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?

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

Give two Friedel-Crafts acylation reactions that could be used to prepare 4-methoxybenzophenone. One of the reactions will occur faster or under milder conditions. OCH3 A. Draw the precursors that would occur faster. B. Draw the precursors that would occur slower. Select Draw Rings More Erase Select Draw Rings More Erase C H. Cl C H. Cl
6. Using just ozone, DMS (dimethyl sulfide), aqueous acid, and methyl magnesium bromide, describe how you might convert cyelohexylidenecyelohexane to 1-methylcyclohexanol. HO. cyclohexylidenecyclohexane 1-methylcyclohexanol
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 CH₂
What is the proper reagent for this transformation?
please do the step by step reaction. thank you
1. Propose multi-step syntheses to make the products shown below. Separate the steps with numbers. You should think about the product after each step you propose to make sure the scheme will work. Use the summary of reactions at the end of Ch 8,9, 10, 11, 17 to help you. Count the number of carbons in the reagents and products. A) OH .CI B) ??? HO. C) H2 .C ??? CH3 CH3CCCH3 H3C `CH3 Но
Identify the correct reagents and conditions to perform this chemoselective reaction: H ရှုံး H Select one: Me e. Reagent(s) and conditions? a. NaBH4 b. BH3 THF Pd/BaSO4, H₂ (1 atm.), quinoline, Pb(OAC)2, MeOH d. Pd/C, H2 (1 atm.), MeOH DIBAL Me H H OH
7. Show reagents that could be used to make the following compound from Grignard reactions. OH X a. Ketone + Grignard reagent b. Different ketone and different Grignard reagent.
4. Write in the reagents that will accomplish the following transformation. Reagents must be placed in the correct order. Show products formed after each step. ?? Br b Br
a. Show the major product for the reaction shown and a mechanism for its formation. Do not use any termination steps in your mechansim .. only propogation steps. Br2 hv b. If sufficient bromine is added and the reaction is allowed to proceed further, another product will form from the first. Show a mechanism for the reaction of the product from part a. to form the final product with two bromines attached.
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?
Choose the best sequence of reagents to synthesize the following ether. 1) CH3SH 2) PhCH(CH3)Br S 1) PhCH(CH3)Br 2) CH3SH 1) CH3SH 2) NaH 3) PhCH(CH3)Br 1) PhCH(CH3)Br 2) NaH 1) PhCH(CH3)SH 2) NaH 3) CH3I 3) CH3SH