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
Question 5.1
![**Question:**
Which direction does the equilibrium below favor and what is the deciding factor?
**Diagram:**
The diagram shows a chemical equilibrium between two compounds.
- **Left side (Reactants):**
- A benzene ring with a methoxy group (OCH₃) attached to it.
- A carboxylic acid group (COOH) attached to the benzene.
- A nitro group (NO₂) attached to the benzene.
- **Right side (Products):**
- The methoxy group becomes an anion (O⁻).
- The carboxylic acid remains unchanged.
- The nitro group remains attached to the benzene.
**Options:**
- ○ reactants, electronegativity
- ○ reactants, resonance
- ○ reactants, induction
- ○ products, electronegativity
- ○ products, resonance
- ○ products, induction](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Faf2aaae6-e5c1-402b-921f-5eab7ac01087%2Fc51f5e9d-2f3e-42ec-9ece-3bc8466d855f%2F2jj8ys5_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Question:**
Which direction does the equilibrium below favor and what is the deciding factor?
**Diagram:**
The diagram shows a chemical equilibrium between two compounds.
- **Left side (Reactants):**
- A benzene ring with a methoxy group (OCH₃) attached to it.
- A carboxylic acid group (COOH) attached to the benzene.
- A nitro group (NO₂) attached to the benzene.
- **Right side (Products):**
- The methoxy group becomes an anion (O⁻).
- The carboxylic acid remains unchanged.
- The nitro group remains attached to the benzene.
**Options:**
- ○ reactants, electronegativity
- ○ reactants, resonance
- ○ reactants, induction
- ○ products, electronegativity
- ○ products, resonance
- ○ products, induction
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