choose the sequence of reagents that provides the most efficient synthesis of 1,2-dicholorobutane starting from butane and using any reagents necessary.
choose the sequence of reagents that provides the most efficient synthesis of 1,2-dicholorobutane starting from butane and using any reagents necessary.
Choose the most efficient synthesis of (halomethyl)cyclohexane starting from cyclohexane and using any reagents needed.24.1 (1).png
Starting from methyl acetoacetate and any other necessary reagents, complete the most efficient threestep synthesis of the ketone, 3-benzyl-5-methylhexan-2-one, by dragging the appropiate compound(s) into the boxes. Only one set of reagents will fit into each box, and all compounds will not be used.
6. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 7. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 8. Starting with benene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there...
1. Starting with benzene and any necessary reagents, design an efficient synthesis of the following compound: 1. Provide a detailed curved-arrow mechanism to account for the transformation below and explain why the only products formed at high and low temperatures are the ones shown. (Show all resonance contributors for all intermediates): HCl, Clos Cocha осн
Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents from the tables. Give route by specifying the number of the starting material followed by the letters of the reagents you would use beginning with the step. Reagents a Mg/dry ether b 1. CO_2 2. acidic workup c NaCN/The or DMF d NaCN/dil. aqueous H_2SO_4 e Aqueous H_2SO_4 at reflux f Conc, HCl or HCl (gas) g PBr_3 h KOH/alcohol i KMnO_4/H_3 O^+ j...
Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents from the tables. Give your route by specifying the number of the starting material followed by the letters of the reagents you would use beginning with the first step. The answer 4fh means treat t-butanol(4) with conc. HCl(f) then treat the product with KOH in alcohol(h). OH OH Starting materials Br Br OH OH Reagents Aqueous H,SO, at rofu f Conc. HCI or HCI...
Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents from the tables. Give your route by specifying the number of the starting material followed by the letters of the reagents you would use beginning with the first step. The answer 4fh means treat t-butanol(4) with conc. HCl(f) then treat the product with KOH in alcohol(h). Mg/dry ether CO_2 acidic workup NaCN/THF or DMF NaCN/dil. Aqueous H_2SO_4 Ethanol, H_2SO_4 [trace) at reflux Conc. HCl...
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
Devise the most efficient synthesis for the carboxylic acid below using a starting material and reagents from the tables. Give your route by specifying the number of the starting material followed by the letters of the reagents you would use beginning with the first step The answer 4th means treat -butanol(4) with conc. HCI(0) then treat the product with KOH in alcohol(h). Br Starting materials Br Br Reagents I KMnO4/H,O j Na2 CrOs/ aqueous H,SO k 1.BH THE a Mg...
Starting with Benzene and using any other necessary reagents of your choice a synthesis for the following compound. Assume that ortho and para isomers can be There may be more than one plausible answer.