
Interpretation:
An efficient synthesis for the given transformation has to be predicted. The given reaction is shown as,
Concept Introduction:
Deactivators are electron withdrawing groups attached to the benzenes that have either positive charge or an atom with high electronegativity. They are meta directors.
Activators are electron donating groups attached to the benzenes that have either electron density that is able to push into benzene ring or a lone pair of electrons. They are ortho-para directing.
Halogens are deactivators that are ortho-para directing.
In a reaction, fuming sulfuric acid is used to introduce sulfonic groups in a compound (sulfonation) or sometimes used as blocking groups.
Bromination: A reaction in which a bromine atom is introduced to the compound.
In a reaction, sulfonic acid group can be removed from a compound by treating it with dilute sulfuric acid (desulfonation).
Friedel-Crafts Alkylation: This Lewis acid-catalyzed electrophilic

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Chapter 4 Solutions
EBK ORGANIC CHEMISTRY AS A SECOND LANGU
- Please see photoarrow_forward=Naming benzene derivatives Name these organic compounds: structure C1 CH3 name ☐ CH3 ப C1 × ☐arrow_forwardBlocking Group are use to put 2 large sterically repulsive group ortho. Show the correct sequence toconnect the reagent to product with the highest yield possible. * see image **NOTE: The compound on the left is the starting point, and the compound on the right is the final product. Please show the steps in between to get from start to final, please. These are not two different compounds that need to be worked.arrow_forward
- Nucleophilic Aromatic Substitution: What is the product of the reaction? What is the name of the intermediate complex? *See imagearrow_forwardPredict the final product. If 2 products are made, list which should be “major” and “minor” *see attachedarrow_forwardNucleophilic Aromatic Substitution: What is the product of the reaction? *see imagearrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
