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0.5 pts Question 4 (10 points) Show how you would synthesize the following aromatic compound from...
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
Problem #3 Show how you would synthesize ethyl benzoate in good yield starting from benzene. You may use any other reagent necessary
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
9- Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents. More than one step is needed. 8 Br OH Bromobenzene, 1-Butene Show hew you weulel Syntfesige 4-Nonanone, begining witA 1-Butanol and any other non- oraanie reagents.(1-Butanol is the only Organic compeonn availabe)
Show how you would synthesize the following compound starting with acetylene and compounds containing no more than two carbon atoms as organic starting material. You may use any additional reagents you need Br H H Br
JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH a) NO2 b) CI c) 4-phenyl-2-pentanol; •DH d) 1-bromo-2-chloro-4-ethylbenzene; 2. Arrange the compounds in each set in order of decreasing reactivity (fastest to slowest) toward EAS. Explain. (2 pts) 0-C-CH3 -C-0-CH3 a) (A) (B) (C) CH2CH3 -NH2 ( C1) do nosotros (B) b) (A) 3. Account for the observation that trifluoromethyl groups is meta directing, as shown in the following example. (1 pt) CF3...
. Show how you would synthesize the following reactions. a. aldol (4 pts.) OH 0 b. condensed aldol reaction (4 pts.)
4. In each reaction show how you would synthesize the product from the reactant. Show the reagents, conditions, and the structures of any important intermediates along the way. Any organic reagent may be used, and more than one step may be used as well. Include mechanism (+-) H Br
וווו והו vide a retrosynthetic analysis to show how you would synthesize the following molecule. As starting erials you may use any alcohols of 5 carbons or less. You may use any necessary solvents and inorganic eagents. There is no need to show reaction mechanisms, just reactants, conditions and products (10 points). HyC
How would you synthesize each of the following from either ethyl acetoacetate or diethyl malonate? Show retrosynthesis and forward synthesis|. a) b)