Explain the mechanism involved in the acid-catalyzed esterification of heptanoic acid with 1-butanol.

Question

Question

Answer 1

Answer #1

CH、了 H3S0 mechanismm sep proto nah om St ttacking dr alcaho CH了 3

cHi HSou

Answer 2

Similar Homework Help Questions

Write a curved arrow mechanism for the acid catalyzed Fischer esterification of benzoic acid...

Write a curved arrow mechanism for the acid catalyzed Fischer esterification of benzoic acid in CH3O*H (that is 0-18 labeled methanol). Show all steps, lone pair of electrons, charges and labeled O atoms through the mechanism.
2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction. 3. Acid-catalyzed hydration...

2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction. 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain.
a) Draw the mechanism (including electron-movement arrows) of the acid-catalyzed esterification + H2O Sulfuric Acetic acid...

a) Draw the mechanism (including electron-movement arrows) of the acid-catalyzed esterification + H2O Sulfuric Acetic acid Isoamyl alcohol acid isoamyl acetatewater (concn.) (glacial)

Please answer all questions and show all work 1. Write a mechanism for the acid-catalyzed esterification...

Please answer all questions and show all work 1. Write a mechanism for the acid-catalyzed esterification that uses cyclopentanol and acetic acid. 2. Tertiary alcohols do not work well in the procedure outlined for this experiment; they give a different product from what you might expect. Explain this and draw the expected product from t-butyl alcohol (2-methyl-2-propanol).
7. Show the mechanism for the following Acid Catalyzed Fisher Esterification | H obrang OH НО-...

7. Show the mechanism for the following Acid Catalyzed Fisher Esterification | H obrang OH НО- H20
What is Zaitsev’s rule? Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol. Give the...

What is Zaitsev’s rule? Give the mechanism for the acid-catalyzed E1 reaction of 2-butanol. Give the mechanism for the base-catalyzed E2 reaction of 2-bromobutane. Draw all possible products. You expect three products from the elimination reaction 2-butanol. What are they? The E2 mechanism is a one-step mechanism. True or False? Explain. Which of these two alcohols would you expect to be more reactive under H3PO4/aqueous conditions? Why? Give the structure of the main product in both cases. 1-phenyl-1-propanol 1 -cyclohexyl-1-propanol...

2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol Show a mechanism for this reaction. 3. Acid-catalyzed hydration...

2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol Show a mechanism for this reaction. 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol
3. Show the detailed mechanism for the Fischer Esterification reaction between acetic acid and sec-butanol. All...

3. Show the detailed mechanism for the Fischer Esterification reaction between acetic acid and sec-butanol. All arrows, charges, structures, etc must be shown neatly and clearly - every little detail counts!
Reaction mechanisms of acid catalyzed esterification of vanillin react with acetic anhydrides

Does anyone know the full mechanism of acid-catalyzed esterification of vanillin when it react with acetic anhydride under acidic condition yielding the product below?

3. The esterification of butanol by sulfuric acid forms butyl hydrogen sulfate (A). This causes side...

3. The esterification of butanol by sulfuric acid forms butyl hydrogen sulfate (A). This causes side products in the synthesis of bromobutane decreasing the yield of the desired product. OH + H2So. - 0-5-OH + H2O A Ö Give the IUPAC name of two possible compounds of different functional groups that are products from this side reaction. Draw a mechanism for each starting from (A). 1) Side Product 1. IUPAC name is Draw Mechanism - 2) Side Product 2, different...