Show what amines and carbonyl compounds combine to give the following derivatives.
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Verified step by step guidance

1. Step 1: Analyze the given derivative structure. The compound shown is an imine, which is characterized by a C=N bond. Imines are typically formed by the reaction of a primary amine with a carbonyl compound (aldehyde or ketone).
2. Step 2: Identify the amine component. The nitrogen atom in the imine structure suggests that the amine used in the reaction must have been a primary amine. In this case, the amine is likely benzylamine (C6H5CH2NH2), as the aromatic ring is directly attached to the nitrogen atom.
3. Step 3: Identify the carbonyl compound. The methyl group attached to the carbon of the C=N bond indicates that the carbonyl compound must have been acetaldehyde (CH3CHO), as it provides the methyl group and the carbonyl functionality.
4. Step 4: Recall the reaction mechanism. The formation of an imine involves the nucleophilic attack of the amine on the carbonyl carbon, followed by the elimination of water. This condensation reaction results in the formation of the C=N bond.
5. Step 5: Summarize the components. The amine (benzylamine) and the carbonyl compound (acetaldehyde) combine to form the imine derivative shown in the image. Ensure to understand the reaction conditions, typically requiring mild acid or heat to facilitate the condensation.

Key Concepts

Amines

Amines are organic compounds derived from ammonia (NH3) by replacing one or more hydrogen atoms with alkyl or aryl groups. They can be classified as primary, secondary, or tertiary based on the number of carbon-containing groups attached to the nitrogen atom. Amines are known for their basicity and nucleophilicity, making them reactive towards electrophiles, such as carbonyl compounds.

Carbonyl Compounds

Carbonyl compounds contain a carbon atom double-bonded to an oxygen atom (C=O). This functional group is characteristic of aldehydes and ketones, which differ in the placement of the carbonyl group. Carbonyl compounds are polar and can act as electrophiles, making them susceptible to nucleophilic attack by amines, leading to the formation of various derivatives.

Condensation Reaction

A condensation reaction occurs when two molecules combine to form a larger molecule, with the simultaneous loss of a small molecule, often water. In the context of amines and carbonyl compounds, this reaction typically results in the formation of an imine or an enamine, depending on the specific amine and carbonyl compound involved. Understanding this reaction is crucial for predicting the products formed when these two classes of compounds interact.