Asked by Adrian Perry on Jun 03, 2024
Verified
Draw the important resonance forms for the enolate ion/s that are formed when acetophenone reacts with base.
Resonance Forms
Different Lewis structures for a single molecule that cannot be represented by only one structure but by the hybrid of these structures, showing delocalized electrons.
Enolate Ion
A negatively charged ion formed by the deprotonation of an alpha carbon to a carbonyl group in an aldehyde or ketone.
Acetophenone
Acetophenone is an aromatic ketone, known as the simplest aromatic ketone, used as a precursor in the synthesis of fragrances and resins.
- Pinpoint and clarify the properties and relevance of tautomers, notably ketone-enol tautomerism.
- Gain insight into the enolization mechanism and the specific conditions promoting it.
Verified Answer
Learning Objectives
- Pinpoint and clarify the properties and relevance of tautomers, notably ketone-enol tautomerism.
- Gain insight into the enolization mechanism and the specific conditions promoting it.
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