2. (14 pts total) Outline a synthesis of the following. Show all necessary reagents for and...
2. (14 pts total) Outline a synthesis of the following. Show all necessary reagents for and the product of each step in your proposed synthesis, a) *Η o b) CH, Br
2. (14 pts total) Outline a synthesis of the following Show all necessary reagents for and the product of each step in your proposed synthesis b)
28. Outline a scheme for accomplishing the following synthesis. Do not show the mechanisms. Show the reagents for each step and show the organic product of each step. 5% 29. Outline a scheme for accomplishing the following synthesis. Do not show the mechanisms. Show the reagents for each step and show the organic product of each step. 5%
4) (2 pts each) Outline a synthesis (i.e., simply show the reagents/reactants for the necessary reactions) for each compound below from the designated starting material. Use reagents you've learned about in Orgo I and II. The number of arrows does not necessarily correspond to the number of steps required. As a general rule, any carbon units in the products that were not in the starting materials should come from molecules containing 7 or fewer carbons. Things that don't end up...
2) Show how you would carry out the following reactions. Write all necessary reagents and solvents for each reaction below. (14 pts) BrR Br - RR R R I Br H R HER Br H Br R
? ? Fill in the reagents for each of the two steps 2.5% 26. Br ? ? Fill in the reagents for each of the two steps 27 . 2.5% 28. Outline a scheme for accomplishing the following synthesis. Do not show the mechanisms. Show the reagents for each step and show the organic product of each step. a 5%6 29. Outline a scheme for accomplishing the following synthesis. Do not show the 29. Outline a scheme for accomplishing the...
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. CI The product should be chloro-3-methylhexane A) Cyclobutane 1) -> 2) 1) 2) Br O B) OH 1) 2)
11. Propose a synthesis for each compound below. You must write in all necessary reactants, reagents, and solvents to receive full credit. Your starting materials must be 3 carbons or less. If you use an ionic or organometallic species, you must show how it was synthesized from a neutral, covalent species. Any species that adds carbon to your product must be synthesized from a molecule of 3 carbons or less. Only show the steps of your synthesis- do not put...
6. Synthesis: (40 pts) Show how you would carry out the following synthesis using inorganic or organic reagents containing four or less carbons. Include the reagents you would need for each step and the structure of the intermediate products formed in each step in the appropriate boxes. Br B) ОН 1) 2) —
1) 2 (CH3),CHCH Br / Cul/ 4 Li? CHỊCH, CHỊCH 2) H30+ 2. Using any necessary reagents, show how the following synthetic transformations may be achieved. Give reagents and conditions for each step. Include all synthetic intermediates compounds produced during the course of multi-step synthesis). NOTE: You may not use HOC OH 1. For each of the following questions, provide the missing reagents that can be purchased) and conditions or predict the MAJOR product. Indicate stereochemistry and identify a racemic...