Retrosynthesis, beneze ring to substituted benzene ring. What are the two steps? Help please.
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Benzene react with methyl chloride in the presence AlCl3 to give methylbenzene via Friedel-Crafts Alkylation reaction
Methylbenzene oxidized with KMnO4 to give benzoic acid
Benzoic acid are meta directing group due to carboxylic acid group are electron withdrawing group.
Benzoic acid undergo bromination in the presence of Br2/FeBr3 via electrophilic substitution reaction to 3-bromobenzoic acid
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benzene undergo bromination in the presence of Br2/FeBr3 via electrophilic substitution to give
bromobenzene
bromo substitution is ortho para directing group,
bromobenzene undergo Friedel-Crafts Alkylation reaction with methyl chloride in the presence AlCl3 to give 1-bromo-2-methylbenzene and 1-bromo-4-methylbenzene
1-bromo-4-methylbenzene product is major product due to stric effct
1-bromo-4-methylbenzene undergo oxidizing reaction with KMnO4 to give 4-bromobenzoic acid
Retrosynthesis, beneze ring to substituted benzene ring. What are the two steps? Help please. Br
Please put all 6 steps. Design a synthesis of 2-bromo-1-chloro-4-nitrobenzene from benzene or any mono-substituted benzene. Cl Br benzene or any mono-substituted benzene NO2 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CI Br NO2
Dihydroxybenzenes are aromatic chemical compounds where two hydroxyl [-OH] groups are substituted onto a benzene ring. Draw the structure for the following: o-dihydroxybenzene – (3 points)
What is the common name for the following substituted benzene? Br Select one: O a. o-bromoanisole o b.o-bromoaniline O c.m-bromoaniline o di m-bromoanisole O e. p-bromotoluene
Please do all parts. 7. Do all parts: a. Starting with benzene propose both a retrosynthesis and a stepwise synthesis for the following compound. (12 points) LOH Br b. Provide a stepwise, curved arrow mechanism points) for the following reaction. (8 AICI3
1. Complete the following exercises: A. Indicate whether each substituted benzene ring will produce predominantly ortho/para or meta products) after electrophilic aromatic substitution: B. Identify the molecule that can undergo nucleophilic aromatic substitution by addition/elimination:
N gCIL Drawing Resonance Contributors of Substituted Benzenes Identify the functional groups attached to the benzene ring as either, being electron withdrawing, electron donating, or neither Drag the appropriate structures to their respective bins. View Available Hint(s) Reset Help CHE che CH, Electron Withdrawing Groups Neither Electron Donating Groups
organic. how would you add a phenyl group to a benzene ring? please show the mechanism and steps (hint was to use grignard)
Based on the mass spectrum. I want to know what are the two substituted functional group to the benzene ring? 1st region info : 108.9 : 691 107.9 , 9878 106.9,9429 2nd peak info : 90.9 , 311 90.0 , 1002 88.7 , 345 (78.0,0) RELATIVE UTENSITY 10000 9000- B000 6000 5000 Mass Spectrum Download spectrum.fi 3000 2000 1000- 100 110 MZ 20130 MS Unknown #18 Benzeme
please help me figure out the steps and reagents for this synthesis problem Br H2N
Give IUPAC name for structure below. i got confused bc this is not a benzene ring so I do not know what to name it. CO2H Br 3- Bro