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 THE
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- 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?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 CNProvide 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 ODraw 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.Draw 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 product of an SN2 reaction shown below. Include all lone pairs. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts. H3C-0: H CH3 CI:iii) 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.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? Recall from Section 3.2A that C6H5 −is a phenyl group, a benzene ring bonded to another group.
- 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 QThe Wolff–Kishner reaction uses hydrazine (H2NNH2) and hydroxide (–OH) to reduce a carbonyl to the alkane. The first steps of the mechanism convert a carbonyl to a hydrazone in a manner similar to imine formation. Draw the mechanism arrows for the reaction from the hydrazone to the alkane. Be sure to add lone pairs of electrons and nonzero formal charges to all species.1) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors (structures), the regiochemistry that results in each case. OMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3