Suggest a plausible scheme (step by step reaction) for the following synthesis.
Suggest a plausible scheme (step by step reaction) for the following synthesis. X CI Br from...
Design a synthesis of n-propylbenzene from benzene. Hint: A one-step synthesis using CH,CH CH Br and AlBr yields a large amount of isopropylbenzene. 4. 5. Design a high-yield synthesis of each target starting from benzene NO2 NH2 NH2 H2N CI CI target target target target
Please describe how each reaction will be accomplished. Alkyne and Nitrile Synthesis Retrosynthesis CH CH2 OH ОН Br HCECH + Synthesis CH CH2 0,0 NMO HCOCH Li NH NaNH Benzyl bromide OH OH Retrosynthesis One-on-o EN Br Synthesis Br KCN er blan NH2 H3C 1) LAH 2) H30* NH CH3 Alkyne and Nitrile Synthesis Retrosynthesis CH CH2 OH OH Br H2=CH + Synthesis CH CH2 0.0 NMO Li NH, NaNH, Benzyl bromide HC SCH OH OH The starting material is...
17. Give the reagents for the following reaction. Write the product for each step. HCECH CH, CH2CH2CH CH, CH.CHOH 18. Give the reagents for the following reaction. Write the mechanism for each step. Br Br HCECH CH.CH -CH2CH3 1 Br Br
Identify the lettered compounds in the following reaction scheme. This reaction was used in the synthesis of a natural product HC CCH OR он CH PBr OR Draw the structures of compounds A, B, and C. Use R for both R and R' in the structures. Only 1 equivalent of alkyne is being used in the reaction. A. edit structure draw structure draw structure
Choose the most appropriate reagent(s) for the final step of the synthesis. 0 CI AlCla Br2 FeBr3 0 Zn(Hg), HC Br NBS, ROOR, heat Br reagent(s) CH3CH20K, CH3CH2OH LiAIH4, diethyl ether C H20 E HCI, H20
Propose a plausible mechanism for the following reaction Br Br 2 ?? Propose a plausible mechanism for the following process, ca tonization:
5. For the following reaction: H9 CH H,Sow, heat to Han> 0 a. Suggest a plausible mechanism for this process; b. What role might the strong acid H2SO4 play? why this reaction use heating? c. Draw the whole energy diagram for this process.
PART III. Mechanism problems 38. Please draw a plausible reaction mechanism of solvolysis reaction by showing poessbility of reermeer ned ntemesatws with the mao prmist. If there isa possibility of rearrangement, please show it for the major product CH3 39. Propose a detailed, step-by-step mechanism for the reaction pathway shown below. 40. CH,CH,CH,Br+NaCCC 41. Plcase draw a plausible reaction mechanism of the following free radical reaction by showing the initiation step, propagation step, and termination step. Bry
Select the major product of the following reaction scheme Reaction Н NaOH HC Acelone, ETOH 25°C А 0 ora CH нс Hc E он о Ho CH HO с нс (No Reaction) P х W N FE 80 BR 74 2 75 # 3 tab $ 4 Q % 5 W 6 E & 7 20 lock А T S Y D
Suggest efficient synthesis for the following compounds from the available starting material(s), specifying necessary reagents for each step NO2 a) OH NH from F Pyo NH2 Br ㅇ from li b) gary