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Specify the reagent you would use in each step of the following synthesis: CH₂ a. LiAlH4 b. H₂SO4 c. HCI d. HBr e. SOCI₂ CH3 step 1 step 2 Reagents Available f. PBr3 k. CH₂CH₂MgBr g. Dess-Martin periodinane (DMP) I. C6H5MgBr h. NaH i. NaOH j. CH3MgBr CH3 (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO3 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2

Specify the reagent you would use in each step of the following synthesis: CH₂ a. LiAlH4 b. H₂SO4 c. HCI d. HBr e. SOCI₂ CH3 step 1 step 2 Reagents Available f. PBr3 k. CH₂CH₂MgBr g. Dess-Martin periodinane (DMP) I. C6H5MgBr h. NaH i. NaOH j. CH3MgBr CH3 (phenylmagnesium bromide) m. (CH3)2CHMgBr n. CrO3 Write the letters of the reagents in the boxes below. Reagent for step 1 Reagent for step 2

Chemistry
Chemistry
10th Edition
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
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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**Specify the reagent you would use in each step of the following synthesis:** **Chemical Transformation Diagram:** - An aromatic ketone (acetophenone) is transformed into an alkene. - **Step 1**: The ketone group is reduced. - **Step 2**: The resulting alcohol undergoes elimination to form the alkene. **Reagents Available:** - a. LiAlH₄ - b. H₂SO₄ - c. HCl - d. HBr - e. SOCl₂ - f. PBr₃ - g. Dess-Martin periodinane (DMP) - h. NaH - i. NaOH - j. CH₃MgBr - k. CH₃CH₂MgBr - l. C₆H₅MgBr (phenylmagnesium bromide) - m. (CH₃)₂CHMgBr - n. CrO₃ **Instructions:** Write the letters of the reagents in the boxes below. - **Reagent for step 1**: [ ] - **Reagent for step 2**: [ ]
Transcribed Image Text:**Specify the reagent you would use in each step of the following synthesis:** **Chemical Transformation Diagram:** - An aromatic ketone (acetophenone) is transformed into an alkene. - **Step 1**: The ketone group is reduced. - **Step 2**: The resulting alcohol undergoes elimination to form the alkene. **Reagents Available:** - a. LiAlH₄ - b. H₂SO₄ - c. HCl - d. HBr - e. SOCl₂ - f. PBr₃ - g. Dess-Martin periodinane (DMP) - h. NaH - i. NaOH - j. CH₃MgBr - k. CH₃CH₂MgBr - l. C₆H₅MgBr (phenylmagnesium bromide) - m. (CH₃)₂CHMgBr - n. CrO₃ **Instructions:** Write the letters of the reagents in the boxes below. - **Reagent for step 1**: [ ] - **Reagent for step 2**: [ ]
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