-Provide the major product of the reaction sequence. If cis/trans isomers are possible, draw only the major isomer. If enantiomers are possible, do not specify configuration. 1) Br₂, heat 2) 2 equiv. NaCN DMF Select Draw Templates More Erase S Q2Q
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- Provide the major product of the reaction sequence. If cis/trans isomers are possible, draw only the major isomer. If enantiomers are possible, do not specify configuration.Provide the major product of the reaction sequence. If cis/trans isomers are possible, draw only the major isomer. If enantiomers are possible, do not specify configuration. Please please help me..$;$;).$?&(&
- Identify the MAJOR product that would be obtained at the end of the following reaction sequence. (ie. the final product not the "isolated intermediate"), Hint- write out the product of each of the three steps and be aware of the stereochemistry in step 2 and 3. NaNH, jsolated intermediate 1) Na, NH, then 2) Clz CI, H + enantiomer CI + enantiomer CI + enantiomer Ci. H + enantiomer CI:$;$;);$:$:$:: draw out neatlyS) Draw the expected major product (except when I explicitly ask for a minor product) in each box NaOCI CH;CO,H : CH,CN : H20 1) `MgBr OH 2) H20 C10H180 C12H240 C12H240 major stereoisomer minor stereoisomer base C13H9F203 "Fiflunisal" NSAID Drug produced by Merck in 1971 NC. CN heat C10H12N2 enant #1 C1OH12N2 enant #2 show "relative stereochemistry" of the methyl groups in the product for full credit. Two enantiomers are produced, draw one in one box, the other in the other box.
- 1. determine the type of pericyclic reaction (sigmatropic, electrocyclic, cycloaddition) 2. draw the mechanism for the reaction using curved arrows, and then use molecular orbital theory to evaluate the appropriate HOMO-LUMO interactions 3. determine the stereochemistry of the product, if necessary CHOOSE TWO OUT OF THE THREE PROBLEMS TO COMPLETE heat A RO, LOR КН, THF RO, в -OH ROH ...OR' 2. МеОн, Н,о OR' heatDraw 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 byproducts. Br₂ CH3OH Drawing Atoms, Bonds and Rings Br Br Br SH Br Charges Br OH 51!!! Br OH Ō Undo Drag To Pan BU Reset Remove Done Ij. 1,2-epoxybutane + acid in methanol Reaction Type(s) Mechanism(s) Product(s). Stereochemistry (if applicable) k. (R)-3-methylbutan-2-ol + TsCl + pyridine in DMSO Reaction Type(s) Mechanism(s) Product(s)_ Stereochemistry (if applicable)