NaN3 DMSO N= N. その Qu

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Draw an alkyl halide that would undergo SN2 reaction to yield this product under the conditions shown below.
**Azide Reaction Explanation**

This image is a depiction of a chemical reaction where a sodium azide (NaN₃) is introduced in the presence of dimethyl sulfoxide (DMSO). This is a common reaction in organic chemistry involving the formation of an azido group.

**Reaction Details:**
- **Reagents:** 
  - Sodium azide (NaN₃)
  - Dimethyl sulfoxide (DMSO)
  
- **Product Formation:**
  - The linear hydrocarbon chain shown is transformed by the addition of the azide functional group, represented as -N⁺=N⁻=N.

**Structure Breakdown:**
- The structure shows a straight hydrocarbon chain with the azido group at the end. The azido group consists of a nitrogen chain with positive and negative charges, indicating resonance and stability in the azide ion.

This reaction is often used as a precursor step in the synthesis of more complex organic compounds, utilizing the azide group for further transformations such as in click chemistry.
Transcribed Image Text:**Azide Reaction Explanation** This image is a depiction of a chemical reaction where a sodium azide (NaN₃) is introduced in the presence of dimethyl sulfoxide (DMSO). This is a common reaction in organic chemistry involving the formation of an azido group. **Reaction Details:** - **Reagents:** - Sodium azide (NaN₃) - Dimethyl sulfoxide (DMSO) - **Product Formation:** - The linear hydrocarbon chain shown is transformed by the addition of the azide functional group, represented as -N⁺=N⁻=N. **Structure Breakdown:** - The structure shows a straight hydrocarbon chain with the azido group at the end. The azido group consists of a nitrogen chain with positive and negative charges, indicating resonance and stability in the azide ion. This reaction is often used as a precursor step in the synthesis of more complex organic compounds, utilizing the azide group for further transformations such as in click chemistry.
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