WHat is the answer to 19.52 (A) 19.52 Suggest routes by which each of the following...
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
3. Draw the structures of each of the following molecules and then provide the reagents needed to convert each of the given starting materials into the required pro a) dimethyl sulfide dimethyl sulfoxide b) phenol methyl phenyl ether c) dimethyl ketone 2-propanol ㅡㅡ
ts of the following question. Provide a synthesis of the following substance from the indicated starting materials. You may assume that you have any needed inorganic reagents. diiodomethane methyl iodide allyl bromide benzaldehyde 1-phenylethene Ph ioniem for each step of the following process: ts of the following question. Provide a synthesis of the following substance from the indicated starting materials. You may assume that you have any needed inorganic reagents. diiodomethane methyl iodide allyl bromide benzaldehyde 1-phenylethene Ph ioniem for...
Please help with A-H Apply retrosynthetic analysis to guide the preparation of each of the following compounds from the indicated starting material, then write out the synthesis showing the necessary reagents. (a) 1-Propanol from 2-propanol (b) 1,2-Dibromopropane from 2-bromopropane (c) 1-Bromo-2-propanol from 2-propanol (d) 1-Bromo-2-methyl-2-propanol from tert-butyl bromide (e) 1,2-Epoxypropane from 2-propanol (1) tert-Butyl alcohol from isobutyl alcohol (g) tert-Butyl iodide from isobutyl iodide (a) 1-Propanol from 2-propanol (b) 1,2-Dibromopropane from 2-bromopropane (C) 1-Bromo-2-propanol from 2-propanol (d) 1-Bromo-2-methyl-2-propanol from tert-butyl...
1. Write a structural formula for each of the following compounds: (36 pts) (a) m-chlorobenzoyl chloride (b) N-ethyl benzamide (c) dibenzalacetone (d) ethyl acetoacetate (e) 2-ethyl-1-butanamine (t) dibenzylamine 2. Write a structural formula for the principal organic product or products of each of the following reactions: (36 pts) (a) propanoyl chloride and sodium propanoate (b) acetic anhydride and 3-pentanol (c) acetaldehyde and sodium ethoxide (CH3CH2ONa) in ethanol solvent (d) cyclohexanone, benzaldehyde, and NaOH (e) 2-aminopropane and acetyl chloride in pyridine...
(7) Suggest an efficient synthesis of each of the following compounds from the indicated starting material. Use any needed reagents and solvents: (80 pts)
10. (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. from and
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
5. (10 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 (use twice)
8. (10 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 (use twice) OH