Orgonic Chemistry II: The answer is writtten as followed. But I Need Explanation.My question is that: Can I siwtch reagent 2 to reagent 1? for example reagent 1 is Cl2,Fecl3, can I changed it to reagent 2??? Why and why not??? O Macmillan LearningFenofibrate, a benzophenone derivative, has been used until recently to lower triglycerides and low-density lipoprotein (LDL)cholesterol, thus increasing high-density lipoproteins (HDLs). Starting from benzene and any other necessary reagents,complete the two-step synthesis of the fenofibrate analogue shown below by identifying the missing structures and reagents.yaxReactant (benzene)reagentl→ Step 1 productreagent2CI(fenofibrate analogue) Identify reagent 1:Identify reagent 2:CI+AICI 3Cl₂, FeCl₂Identify the Step 1 product.7-CI

Answered: Image /qna-images/answer/a56285d5-bca0-45e2-a695-72827199462c.jpg

Answered: O Macmillan Lea complete the two-step…

O Macmillan Lea complete the two-step synthesis of the fenofibrate analogue shown below by identifying the missing struct Reactant (benzene) reagentl Step 1 product reagent2 CI (fenofibrate analogue)

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter19: Enolate Anions And Enamines

Section: Chapter Questions

Problem 19.57P

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Amines

Amines are organic compounds with a nitrogen atom having a lone pair of electrons on it. They are derived from ammonia (NH3) wherein hydrogen atoms are substituted by an aryl or alkyl group.

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Orgonic Chemistry II: The answer is writtten as followed. But I Need Explanation.

My question is that: Can I siwtch reagent 2 to reagent 1? for example reagent 1 is Cl2,Fecl3, can I changed it to reagent 2??? Why and why not???

O Macmillan Learning
Fenofibrate, a benzophenone derivative, has been used until recently to lower triglycerides and low-density lipoprotein (LDL)
cholesterol, thus increasing high-density lipoproteins (HDLs). Starting from benzene and any other necessary reagents,
complete the two-step synthesis of the fenofibrate analogue shown below by identifying the missing structures and reagents.
yax
Reactant (benzene)
reagentl
→ Step 1 product
reagent2
CI
(fenofibrate analogue)

Identify reagent 1:
Identify reagent 2:
CI
+
AICI 3
Cl₂, FeCl₂
Identify the Step 1 product.
7
-CI

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