the most efficient synthesis possible 6. Synthesis propose to make the compound shown below Starting from...
Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. *Note: This will require more than 3 steps* ohin 3...
Retrosynthesis. Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. "Note: This will require more than 3 steps BrMg
yeah Retrosynthesis. Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the intermediates formed. *Note: This will require more than 3 steps HH BrMg
Retrosynthesis. Propose the most efficient synthetic route to make the following compound starting from the indicated reagents and any other reagents, clearly identifying the reaction conditions at each step and the structure of the Intermediates formed. *Note: This will require more than 3 steps BIO o 3 by BrMg
Propose a synthesis for the compound D shown below, starting with benzene. Identify appropriate reagents, reaction conditions and give the detailed mechanism for the formation of the azo bond.
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.
Synthesis 10. Give a reasonable synthesis for the following compound from the indicated starting material. You may use any other organic or inorganic reagents you wish unless otherwise indicated. The desired product for each reaction you propose must be the one of the predominant products. Give the reactants, conditions (where appropriate) and products of each synthetic step. NO MECHANISMS! [6 points) Make med og som en ons starting with SO3H
3. SURResta synthesis for each of the compounds shown below, beginning with the compound shown on the left. Clearly show all required reagents and intermediates Mehr HO но NO NHL-NH.KOH NH, NHL-NHKOH I reali HO CH.CH COH SOA NH Сн,CH, 2 CHOH Nathanol Η O' 1,0 4. Suggest a synthesis for each of the compounds shown below, beginning with the starting material shown on the left. Clearly show all intermediates and reaction conditions. Multiple steps are likely to be required....
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
6. Provide the most efficient synthesis possible by matching the reagents to the reaction. Write the letter(s) over or adiacent to the corresponding reaction arrow. As many as three steps represented by each letter may be needed. Assume intermediate products are isolated and purified or used in situ as appropriate. A. H2/Ni B. KI $ C. CuCN NH D. HBF4 E. HO F. Cuci G. LAH/THF Q-- H. HONO2/ H2SO4 I. H3PO2 J. CH3COCI/ AICI: K. NaNO2/H2SO4