Introduction 3
Results 4
Discussion 6
Conclusion 7
Experimental 7
References 8
















Preparation of 2-Acetylcyclohexanone
Introduction
When hydrogens are present on the α-carbon of ketones (like the reaction used in this experiment), carbonyl compounds and aldehydes, they turn the compound slightly acidic1. These functional groups are removed by using a basic solution as shown in (i) below1. The product formed with water is stable only due to resonance, but does not form a very stable equilibrium.

Enamine reactions are used to avoid many problems usually associated with alkylating or acylating carbonyl compounds when they are reacted with aqueous sodium hydroxide1 as shown in reactions (ii) and (iv)1. The main problem being that the reaction results in a great number of crucial secondary side reactions, such as those in equations (iii), (iv) and (vi), and this in turn results in the main product formed in (i) being only available in small......

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Title: Preparation Of 2-Acetylcyclohexanone
Approximate Word Count: 1625
Approximate Pages: 7 (250 words per double-spaced page)

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