What alcohol must react with propionic acid then trreated with H2SO4 and heat to yield isobutyl acetate ? Please show the reaction mechanism.
What alcohol must react with propionic acid then trreated with H2SO4 and heat to yield isobutyl...
4. 20 points Acetic acid (CH,CO,H) reacts with isobutyl alcohol (C.H100) to yield isobutyl acetate (C H202), a fragrant substance with the scent of raspberries or pears (depending on the concentration), via the balanced reaction: CH,CO,H(aq) + C,H,O(aq) -CH202 (aq) + H20() If the yield of this reaction is 51%, how many grams of isobutyl acetate are formed from 4.00 g of acetic acid and 6.00 g of isobutyl alcohol?
7.5
mL isobutyric acid
10mL isobutyl alcohol
2. Chemical Reaction and Yield (7 points): In the space below, calculate the theoretical yield (in grams and ml) of the ester product (d = 0.855 g/ml for the ester product). H2SO4 lot + Hoy 1.0 H2O он + но Y т y . 40 reflux
Calculate the theoretical yield of 1mL of isopropanol, 1.5mL propionic acid and 4 drops of sulfuric acid to form isopropyl propanoate. Also, provide a reaction mechanism of the reaction. Include lone electron pairs, electron flow, and arrows. Please and thank you!!!
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2Cr04 D) CH3MgBr, followed by HCI - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) sec-butyl alcohol D) n-butyl alcohol 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation of an...
H2SO4 (cat) OH n-butanol HO propionic acid homoly od 10.my mol no H₂O n-butyl propionate cal concenteNucleophilie gewl substiti Diabanidaataifianti 3. Answer the following questions: a. For only the ester you are making, please draw a detailed electron-pushing mechanism to show the formation of the compound. There are many resources available to you on the web, etc) for the mechanism of the Fischer esterification reaction. latest some of one of obol whichever one will be using to
14) Which of the following reagents would react with a primary alcohol to produce an aldehyde as the final product? A) PCC B) H2SO4 C) H2C704 D) CH3MgBr, followed by HCI 15) - 15) Which one of the following is not oxidized by K2Cr2O7 in H2SO4/H20? A) isobutyl alcohol B) tert-butyl alcohol C) seo-butyl alcohol D) n-butyl alcohol 16) 16) Which of the following methods will NOT produce an alcohol as the product? A) hydroboration-oxidation of an alkene B) oxidation...
Draw a Fischer esterification reaction of: Propyl propionate (alcohol) and propionic acid (acetic acid) ( include lone pairs, arrows electron flow)
If 4.46 g of acetic acid and 2.19 g of isopentyl alcohol are used in the reaction, what is the limiting reagent? What is the theoretical yield? What is the percent yield if 2.50 g of isopentyl acetate are obtained? (please show all calculations!!!)
If the yield from the reaction of acetic acid with isopentyl alcohol is 45%, how many grams of isopentyl acetate are formed from 3.58 g of acetic acid and 4.70 g of isopentyl alcohol? The reaction is: CH3CO2H+C5H12O→C7H14O2+H2O Express your answer using two significant figures.
Show the mechanism of the acid catalyzed reaction of an alcohol
with acetic anhydride, indicating the involvement of the strong
acid catalyst in the reaction.
H2SO4 (cat.) R'OH ROR ROH ROD +