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- Given the following reaction sequence, determine the structures of A and B, including proper stereochemistry. Br NaOH A DMSO 1. CH3(CH)3Li В 1. NaH 2. CI- Br 2.Draw the products of the following reactions, indicating both regiochemistry and stereochemistry when appropriate. H3C. KMnO4 H3O*4) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors, the regiochemistry that results in each case. ỌMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3
- Give the major product of the following reaction. مشن Ph-CEC-H 1) NaNH, 2) CH3CH2CH2CI, ? O There is no reaction under these conditions or the correct product is not listed here.Aa.47. Please write final answer in bond line form and circle it.Each of these reaction produces ONE MAJOR PRODUCT. In each case, draw this product in the boxprovided, including appropriate stereochemistry when applicable. For multi-step reactions, just give theFINAL product, no intermediates.
- Show the detailed mechanism of this in 3D structure, and predict the major regioisomer and the major stereoisomer with a stepwise explanation. show the final major product in Newman projection.Your task is to convert 2-bromobutane to 1-butene in highest yield. Which reagents would you use? O KOH/H2O O KOH/CH,OH O CH3CH2ONA/CH3CH2OH O CH3ONA/CH3OH O (CH3)3COK/(CH3)3COH3. Propose a mechanism and predict the product. Include any relevant stereochemistry. a) HCI b) CH,N2 CH,N2 = H2C-NEN HO,
- Predict the major product in the following reaction. Be sure to draw it with well-defined stereochemistry as necessary. cat. OsO4, NMO1) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors (structures), the regiochemistry that results in each case. OMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3Consider the nucleophilic substitution reaction shown here. Based on the stereochemistry, does it proceed by an Sy1 or Sy2 mechanism? Explain. OH KOCH3 Enantiomer CH;OH `OCH3