Identify the reagents necessary to achieve the transformation below. You will need to use at least one reaction from this chapter a at least one reaction from the previous chapter. The essence of this problem is to choose reagents that will achieve the desired stereochemical outcome: Br The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagent(s) in the correct order, as a string of letters (without spaces or punctuation, such as “EBF"). If there is more than one corre solution, provide just one answer. A xs HBr xs HBr, ROOR 1) xs NaNH2; 2) H20 D E F Br2 H2, Lindlar's cat. Na, NH3 (1)

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**Title: Identifying Reagents for Stereochemical Transformations**

**Objective:**
Identify the reagents necessary to achieve the transformation depicted below. Incorporate at least one reaction from this chapter and one from the previous chapter, selecting reagents that will result in the desired stereochemical outcome.

**Chemical Transformation:**
- **Reactant:** Alkyne
- **Product:** Alkane with vicinal dibromide

**Instructions:**
The transformation can be achieved using the reagents listed. Select the necessary reagent(s) in the correct order, represented by their corresponding letters, without spaces or punctuation (e.g., “EBF”). Provide just one solution, even if multiple correct answers exist.

**Reagents:**
- **A:** Excess HBr
- **B:** Excess HBr, ROOR
- **C:** 1) Excess NaNH₂; 2) H₂O
- **D:** Br₂
- **E:** H₂, Lindlar’s catalyst
- **F:** Na, NH₃ (l)

**Approach:**
Review the chemical equation and structure to determine the appropriate reagents that will lead to the formation of a vicinal dibromide with the specified alkyne as the starting material. Consider each reagent's role in modifying the molecular structure, paying special attention to the stereochemistry of the final product.

**Conclusion:**
Select the correct sequence of reagents to achieve the desired transformation while ensuring the stereochemistry aligns with the target structure.
Transcribed Image Text:**Title: Identifying Reagents for Stereochemical Transformations** **Objective:** Identify the reagents necessary to achieve the transformation depicted below. Incorporate at least one reaction from this chapter and one from the previous chapter, selecting reagents that will result in the desired stereochemical outcome. **Chemical Transformation:** - **Reactant:** Alkyne - **Product:** Alkane with vicinal dibromide **Instructions:** The transformation can be achieved using the reagents listed. Select the necessary reagent(s) in the correct order, represented by their corresponding letters, without spaces or punctuation (e.g., “EBF”). Provide just one solution, even if multiple correct answers exist. **Reagents:** - **A:** Excess HBr - **B:** Excess HBr, ROOR - **C:** 1) Excess NaNH₂; 2) H₂O - **D:** Br₂ - **E:** H₂, Lindlar’s catalyst - **F:** Na, NH₃ (l) **Approach:** Review the chemical equation and structure to determine the appropriate reagents that will lead to the formation of a vicinal dibromide with the specified alkyne as the starting material. Consider each reagent's role in modifying the molecular structure, paying special attention to the stereochemistry of the final product. **Conclusion:** Select the correct sequence of reagents to achieve the desired transformation while ensuring the stereochemistry aligns with the target structure.
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