Specify the reagent(s) suitable for converting 2-methyl-2-butene to 2-bromo-3-methylbutane. Check all that apply. H₂ HBr Peroxides BH3 NaBr Br₂ Peroxyacetic acid None of the above × 5
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- 15 eBook Print References 3 attempts left Check my work Specify reagents suitable for converting 3-ethyl-2-pentene to 2,3-dibromo-3-ethylpentane. Select the single best answer. HBr, peroxides NaBr, acetone Br2, CC14 1. B₂H6; 2. H₂O₂, HO™ HBrHW9 #2What are the reagents and intermediate products of these compounds?Please start from benzene. Show complete solution and steps. No shortcuts
- 9B Explain why the products of the following reactions are incorrect while giving the correct ones. OH H3C H д 1. TsCl, Py 2. CH3S* Na+ CH3O- Na+ CH3OH SCH 3 H3C H OCH3 OHDraw the structure of the major organic product of the reaction below. ● + CHCI3 MILL KOH Use the wedge/hash bond tools to indicate stereochemistry where it exists. Show stereochemistry in a meso compound. If the reaction produces a racemic mixture, just draw one stereoisomer. ▼ n [F ? ChemDoodleⓇCan i get help please
- 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.HW8 #10Br Brz CH3 CH3 H3C CH2CI2 H3C Br Electrophilic addition of bromine, Br2; to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH,Cl). In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br: :Br: .CH3 H3C H3C CH3 Br: