Complete the following reaction scheme. HO pyridine ·K=.=. F + Cl- S O C F F A LiBr acetone B

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Complete the following reaction scheme.

Draw the structure for compound A. Be sure to show stereochemistry and do not include any byproducts.

Draw the structure for compound B. Be sure to show stereochemistry and do not include any byproducts.

**Title: Reaction Scheme Completion**

**Objective:**
Complete the following reaction scheme.

**Reaction Scheme:**

- **Reactants:**
  - The first reactant is an alcohol, specifically a bicyclic compound with a hydroxyl (OH) group.
  - The second reactant is a sulfur-based compound: Chlorosulfonyl isocyanate with a structure of Cl-SO2-CF3.

- **Conditions:**
  - The reaction proceeds in the presence of pyridine, leading to intermediate **A**.

- **Further Reaction:**
  - Intermediate **A** reacts with lithium bromide (LiBr) in acetone to produce the final product, **B**.

**Instructions:**
- Identify the chemical transformations occurring at each stage.
- Determine the structures of intermediate **A** and final product **B** based on known reactions involving the given reactants and conditions.

**Diagram Explanation:**
- The reaction scheme features two main stages with conditions labeled.
- Structural formulas are used for the reactants and intermediate steps, depicting functional groups and connectivity. 

Use this information to analyze and predict the structural changes occurring during each reaction step.
Transcribed Image Text:**Title: Reaction Scheme Completion** **Objective:** Complete the following reaction scheme. **Reaction Scheme:** - **Reactants:** - The first reactant is an alcohol, specifically a bicyclic compound with a hydroxyl (OH) group. - The second reactant is a sulfur-based compound: Chlorosulfonyl isocyanate with a structure of Cl-SO2-CF3. - **Conditions:** - The reaction proceeds in the presence of pyridine, leading to intermediate **A**. - **Further Reaction:** - Intermediate **A** reacts with lithium bromide (LiBr) in acetone to produce the final product, **B**. **Instructions:** - Identify the chemical transformations occurring at each stage. - Determine the structures of intermediate **A** and final product **B** based on known reactions involving the given reactants and conditions. **Diagram Explanation:** - The reaction scheme features two main stages with conditions labeled. - Structural formulas are used for the reactants and intermediate steps, depicting functional groups and connectivity. Use this information to analyze and predict the structural changes occurring during each reaction step.
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