Isoamyl Acetate because of its distbanana avor. Its avoring compound called ester is umany foods and drins. Also* it is one of the ma/or

    components of fermented alcoholic beverages.

    The extent of this experiment is till the percent yield o

  • 7/25/2019 Preparation of Fruit Flavors

    4/12

    -b/ectives

    0ynthesize isoamyl acetate

    1earn the reux techni%ue

    Perform li%uid2li%uid extraction

    $alculate percent yield of a reaction

  • 7/25/2019 Preparation of Fruit Flavors

    5/12

    3sters 2

    3sters are derived from carboxylic acids. A carboxylcontains the 2$--4 group* and in an ester the hydroin this group is replaced by a hydrocarbon group of ind. This could be an alyl group lie methyl or eth

    one containing a benzene ring lie phenyl. -rganic compound formed in a reaction between an

    and an alcohol with the elimination of water.

    3sters can be formed from both organic and inorganacids and the process of producing an ester is calledFischer 5eaction.

  • 7/25/2019 Preparation of Fruit Flavors

    6/12

    Fischer reaction

    )hen alcohols are combined with carboxylic acids inpresence of an acid catalyst an esterication reactiooccurs to form esters and water.

  • 7/25/2019 Preparation of Fruit Flavors

    7/12

    Theoretical yield

    6moles of the 1imiting reagent7 x 68olecular weighisoamyl acetate7

    1imiting reagent 9 &."ml x ".#"': x ; mol x ;mol of alcohol x ;!

    ml ##.:g ; mol of acetate mo

    9 &.'( alcohol 1imiting reagent 9 &.:ml x ;."#:"' x ; mol x ;mol of anhydride

    ml ;":.;g ; mol of acetate

    9 (.;(& acetic anhydride

  • 7/25/2019 Preparation of Fruit Flavors

    8/12

    5eux

    8ethod of heating li%uid so that escaping vapor iscondensed and returned to li%uid.

    )ith the use of the condenser any vapors given o< acooled bac to li%uid* and fall bac into the reaction

    vessel. The vessel is then heated vigorously for the cof the reaction. The purpose is to thermally accelerareaction by conducting it at an elevated temperature

  • 7/25/2019 Preparation of Fruit Flavors

    9/12

    =oiling $hips

    =oiling chips are small* insoluble* porous stones madcalcium carbonate or silicon carbide. These stones hpores inside which provide cavities both to trap air aprovide spaces where bubbles of solvent vapor can f

    These bubbles ensure even boiling and prevent bumand boiling over and loss of the solution.

  • 7/25/2019 Preparation of Fruit Flavors

    10/12

    >rying Agents

    3xtraction with ?a$l was used to remove the buls water remaining in the mixture.

    The salt water wors to pull the water from the orgalayer to the water layer. This is because the concent

    salt solution wants to become more dilute and becausalts have a stronger attraction to water than to orgsolvents.

  • 7/25/2019 Preparation of Fruit Flavors

    11/12

    0odium =icarbonate

    used as a wash to remove any acidic impurities fromcrude li%uid* producing a purer sample.

  • 7/25/2019 Preparation of Fruit Flavors

    12/12

    Anhydrous 0ulfate

    is used to dry the mixture from the water.