(7) Suggest an efficient synthesis of each of the following compounds from the indicated starting material....
PLEASE ANSWER ASAP 4. Suggest an efficient synthesis of each of the following compounds, starting from the compound indicated and any other needed reagents and solvents. (72 pts) (a) 2-pentanol, from 1-chloropropane (b) 2-butanone, from 2-butanol (c) 1,3,5-tribromobenzene, from benzene (d) benzoic acid, from chlorobenzene (e) benzyl tert-butyl ether (C6H3CH2OC(CH3)3, from benzyl alcohol and tert-butyl alcohol (1) acetyl chloride, from ethanol
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
3 e f g 3. Suggest efficient syntheses for the following compounds, starting from the compound indicated and any other needed reagents. (98 pts) e) benzonitrile (C HsCEN) starting from benzene. (f) octanoic acid, from 1-hexanol. (g) phenol, from aniline (CsHsNH:).
(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....
Devise a synthesis of the following compound from the indicated starting material, organic compounds containing one or two carbons, and any other required reagents. Be sure to answer all parts. Devise a synthesis of the following compound from the indicated starting material, organic compounds containing one or two carbons, and any other required reagents. Be sure to answer all parts. (+ enantiomer) CECH edit structure ... CH,CI edil structure. edit structure
Give a reasonable synthesis for each of the following compounds from the indicated starting materials. 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. If equal mixtures are anticipated (i.e. ortho / para products) then indicate where separations are needed. NO MECHANISMS! [6 points 2. Give a...
(8 pts) Suggest an efficient reaction sequence for the preparation of each of the following compound from the indicated starting materials and any other necessary reagents 2. from and Br
Design a multi-step synthesis for each of the following target molecules from the indicated starting material. Show the reagents needed for each step and the product of each step. Do not show any mechanisms. Draw the structures of the diene and the dienophile that reacted to form the Diels-Alder product shown. Provide the missing reagents in this multistep synthesis.
7. (12 pts) Suggest an efficient reaction sequence for the preparation of each of the following compound from the indicated starting materials and any other necessary reagents. from and HO OH
need D,E & G. outline a reaction sequence for synthesis of each of the following compounds from the indicated starting material & any other organic or inorganic reagents needed. Outline a reaction sequence for synthesis of each of the following compounds from the indicated starting material and any other organic or inorganic reagents needed. (a) 0 0 0 он OEt он ,EUA 853 PROBLEMS NH+ (g) O OEt OE Outline a reaction sequence for synthesis of each of the following...