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- Draw the products of these reactions clearly showing stereochemistry in each case if necessary. If the product is formed as a racemic mixture, clearly draw one stereoisomer with dash/wedge bonds and write “+en”. Circle whether each reaction occurs by an SN1 or SN2 pathway.Which keto product would be isolated from the reaction shown? A B C D EWhich set of reagents are most likely to affect the E2 elimination? a. CH3CH2O-, CH3CH2OH b. (CH3)3CO-, (CH3)3COH
- Given that an E2 reaction proceeds with anti periplanar stereochemistry, draw the products of each elimination. The alkyl halides in (a) and (b) are diastereomers of each other. How are the products of these two reactions related?What alkene is required to synthesize each of the following compounds? b. What other epoxide is formed in each synthesis? c. Assign an R or S configuration to each asymmetric center.What are the major products (include stereoisomers) of the following reaction? The peroxide works as light, hν. So, read “NBS/hν.”
- Draw the elimination products obtained E2 condiitons for each of the following alkyl halides.If the following sesquiterpene is synthesized in a medium containing acetate with a 14C-labeled carbonyl carbon, which carbons will be labeled?Determining the Alkene That Forms a Set of Oxidative Cleavage Products What alkene forms the following products after reaction with O3 followed by CH3SCH3?
- What are products formed from the below reaction?Draw the stereoisomers and name them.(Hint: There are two different constitutional isomers and each constitutional isomer has 2nstereoisomers.Draw the major product (with stereochemistry) of the following reaction. Draw only one enantiomer for a racemic mixture.Predict the elimination products for the following reaction. Identify the major and minor stereoisomers and draw them in the indicated box.