#31 help **Exercise Instructions:**1. **Objective**: Draw the tautomer of the given aldehyde. Make sure to include all lone pairs in your drawing. You should ignore inorganic byproducts in this process.2. **Chemical Structure Provided**: - The chemical structure showcases an aldehyde with a benzene ring (phenyl group) attached to a propanal group (three-carbon chain ending with an aldehyde functional group).3. **Reaction Condition**: - The conversion is to be performed in the presence of H₃O⁺ (hydronium ion), which acts as a catalyst for the tautomerization reaction.4. **Response to Input**: - The initial attempt has been marked incorrect, with a reminder that 2 attempts remain.5. **Diagram Details**: - **Initial Structure**: The image depicts the aldehyde with lone pairs on the oxygen atom. - **Attempted Tautomer Structure**: The drawing reflects an incorrect enol form, where an -OH group is attached to a carbon that was originally near the double-bonded oxygen.6. **Instruction Visuals**: - The visual representation includes a large arrow indicating the transformation process from the aldehyde to the enol form. - An error indication is shown in the form of a red cross suggesting the attempted tautomer formation is incorrect.**Guidance for Attempts**:- Reevaluate the placement of hydrogen and hydroxyl groups.- Ensure the enol form respects the proper keto-enol tautomerization mechanism, focusing on the proton shift and formation of a new double bond adjacent to the hydroxyl group.

Tautomers are the isomers which involve the interchange of H-atom.

Answered: :O: H3O+ OH H I 'Н Draw Tautomer X

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Chemistry

:O: H3O+ OH H I 'Н Draw Tautomer X

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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Question

#31 help

**Exercise Instructions:**

1. **Objective**: Draw the tautomer of the given aldehyde. Make sure to include all lone pairs in your drawing. You should ignore inorganic byproducts in this process.

2. **Chemical Structure Provided**:
- The chemical structure showcases an aldehyde with a benzene ring (phenyl group) attached to a propanal group (three-carbon chain ending with an aldehyde functional group).

3. **Reaction Condition**:
- The conversion is to be performed in the presence of H₃O⁺ (hydronium ion), which acts as a catalyst for the tautomerization reaction.

4. **Response to Input**:
- The initial attempt has been marked incorrect, with a reminder that 2 attempts remain.

5. **Diagram Details**:
- **Initial Structure**: The image depicts the aldehyde with lone pairs on the oxygen atom.
- **Attempted Tautomer Structure**: The drawing reflects an incorrect enol form, where an -OH group is attached to a carbon that was originally near the double-bonded oxygen.

6. **Instruction Visuals**:
- The visual representation includes a large arrow indicating the transformation process from the aldehyde to the enol form.
- An error indication is shown in the form of a red cross suggesting the attempted tautomer formation is incorrect.

**Guidance for Attempts**:
- Reevaluate the placement of hydrogen and hydroxyl groups.
- Ensure the enol form respects the proper keto-enol tautomerization mechanism, focusing on the proton shift and formation of a new double bond adjacent to the hydroxyl group.

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