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Analyze the two (2) SN2 reactions by responding to the questions. Rxn →>> Question Draw a Lewis structure for the nucleophile used in this rxn which takes into account the spectator ion. Draw a rocopango NaNCS H3C H3C SCN ¡Ⓒ NaNCO H3C H3C NCO + 0

Analyze the two (2) SN2 reactions by responding to the questions. Rxn →>> Question Draw a Lewis structure for the nucleophile used in this rxn which takes into account the spectator ion. Draw a rocopango NaNCS H3C H3C SCN ¡Ⓒ NaNCO H3C H3C NCO + 0

Chemistry
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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Analyze the Sn2 reactions by filling out the chart and answering the questions 

**Educational Website Transcript:** **Analyzing Two S<sub>N</sub>2 Reactions** The table below provides a detailed analysis of two S<sub>N</sub>2 reactions through a series of questions. Each question corresponds to specific concepts in organic chemistry, focusing on nucleophile behavior, Lewis structures, resonance structures, and reaction mechanisms. | Rxn → | NaNCS | H<sub>3</sub>C | I → | H<sub>3</sub>C | SCN + | ⦵ | NaNCO | H<sub>3</sub>C | I → | H<sub>3</sub>C | NCO + | ⦵ | |----------------------------------|----------------|-------------------------|-------------------|-------------------------|------------|-------------------------------|-----------------|------------------------|------------|-------------------------|------------|----------------------------| | **Question ↓** | | | | | | | | | | | | | | **Draw a Lewis structure for the nucleophile used in this rxn which takes into account the spectator ion.** | | | | | | | | | | | | | **Draw a resonance structure that shows an additional site of nucleophilicity in the nucleophile.** | | | | | | | | | | | | | **Draw an S<sub>N</sub>2 mechanism for the given rxn.** | | | | | | | | | | | | | **Why did the nucleophile attack from the site it did?** | | | | | | | | | | | | | **Which rxn do you think is faster/slower than the other?** | | | | | | | | | | | | | **Why do you think each rxn is faster/slower than the other?** | | | | | | | | | | | | **Description of Reactions:** - **Reactants and Products:** - The first reaction involves NaNCS with CH<sub>3</sub>I, resulting in CH<sub>3</sub>SCN and a by-product. - The second reaction involves NaNCO with CH<sub>3</sub>I, resulting in CH<sub>3</sub>NCO and a by-product. **Graph and Diagram
Transcribed Image Text:**Educational Website Transcript:** **Analyzing Two S<sub>N</sub>2 Reactions** The table below provides a detailed analysis of two S<sub>N</sub>2 reactions through a series of questions. Each question corresponds to specific concepts in organic chemistry, focusing on nucleophile behavior, Lewis structures, resonance structures, and reaction mechanisms. | Rxn → | NaNCS | H<sub>3</sub>C | I → | H<sub>3</sub>C | SCN + | ⦵ | NaNCO | H<sub>3</sub>C | I → | H<sub>3</sub>C | NCO + | ⦵ | |----------------------------------|----------------|-------------------------|-------------------|-------------------------|------------|-------------------------------|-----------------|------------------------|------------|-------------------------|------------|----------------------------| | **Question ↓** | | | | | | | | | | | | | | **Draw a Lewis structure for the nucleophile used in this rxn which takes into account the spectator ion.** | | | | | | | | | | | | | **Draw a resonance structure that shows an additional site of nucleophilicity in the nucleophile.** | | | | | | | | | | | | | **Draw an S<sub>N</sub>2 mechanism for the given rxn.** | | | | | | | | | | | | | **Why did the nucleophile attack from the site it did?** | | | | | | | | | | | | | **Which rxn do you think is faster/slower than the other?** | | | | | | | | | | | | | **Why do you think each rxn is faster/slower than the other?** | | | | | | | | | | | | **Description of Reactions:** - **Reactants and Products:** - The first reaction involves NaNCS with CH<sub>3</sub>I, resulting in CH<sub>3</sub>SCN and a by-product. - The second reaction involves NaNCO with CH<sub>3</sub>I, resulting in CH<sub>3</sub>NCO and a by-product. **Graph and Diagram
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