15. Predict the product. Be sure to show stereochemistry Os04 H202 mCPBA H2SO4 (aq) mCPBA 16....
please help 15. Predict the product. Be sure to show stereochemistry OsO4 H2O2 mCPBA H2SO4 (aq) mCPBA 16. Draw out the complete mechanism for the chlorination of What is the name of the intermediate? 17. Draw the product(s) from ozonolysis of > I T Op> (CH3), 18. Draw the product KMnO4 KMnO4 dilute -OH
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 ? ????
the following reactions, predict the product. Be sure to show stereochemistry where nncessary /6 points each) 4) For sOC, TEA I. HNO, H SO, 2. Br,, FeBr 3. H2SO4, SO 2 eq. NH, d. LiAIH
3. Predict the major product(s) for the following reactions. Show the stereochemistry of the product(s) when applicable. (a) (e) Br2, H20 H2 PL (1) Os04 (2) NaHSO4, H20 (1) 03 (2) DMS (1) CH2CO3H (2) H30*
Predict the (major) product(s), clearly indicating stereochemistry mCPBA Me Me Xs H2, Pd/C CH3 H3C H2, Pd/C Me Draw the lowest energy chair conformer
5. Draw an arrow-pushing mechanism for the following reaction, and predict the stereochemistry of the product(s). If more than one stereoisomer is formed, state which stereoisomers will be formed in equal quantities and which will be formed in unequal quantities. cat. H2SO4 HO Draw an arrow-pushing mechanism for the following reaction, and predict the stereochemistry of the product(s). If more than one stereoisomer is formed, state which stereoisomers will be formed in equal quantities and which will be formed in...
For the reactions below, provide the missing product, reactant or reagent(s). Show the stereochemistry where appropriate. OH ''OH racemic Os04 H202 ao COZH Zn, H30+ + CO2
2P (a) Draw/predict the major elimination product(s) of the following proposed reaction. Be sure to indicate correct stereochemistry when appropriate in the product. (b) Provide a mechanism that describes the formation of your drawn product. Show how (Newman Projection) any stereochemistry within the mechanism/product results. CHз Br NAOCH3 "CH-CHз
5. Predict the major product(s) for each of the following reactions. Show stereochemistry where appropriate. H2 Pc 0.0, NMO Acetone 0 CHI, (ii) ~ ZnCu) mCPBA
4. (15) Predict the major organic product, including any appropriate stereochemistry, for each of these reactions: NaSH H 2 Pi > 1) BH 3 2) NaOH, H202 n g hanisms to explain these transformations: