6. Draw the arrow-pushing mechanism for this transformation. 2 NaOH(aq) 7. Propose routes to make the...
6. Draw the arrow-pushing mechanism for this transformation 2 NaOH(aq) 7. Propose routes to make the products shown from the reactants. Give all reagents required and draw all stable, neutral intermediate compounds. You will need more than one step in each case. OH CH CH3 CH3 HyC H3C н,с Br он Br CH3 Brunker CHEM332
Chem 306 Unit 2 Exam Page 5 of 6 7. Draw a reasonable arrow-pushing mechanism to show how the reactant transformed into the final products: (First arrow shown: 14 pts if all correct) Products Reactants 0 + H₂O он (cat.) HO 0 + H₂O H-0 + Ho H . H 1 0 o Hº 0 H 8. a) Consider the polymer below. Circle all reasonable reactants that can be used to make the indicated polymer A. (8 pts) Possible monomers...
Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) OME B OMe NaOH Me Me H2O2 Me H Me
3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) ОMe NaOH Me Ме. B OMe H2O2 Me H Me
3. Draw a detailed arrow-pushing mechanism for the following transformation. (4 pts) ОMe NaOH Me Me B ОMe H2O2 Me H Me
7. Provide a complete, arrow-pushing mechanism for each of the reactions below.(7 pts. each) NaOH (aq) then heat (a) HO NaOH ini EtOH/H20 (b)
4) Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for every step, writing statements like "proton transfer without showing the arrows for that step is not an acceptable answer NOE, EIH
Write the product and a complete arrow-pushing mechanism and propose (the) major product(s) for the following transformation. After a Grignard reaction. .... Each of the Grignard reactions we have studied so far produces an alcohol as the major organic product. Alcohols can be used as starting materials for a number of organic reactions. Use this exercise to consider the range of reactions that can be performed after a Grignard reaction. For each reaction sequence below, suggest a Grignard reagent and...
Curved Arrow Pushing 5. For each transformation below, complete the mechanism by drawing the proper arrows. Show all lone pairs in the reactants and products. X -- d .o.o. OX C. @s-CH2-CH2-CH2CH2-Br- - R H Ho H. :-- -- ::-- .Com -- 0.00u . осн HOCH . CH3 CH + Ho CH3 대 CH3 5. For each transformation below, complete the mechanism by drawing the proper arrows. Show all lone pairs in the reactants and products. X X - separowangen...
Propose a complete, stepwise, curved-arrow reaction mechanism for this base-catalyzed retro-aldo transformation. You do not need to worry about stereochemistry. Draw the best resonance contributor for each proposed intermediate excess NaOH mele H,O, Heat Өон Yo- 21