1. Write the reaction that you will do this week for the Williamson ether synthesis. Label the nucleophile and the electrophile, the nucleophilic atom and the electrophilic atom. 2. Mechanistically, what type of reaction is the ether synthesis that you will perform this week? 3. An extraction is done for the work-up. What liquids will be used for the extraction? In which liquid will the product be? Will the product be in the top layer or the bottom layer?

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1. Write the reaction that you will do this week for the Williamson ether synthesis. Label the nucleophile and the electrophile, the nucleophilic atom and the electrophilic atom.

2. Mechanistically, what type of reaction is the ether synthesis that you will perform this week?

3. An extraction is done for the work-up. What liquids will be used for the extraction? In which liquid will the product be? Will the product be in the top layer or the bottom layer?

 

**Transcription for Educational Website:**

This diagram illustrates the Williamson Ether Synthesis, a reaction that produces an ether from an alkoxide and a haloalkane. 

**Reactants:**
- **Sodium ethoxide (\(C_2H_5ONa\))**: A base that contributes the ethoxide ion.
- **1-Bromobutane (\(C_4H_9Br\))**: A reactant with a boiling point of 101°C and a density of 1.27 g/mL.

**Reaction Conditions:**
- The reaction takes place in ethanol as the solvent at a temperature of 90°C.

**Products:**
- **1-Ethoxybutane (\(C_6H_{14}O\))**: The target ether product, with a boiling point of 91-92°C and a density of 0.75 g/mL.
- **Sodium bromide (NaBr)**: A byproduct of the reaction.

**Reaction Pathway:**
- The ethoxide ion from sodium ethoxide attacks the electrophilic carbon in 1-bromobutane, resulting in the formation of 1-ethoxybutane and the release of sodium bromide.

This reaction is an example of nucleophilic substitution and demonstrates the classic method for synthesizing ethers.
Transcribed Image Text:**Transcription for Educational Website:** This diagram illustrates the Williamson Ether Synthesis, a reaction that produces an ether from an alkoxide and a haloalkane. **Reactants:** - **Sodium ethoxide (\(C_2H_5ONa\))**: A base that contributes the ethoxide ion. - **1-Bromobutane (\(C_4H_9Br\))**: A reactant with a boiling point of 101°C and a density of 1.27 g/mL. **Reaction Conditions:** - The reaction takes place in ethanol as the solvent at a temperature of 90°C. **Products:** - **1-Ethoxybutane (\(C_6H_{14}O\))**: The target ether product, with a boiling point of 91-92°C and a density of 0.75 g/mL. - **Sodium bromide (NaBr)**: A byproduct of the reaction. **Reaction Pathway:** - The ethoxide ion from sodium ethoxide attacks the electrophilic carbon in 1-bromobutane, resulting in the formation of 1-ethoxybutane and the release of sodium bromide. This reaction is an example of nucleophilic substitution and demonstrates the classic method for synthesizing ethers.
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