1. Devise a synthesis of 2-propylhexanenitrile (structure below) from butanol as the only starting material. CN
For the compounds named below, (1) draw the structure of each compound (2) using benzene or toluene as the only aromatic starting material devise a synthesis of each compound. b. p-nitroethylbenzenec. p-bromonitrobenzene d. p-isopropylbenzenesulfonic acid
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
1) Outline a synthesis for the product shown below from the given starting material ОН CN
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...
1) Outline a synthesis for the product shown below from the given starting material. OH CN 2) Provide an arrow-pushing mechanism for each of the transformations shown below. HBr H2SO4 H20
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). a Mg/dry ether b 1. CO_2 2. Acidic workup c NaCN/THF or DMF d NaCN/dil. Aqueous H_2SO_4 e...
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...
Devise a 4-step synthesis of the product from the starting material shown. 1. reagent 1 2. reagent 2 3. reagent 3 4. reagent 4 HOT Identify reagent 1. Identify reagent 2. Identify reagent 3. Identify reagent 4.
2. Devise a multistep synthesis of the target molecule from the starting material shown. Show the reagents needed for each step and the product of each step. Do not show any mechanisms.
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...