Draw one of the two enantiomers of the major product from this reaction. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.
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- Draw two major products of this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore 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.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.
- Predict mechanistically what stereoisomers of 3-chloro-5-methylcyclohexene should form when (image below) is treated with Lucas reagent (ZnCl2/H30+Cl-).Fill in the missing reagents or major products to complete the transformations. Be sure to pay carefulattention to stereochemistry where appropriate. If the major product is a pair of enantiomer you mayshow one of them and indicate + enantiomer. If the products are diasteromers, show them both.Draw the products of this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.
- For the given ee values, calculate the percentage of each enantiomer present.a. 90% eeb. 99% eec. 60% eeFor the given ee values, calculate the percentage of each enantiomer present. Q: 99% eeDraw 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.
- Draw 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.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 products resulting from addition of a Grignard reagent to an aldehyde. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicableIgnore any inorganic byproducts.