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with mechanism please! H Ph NaOH HO mCPBA Oz. DMS Br 09 Br Show transcribed image...
H (€10,BCH,Ph (Eto)PCH,Ph cat. Bu,N+ Br* 50% NaOH hexanes ?
1. The 1,4-endoperoxide is treated with Dimethyl Sulfide (DMS). Please show the mechanism and arrow-pushing of how the product (epoxide) was created as a result of the DMS. Thank you! CH3 С. С НО — О О HO С НЫС S— СН3 О M О О H
For each reagent, predict the major product(s). 1) MCPBA n 1) Os04 H OH HO H A. 2) H30* D. 2) NaHSO3/H2O 3. TOM B. Os04 (catalytic), NMO E. KMnO4, NaOH, cold H OH HO H HO HoT F. OsO4 (catalytic) c.) J OH 2) H30+ ????, NaOH <mo ? ????
Draw a reasonable mechanism for this reaction: H-CI NH HO H-: но NH3
-Br mglether º H₂O+ H₂Criou a) b) Hoc) H •OH DRA HO.
Draw the arrow pushing mechanism for the following reaction in bond line H-Br
identify the mechanism this reaction is going though and write mechanism. H D Br NaOH CH COCH
(10 pts) Predict the major product for each of the following reactions. 2. Ho Br 1. NaOH/Br 2. H,O NaOH/H20 1. NaOCH,CH 2. H,0 1. NaOCH,CH, 2 HO (10 pts) Predict the major product for each of the following reactions. 2. Ho Br 1. NaOH/Br 2. H,O NaOH/H20 1. NaOCH,CH 2. H,0 1. NaOCH,CH, 2 HO
with mechanism please! H H / H20 ОН B.
Draw the product(s) Br NaOH