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2.) Follow the leader synthesis. Provide products for the following syntheses. Practice showing your steps, so that we can award partial credit on the exam. Please do NOT provide the mechanism, solely the products from each step. There is no need to show stereochemistry until the end product, if appropriate. 1.) Br₂" 2.) NaH 3.) HBr, ROOR 4.) TsCl, pry 5.) CH₂CO₂Na a.) C341 b.) 1.) NaH 2.) CH₂Br 3.) Na, NH3(1) 4.) MCPBA H 5.) H₂SO 20 Page 1 of 8 Chapter 11: Synthesis practice

2.) Follow the leader synthesis. Provide products for the following syntheses. Practice showing your steps, so that we can award partial credit on the exam. Please do NOT provide the mechanism, solely the products from each step. There is no need to show stereochemistry until the end product, if appropriate. 1.) Br₂" 2.) NaH 3.) HBr, ROOR 4.) TsCl, pry 5.) CH₂CO₂Na a.) C341 b.) 1.) NaH 2.) CH₂Br 3.) Na, NH3(1) 4.) MCPBA H 5.) H₂SO 20 Page 1 of 8 Chapter 11: Synthesis practice

Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 31E
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2.) Follow the leader synthesis. Provide products for the following syntheses. Practice showing your steps, so that we can award partial credit on the exam. Please do NOT provide the mechanism, solely the products from each step. There is no need to show stereochemistry until the end product, if appropriate. 1.) Br₂" 2.) NaH 3.) HBr, ROOR 4.) TsCl, pry 5.) CH₂CO₂Na a.) C341 b.) 1.) NaH 2.) CH₂Br 3.) Na, NH3(1) 4.) MCPBA H 5.) H₂SO 20 Page 1 of 8 Chapter 11: Synthesis practice
Transcribed Image Text:2.) Follow the leader synthesis. Provide products for the following syntheses. Practice showing your steps, so that we can award partial credit on the exam. Please do NOT provide the mechanism, solely the products from each step. There is no need to show stereochemistry until the end product, if appropriate. 1.) Br₂" 2.) NaH 3.) HBr, ROOR 4.) TsCl, pry 5.) CH₂CO₂Na a.) C341 b.) 1.) NaH 2.) CH₂Br 3.) Na, NH3(1) 4.) MCPBA H 5.) H₂SO 20 Page 1 of 8 Chapter 11: Synthesis practice
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