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Q: Draw the products of each reaction, indicating the stereochemistry around any stereogenic centers.
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Q: Draw the products of each reaction. Include all stereoisomers formed.
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Q: Draw the products of attached reaction and indicate stereochemistry around stereogenic centers.
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- What epoxide is formed when each alkene is treated with mCPBA?Draw the products formed when (CH3)2C=CH2 is treated with each reagent.a. HBrb. H2OH2SO4c. CH3CH2OH, H2SO4d. Cl2e. Br2, H2Of. NBS (aqueous DMSO)g. [1]BH3;[2]H2O2, HO-Draw the products formed when attached alkene is treated with BH3 followed by H2O2, HO−. Include the stereochemistry at all stereogenic centers
- (a) What product(s) are formed when the E isomer of C6H5CH = CHC6H5 is treated with Br2, followed by one equivalent of KOH? Label the resulting alkene(s) as E or Z. (b) What product(s) are formed when the Z isomer of C6H5CH = CHC6H5 is subjected to the same reaction sequence? (c) How are the compounds in parts (a) and (b) related to each other?What product is formed when D-Gulose is treated with a. CH3I, Ag2O b. The product in (a), then H3O+ c. The product in (b), then C6H5CH2Cl, Ag2OWhat is the major stereoisomer formed when attached alkyl halide is treated with KOC(CH3)3?
- Draw the products of each SN1 reaction and indicate the stereochemistry of any stereogenic centers.Draw the products formed when A or B is treated with each reagent. In some cases, no reaction occurs. [1] C6H5Li (excess); [2] H2ODraw the products formed when hex-1-yne is treated with each reagent. a. HCl (2 equiv) b. HBr (2 equiv) c. Cl2 (2 equiv) d.H2O + H2SO4 + HgSO4 e. [1] R2BH; [2] H2O2, HO− f. NaH g. [1] −NH2; [2] CH3CH2Br