Draw product C given the following reagents/conditions. Show stereochemistry when necessary. C 1. B = Br2, CH2CI2 2. B = KMNO4, H3O* 3. B = (1) 03 (2) Zn / H3O* 4. B = H2, Pd/C
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- write the correct product for each and indicate stereochemistry if necessary.a.What product(s) (excluding stereoisomers) are formed when Y is heated with Cl2? b.What product(s) (excluding stereoisomers) are formed when Y is heated with Br2? c.What steps are needed to convert Y to the alkene Z?Please identify priorities of functional groups and name following molecules based on thier stereochemistry as R or S
- What organic product is formed when 1‑methylcyclopentene is treated with NMMO in the presence of H2O and a catalytic amound of OsO4? Clearly show stereochemistry by drawing a wedge and dashed bond for each chiral carbon. Only draw one stereoisomer if more than one can be formed.Draw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3I; (b) TsCl and pyridine, followed by NaOCH3; (c) PBr3, followed by NaOCH3. Which two routes produce identical products?Spiderweb chemistry . Reagents needed to get the major product and show stereochemistry.
- Consider a reaction where cis-but-2-ene is treated with OsO4 followed by NaHSO3/H2O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.Predict mechanistically what stereoisomers of 3-chloro-5-methylcyclohexene should form when (image below) is treated with Lucas reagent (ZnCl2/H30+Cl-).Provide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the help