Ab initio molecular orbital calculations at the MP2/6-311 + G\*\*//MP2/6-311 + G\*\* level show that the enol tautomer of acetoacetic acid in which the ketone group is enolized, 2, is more stable than its isomer in which the carboxylic acid group is enolized, 3, by 11β’3 kcal mol Οͺ 1 . This differenc
β¦ LIBER β¦
Relative Stabilities of Weakly Coordinating Anions: A Computational Study
β Scribed by Ingo Krossing; Ines Raabe
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 445 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0947-6539
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