3. Provide the missing reagents for the following reactions CH3 a. b. с. d. HC HC CH3 H.C. CH3 CH3 ? ? CH3 ? CH3 Br поче H₂C он CH3 на Br H3C ? H3C. CH3 H3C CH3 + HC CH3 CH3 Br OH
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Solved in 2 steps with 2 images
- Which compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaFSupply the missing reagent in the following reaction: (see attachment) A. Lindlar, H2, mCPBA B. O3 or KMnO4 C. fused KOH D. NH3 E. NaNH2Which of the following reagent best accomplish this transformation below? a. BH3, THF, H2O2 b. NaNH2, NH3 c. H2SO4, H2O, HgSO4 d. H2, Lindlar
- What major product is expected from the reaction shown in Image 18?Please label all the steps and reagents with their corresponding letter. Thanks!Which of the following will give just 1 product when reacted with a Grignard reagent (R-MgBr)? asymmetric ketone ?,? -unsaturated ketone generic aldehyde symmetric ketone
- For butenafine, develop a synthesis that starts with napthalene and benzene. (aromatic methyl groups can be converted to alkyl bromides using Br2/light, and aldehydes by heating the alkyl bromide in DMSO, eg. ArCH3 to ArCH2Br then to ArCHO).Why is this considered an Elimination E2 reaction? C₃H₈O (l) → C3H6 (g) + H2O (l) propan-1-ol → propene + waterDetermine reagents C and D from the reaction scheme below.