Opts) Propose a synthesis for the compounds below using acetylene and any other necessary reagent Show your work cl...
7. Propose the scheme of the synthesis of the compounds a) A and b) B from acetylene (CH-CH), cyclohexane and other necessary reagents out more
Complete the synthesis of muscalure from acetylene and other compounds. Your synthesis must give specifically the cis isomer of muscalure. Identify the reagents by dragging the appropriate labels to their respective targets. Reset Help CHz(CH), Br H, Lindlar's catalyst NaNH2 Na, NH3 CH3(CH)2Br H-C= -H CH3CH2-CEC-H CHz(CH2) (CH),2CH3 C=c CH3CH2-CEC-(CH2CH3 H muscalure
Propose an efficient synthesis of the compound shown below, starting from acetylene and methyl iodide. You may use any other reagents as necessary, but all carbons in the product must originate from acetylene and methyl iodide.
12. Propose a synthesis for the following compound using benzene or toluene and any other reagents necessary. Show all major intermediate compounds that would probably be isolated during the course of your synthesis. (6 points)
Page 4 Propose reasonable syntheses for the following compo compounds and using any other necessary organic intermediates formed to receive full credit. Assume separated. ng compounds beginning with the indicated organic or inorganic reagents. Show all sume any isomers formed can easily be [3% +6% marks] c. Provide any required reagents and give the stru following synthetic scheme. If more than one reaga steps. ve the structures of the intermediates in the one reagent is required, please number the Bra,...
please show work
20. Starting from benzene or anisole and any other reagent of your choice, design a synthesis for each of the following compounds. (18 pts) TO ) сон CBry
Please explain the mechanisms!
1. Propose a synthesis for each of the following problems starting with reagent shown and using any other organic or inorganic reagents allowed in each problem. Multiple steps are required. The number of steps you use does not matter. Reactions should give the desired product as a major product. For full credit show the product of each step (reaction). If you make use of organometallic reagents such as Grignard, Wittig, organolithium, organosodium, organocopper, etc. you must...
Synthesis. Use suitable nitrile precursors and any other necessary reagents to propose a synthesis route to each compound below. & NH2
2. Propose an elegant synthesis of the following molecule starting from terminal alkyne compounds of five carbons or fewer as your only source of carbon. You may use any other reagent necessary. CH3 CH3 H3C CH3
2) Propose a synthesis for the transformation below. You may use any reagent discussed in the course notes or textbook, as well as any additional compound with 2 or fewer C atoms in your solution. (5 marks)