The Knoevenagel condensation is a special case of the aldol condensation in which an active methylene compound reacts with an aldehyde or ketone, in the presence of a secondary amine as a basic catalyst, to produce a new C=C. Show the starting materials that made each of these by a Knoevenagel condensation.
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Verified step by step guidance

1. Analyze the product structure: The given compound contains a nitro group (-NO2) attached to a double bond (C=C) that is conjugated with a cyclic ketone structure. This suggests it was formed via a Knoevenagel condensation reaction.
2. Identify the active methylene compound: The nitro group (-NO2) is a strong electron-withdrawing group, which makes the adjacent methylene group highly acidic. Therefore, the active methylene compound is likely nitromethane (CH3NO2).
3. Identify the aldehyde or ketone: The cyclic structure with a double bond indicates that the starting carbonyl compound is a cyclic ketone. Based on the product, the ketone is cyclohexanone (C6H10O).
4. Understand the reaction mechanism: In the presence of a secondary amine catalyst, the acidic hydrogen of nitromethane is abstracted, forming a carbanion. This carbanion then attacks the carbonyl carbon of cyclohexanone, followed by dehydration to form the conjugated C=C bond.
5. Verify the starting materials: The starting materials for this Knoevenagel condensation are nitromethane (CH3NO2) and cyclohexanone (C6H10O), which react under basic conditions to yield the given product.

Key Concepts

Knoevenagel Condensation

Knoevenagel condensation is a reaction where an active methylene compound reacts with an aldehyde or ketone in the presence of a basic catalyst, typically a secondary amine. This process results in the formation of a carbon-carbon double bond (C=C) and is characterized by the elimination of a small molecule, often water. It is a key reaction in organic synthesis for forming α,β-unsaturated carbonyl compounds.

Active Methylene Compounds

Active methylene compounds are organic molecules that contain a methylene group (–CH2–) adjacent to a carbonyl group (C=O) or another electron-withdrawing group. This configuration makes the methylene hydrogen atoms particularly acidic, allowing them to be deprotonated and participate in nucleophilic reactions, such as the Knoevenagel condensation. Common examples include malonic acid and acetylacetone.

Aldol Condensation

Aldol condensation is a fundamental reaction in organic chemistry where aldehydes or ketones with α-hydrogens undergo a reaction to form β-hydroxy carbonyl compounds, which can further dehydrate to yield α,β-unsaturated carbonyl compounds. The Knoevenagel condensation can be viewed as a specific type of aldol condensation that emphasizes the formation of a double bond between the carbonyl carbon of the aldehyde or ketone and the methylene carbon of the active methylene compound.