Br OCH 3

Chemistry
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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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Propose a synthesis for the compounds below using the reagents given below. 

### Reagents (not necessarily a complete list):

- **PCC**
- **1. OsO₄; 2. KHSO₃**
- **MsCl (or TsCl), pyridine**
- **1. LiAlH₄; 2. H₃O⁺**
- **NaH**
- **SOCl₂**
- **TBDMS-Cl or TMS-Cl, Et₃N**
- **1. RSH, H⁺; 2. Raney Ni**
- **1. Hg(O₂CCF₃)₂, ROH; 2. NaBH₄**
- **POCl₃, pyridine**
- **PBr₃**
- **1. RMgX or RLi; 2. H₃O⁺**
- **NaBH₄**
- **mCPBA**
- **CrO₃, H₂SO₄, H₂O**
- **H⁺, ROH**
- **NaIO₄**
- **HX (X = Halogen)**
- **X₂**
- **1. Hg(OAc)₂, H₂O; 2. NaBH₄**
- **1. H⁺, H₂NNH₂; 2. NaOH**
- **H₂, Lindlar’s catalyst**
- **NaNH₂**
- **1. O₃; 2. Zn, HOAc**
- **1. BH₃-THF; 2. H₂O₂, NaOH**
- **H₂, Pd/C**
- **1. O₃; 2. H₂O**
- **Na, NH₃** 

This list includes a variety of reagents commonly used in organic chemistry for different reactions such as oxidation, reduction, protection, and other transformations.
Transcribed Image Text:### Reagents (not necessarily a complete list): - **PCC** - **1. OsO₄; 2. KHSO₃** - **MsCl (or TsCl), pyridine** - **1. LiAlH₄; 2. H₃O⁺** - **NaH** - **SOCl₂** - **TBDMS-Cl or TMS-Cl, Et₃N** - **1. RSH, H⁺; 2. Raney Ni** - **1. Hg(O₂CCF₃)₂, ROH; 2. NaBH₄** - **POCl₃, pyridine** - **PBr₃** - **1. RMgX or RLi; 2. H₃O⁺** - **NaBH₄** - **mCPBA** - **CrO₃, H₂SO₄, H₂O** - **H⁺, ROH** - **NaIO₄** - **HX (X = Halogen)** - **X₂** - **1. Hg(OAc)₂, H₂O; 2. NaBH₄** - **1. H⁺, H₂NNH₂; 2. NaOH** - **H₂, Lindlar’s catalyst** - **NaNH₂** - **1. O₃; 2. Zn, HOAc** - **1. BH₃-THF; 2. H₂O₂, NaOH** - **H₂, Pd/C** - **1. O₃; 2. H₂O** - **Na, NH₃** This list includes a variety of reagents commonly used in organic chemistry for different reactions such as oxidation, reduction, protection, and other transformations.
The image depicts a chemical reaction involving organic compounds. 

On the left side, there is a reactant: a benzene ring attached to a bromine atom (C6H5-CH2-Br), commonly referred to as benzyl bromide.

The reaction is shown with a rightward arrow, indicating the transformation of the reactant into a product.

On the right side, the product is shown: a benzene ring attached to a propyl group terminating in a methoxy group (C6H5-CH2-CH(CH3)-OCH3). 

This reaction suggests a substitution process where the bromine in benzyl bromide is replaced by a methoxypropyl group. 

The diagram does not include specific conditions or reagents necessary for the reaction, such as catalysts, solvents, temperature, or pressure, which are essential for carrying out the substitution.
Transcribed Image Text:The image depicts a chemical reaction involving organic compounds. On the left side, there is a reactant: a benzene ring attached to a bromine atom (C6H5-CH2-Br), commonly referred to as benzyl bromide. The reaction is shown with a rightward arrow, indicating the transformation of the reactant into a product. On the right side, the product is shown: a benzene ring attached to a propyl group terminating in a methoxy group (C6H5-CH2-CH(CH3)-OCH3). This reaction suggests a substitution process where the bromine in benzyl bromide is replaced by a methoxypropyl group. The diagram does not include specific conditions or reagents necessary for the reaction, such as catalysts, solvents, temperature, or pressure, which are essential for carrying out the substitution.
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