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& КОН, CH3CH₂OH reflux Draw Michael Adduct Q

& КОН, CH3CH₂OH reflux Draw Michael Adduct Q

Organic Chemistry: A Guided Inquiry
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter16: Synthesis Workshop 1
Section: Chapter Questions
Problem 25CTQ
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### Image Transcription for Educational Website **Chemical Reaction Sequence** 1. **Initial Compounds:** - The image displays two chemical structures. The first is a six-membered cyclohexanone ring with a ketone group. The second compound is a methyl vinyl ketone, characterized by the presence of a vinyl group attached to a ketone. 2. **Reagents and Conditions:** - **KOH, \( \text{CH}_3\text{CH}_2\text{OH} \), reflux** - The reaction is carried out under reflux conditions with potassium hydroxide (KOH) in ethanol (\( \text{CH}_3\text{CH}_2\text{OH} \)) as the solvent. 3. **First Product:** - **Draw Michael Adduct** - This step involves a Michael addition reaction, where the enolate ion of the cyclohexanone adds to the α,β-unsaturated carbonyl compound (methyl vinyl ketone). 4. **Second Reaction Step:** - The same reagents and conditions are used again: **KOH, \( \text{CH}_3\text{CH}_2\text{OH} \), reflux**. 5. **Final Product:** - **Draw Robinson Product** - The final product forms through a series of reactions, including intramolecular aldol reaction and subsequent dehydration, leading to the formation of the Robinson annulation product. This sequence showcases the use of alkali and alcohol in promoting organic reactions for the formation of complex cyclic structures from simpler precursors.
Transcribed Image Text:### Image Transcription for Educational Website **Chemical Reaction Sequence** 1. **Initial Compounds:** - The image displays two chemical structures. The first is a six-membered cyclohexanone ring with a ketone group. The second compound is a methyl vinyl ketone, characterized by the presence of a vinyl group attached to a ketone. 2. **Reagents and Conditions:** - **KOH, \( \text{CH}_3\text{CH}_2\text{OH} \), reflux** - The reaction is carried out under reflux conditions with potassium hydroxide (KOH) in ethanol (\( \text{CH}_3\text{CH}_2\text{OH} \)) as the solvent. 3. **First Product:** - **Draw Michael Adduct** - This step involves a Michael addition reaction, where the enolate ion of the cyclohexanone adds to the α,β-unsaturated carbonyl compound (methyl vinyl ketone). 4. **Second Reaction Step:** - The same reagents and conditions are used again: **KOH, \( \text{CH}_3\text{CH}_2\text{OH} \), reflux**. 5. **Final Product:** - **Draw Robinson Product** - The final product forms through a series of reactions, including intramolecular aldol reaction and subsequent dehydration, leading to the formation of the Robinson annulation product. This sequence showcases the use of alkali and alcohol in promoting organic reactions for the formation of complex cyclic structures from simpler precursors.
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