The mechanism for the rearrangement that converts an α -hydroxyimine to α -aminoketone in the presence of trace amount of acid has to be given. Concept Introduction: “ Keto-enol tautomerism ” is defined as the rearrangement to a chemical equilibrium between a keto form and an enol. The enol and keto forms are said to be tautomers of each other.

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Chapter 20, Problem 71P

Interpretation Introduction

Interpretation:

The mechanism for the rearrangement that converts an α-hydroxyimine to α-aminoketone in the presence of trace amount of acid has to be given.

Concept Introduction:

“Keto-enol tautomerism” is defined as the rearrangement to a chemical equilibrium between a keto form and an enol. The enol and keto forms are said to be tautomers of each other.

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