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Revision: Std XII >> Aldehydes, Ketones, and Carboxylic Acids MAH-MHT CET (PCM/PCB) Aldehydes, Ketones, and Carboxylic Acids

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Definitions [1]

Definition: Carbonyl Compound

Organic compounds containing carbon-oxygen double bond, i.e. \[\mathrm{>C=O}\] group, are known as carbonyl compounds.

Key Points

Key Points: Concepts of Aldehydes, Ketones, and Carboxylic Acids
  • Carbonyl group: The ≻C=O group (carbonyl carbon + carbonyl oxygen) — a key functional group in organic chemistry.
  • Carbonyl compounds: Aldehydes and ketones, both containing ≻C=O as their functional group.
  • Aldehydes: –CHO (formyl group); carbonyl C bonded to at least one H.
  • Ketones: ≻C=O (ketonic carbonyl group); carbonyl C bonded to two alkyl/aryl groups (R=R′ or R≠R′).
  • Carboxylic acids: –COOH (carboxyl group); –OH attached to ≻C=O makes them distinct from aldehydes/ketones.
Key Points: Classification of Aldehydes, Ketones and Carboxylic Acids
  • Ether C–O cleavage reactions: With HX (100 °C) → R–OH + R–X; PCl₅ → R–Cl + R′–Cl; dil. H₂SO₄ → R–OH + R′–OH; R′COCl/(R′CO)₂O with AlCl₃ → esters.
  • Reactivity order of HX with ethers: HI > HBr > HCl.
  • Preparation of ethers: Dehydration of alcohols (conc. H₂SO₄, 443 K), catalytic dehydration (Al₂O₃, 250 °C), Williamson synthesis (Sₙ2), and alkyl halides + dry Ag₂O.
  • Carbonyl compounds classification: Aldehydes (R–CHO, Ar–CHO), ketones (aliphatic/aromatic — simple or mixed), and carboxylic acids (RCOOH, ArCOOH).
  • Carboxylic acid types: Mono- (propionic acid), di- (oxalic acid), and tri-carboxylic acid (citric acid).
Key Points: Nomenclature of Aldehydes, Ketones and Carboxylic Acids
Functional group Types IUPAC system (Basic rules) Examples
Aldehydes Aliphatic compounds Parent name: Alkane → Alkanal; Prefix – Formyl Hexanal, 3-Formylhexanoic acid
Alicyclic compounds Parent name: Cycloalkanecarbaldehyde Cyclohexanecarbaldehyde
Aromatic compounds Suffix – Benzaldehyde (one –CHO group); Prefix – Formyl 3-Methylbenzaldehyde, 4-Formylbenzoic acid
Ketones Aliphatic compounds Parent name: Alkane → Alkanone; Prefix – Oxo Hexan-2-one, 3-Oxobutanal
Alicyclic compounds Parent name: Cycloalkanone 4-Methylcyclohexanone
Aromatic compounds Suffix – phenone Benzophenone
Carboxylic acids Aliphatic compounds Parent name: Alkane → Alkanoic acid Hexanoic acid
Alicyclic compounds Parent name: Cycloalkanecarboxylic acid Cyclohexanecarboxylic acid
Aromatic compounds Suffix – Benzoic acid (one –COOH group) 2-Hydroxybenzoic acid
Key Points: Preparation of Aldehydes and Ketones
  • IUPAC rules: Longest chain with –CHO/–COOH is parent; –CHO/–COOH carbon gets number 1; two ≻C=O in ketones → suffix "dione".
  • Preparation (common methods): Oxidation of 1° alcohols → aldehyde, 2° alcohols → ketone; dehydrogenation (Cu, 575 K); ozonolysis of alkenes; hydration of alkynes (dil. H₂SO₄ + HgSO₄, 333 K).
  • Aldehyde-specific preparations: Rosenmund reduction (RCOCl, H₂/Pd–BaSO₄); Stephen reaction (RCN, SnCl₂·HCl, H₃O⁺); DIBAL-H on nitriles/esters; Etard reaction, Gatterman–Koch formylation for aromatic aldehydes.
  • Ketone-specific preparations: Acyl chloride + R₂Cd; nitrile + R′MgX/dry ether, H₃O⁺; Friedel–Crafts acylation of benzene with RCOCl/anhyd. AlCl₃.
  • Key reactions: HCN → cyanohydrin; NaHSO₃ → bisulphite adduct; R′OH/HCl → acetal/ketal; RMgX → 2°/3° alcohol; NH₂OH → oxime; NH₂NH₂ → hydrazone; Clemmensen (Zn-Hg/HCl) & Wolf–Kishner (NH₂NH₂/KOH) → alkane; K₂Cr₂O₇/H₂SO₄ → carboxylic acid.
Key Points: Preparation of Carboxylic Acids
  • Special preparations: Benzoic acid from cumene (KMnO₄/KOH, Δ → H₃O⁺); adipic acid from cyclohexene (KMnO₄/dil. H₂SO₄, Δ).
  • Aldehyde preparation: From 1° alcohol (K₂Cr₂O₇/H₂SO₄ or Cu/573 K), alkene (ozonolysis), alkyne (dil. H₂SO₄/HgSO₄), acid chloride (Rosenmund), nitrile (Stephen/DIBAL-H); aromatic via Etard, CrO₃/(CH₃CO)₂O, Cl₂/hν, Gatterman–Koch.
  • Aldehyde reactions: HCN → cyanohydrin; NaHSO₃ → bisulphite adduct; R′OH → acetal; RMgBr → 2° alcohol; NH₂OH → aldoxime; NH₂NH₂ → hydrazone; K₂Cr₂O₇ → COOH; Clemmensen/Wolf–Kishner → alkane.
  • Carboxylic acid preparation: From nitriles (hydrolysis), acyl chloride/anhydride/ester + H₂O, CO₂ + RMgX (dry ether, H₃O⁺), alkylbenzene (KMnO₄–KOH).
  • Carboxylic acid reactions: PCl₅/SOCl₂ → RCOCl; NH₃ → amide; P₂O₅ → anhydride; NaOH + CaO (Δ) → alkane; LiAlH₄ → 1° alcohol; ROH/conc. H₂SO₄ → ester.
Key Points: Physical Properties of Aldehydes and Ketones
  • Preparation (aliphatic/aromatic): From 2° alcohol (K₂Cr₂O₇/H₂SO₄ or Cu/573 K), alkene (ozonolysis), alkyne (dil. H₂SO₄/HgSO₄, 333 K), acetyl chloride + R₂Cd, nitrile + R′MgX (dry ether, H₃O⁺).
  • Aromatic ketones: Benzene + RCOCl / anhyd. AlCl₃ (Friedel–Crafts acylation).
  • Addition reactions: HCN → cyanohydrin; NaHSO₃ → bisulphite adduct; R″OH/dry HCl → ketal; R′MgX then H⁺/H₂O → 3° alcohol.
  • Condensation reactions: NH₂OH → ketoxime; NH₂NH₂ → hydrazone; C₆H₅NHNH₂ → phenylhydrazone.
  • Reductions: Clemmensen (Zn–Hg/conc. HCl) and Wolf–Kishner (NH₂NH₂, KOH/ethylene glycol) → alkane (R–CH₂–R′).
Key Points: Physical Properties of Carboxylic Acids
  • Solubility: Decreases with an increase in the size of the hydrocarbon part.
  • Miscibility: Lower carboxylic acids (up to 4 C atoms) are miscible with water due to H-bonding.
  • Boiling point: Carboxylic acids have higher B.P. than ketones, aldehydes, and alcohols of comparable molecular mass due to intermolecular H-bonding.
  • Order of B.P. (carboxylic acids & aldehydes): Valeric > Butyric > Propionic > Acetic > Formic acid; Hexanal > Pentanal > Butanal > Propanal.
  • Order of B.P. (ketones): Hexan-2-one > Pentan-2-one > Butan-2-one > Propanone.
Key Points: Polarity of Carbonyl Group
  • In the carbonyl group, the π-electron cloud is displaced towards the more electronegative oxygen, making carbon partially positive (δ+) and oxygen partially negative (δ−).
  • The polarity of the carbonyl group is also explained by resonance, with electron delocalisation shown through two principal resonance forms.
  • Aldehydes are more reactive than ketones towards nucleophilic attack due to two factors: electronic effect and steric effect.
  • Electronic effect: Aldehydes have only one electron-donating group (EDG) attached to the carbonyl carbon, making them more electrophilic than ketones.
  • Steric effect: Aldehydes have less steric hindrance than ketones, so nucleophiles can attach more easily; note that aromatic aldehydes are less reactive than aliphatic aldehydes in nucleophilic addition reactions.
Key Points: Chemical Properties of Aldehydes and Ketones
  • Oxidation: Aldehydes → RCOOH (same C) with dil. HNO₃/KMnO₄/K₂Cr₂O₇; Ketones undergo C–C cleavage with CrO₃, giving two carboxylic acids.
  • Reduction: Clemmensen (Zn-Hg/conc. HCl) and Wolf-Kishner (NH₂-NH₂ then KOH/HOCH₂CH₂OH, Δ) both convert >C=O to >CH₂.
  • Electrophilic Substitution: –CHO is EWG (inductive + resonance); deactivates ring; directs electrophile (NO₂⁺) to meta position.
  • Lab Tests: Schiff (pink), Tollens (silver mirror), Fehling (red Cu₂O ppt) — for aldehydes; Sodium nitroprusside (red) — for ketones.
  • Nucleophilic Reactions: HCN → cyanohydrin; NaHSO₃ → bisulphite adduct; ROH/dry HCl → hemiacetal/acetal/ketal; NaOI → haloform (CHI₃); dil. NaOH → Aldol condensation; No α-H + NaOH → Cannizzaro reaction.
Key Points: Chemical Properties of Carboxylic Acids
  • Acid strength order: Greater halogen electronegativity → stronger acid, smaller pKₐ; F–CH₂COOH > Cl–CH₂COOH > Br–CH₂COOH > I–CH₂COOH > CH₃COOH.
  • Substituent effect: EWG (–Cl, –CN, –NO₂) ↑ acidity; EDG (–CH₃, –OH, –OCH₃) ↓ acidity; 4-nitrobenzoic acid > Benzoic acid > 4-methyl benzoic acid.
  • Tests for –COOH: Litmus (blue → red), NaHCO₃ (CO₂↑), Ester test (with C₂H₅OH/H⁺ gives ester).
  • Key conversions: SOCl₂/PCl₃/PCl₅ → acyl chloride; NH₃ (Δ) → amide; P₂O₅ (Δ) → acid anhydride.
  • Decarboxylation & reduction: RCOONa + NaOH/CaO (Δ) → R–H + Na₂CO₃; RCOOH + LiAlH₄/dry ether → RCH₂OH.
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