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

Chapter10: Alcohols

Section: Chapter Questions

Problem 10.50P

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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?
Show reaekson and don't use hend raiting and step by step solutions
10. Use retrosynthesis to propose a method of producing 2-chloro-2,3-dimethylhexan-3-ol from 3,3-dimethylhexan-1-ol. Include all needed reagents at each step. This is not a one step synthesis.
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!
1. Show the steps necessary to make this compound using a Wittig reaction. Start with triphenylphosphine and an alkyl halide. After that you may use any other organic or inorganic reagents. H₂C H₂C CH₂ CH3
1. Williamson Ether Synthesis Questions for lab , Synthesize phenacetin from acetaminophen (Tylenol) via a Williamson ether synthesis. a.Find the missing reagent:CH3CH2OH +? → C2H5OC2H5 H2SO4, H2O HNO3, H2CO3 b.What is the nucleophile in this reaction? H2O Nu- RO- ROH c.If you wanted to prepare Guaifenesin (present in OTC cough meds), choose the alcohol you would start with? 2 methoxy benzoinc acid 2-methoxy benzaldehyde 2-methoxyphenol 2 methoxy anisole d.What was the mechanism of the reaction you used to prepare the ether? SN1 SN2 E1 E2 e.The reaction given below is known as by which o the following reaction? C2H5ONa+IC2H5→C2H5OC2H5+NaI Oxidation reaction Williamson reduction reaction Williamson ether synthesis Wittig synthesis f.Chloroethane reacts with X to form diethyl ether. What is X?…
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1. Design a synthetic route to demonstrate how you can convert 1-propanol into 2- hexyne. You must use 1-propanol as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way. НО.
1. Design two syntheses of the compound below using the Grignard reagent and a carbonyl compound. Show all reagents and intermediates. Of the two, which is the better synthesis. Explain your reasoning. H 2 Design two syntheses of the compound below using the Wittig reagent and a carbonyl compound. Show all reagents and intermediates. Of the two, which is the better synthesis. Explain your reasoning.
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In this lab, you will be adding hydrochloric acid to a mixture of p-chloroaniline and biphenyl. What is the purpose of hydrochloric acid? To deprotonate the p-chloroaniline To protonate the biphenyl To protonate the p-chloroaniline To make water soluble sodium salt of biphenyl