Just number 3 please 2. Name these aromatic compounds properly.a)b)4. Write in the reagents need to transform benzene into this product.Benzene->4. Write out all the steps in the mechanism of this electrophilic aromatic substitutionreaction. Include all resonance contributors.Cl2Benzene→ chlorobenzeneFeCl322tvMacBook888DIIF4F5F6F7F9F1F2F3@#$%&*2456.78WERTYSFGHJKCV* 00

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Answered: 2. Name these aromatic compounds…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter13: Substitution

Section: Chapter Questions

Problem 4E

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Provide a short paragraph that relates the most essential elements of theory (reactivity, regiochemistry and rate etc) behind the EAS reaction. (Electrophilic Aromatic Substitution Reactions)
as a follow-up question can explain this mechanism
Please propose a synthesis of the target molecule using as many steps or reagents and answer these questions. 1. Why use chemoselectivity as the functional group and not another? 2. Why regioselectivity? 3. Why stereoselectivity? 4. What are the changes in the oxidation state?
Why does the carbomethoxy group directs the reaction to positions that are meta to it ?b) Why the formation of dinitrobenzaote is substantially disfavored ?c) Would you expect small amounts of the ortho and para substituted product ? How would you remove them if they are formed ?d) Why does water have a retarding effect on the nitration ?e) Explain why Benzene has lower reactivity in electrophilic addition reactions than cyclohexene?
While designing a synthesis, define Reactions that convert one functional group to another—that is, functional group interconversions ?
By which substitution mechanism (SN1 or SN2) did the reaction occur? How did you know? For what reason does the substitution occur at only one of the bromine atoms, and in particular the bromine atom that it did?
p-Fluoronitrobenzene is more reactive toward hydroxide ion than is p-chloronitrobenzene. What does this tell you about the rate-determining step for nucleophilic aromatic substitution?
Which of the following is statements is/are TRUE about the experiment on the relative rates of electrophilic aromatic substitution?I. The experiment must be performed in dark conditions. II. Using the same solvents, a faster decolorization will be observed in aniline as compared to ethylbenzene. III. Chlorobenzene will react faster than methoxybenzene. IV. The use of AlCl3 in the halogenation of aromatic compounds using elemental bromine could hasten the reaction.
How does increasing base, solvent, or alkyl halide or aptly halide + base affect or decreasing them affect the reaction rate for e2/e1 and sn2/sn1? Please provide examples
Working Backwards Parte Deux. a.First, identify which functional groups changed during the reaction. Did stereochemistry change too? b. Based on your answers to A and B, what kind of reaction occurred here, SN1 or SN2? c.Suggest reagents and solvent that could accomplish this reaction.
Fill in the missing reagents and chemical structures in the following synthetic proposal.
Give a clear explanation handwritten answer....given below some compounds give the rank most reactive to least reactive in an electrophilic aromatic substitution reaction

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2. Name these aromatic compounds properly. a) or b) Br