f.) се , десяцу Ь 2.) Hz604, HNO3

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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Fill in the missing structure(s) for the reaction pathways shown below. Provide
all starting material(s), reagent(s), or product(s). If more than one product can be
formed, draw all major products. If more than one starting material or reagent is
possible, write all starting materials or reagents. Include stereochemistry in your
answer, if applicable, and draw all stereoisomers.

Certainly! Here's a transcription suitable for an educational website:

---

**Chemical Reaction Illustration (Section f):**

In this reaction, we start with a benzene ring as the primary reactant. The reaction involves two main steps:

1. **First Step:**
   - Reagents: Acetyl chloride (represented as "C=O with a Cl attached") and aluminum chloride (AlCl₃) are used.
   - Purpose: This step likely involves an acylation process, where the acetyl group is introduced to the benzene ring using AlCl₃ as a catalyst.

2. **Second Step:**
   - Reagents: Sulfuric acid (H₂SO₄) and nitric acid (HNO₃) are involved.
   - Purpose: This step indicates a nitration reaction, where a nitro group might be introduced to the benzene derivative.

The image ends with an arrow pointing to a blank rectangle, which possibly represents the final product following these transformations. This placeholder suggests the need for further elaboration or completion of the product's chemical structure.

---
Transcribed Image Text:Certainly! Here's a transcription suitable for an educational website: --- **Chemical Reaction Illustration (Section f):** In this reaction, we start with a benzene ring as the primary reactant. The reaction involves two main steps: 1. **First Step:** - Reagents: Acetyl chloride (represented as "C=O with a Cl attached") and aluminum chloride (AlCl₃) are used. - Purpose: This step likely involves an acylation process, where the acetyl group is introduced to the benzene ring using AlCl₃ as a catalyst. 2. **Second Step:** - Reagents: Sulfuric acid (H₂SO₄) and nitric acid (HNO₃) are involved. - Purpose: This step indicates a nitration reaction, where a nitro group might be introduced to the benzene derivative. The image ends with an arrow pointing to a blank rectangle, which possibly represents the final product following these transformations. This placeholder suggests the need for further elaboration or completion of the product's chemical structure. ---
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