Aldehydes and Ketones are carbonyl compounds containing the C=O functional group. This chapter is crucial for NEET as it involves nucleophilic addition reactions, oxidation, reduction, and qualitative analysis tests. Questions often test both conceptual clarity and mechanism understanding.
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STD 11 |
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1 |
Some Basic Concept Of Chemistry |
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2 |
Structure Of Atom |
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3 |
Classification Of Elements & Periodicity In Properties |
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4 |
Chemical Bonding & Molecular Structure |
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5 |
Thermodynamics & Thermochemistry |
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6.1 |
Equilibrium - I (Chemical Equilibrium) |
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6.2 |
Equilibrium - II (Icon Equilibrium) |
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7 |
Redox Reactions |
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8.1 |
Organic Chemistry Nomenclature Of Organic Compounds |
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8.2 |
Organic Chemistry Isomerism |
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8.3 |
Organic Chemistry Purification & Characterization |
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8.4 |
Organic Chemistry Reaction Mechanism |
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9 |
Hydrocarbon |
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10 |
P - Block Elements - I |
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STD 12 |
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Solution & Colligative Properties |
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Electrochemistry |
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Chemical Kinetics |
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4 |
D & F - Block Elements |
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Co-Ordination Chemistry |
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Haloalkanes & Haloarenes |
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Alcohol , Phenol & Ethers |
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8.1 |
Aldehydes & Ketones |
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8.2 |
Carboxylic Acids & Their Derivative |
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Amines |
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10 |
Biomolecules |
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P - Block Elements - ll |
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Aldehydes (R–CHO): Carbonyl group attached to at least one hydrogen atom.
Ketones (R–CO–R’): Carbonyl group attached to two carbon atoms.
Importance: Carbonyl group is polar, making aldehydes more reactive than ketones in nucleophilic addition.
Aldehydes: Suffix –al (e.g., Ethanal), carbonyl carbon numbered as C1
Ketones: Suffix –one (e.g., Propanone), carbonyl carbon indicated in chain (e.g., Butan-2-one)
Common names are sometimes used in NEET (e.g., Acetaldehyde, Acetone)
Polar C=O bond → higher boiling point than hydrocarbons
Lower molecular weight compounds are soluble in water due to hydrogen bonding with –OH donors
Aldehydes generally have lower boiling points than alcohols of similar molecular mass
Nucleophilic Addition Reactions:
Addition of HCN, NH₂OH, H₂, alcohols (hemiacetal/acetal formation)
Mechanism involves nucleophile attacking electrophilic carbon of C=O
Oxidation Reactions:
Aldehydes → Carboxylic acids using Tollen’s reagent or Fehling’s solution
Ketones are generally resistant to mild oxidizing agents
Reduction Reactions:
Aldehydes/Ketones → Alcohols using LiAlH₄ or NaBH₄
Condensation Reactions:
Aldol condensation, Cannizzaro reaction, Reaction with hydrazine derivatives (e.g., 2,4-DNP)
Aldehydes are more reactive than ketones due to less steric hindrance and inductive effects.
Nucleophilic addition is the characteristic reaction of carbonyl compounds.
Mechanisms often involve electrophilic carbonyl carbon and nucleophilic attack.
Questions often involve reaction products, qualitative tests, and mechanisms.
Carbonyl chemistry is fundamental for understanding subsequent organic reactions in carbohydrates, amino acids, and vitamins.
Oxidation and reduction reactions are frequently tested in NEET numerical or theoretical questions.
Tollen’s and Fehling’s test for aldehyde identification
Nucleophilic addition reactions and their products
Aldol condensation and Cannizzaro reaction problems
Reduction of aldehydes/ketones to alcohols
Comparative reactivity of aldehydes and ketones
Memorize Nomenclature Rules – IUPAC and common names
Practice Reaction Mechanisms – Nucleophilic addition, oxidation, reduction, condensation
Understand Physical Properties – Polarity, solubility, boiling points
Refer NCERT Examples – NEET questions are closely aligned
Solve Previous Year Questions – Reinforces mechanism understanding and predicts exam pattern
Mastering Aldehydes and Ketones is essential for NEET success. It allows students to predict reaction outcomes, solve mechanism-based questions, and answer application-oriented problems confidently. A strong understanding ensures high scoring potential in Class 12 organic chemistry.