#9 "Complete the mult step Bynthesis below Farting with benzene. No Mechanisms are needed just write...
9. (7) Write a complete multi-step synthetic route for the following transformations, using only the given starting material(s) as the sole source(s) of carbon. You do not have to show the synthesis of solvents or reagents if they are not incorporated into the final product. Clearly (in) Show all intermediate steps and reagents, but do not show any mechanisms or transition states. (24 points): a) Y. I-oyar onbino - we
9. P ropose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step. [It is not necessary to show any mechanisms.] OH 10. Propose a multi-step synthesis to accomplish the overall transformation shown below (make the molecule on the right starting with the molecule on the left). Show all necessary reagents and products for each forward step....
3. MECHANISMS: Provide complete, arrow-pushing mechanisms for each of the reactions shown below. Only TWO of these will be graded but YOU MUST COMPLETE ALL FOUR TO EARN ANY CREDIT! (8 pts.) (note: only mechanism for step 1) 1. Hg(OAc), CH3OH H20 H2SO4 tocha 2. NaBH
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction mechanism. Be sure to include important intermediate compounds, electron flow arrows, and formal charges for full credit. ОН 1. SOCl2, pyridine 2. CH3NH2 (10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with Correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10...
Please try to show/explain every step! 22. Complete the following reactions by clearly writing out the products and state if the product is a water soluble molecule or not. (3 pts cach/15 pts total) HO NH,Br. H,804 HAPO, 200 °C HBE No peroxides CH,CH 23. Complete the following reactions and show the mechanism of how the reaction occurred. You must identify at least one nucleophile and one electrophile in cach mechanism that you draw. Only do ONE of the two...
10. Write the complete mechanisms for the reactions below (3 points each) 1. NaBH4 OH NH 2. H2O Li 11. Rank the following nucleophiles in terms of nucleophile strength where 1 the strongest nucleophile and 5 = the weakest nucleophile (5 points) он 10. Write the complete mechanisms for the reactions below (3 points each) 1. NaBH4 OH NH 2. H2O Li 11. Rank the following nucleophiles in terms of nucleophile strength where 1 the strongest nucleophile and 5 =...
A complete step by step solution please Kerosene Air Benzene 40 cm 9 cm 20 cm 14 cm 8 cm Mercury Water Q5: In the figure, determine Ap between points A and B. All fluids are at 20°C. Given: Ywater = 9790 N/m? Ymercury 133100 N/m3 Ybenzene 8640 N/m3 Ykerosene = 7885 N/m2 Yair12.0 N/m3
organic chemistry 7. How many arrow are needed to complete the mechanism (steps 1 through 4)? step H:0 step 4 a. 4 b. 5 c. 6 d. 7 1. 8 8. Using only the oxidation and reduction reagents shown below, complete the following synthetic transformation. H2Cro 1. NaBHA 1. LIAIHA 1. DIBAL-H PCC H2O, acetone 2. H20 2. H20 2. H2O A. 4 only B. 5 only C. 2, then 5 D. 4, then 3 E. 5, then 1 F....
how do you solve for these? HOW DO YOU SOLVE THESE QUESTIONS STEP BY STEP MECHANISMS 3. Show a mechanism for the following (Grant Challenge). Hint at end with * if you need it. - this is for the people that want a big challenge and who are already very comfortable with mechanisms. 3. Na2CO3, H, 0 0 4. Propose a synthesis for the following, starting from methanolas your only carbon-based starting material. ool logo Me 5. Classify the following...