Draw the starting structure that would lead to this major product (and its enantiomer) under these conditions. Draw the product of this reaction. Ignore inorganic byproducts. Br2 Cl2 Br
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- Ketones react with alcohols to yield products called acetals. Why does the all-cis isomer of 4-tert-butyl-1,3-cyclohexanediol react readily with acetone and an acid catalyst to form an acetal, but other stereoisomers do not react? In formulating your answer, draw the more stable chair conformations of all four stereoisomers and the product acetal for each one.When carbonyl compounds are reduced with a reagent such as LiAlH4 or NaBH4 and a new stereogenic center is formed, what will the composition of the product mixture be? Forms more of one enantiomer than another because of steric reasons around the carbonyl Forms more of one enantiomer than another depending on the temperature of the reaction Forms different products depending on the solvent used Forms a racemic mixture of the two possible enantiomersa.Draw three-dimensional representations for all stereoisomers of 2chloro-3-methylpentane, and label pairs of enantiomers. b. Considering dehydrohalogenation across only C2 and C3, draw the E2 product that results from each of these alkyl halides. How many different products have you drawn? c. How are these products related to each other?
- 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 byproductsConsider 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.Draw two major products of this reaction. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts.
- Please assign priority groups and assign R or S stereochemistry for eachFill in the missing starting material, reaction conditions, or products for each reaction shown below. Take care to indicate if two sets of reagents have been added sequentially (using 1. ___ and 2.___ above the arrow), and also to show all MAJOR products and indicate stereochemistry. In cases where a pair of enantiomers are produced or stereochemistry is not controlled you can write “+ enantiomer” or use squiggly lines, as appropriate.(a) Show how you would synthesize the pure (R) enantiomer of 2-butyl methyl sulfide, starting with pure (R)-butan-2-oland any reagents you need.(b) Show how you would synthesize the pure (S) enantiomer of the product, still starting with (R)-butan-2-ol and anyreagents you need.
- a. Draw three-dimensional representations for all stereoisomers of 2-chloro-3- methylpentane, and label pairs of enantiomers.b. Considering dehydrohalogenation across C2 and C3 only, draw the E2 product that results from each of these alkyl halides. How many different products have you drawn?c. How are these products related to each other?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.what are the products? please indicate the relative stereochemistry for the following transformations and indicate the major product.