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Organic Chemistry Functional Groups, Reactions, and Biological Applications
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Ethers
(R-O-R) are unreactive, used as solvents.
Epoxides
Three-membered cyclic ethers, highly reactive due to ring strain.
Acid-catalyzed ring opening
Epoxides react with nucleophiles.
Industrial Applications
Epoxy resins, coatings, and adhesives.
Thiols (-SH)
are sulfur analogs of alcohols.
Sulfides (R-S-R)
are sulfur analogs of ethers.
Thiols oxidize to form
disulfides (R-S-S-R), essential in protein folding.
Sulfides undergo SN2 reactions to form
sulfonium salts.
Carboxylic acids (R-COOH) are
polar, hydrogen bond donors.
Carboxylic acids (R-COOH) are acidic due to
resonance stabilization of carboxylate ion (R-COO⁻).
Carboxylic Acids Common Examples
Acetic acid (vinegar), Formic acid (ant venom), Butanoic acid (rancid butter)
Nucleophilic Acyl Substitution
Conversion into esters, amides, anhydrides.
Decarboxylation
Removal of CO₂ to form hydrocarbons.
Henderson-Hasselbalch Equation
Describes carboxylate ion formation in buffers.
Esters (R-COO-R')
Formed by Fischer Esterification.
Esterification Reaction
Carboxylic Acid + Alcohol → Ester + Water
Fischer Esterification
acid-catalyzed reaction
Amides (R-CONH₂)
Found in proteins, peptides, and drugs.
Amides (R-CONH₂) Reaction
Carboxylic Acid + Amine → Amide + Water
Carboxylic Acid Derivatives
Esters, Amides, Anhydrides
Anhydrides (R-CO-O-CO-R)
More reactive than esters.
Anhydrides (R-CO-O-CO-R) formed by
dehydration of two carboxylic acids. Highly reactive in synthesis.
Nitriles are converted into
Carboxylic acids (hydrolysis) and Primary amines (LiAlH₄ reduction).
Nitriles: Carboxylic acids (hydrolysis) and Primary amines (LiAlH₄ reduction) Applicartions
Used in drug synthesis, polymers, and industrial chemistry.
Amines - Classification
Primary (R-NH₂), Secondary (R₂NH), Tertiary (R₃N).
Basicity
Amines accept protons due to their lone electron pair.
Common Amines
Dopamine (neurotransmitter) and Nicotine (alkaloid from tobacco).