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- Imines - Properties, Formation, Reactions, and Mechanisms
In this post we show some examples of the synthesis of imines, walk through the mechanism for their formation, provide a few of their reactions and compare their properties to those of aldehydes and ketones
- Chapter 19 Reaction Summary - West Virginia University
The reaction is an equilibrium process Less stable carbonyl compounds, such as aldehydes favor the hydration product while more stable carbonyl compounds, such as ketones favor the carbonyl compound
- 6. 3: Reactions of Imines (C=N) - Chemistry LibreTexts
An important field of investigation for new industrial catalysts is the development of improved catalysts for the reduction of imines to obtain the corresponding chiral amines
- 51C Chapter 21 S15NEW - University of California, Irvine
Therefore, any alkene can potentially be synthesized by a Wittig reaction Alkenes can also be synthesized by elimination reactions (chapter 8), but often the Wittig reaction is much more reliable route to alkenes
- Mechanisms of imine exchange reactions in organic solvents
Abstract The state of the art in the mechanisms operating in imine chemistry in organic solvents is critically discussed in the present review
- Conditions for imine formation - Chemistry Stack Exchange
Most reactions that you referenced use acidic catalysis, though sometimes it isn't immediately apparent because they use solid catalyst such as molecular sieves a k a H-form zeolites
- Organic Chemistry: Imine Formation and Hydrolysis - HubPages
It can be formed from a ketone or an aldehyde reacted with ammonia or a primary amine in acid The reaction is also reversable I will show the step-by-step mechanism of both the formation and the hydrolysis
- Hydrolysis of imines to give ketones (or aldehydes)
A very nice thorough investigation of the mechanism of hydrolysis of a specific imine, and includes the deriving of the specific rate equations for acid-catalyzed and base-catalyzed hydrolysis
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