dict the organic products of the following reaction. Show stereochemistry clearly. The (R) or (S) designation Tor each stereocenter carbon atom is specified adjacent to the answer box, please draw the products accordingly (1S,2R) 1) OsO4, pyridine 2) Na2SO3 or NaHSO3 in H20 Н (1R,2S)
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- The molecules below react in a displacement reaction. Determine the products) and assign configuration (R/S) to any stereogenic centers in the product. The Cahn-Ingold - Prelog rules can be used to assign priority to the four different groups on a stereogenic center.Draw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic no stick structure don't understand 3,4-dimethylhex-3-ene with BH3. After reaction is complete, add H2O2, –OH, and H2OPlease explain it. For each stereoisomer, draw the interconversion of chairs and identify the most stable. Give handwritten answer. ASAP
- Complete the following reactions with the majority products and the missing reaction conditions. Indicate stereochemistry if applicable. Also indicate the type of reaction that took place (SN1, SN2, E1, E2, E1bc)Show the structures for the major/significant organic product(s) expected for the following eleven reactions or sequences of reactions. If there is a major and minor productcircle the major product. Show all relevant stereochemistry.For the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product(s) resulting from elimination involving C2–C3 (i.e., the carbon atoms depicted with stereobonds). Show the product stereochemistry clearly. If there is more than one organic product, both products may be drawn in the same box. Ignore elimination involving C2 or C3 and any carbon atom other than C3 or C2.
- what are products of the following reactions. include close attention to regio and stereochemistryProvide the mechansim using curved arrows of the reaction of p-t-butyl phenol treated with acetic anhydride in AlCl3. Include resonance stabilized intermediates and if more than one product is formed, label them as major, minor, etc. thank you for the help1-methylcyclohexene is reacted with the following reactants. Write products. Write which stereochemistry is valid (syn/anti, racemization, antimarkovnikof, etc). 1- Br2/ H2O 2- CH2N2/heat
- In some nucleophilic substitutions under SN1 conditions, complete racemization does not occur and a small excess of one enantiomer is present. For example, treatment of optically pure 1-bromo-1-phenylpropane with water forms 1-phenylpropan-1-ol. (a) Calculate how much of each enantiomer is present using the given optical rotation data. (b) Which product predominates—the product of inversion or the product of retention of configuration? (c) Suggest an explanation for this phenomenon.The synthesis above can be performed with some combination of the reagents listed below. Give the necessary reagents in the correct order. Be sure to consider stereochemistry and regiochemistry.A. NaOHB. mCPBAC. OsO4, tBuOOHD. NaHE. H2, LindlarF. CH3CH2CH2BrG. CH3CH2ClH. NaNH2I. H3O+J. Na, NH3(l)Provide the complete mechanism using Curved Arrow Formalism for the reaction of 1-chloro-1-methylcyclopentane treated with NaOMe in MeOH. If more than one product is formed, which is the major, minor, and very minor product? Is the reaction SN1, SN2, E1, or E2. I appreciate the help on this question.