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- Draw the products formed when hex-1-yne is treated with each reagent. Show arrow pushing as well. [1] R2BH; [2] H2O2 , HO−When HCl is added to an alkene in a Markovnikov reaction, the product will have a higher boiling point than the alkene from which it was made. Please explain why this happens.Draw the skeletal structure for the product at the end.
- Draw the structure(s) for the major final product(s) formed in the following reaction sequence. CN ༼་་ SO 503 H₂SO4 Cl FeCl3 Click and drag to start drawing a structure.In the reaction given below, what type of reaction is used? n-Pentane → Isopentane нннн H ITH Н—С—с—С—с —О —Н Н—с—с— с-с—н ||| | H нн H Addition Elimination Substitution RearrangementWhich of the following is an anti addition? O Addition of C12 and H2O across an alkene Addition of H2 across an alkene O Dihydroxylation of an alkene using OsO4 o Formation of an epoxide from an alkene using mCPBA
- Question 7: Draw the products formed when each alkene is treated with O3 followed by Zn, H₂O. 4Draw the alkene that can form the alcohol shown via an acid-catalyzed hydration reaction that does NOT require a rearrangement. Draw the starting alkene. OH H3O*● Draw the structures for the three major alkene products that result when 1-pentene is treated with Grubbs catalyst.