8 Raph 152 Min Quick 21 34 Mix What Is The Nucleophile In This Experiment Why Is The Reaction Considered Regioselectiv 1 (63.73 KiB) Viewed 41 times
8 Raph 152 Min Quick 21 34 Mix What Is The Nucleophile In This Experiment Why Is The Reaction Considered Regioselectiv 2 (16.69 KiB) Viewed 41 times
8 raph 152 MIN QUICK 21. 34 MIX What is the nucleophile in this experiment? Why is the reaction considered regioselective? 4. (1 Hydroboration - 2 For this assignment, the target compound that you should synthesize is trans-2-methyl-cyclohexanol. Again, this is an electrophilic alkene addition reaction. Examine the product to determine the location of the new functionality. The regioselectivity is still dictated by placement of the electrophile at the terminal position. List the reactants, solvent, reagent, and products formed: What are the components in the aqueous and organic layer? What type of carbocation is form in this reaction primary, tertiary or secondary? 5pts 10pts Styles 5. 10pts 10pts 5pts Focus no
What are the components in the aqueous and organic layer? How long did the reaction take to go to completion? 5pts 5pts 10pts
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