HW11#5 **Title: Enol and Ketone Formation from Pent-2-yne****Instructions:**Click the "draw structure" button to launch the drawing utility.**Question:**Ignoring E and Z isomers, what two enols are formed when pent-2-yne is treated with H₂O, H₂SO₄, and HgSO₄? Draw the second ketone formed from these enols after tautomerization.**Chemical Reaction:**- **Starting Material:** Pent-2-yne- **Reagents:** H₂O, H₂SO₄, HgSO₄- **Products:** Two ketones, with one shown as a specific structure and the second labeled "Product A."**Diagram Explanation:**- The reaction starts with the structural depiction of pent-2-yne, represented by a carbon chain with a triple bond between the second and third carbon atoms.- The reaction conditions (H₂O, H₂SO₄, HgSO₄) are indicated above the reaction arrow.- The primary product is shown as a ketone resulting from tautomerization, with the carbonyl group (C=O) on the second carbon.- There is a second product, labeled as "Product A," which is unspecified in structure but indicated with a prompt for the user to "edit structure."**Interactive Element:**- A button labeled "edit structure" within a dashed box invites users to draw and submit their proposed structure for Product A.

Alkyne gives a hydration reaction in the presence of mercuric sulfate and sulfuric acid to form an…

Click the "draw structure" button to launch the drawing utility. Ignoring E and Z isomers, what two enols are formed when pent-2-yne is treated with H₂O, H₂SO4, and HgSO4? Draw the second ketone formed from these enols after tautomerization. H₂O H₂SO4, HgSO4 + Product A

Click the "draw structure" button to launch the drawing utility. Ignoring E and Z isomers, what two enols are formed when pent-2-yne is treated with H₂O, H₂SO4, and HgSO4? Draw the second ketone formed from these enols after tautomerization. H₂O H₂SO4, HgSO4 + Product A

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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HW11#5

**Title: Enol and Ketone Formation from Pent-2-yne**

**Instructions:**

Click the "draw structure" button to launch the drawing utility.

**Question:**

Ignoring E and Z isomers, what two enols are formed when pent-2-yne is treated with H₂O, H₂SO₄, and HgSO₄? Draw the second ketone formed from these enols after tautomerization.

**Chemical Reaction:**

- **Starting Material:** Pent-2-yne
- **Reagents:** H₂O, H₂SO₄, HgSO₄
- **Products:** Two ketones, with one shown as a specific structure and the second labeled "Product A."

**Diagram Explanation:**

- The reaction starts with the structural depiction of pent-2-yne, represented by a carbon chain with a triple bond between the second and third carbon atoms.
- The reaction conditions (H₂O, H₂SO₄, HgSO₄) are indicated above the reaction arrow.
- The primary product is shown as a ketone resulting from tautomerization, with the carbonyl group (C=O) on the second carbon.
- There is a second product, labeled as "Product A," which is unspecified in structure but indicated with a prompt for the user to "edit structure."

**Interactive Element:**

- A button labeled "edit structure" within a dashed box invites users to draw and submit their proposed structure for Product A.

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Step 1: Hydrolysis of alkyne

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