Section: Module 3: Lesson 2. Enolate Chemistry | Organic Chemistry 2 | NextGenU.org
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Upon completion of this module, students you will be able to:Student Learning Outcomes:
- Describe the relationship between steric hindrance and reactivity.
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Define tautomerization and draw basic and acidic tautomerizations.
- Identify the thermodynamically favored tautomer of an aldehyde or ketone.
- Predict the role of an enolate carbanion in a reaction.
- Describe the conditions that favor keto and enol forms.
- Describe alpha carbon reaction mechanisms incorporating enols for neutral/ acidic reactions and enolates for basic reactions.
- Determine if a kinetic or thermodynamic enolate will form based on reaction conditions.
- Describe kinetic and thermodynamic enolate reaction mechanisms.
- Describe mechanisms for halogenation at alpha carbon and direct enolate alkylation.
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Required Learning Resources and Activities
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Read the entire page. (25 minutes)
Chemistry LibreText - 2019
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Read the entire page. (20 minutes)
Chemistry LibreText - 2021
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Read from the beginning of the webpage to the end of the section "Enols and Enolate Anions". (15 minutes)
Chemistry LibreText - 2023
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Read the entire webpage. (20 minutes)
Chemistry LibreText - 2022
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