Br OCH 3

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...
icon
Related questions
Question

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.
Expert Solution
steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Alcohols
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY