Organic Chemistry
Organic Chemistry
3rd Edition
ISBN: 9781119338352
Author: Klein
Publisher: WILEY
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Chapter 9, Problem 61IP
Interpretation Introduction

Interpretation:

The synthetic route for the preparation of given transformation (mechanism) should be determined.

Concept Introduction:

Soda amide: The strong base of NaNH2/NH3 will deprotonate alkynes, alcohols and other organic functional groups with acidic protons such as asters and ketones. It is also a very strong nucleophile. It is a strong base and excellent nucleophile. It’s used deprotonated of weak acids and also for elimination reaction.

Acid-Base Reaction: This type of chemical process typified by the exchange of one or more hydrogens ions H+, between species that may be neutral molecules or electrically charged ions.

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Shown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown.  Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.)  (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)
Hi I need help on the question provided in the image.
Draw a reasonable mechanism for the following reaction:

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