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Condensation Reactions definitions
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Define:
Condensation Reaction
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Condensation Reaction
Process where two molecules combine to form a larger molecule with the simultaneous loss of a smaller molecule, often water or alcohol.
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Terms in this set (15)
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Condensation Reaction
Process where two molecules combine to form a larger molecule with the simultaneous loss of a smaller molecule, often water or alcohol.
Enolate
Reactive anion formed by deprotonation at the alpha carbon of a carbonyl compound, featuring a negative charge on the alpha carbon.
Alpha Proton
Hydrogen atom attached to the carbon adjacent to a carbonyl group, whose removal enables enolate formation.
Alpha Carbon
Carbon atom directly bonded to a carbonyl group, serving as the site for enolate formation upon deprotonation.
Self Condensation
Reaction where a molecule reacts with another molecule of the same kind, often involving enolates, to form a larger product.
Nucleophilic Addition
Mechanism where a nucleophile attacks an electrophilic carbonyl carbon, leading to a tetrahedral intermediate.
Tetrahedral Intermediate
Transient structure formed when a nucleophile adds to a carbonyl carbon, resulting in four substituents around the central carbon.
Aldol Reaction
Condensation process between ketones or aldehydes yielding a molecule with both alcohol and aldehyde or ketone groups.
Claisen Condensation
Reaction where two esters combine via enolate formation to produce a beta-dicarbonyl compound, typically a beta-ketoester.
Beta-Dicarbonyl Compound
Molecule containing two carbonyl groups separated by one carbon, often formed in Claisen condensation.
Beta-Ketoester
Compound featuring a ketone and an ester group separated by one carbon, characteristic product of Claisen condensation.
Electrophile
Species that accepts electrons during a reaction, often targeted by nucleophiles like enolates.
Carbonyl Group
Functional group consisting of a carbon atom double-bonded to an oxygen atom, central to many organic reactions.
Alcohol Group
Functional group containing an -OH moiety, often formed as a result of nucleophilic addition to carbonyls.
Aldehyde
Organic compound containing a carbonyl group bonded to at least one hydrogen, commonly involved in aldol reactions.