"Ethyl acetate" Essays and Research Papers

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    Hand Sanitiser

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    Solvents used were water‚ methanol‚ n-butanol‚ ethylene glycol‚ acetone‚ hexane‚ toluene‚ ethyl acetate‚ and dichloromethane. Then added to the vials was 0.5 mL of isooctane in each one. The vials were then swirled and observed to determine solubility. In part two of the experiment‚ 0.5 mL of concentrated sulfuric acid was added into two sample

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    there are two esters that are very close in molar mass‚ methyl acetate and ethyl formate. The methyl acetate and the ethyl formate both have a molar mass of 74.08 g/mol [5][6]. The last step is to distinguish between the two. Both methyl acetate and ethyl formate are described as having a “fruity odour”‚ relatively close boiling points and the same colourless appearance [5][6]. However‚ there is one source that says that methyl acetate has a “characteristically pleasant smell reminiscent of some glues

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    and adsorbent used‚ molecules will experience the interaction during dynamic equilibrium. On a TLC plate‚ capillary tube is used to transfer o- and p- hydroxyacetopheone‚ taking advantage of capillary force to make small spotting. A 30:70 ether acetate: petroleum ether is used as a solvent‚ which will not interact with surface of the silica gel due to a characteristic of non-polar. When they are desorbed‚ that is‚ when there is no interaction between the surface of the silica gel and the molecules

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    (-OCH3). Similarly‚ ethyl acetate (CH3CO-OCH2CH3) is made up of acetic acid (CH3CO-OH) in which the hydroxy group has been replaced by an ethoxy group (-OCH2CH3) Although esters can be produced by many mechanisms‚ the most commonly used method is called esterification‚ which is a condensation reaction between an alcohol and an acid‚ typically in the presence of a strong acid catalyst‚ such as sulfuric acid. For example‚ ethyl acetate can be produced by reacting ethanol (ethyl alcohol) with acetic

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    Effect of Organic Solvents

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    SYNTHETIC EXPLOITATION OF ENZYMES: BIOCATALYSIS IN ORGANIC SOLVENTS: FUNDAMENTALS ENZYMES IN ORGANIC SYNTHESIS 1. Enzymes catalyze a broad spectrum of reactions with high turnover numbers. Rate enhancements approach 1012 fold. 2. Enzymes may accept a wide range of substrates. 3. Enzymes are highly regio and stereoselective. 4. Enzyme reactions take place under mild conditions; this minimizes problems of isomerization and racemization. 5. Enzymatic processes are less hazardous and polluting

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    stirred tank reactor for the saponification of ethyl acetate with dilute sodium hydroxide. To determine the effect of temperature on reaction rate constant. To find the values of rate constant and Arrhenius parameters. Equipment used Arm field batch stirred tank reactor A stop clock A conductivity meter Water bath (tank) with a thermostat Funnel A heat controller Two flasks of one litre each and Stock solutions (0.1M sodium hydroxide and 0.1M ethyl acetate). The key results obtained include Table showing

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    as the solution cools and begins to come out of the solution. The acetylsalicylic acid is further purified through recrystallization with ethyl acetate. MATERIALS USED: Test Tubes Pasteur Pipette Salicylic acid acetic anhydride Sulfuric acid 125 mL Erlenmeyer flask Scale Water Hot water bath Ice Bath Buchner Fünnel 1% Ferric Chloride Ethyl acetate Glass Rod Iodine Aspirin Tablet Commercial Aspirin tablet METHODS Part A 1. 2.0 g of salicylic acid was placed in a 125 mL Erlenmeyer

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    mL of distillate was collected in the receiving flask. The distillate was added to a separatory funnel to perform an extraction with 5 mL of ethyl acetate. The ethyl acetate extract was then dried by adding 0.6102 grams of anhydrous calcium chloride to remove the water. The contents were filtered to remove the anhydrous calcium chloride from the ethyl acetate extract. This liquid contained the extracted limonene‚ and it was placed on a hot plate to boil off the solvent (leaving pure limonene extract

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    3 1.23 NaCl 58.44 1 800.7 36 H2O 18.02 1 0.0 1.00 Experimental procedure: Aspirin (1.30 g ‚ 0.00722 mol)‚ Caffeine (0.00666 g‚ 0.000350 mol) and Salicylamide (0.390 g‚ 0.00284 mol) were combined in a 100 mL beaker. To this beaker‚ ethyl acetate (20 mL) and saturated NaHCO3 (10 mL) were added. The organic and aqueous layers were allowed time to separate before the organic layer was removed and put aside. An additional portion of NaHCO3 solution (10 mL) was added and the separation was

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