(c) Br NaOCH, HOCH3 Br CH3ONA CH;OH (c)

Chemistry
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Chapter1: Chemical Foundations
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What are the major products of these reactions? Show the mechanisms. 

### Chemical Reaction Diagrams

#### Example (c):

**Diagram 1:**

This diagram shows a chemical reaction where a bromocyclopentane compound is transformed. The reactant is a cyclopentane ring with a bromine (Br) substituent. The reaction involves sodium methoxide (NaOCH₃) in methanol (HOCH₃) as the reagents. The arrow indicates the transformation process under these conditions.

**Diagram 2:**

This diagram illustrates another organic reaction. The reactant is a linear alkyl chain with a bromine (Br) atom attached to a more substituted carbon, indicating a tertiary bromide. The reaction occurs in the presence of sodium methoxide (CH₃ONa) in methanol (CH₃OH). The arrow denotes the direction of the chemical transformation.

### Explanation:

Both diagrams highlight nucleophilic substitution reactions commonly observed in organic chemistry. Sodium methoxide is a strong nucleophile and base, typically leading to either substitution or elimination reactions, depending on the structure of the substrate and reaction conditions.
Transcribed Image Text:### Chemical Reaction Diagrams #### Example (c): **Diagram 1:** This diagram shows a chemical reaction where a bromocyclopentane compound is transformed. The reactant is a cyclopentane ring with a bromine (Br) substituent. The reaction involves sodium methoxide (NaOCH₃) in methanol (HOCH₃) as the reagents. The arrow indicates the transformation process under these conditions. **Diagram 2:** This diagram illustrates another organic reaction. The reactant is a linear alkyl chain with a bromine (Br) atom attached to a more substituted carbon, indicating a tertiary bromide. The reaction occurs in the presence of sodium methoxide (CH₃ONa) in methanol (CH₃OH). The arrow denotes the direction of the chemical transformation. ### Explanation: Both diagrams highlight nucleophilic substitution reactions commonly observed in organic chemistry. Sodium methoxide is a strong nucleophile and base, typically leading to either substitution or elimination reactions, depending on the structure of the substrate and reaction conditions.
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