Specify the reagent you would use in each step of the following synthesis: a. LIAIH4 b. H₂SO4 c. HCI d. HBr e. SOCI₂ step 1 step 2 Reagents Available f. PBr3 k. CH3CH₂MgBr g. Dess-Martin periodinane (DMP) 1. C6H5MgBr h. NaH i. NaOH j. CH3MgBr (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: a. LIAIH4 b. H₂SO4 c. HCI d. HBr e. SOCI₂ step 1 step 2 Reagents Available f. PBr3 k. CH3CH₂MgBr g. Dess-Martin periodinane (DMP) 1. C6H5MgBr h. NaH i. NaOH j. CH3MgBr (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

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section19.8: Conjugate Addition To A,b-unsaturated Carbonyl Compounds

Problem 19.13P

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