O2 CHO CI Starting from unsubstituted benzene, provide the reagents that would be required to synthesize...
ОН Starting from unsubstituted benzene, provide the reagents that would be required to synthesize the aromatic molecule shown. Please correct order.
You are told synthesize cumene starting from benzene and any other reagents. You find 1- chloropropane in the lab and decide to attempt a Fridel Crafts alkylation. Upon completion of the experiment, a H-NMR reveals two products: a minor product with six signals and a major product with 5 signals. Provide the mechanism for the formation of both products. 2. Provide the reaction for chlorination of benzene using electrophilic aromatic substitution, it's complete mechanism including formation of "super" electrophile, and...
The reagents required to synthesize the desired compound from benzene are listed below. Arrange them in the appropriate order. QUESTION 4 The synthesis below can be accomplished using reactions you have learned in CHEM 241b. OH The reagents required to synthesize the desired compound from benzene are listed below. Arrange them in the appropriate order. - BH3 THE - (H2C=CH)2Culi - i-PrCI, AICI: - H2O2, NaOH 12, HNO3 -
Starting with benzene and any reagents you need, synthesize compound shown. More than one step is required. Assume you can separate ortho and para-isomers. (12 pts) _CH₂
Name: 4. Starting with benzene and any inorganic or organic reagents, outline all steps in the synthesis of the following compounds. No mechanisms required but correct order is. (HINT: think clectrophilic aromatic substitution) (10 points): (A) (B)
. Starting with acetylene, any halide ($4C), and any other reagents required, synthesize the target molecule. (8 pts) TM Starting with acetylene, any halide (S4C), and any other reagents required, synthesize the target molecule. (7 pts) 2. OH TM
9. Propose an efficient synthesis of each molecule below starting from benzene and any other reagents needed (organic or inorganic) A. CI B. CI NO2 Br
Name: 4. Starting with benzene and any inorganic or organic reagents, outline all steps in the synthesis of the following compounds. No mechanisms required but correct order is. (HINT: think clectrophilic aromatic substitution) (10 points): (A) (B)
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
Answer all parts quckily thank you 4. Starting with benzene and any inorganic or organic reagents, outline all steps in the synthesis of the following compounds. No mechanisms required but correct order is. (HINT: think electrophilic aromatic substitution) (10 points): (B)