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Identify the reagents needed to complete this multistep synthesis.

Identify the reagents needed to complete this multistep synthesis.

Chemistry
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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Identify the reagents needed to complete this multistep synthesis. 

The image displays a flowchart of a chemical synthesis process, featuring benzene and an alcohol derivative reacting to form a brominated compound. The process involves several reactions that are to be completed using specified reagents. ### Reagents: - **PCC (Pyridinium chlorochromate)** - **Jones Reagent** - **Br₂/FeBr₃ (Bromine and Iron(III) bromide)** - **H₃O⁺ (Hydronium ion)** - **HCl/Zn(Hg) (Hydrochloric acid and zinc amalgam)** - **LAH (Lithium aluminium hydride)** - **H₂SO₄ (Sulfuric acid)** - **SOCl₂ (Thionyl chloride)** ### Chemical Structures and Arrows: 1. **Benzene** is shown reacting with an alcohol derivative. 2. **Br₂/FeBr₃** reagent is indicated to be responsible for transforming the compound into a brominated benzene ring. 3. An intermediate with a hydroxy group suggests a possible nucleophilic substitution or elimination step. 4. **AlCl₃ (Aluminum chloride)** is used further along in the pathway, possibly indicating a Friedel-Crafts alkylation or acylation. 5. Several other reaction steps with empty placeholders indicate directions where different reagents from the list might be applied. The intention is to fill in these reaction steps with appropriate reagents and intermediates based on knowledge of organic chemistry reactions and mechanisms. The flowchart should be explored to understand how reagents interact to carry out specific transformation steps in synthesis.
Transcribed Image Text:The image displays a flowchart of a chemical synthesis process, featuring benzene and an alcohol derivative reacting to form a brominated compound. The process involves several reactions that are to be completed using specified reagents. ### Reagents: - **PCC (Pyridinium chlorochromate)** - **Jones Reagent** - **Br₂/FeBr₃ (Bromine and Iron(III) bromide)** - **H₃O⁺ (Hydronium ion)** - **HCl/Zn(Hg) (Hydrochloric acid and zinc amalgam)** - **LAH (Lithium aluminium hydride)** - **H₂SO₄ (Sulfuric acid)** - **SOCl₂ (Thionyl chloride)** ### Chemical Structures and Arrows: 1. **Benzene** is shown reacting with an alcohol derivative. 2. **Br₂/FeBr₃** reagent is indicated to be responsible for transforming the compound into a brominated benzene ring. 3. An intermediate with a hydroxy group suggests a possible nucleophilic substitution or elimination step. 4. **AlCl₃ (Aluminum chloride)** is used further along in the pathway, possibly indicating a Friedel-Crafts alkylation or acylation. 5. Several other reaction steps with empty placeholders indicate directions where different reagents from the list might be applied. The intention is to fill in these reaction steps with appropriate reagents and intermediates based on knowledge of organic chemistry reactions and mechanisms. The flowchart should be explored to understand how reagents interact to carry out specific transformation steps in synthesis.
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We have to identify the reagents needed to complete the following multistep synthesis :

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