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Propose an efficient and elegant synthesis of the molecule
using only a benzene as your starting...
Propose an efficient and elegant synthesis of each of the following molecules using either diethyl malonate...
Propose an efficient and elegant synthesis of each of the following molecules using either diethyl malonate or ethyl acetoacetate as your starting material. You may use any alkyl halide or alcohol as your other sources of carbon, and you may use any reagent you deem necessary. CH3 EN CH₂ HCO CH, Hgc CH, CHA CH₃ -CHS
2. Propose an elegant synthesis of the following molecule starting from terminal alkyne compounds of five...
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
Extra Credit Propose an elegant and efficient synthesis of the following amine using benzene and alcohols...
Extra Credit Propose an elegant and efficient synthesis of the following amine using benzene and alcohols of 4 carbons or less as your only source of carbon
Extra Credit Propose an elegant and efficient synthesis of the molecule show below. You may use...
Extra Credit Propose an elegant and efficient synthesis of the molecule show below. You may use alcohols of 4 carbons or less as your only source of carbon. H3C CH3 HBr CHs
Propose a synthesis of the following molecule starting with the indicated starting moleucles as the only...
Propose a synthesis of the following molecule starting with the indicated starting moleucles as the only allowed carbon sources and any needed inorganic reagents. Cl anisole ← H3CO Cl
Starting with benzene, carbon dioxide, and 2-propanol as your sources of carbon, purpose and efficient synthesis...
Starting with benzene, carbon dioxide, and 2-propanol as your
sources of carbon, purpose and efficient synthesis for propanoyl
benzoate:
1) Starting with benzene, carbon dioxide, and 2-propanol as your sources of carbon, propose an efficient synthesis for propanoyl benzoate: CH он AND CO, AND
Propose a synthesis of the following molecule starting with the indicated starting molecules as the only...
Propose a synthesis of the following molecule starting with the
indicated starting molecules as the only allowed carbon sources and
any needed inorganic reagents.
Br B(OH)2 + ethyne ethyl iodide
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformati...
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents...
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
4. Propose an efficient synthesis of the molecule below starting with benzene. You can use any...
4. Propose an efficient synthesis of the molecule below starting with benzene. You can use any other reagents you want. NOTE: Some reactions produce ortho- and para-products. It is allowable to just take ONE of the products and use it in the next synthesis or claim it as the final product (we assume that ortho- and para-products can be separated). (3 points) CH2CH2CH Br
Propose an efficient and elegant synthesis of each of the following molecules using either diethyl malonate or ethyl acetoacetate as your starting material. You may use any alkyl halide or alcohol as your other sources of carbon, and you may use any reagent you deem necessary. CH3 EN CH₂ HCO CH, Hgc CH, CHA CH₃ -CHS
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
Extra Credit Propose an elegant and efficient synthesis of the following amine using benzene and alcohols of 4 carbons or less as your only source of carbon
Extra Credit Propose an elegant and efficient synthesis of the molecule show below. You may use alcohols of 4 carbons or less as your only source of carbon. H3C CH3 HBr CHs
Propose a synthesis of the following molecule starting with the indicated starting moleucles as the only allowed carbon sources and any needed inorganic reagents. Cl anisole ← H3CO Cl
Starting with benzene, carbon dioxide, and 2-propanol as your
sources of carbon, purpose and efficient synthesis for propanoyl
benzoate:
1) Starting with benzene, carbon dioxide, and 2-propanol as your sources of carbon, propose an efficient synthesis for propanoyl benzoate: CH он AND CO, AND
Propose a synthesis of the following molecule starting with the
indicated starting molecules as the only allowed carbon sources and
any needed inorganic reagents.
Br B(OH)2 + ethyne ethyl iodide
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI. Devise a synthesis that will accomplish the following transformation in good yield. Use the given compounds as the only organic source of carbon atoms. You may use any common organic solvents as well as any needed inorganic reagents
(14) V. Starting from benzene and any other reagents you need, propose an efficient synthesis of th following compound. (10) VI....
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
4. Propose an efficient synthesis of the molecule below starting with benzene. You can use any other reagents you want. NOTE: Some reactions produce ortho- and para-products. It is allowable to just take ONE of the products and use it in the next synthesis or claim it as the final product (we assume that ortho- and para-products can be separated). (3 points) CH2CH2CH Br
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