2. Devise a synthesis of p-nitro-tert-butylbenzene from benzene.
3. Classify the compounds below as aromatic or nonaromatic.
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 molecule FROM benzene. Please start with benzene and list all reagents/transformations. Thank you! но
In the reactions below you are given a product and enough the starting materials information about the formation of the product to provide 1. Th followling as munde usiig a Dicls-Alder reuction Provide the rouctants and reaction conditiows The foliowing product was made starting with benzene -provide all steps of the reaction and reaction conditions 2. 3. The following was made in an enamine synthesis-provide the starting materials and reaction condit Aromaticity-3 points each Please classify the following compounds us...
Provide a retrosynthesis and forward synthesis for butylbenzene. You may only use benzene, any alkane with 3 or fewer carbons, cyanide or carbon dioxide as carbon sources.
(nasal decongestant) 25.71 Devise a synthesis of each compound from benzene, any organic alcohols having four carbons or fewer, and any required reagents a. CI ん CN (nasal decongestant) 25.71 Devise a synthesis of each compound from benzene, any organic alcohols having four carbons or fewer, and any required reagents a. CI ん CN
(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....
solve the following Create a mechanism to produce 4-tert-Butylbenzene-1, 2-dicarboxylic acid from o-Xylene possible to get multiple products from used mechanisms. Use only the reaction path that yields the final desired product СОН tert Buty benzene 12 licarbon and 6) Chose the starting material from the table and create m-nitroacetophenone. Does it matter which functional group is attached to your starting material first? Give a reason to support your responce 7) Make 3-Bromo-5-nitrobenzoic acid from toluene using reactions from the...
HO Devise a synthesis and propose a mechanism starting with benzene and any 2 carbon compound.
30 Design a synthesis of m-bromostyrene from benzene. points Br Part 1 out of 12 Choose the best option for the immediate precursor to the target molecule. Br points НО 23 Design a synthesis of p-t-butylacetophenone from benzene. points Choose the best option for the immediate precursor to the target molecule. Part 2 out of 6 Choose the best option for the precursor to t-butylbenzene. 2 points NH2 OH 23 points NH2 он
Perform a retrosynthetic analysis of the compounds below and then devise their synthesis from readily available starting compounds and any inorganic and/ or organic reagents. Your answer should include a complete retrosynthetic analysis, synthesis pathway with reagents and reaction conditions. Ph Ph from Ph Ph from