Draw two major products of this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts. H2 Pt ⑤
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- Draw the products of this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.Draw the possible products of this epoxied ring opening reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, Ignore any inorganic byproducts.a. With attention to stereochemistry, indicate the product of the SN2 reaction of cis-1-bromo-2methylcyclohexane. b. Draw and identify (R) and (S) enantiomers of lactic acid, CH3CH(OH)COOH. Use the proper conventions to draw Fischer projections.
- draw one of the two enantiomers of the major product from this reaction. use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. ignore inorganic byproductsDraw the products of this halogenation reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.Can someone please explain the logic of 2 vs 3 for stereochemistry? They are both C-C so I don't understand how to rank 2 vs 3. Thank you!
- 4-Chloro-2-pentene has a double bond that can have either the E or the Z configuration and a stereogenic center that can have either the R or the S configuration. How many stereoisomers arepossible altogether? Draw the structure of each, and group the pairs of enantiomers.The substitution product of (S)-3-chloro-3-phenyl-heptane in methanol will be _______________. a racemix mix the (S)-enantiomer the (R)-enantiomer not chiralDraw the product of an SN2 reaction shown below. Use the dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.
- Consider the E2 elimination of Compound A, and answer the following questions: (a) Label each stereocenter in Compound A with the correct R or S configuration. (b) Draw the structures of the major product with correct stereochemistry. Assume D and H have the same reactivity.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.Draw the structures for (Z)-3-methylhex-3-ene and the two major organic products for its reaction with HBr. Be sure to show all stereoisomers using wedge and dash stereochemistry at any chirality center.