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-nitroethylbenzene
c. p-bromonitrobenzene
d. p-isopropylbenzenesulfonic acid
using benzene or toluene as the only aromatic starting material devise a synthesis of each compound.
Starting with benzene or toluene, outline a synthesis of each of the following compounds using diazonium salts as intermediates a) 3,4,5-Tribromobenzonitrile b) 2,6-Dibromobenzoic acid
Starting with benzene as your only source of aromatic compounds, how would you synthesize the following substances? Assume that you can separate ortho and para isomers if necessary. p-Chlorotoluene m-Bromonitrobenzene o-Bromobenzenesulfonic acid m-Chlorobenzenesulfonic acid Starting with either benzene, phenol, or toluene, how would you synthesize the following substances? Assume that ortho and para isomers can be separated 2-Bromo-4-methylphenol 1,3,5-Trinitrobenzene 2,4,6-Tribromoaniline 2-Chloro-4-nitrotoluene
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
2. Devise a synthesis of p-nitro-tert-butylbenzene from benzene. 3. Classify the compounds below as aromatic or nonaromatic.
1. Devise a synthesis of 2-propylhexanenitrile (structure below) from butanol as the only starting material. CN
HO Devise a synthesis and propose a mechanism starting with benzene and any 2 carbon compound.
(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....
Synthesis starting with toluene starting with benzene and using a protecting group at some point in your synthesis
Using benzene as the only organic starting material, design a synthesis(no mechanism) for the following (use any other reagents that you need). Please disregard the orange box that is in the structure. Na
4) Devise a synthesis (series of reactions) to transform each starting material the given product into desired using the starting any necessaryand aromatic source and reagents Show reaction . all steps their resulting intermediate products. Or Or 18 OH 18 O - OAO /10 131