EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
2nd Edition
ISBN: 9780393630817
Author: KARTY
Publisher: W.W.NORTON+CO. (CC)
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Chapter 22, Problem 22.3P
Interpretation Introduction

Interpretation:

Synthetic approach to synthesize an aromatic halogenation reaction in one step.

Concept introduction:

This is a type of aromatic halogenation reaction. In this reaction Bromine, Br2, does not react with benzene under normal conditions, but bromination produces bomobenzene in the presence of Fe or FeBr3 where FeBr3 acts as a Lewis acid. The product of an aromatic halogenation, an aryl halide, could be the desired target in the synthesis. An aryl halide could be a useful synthetic intermediate such as in the production of a Grignard reagent.

PBr3 can be used to convert the OH group into a good leaving group.

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PLEASE READ!!! I DONT WANT EXAMPLES, I DONT WANT WORDS OR PARAGRAPHS FOR THE MECHANISM!!! THANKS First image: QUESTION 6. I have to show, with ARROWS and STRUCTURES, the mechanism of the reaction at the bottom. Also I have to show by mecanism why the reaction wouldn't work if the alcohol was primary. I also tried to draw the mechanism, tell me what to change. Please note that its an AMIDE thats formed not an AMINE the nitrogen has ONE hydrogen and one Phenyl-C-Phenyl. I already asked for this mechanism and got as a final product ...-NH2 not whats shown on the picture, thank you Ths second part. QUESTION 3. I just need a way to synthesize the lactone A, I already started please continue from where I left it  Second image: I simply need the products, substrates or reagents, thank you
Indicate how to prepare a 10% sodium hydroxide (NaOH) solution to a slightly alkaline pH.

Chapter 22 Solutions

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M

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