How will you collect data for this experiment? (39pts) Report Sheet From the procedure Choose four of the esters listed

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How will you collect data for this experiment? (39pts) Report Sheet From the procedure Choose four of the esters listed in Table E.1 in the lab mnaual that have a fragrance and determine the appropriate acid or acid anhydride and alcohol to prepare the ester. Use the relevant procedure based on whether starting with an acid or an acid anhydride. Refer to the lab manual for the synthetic procedures for the synthesis of esters from acetic anhydrides and the synthesis of esters from acids. In the table below, choose the four unique esters you want to synthesize. For each ester, select the method of preparation (synthesis from an acid anhydride and synthesis from an acid). Based on the method used, select the necessary reactants that will produce your chosen ester. Report Table E.1: Synthesis of Esters Synthesis of Esters Ester Chosen Preparation Used virtually Reactant 1 teid ne zabudridet Table view List view Reactant 2 datustest
Synthesis of Esters 1 W N 3 4 Ester Chosen Choose ethyl butyrate Choose amyl acetate Choose 1-octyl acetate ▸ C Choose isobutyl formate- Preparation Used Choose... From acid Choose From acid Choose From acid Choose From acid Reactant 1 (acid or anhydride) Choose butyric acid Choose acetic acid Choose acetic acid Choose formic acid Y Choose Choose... Reactant 2 (alcohol) Choose amyl alcohol Choose 1-octyl alcohol Choone isobutyl alcohol (5pts) Describe the procedure for the preparation you chose for each ester. Make sure the procedure matches the method you selected above and that you include all reagents.
(5pts) Describe the procedure for the preparation you chose for each ester. Make sure the procedure matches the method you selected above and that you include all reagents, Normal : BIUX, X === fx Ester 2 Same as above but the acid and alcohol are different Ester 3 Same as above but thed acid and alcohol are different 8 Ester 1 Formic acid and butylalchohol and catalytic H2504 are heated which creates the butyformate The reaction is neutralized by using aqueous NaOH. The diethyl ether rids of the reaction mass. The ether is then distilled to get rid of the crude butyl formate, the crude is purified by distillation Ester 4 Same as above but the4 acid and alcohol are different C 0₂ EBT & IT Saved
Characterization of Ester Product 13. Obtain a mass and spectral data for one of your purified esters. (1pts) Synthesized ester chosen to characterize: (17pts) Calculation of Yields For the ester you selected to characterize, complete the following calculation of yields. Choose... Choose... Synthesized ester 1 Synthesized ester 2 Synthesized ester 3 Synthesized ester 4 Refer to the appropriate procedure in the lab manual PDF to find the masses of the reactants that would be used if you synthesized this ester. (1pts) Mass of acid or anhydride used (0)
(1pts) Mass of acid or anhydride used (9) (1pts) Molar mass of acid or anhydride used (g/mol) (2pts) Moles of acid or anhydride used (mol) (1pts) Mass of alcohol used (g) (1pts) Molar mass of alcohol used (g/mol) (2pts) Moles of alcohol used (mol) Choose.... Choose...
(1pts) Molar mass of alcohol used (g/mol) (2pts) Moles of alcohol used (mol) (2pts) Select the limiting reagent (1pts) Molar mass of ester product (g/mol) (3pts) Ester theoretical yield (g) (1pts) Since you are collecting data virtually calculate the mass of product that you Choose... Choose... Choose... Choose... 102.13 130.19 172.26 116.16 158.24 152.15
(1pts) Since you are collecting data virtually, calculate the mass of product that you would have obtained if your reaction had percent yield of 90% and enter it here. Mass of ester product obtained (g) (2pts) Product percent yield (%) (10pts) IR Analysis