For the given SN2 reaction, draw the organic and inorganic products of the reaction, and identify the nucleophile, substrate, and leaving group. Include wedge-and-dash bonds and draw hydrogen on a stereocenter. Hl :cEN Organic product Inorganic product +

Chemistry
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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
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For the given S<sub>N</sub>2 reaction, students are tasked with drawing the organic and inorganic products of the reaction. They must identify the nucleophile, substrate, and leaving group, and ensure to include wedge-and-dash bonds along with a hydrogen on the stereocenter.

### Reaction Overview:
- **Reactants:**
  - A molecular structure with a chlorine atom (Cl) as the leaving group.
  - A cyanide ion (^-C≡N) as the nucleophile.
- **Products:**
  - An organic product with a specified structural change.
  - An inorganic product which likely involves the released chloride ion.

### Interface Components:
- **Drawing Tools:**
  - Options to select and draw using line structures, with wedge-and-dash bond representations for three-dimensionality.
  - Atom elements available: Carbon (C), Hydrogen (H), Nitrogen (N), and Chlorine (Cl).
- **Two Input Areas:**
  - **Organic Product:** Area for the student to draw the resulting molecular structure after nucleophilic substitution.
  - **Inorganic Product:** Area to illustrate the inorganic portion, typically the ion released during the reaction. 

Students are expected to understand the mechanics of an S<sub>N</sub>2 reaction, particularly how the nucleophile attacks the substrate and the leaving group is expelled, resulting in the inversion of configuration at the stereocenter.
Transcribed Image Text:For the given S<sub>N</sub>2 reaction, students are tasked with drawing the organic and inorganic products of the reaction. They must identify the nucleophile, substrate, and leaving group, and ensure to include wedge-and-dash bonds along with a hydrogen on the stereocenter. ### Reaction Overview: - **Reactants:** - A molecular structure with a chlorine atom (Cl) as the leaving group. - A cyanide ion (^-C≡N) as the nucleophile. - **Products:** - An organic product with a specified structural change. - An inorganic product which likely involves the released chloride ion. ### Interface Components: - **Drawing Tools:** - Options to select and draw using line structures, with wedge-and-dash bond representations for three-dimensionality. - Atom elements available: Carbon (C), Hydrogen (H), Nitrogen (N), and Chlorine (Cl). - **Two Input Areas:** - **Organic Product:** Area for the student to draw the resulting molecular structure after nucleophilic substitution. - **Inorganic Product:** Area to illustrate the inorganic portion, typically the ion released during the reaction. Students are expected to understand the mechanics of an S<sub>N</sub>2 reaction, particularly how the nucleophile attacks the substrate and the leaving group is expelled, resulting in the inversion of configuration at the stereocenter.
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