Chemistry
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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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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Transcribed Image Text:**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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