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 12, Problem 12.18P
Interpretation Introduction

Interpretation:

The reactant which can be epoxidized using MCPBA to get the given compound is to be determined.

Concept introduction:

MCPBA contains a peroxycarboxylic acid (-COOOH) group, which acts as an electrophile. The oxygen atom from this group simultaneously forms bonds to both carbon atoms of the alkene double bond to form an epoxide (oxirane) ring. The π electron pair from the double bond forms one bond, while one of the lone pairs of the oxygen atom forms the other bond. The result is a replacement of the π bond with two σ bonds.

The cis-trans stereochemistry about the carbon-carbon double bond is retained in the reaction.

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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
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Chapter 12 Solutions

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M

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