Suggest reactants/reagents to make compounds 1 and 2 from 2-butanone. Each method could contain one or...
5. Suggest reagents that could be used to synthesize each of the following compounds. OH OH (3 methods) and b а.
66. Suggest a synthetic route by which one could produce the following compound from benzene. Provide all necessary reagents needed for each transformation. (10 pts) SO3H 66. Suggest a synthetic route by which one could produce the following compound from benzene. Provide all necessary reagents needed for each transformation. (10 pts) SO3H
4) (2 pts each) Outline a synthesis (i.e., simply show the reagents/reactants for the necessary reactions) for each compound below from the designated starting material. Use reagents you've learned about in Orgo I and II. The number of arrows does not necessarily correspond to the number of steps required. As a general rule, any carbon units in the products that were not in the starting materials should come from molecules containing 7 or fewer carbons. Things that don't end up...
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
1- Suggest a retrosynthetic analysis for each of the following target molecules In each case identify the latent polarity and the type of disconnection . 2-suggest synthons, synthetic equivalents, and reagents for the forward synthesis (a single disconnection is required ) ((resynthetic steps) , ((synthetic steps))
WHat is the answer to 19.52 (A) 19.52 Suggest routes by which each of the following compounds could be synthesized from the indicated starting materials and any other reagents (a) 1-phenyl-1-butanone (butyrophenone) from butyraldehyde |(b) 2-cyclohexyl-2-propanol from cyclohexanone (c) cyclohexyl methyl ether (methoxycyclohexane) from cyclohexanone (d) PhCH20CH,Ph (dibenzyl ether) from benzaldehyde as the only carbon source
7.40 Suggest reagents that could be used to synthesize each of the following from an aldehyde or ketone. a) ОН (3 methods) Groups ОН b) (2 methods) ОН
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...
"uctions down Question 1 Pe Which reagents would favor the formation of 3-methyl 2-butanone from 2-butanone? 1. Nah, 25°C 2.CHgBr O H20 / CH2BE O 1. LDA -78°C 2.CH3Br O Both A and B all the reagents would give that product Question 2 2.5 pts
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...