Draw an alkyl halide that would undergo an SN2 reaction to yield this product under the conditions shown below. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts. Drawing NaSCH THE D
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- Draw an alkyl halide that would undergo an SN2 reaction to yield this product under the conditions shown below. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts. S Drawing NaSCH THEiii) 2-Bromo-2-cyclopropylpropane will undergo an SN1 reaction called solvolysis in methanol to give several products, two of which are shown below. Use curly arrows to show how the formation of these two products occurs mechanistically.Draw an alkyl halide that would undergo an SN2 reaction to yield this product under the conditions shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. NaCN acetonitrile CN
- Do hydration reactions like this one have Markovnikov and anti-Markovnikov products? I know that for addition of halides on alkene double bonds, there are Markovnikov products becasue of 1,2-halide/methyl shifts, but there usually aren't shifts in hydration reactions. Essentially, would the Markovnikov/major product for this reaction have a hydroxy group attached to the tertiary carbocation and the anti-Markovnikov/minor product for this reaction have a hydroxy group attached to the adjacent secondary carbocation?3. Substitution and Elimination. Consider the 2° alkyl halide shown below. Draw all major product(s) if it were to be treated with the following reagents. Be sure to consider stereochemistry and include structures of stereoisomers if present. H₂O Na OCH3. Acetonitrile CH3 ~Ire H3C- CH3 -OK* H3CS Na Acetonitrile BrDraw the major and minor neutral organic products that would form when the alkene below undergoes acid-catalyzed hydration. ignore the stereochemistry, so your two products should be regioisomers.
- Complete the reaction scheme below. Show all reagents and intermediates. No reaction is a possible answer. Do not neglect stereochemistry. NaCN DIBAL Br в A "OCH3 (sodium cyanide)Provide the E2 mechanism for β-elimination reactionemploying 2-chloro-2-methylbutane to prepare 2-methyl-2-butene and 2-methyl-1-butene reaction. Use the actual structures of thereactants and products. Explain which of the alkenes is the major product ofthis reaction ?Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the product of this elementary step in an E1cb mechanism. Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore methanol and inorganic byproducts. : OH CH3C H H Na :O: NaOCH3 heat O
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the product of an SN2 reaction shown below. Include all lone pairs and charges as appropriate. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. N=C: H3C H Br: THF Select to Draw QDraw the product of an SN2 reaction shown below. Include all lone pairs. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. : NEC: H3C Br:Draw the major products of the SN1 reaction shown below. Use a dash or wedge bond to indicate stereochemistry of substituents on asymmetric centers, where applicable. Ignore any inorganic byproducts. H OH HCI ✓