Draw the product, please shows step by step in details 2.Explain if (CH3)2CH in this reaction can attach in ortho positon in Friedel Craft Alkylation?? why or why not???
Draw the product, please shows step by step in details 2.Explain if (CH3)2CH in this reaction can attach in ortho positon in Friedel Craft Alkylation?? why or why not???
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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1.Draw the product, please shows step by step in details
2.Explain if (CH3)2CH in this reaction can attach in ortho positon in Friedel Craft Alkylation?? why or why not???

Transcribed Image Text:The image depicts a chemical reaction process involving a benzene ring with a methyl group.
**Reaction Steps:**
1. **Friedel-Crafts Alkylation:**
- Reagents: \((\text{CH}_3)_2\text{CHCl, AlCl}_3\)
- Purpose: Introduction of an isopropyl group onto the benzene ring via electrophilic aromatic substitution.
2. **Nitration:**
- Reagents: \(\text{HNO}_3, \text{H}_2\text{SO}_4\)
- Purpose: Nitration of the benzene ring to introduce a nitro group.
3. **Oxidation and Hydroxylation:**
- Reagents: \(\text{KMnO}_4, \text{NaOH}, \Delta\)
- Purpose: Oxidation of the side chain and introduction of oxygen functionalities.
4. **Acidic Workup:**
- Reagents: \(\text{H}^+, \text{H}_2\text{O}\)
- Purpose: Acidic hydrolysis to finalize any required transformations and stabilize the compound.
This sequence of reactions demonstrates a complex transformation involving alkylation, nitration, and oxidation of an aromatic compound.
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