Draw curved arrows to indicate the movement of electrons in the following reaction. H HO: Arrow-pushing Instructions HỌ: ANC↔XT H H----C—CI H H- H -CI HO H HO-C- H -CH H H H :CI:

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The image contains a chemical reaction diagram where the movement of electrons is to be illustrated with curved arrows. The reaction involves a hydroxide ion (\( \text{HO}^- \)) and a chloromethane molecule (\( \text{CH}_3\text{Cl} \)), which transforms into methanol (\( \text{CH}_3\text{OH} \)) and a chloride ion (\( \text{Cl}^- \)).

### Diagram Explanation

1. **Reactants:**
   - **Hydroxide ion (\( \text{HO}^- \))**: Shown on the left with a lone pair of electrons around the oxygen atom.
   - **Chloromethane (\( \text{CH}_3\text{Cl} \))**: Depicted in the center with three hydrogen atoms bonded to a central carbon atom, which is also bonded to a chlorine atom.

2. **Products:**
   - **Methanol (\( \text{CH}_3\text{OH} \))**: Shown on the right side with hydroxyl (\(\text{OH}\)) bonded to the central carbon.
   - **Chloride ion (\( \text{Cl}^- \))**: Present as a separate ion with a full set of valence electrons.

3. **Reaction Arrow:**
   - An arrow between the reactants and products denotes the chemical transformation.

### Arrow-Pushing Instructions

Below the diagram, there is a box titled “Arrow-pushing Instructions” showing:
- A series of curved arrows used to indicate electron movement in chemical reactions.
- The notation shows how electrons are transferred from the lone pair of the hydroxide ion to the carbon atom, and from the carbon-chlorine bond to the chlorine atom.

Understanding this electron movement is crucial for illustrating how the hydroxide ion acts as a nucleophile, attacking the electrophilic carbon in chloromethane, resulting in the substitution reaction that forms methanol and releases a chloride ion.
Transcribed Image Text:The image contains a chemical reaction diagram where the movement of electrons is to be illustrated with curved arrows. The reaction involves a hydroxide ion (\( \text{HO}^- \)) and a chloromethane molecule (\( \text{CH}_3\text{Cl} \)), which transforms into methanol (\( \text{CH}_3\text{OH} \)) and a chloride ion (\( \text{Cl}^- \)). ### Diagram Explanation 1. **Reactants:** - **Hydroxide ion (\( \text{HO}^- \))**: Shown on the left with a lone pair of electrons around the oxygen atom. - **Chloromethane (\( \text{CH}_3\text{Cl} \))**: Depicted in the center with three hydrogen atoms bonded to a central carbon atom, which is also bonded to a chlorine atom. 2. **Products:** - **Methanol (\( \text{CH}_3\text{OH} \))**: Shown on the right side with hydroxyl (\(\text{OH}\)) bonded to the central carbon. - **Chloride ion (\( \text{Cl}^- \))**: Present as a separate ion with a full set of valence electrons. 3. **Reaction Arrow:** - An arrow between the reactants and products denotes the chemical transformation. ### Arrow-Pushing Instructions Below the diagram, there is a box titled “Arrow-pushing Instructions” showing: - A series of curved arrows used to indicate electron movement in chemical reactions. - The notation shows how electrons are transferred from the lone pair of the hydroxide ion to the carbon atom, and from the carbon-chlorine bond to the chlorine atom. Understanding this electron movement is crucial for illustrating how the hydroxide ion acts as a nucleophile, attacking the electrophilic carbon in chloromethane, resulting in the substitution reaction that forms methanol and releases a chloride ion.
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