2. Starting with 2-methyl-1-phenylpropan-1-one, show how you can convert this to 2-methyl-1- phenylpropan-1-ol. What reagent did you choose and why? Show all steps and draw the product. Is this addition to benzene an activator or deactivator? 3. Using the product from step 2. Show how using the tosyl chloride reagent from the alcohol reactions powerpoints how this can be converted to this molecule, isobutyl benzene: Is this addition to benzene an activator or deactivator?

2. Starting with 2-methyl-1-phenylpropan-1-one, show how you can convert this to 2-methyl-1- phenylpropan-1-ol. What reagent did you choose and why? Show all steps and draw the product. Is this addition to benzene an activator or deactivator? 3. Using the product from step 2. Show how using the tosyl chloride reagent from the alcohol reactions powerpoints how this can be converted to this molecule, isobutyl benzene: Is this addition to benzene an activator or deactivator?

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter9: Nucleophilic Substitution And Β-elimination

Section: Chapter Questions

Problem 9.54P

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2. Starting with 2-methyl-1-phenylpropan-1-one, show how you can convert this to 2-methyl-1- phenylpropan-1-ol. What reagent did you choose and why? Show all steps and draw the product. Is this addition to benzene an activator or deactivator? 3. Using the product from step 2. Show how using the tosyl chloride reagent from the alcohol reactions powerpoints how this can be converted to this molecule, isobutyl benzene: Is this addition to benzene an activator or deactivator?
Please provide a clear drawing and any explainatin you feel is needed. Also any tips you may have. I am having trouble with this topic. Thank you for help!
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