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:
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:
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...
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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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