Identify reagents that can be used to achieve the following transformation: 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 correct solution, provide just one answer. A В C H20, H2SO4, HgSO4 Br2 HC=CNa E F 1) O3 H2, Lindlar's catalyst 1) R2BH 2) H2О2. NaOH 2) DMS H 1) xs NaNH2 t-BUOK H2, Pd 2) H20

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**Task:** Identify reagents that can be used to achieve the following transformation:

**Chemical Transformation:**
- Starting material: An alkyne
- Target product: An aldehyde

**Instructions:**
The transformation can be performed with some reagent or combination of the reagents listed below. Provide 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 correct solution, provide just one answer.

**Reagents Options:**

- **A:** H₂O, H₂SO₄, HgSO₄
- **B:** Br₂
- **C:** HC≡CNa
- **D:** 
  1) O₃ 
  2) DMS
- **E:** H₂, Lindlar's catalyst
- **F:** 
  1) R₂BH 
  2) H₂O₂, NaOH
- **G:** 
  1) xs NaNH₂ 
  2) H₂O
- **H:** t-BuOK
- **I:** H₂, Pd

**Diagram Explanation:**
There are no graphs or diagrams presented apart from the chemical structures represented for transformation. The initial molecule is an alkyne, and the product is an aldehyde, suggesting the need for hydroboration-oxidation or similar reactions.
Transcribed Image Text:**Task:** Identify reagents that can be used to achieve the following transformation: **Chemical Transformation:** - Starting material: An alkyne - Target product: An aldehyde **Instructions:** The transformation can be performed with some reagent or combination of the reagents listed below. Provide 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 correct solution, provide just one answer. **Reagents Options:** - **A:** H₂O, H₂SO₄, HgSO₄ - **B:** Br₂ - **C:** HC≡CNa - **D:** 1) O₃ 2) DMS - **E:** H₂, Lindlar's catalyst - **F:** 1) R₂BH 2) H₂O₂, NaOH - **G:** 1) xs NaNH₂ 2) H₂O - **H:** t-BuOK - **I:** H₂, Pd **Diagram Explanation:** There are no graphs or diagrams presented apart from the chemical structures represented for transformation. The initial molecule is an alkyne, and the product is an aldehyde, suggesting the need for hydroboration-oxidation or similar reactions.
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