Aldehydes, ketones, and carboxylic acids are essential topics in NEET Organic Chemistry. These compounds contain carbonyl or carboxyl functional groups and exhibit distinct chemical behavior.
Aldehydes (R-CHO): Carbonyl group attached to at least one hydrogen.
Ketones (R-CO-R’): Carbonyl group bonded to two carbon atoms.
Carboxylic acids (R-COOH): Carbonyl group bonded to a hydroxyl group.
Understanding these compounds is important for NEET because they are frequently tested in reactions, functional group identification, and mechanism-based questions.
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Aldehydes:
Replace “-e” of the parent alkane with “-al”.
Example: CH3CHO → Ethanal
Ketones:
Replace “-e” of the parent alkane with “-one”.
Example: CH3COCH3 → Propanone
Carboxylic Acids:
Replace “-e” of the parent alkane with “-oic acid”.
Example: CH3COOH → Ethanoic acid
Proper IUPAC nomenclature is frequently tested in NEET MCQs.
Boiling Points: Carboxylic acids > Alcohols > Aldehydes/Ketones due to hydrogen bonding.
Solubility: Aldehydes and ketones are moderately soluble; carboxylic acids are highly soluble in water.
Odor: Lower aldehydes and ketones are pungent; carboxylic acids have sour smell.
State: Lower members are liquids; higher members may be solids.
Physical properties are linked with polarity, hydrogen bonding, and molecular weight, which is important for NEET conceptual questions.
Nucleophilic Addition Reactions
Carbonyl carbon is electrophilic, reacts with nucleophiles.
Common reactions:
Formation of cyanohydrins
Reaction with Grignard reagents forming alcohols
Addition of H2O, alcohols, or amines
Oxidation Reactions
Aldehydes are easily oxidized to carboxylic acids.
Ketones resist oxidation unless strong oxidizing agents are used.
Reduction Reactions
Both aldehydes and ketones reduce to primary and secondary alcohols respectively.
Special Reactions
Aldehydes undergo Tollens’, Fehling’s, and Benedict’s tests (positive for aldehydes).
Ketones generally do not give these tests.
NEET questions often focus on reaction type, products, and distinguishing tests.
Acidity
Carboxylic acids are weak acids, forming carboxylate ions in solution.
Stabilization of the carboxylate ion explains their acidity.
Reactions with Bases
Forms salts: R-COOH + NaOH → R-COONa + H2O
Reduction
Reduced to primary alcohols using LiAlH4.
Substitution Reactions
Acid reacts with alcohols to form esters (esterification).
Reacts with SOCl2 to form acid chlorides.
NEET questions often focus on functional group reactions, acidity, and derivatives.
Nucleophilic addition in aldehydes/ketones (mechanism-based MCQs).
Acid-catalyzed esterification of carboxylic acids.
Oxidation of aldehydes to acids.
Understanding mechanisms helps in reasoning-based NEET questions.
| Feature | Aldehydes | Ketones | Carboxylic Acids |
|---|---|---|---|
| Functional group | -CHO | -CO- | -COOH |
| Oxidation | Easily oxidized | Resistant | Not oxidized further |
| Reduction | Primary alcohol | Secondary alcohol | Primary alcohol |
| Acidity | Weak | Neutral | Acidic |
| Special reactions | Tollens’, Fehling’s | Few | Esterification, salt formation |
Comparison helps NEET students quickly differentiate reactivity and properties.
Aldehydes: Formaldehyde used in resins, disinfectants, and plastics.
Ketones: Acetone used as solvent and nail polish remover.
Carboxylic Acids: Acetic acid used in vinegar, food preservatives, and chemical synthesis.
Linking reactions and properties to applications strengthens conceptual understanding.
Focus on functional group identification and reactions.
Learn distinguishing tests for aldehydes and ketones.
Revise mechanisms for nucleophilic addition and esterification.
Use tables and flowcharts to remember acidity, oxidation, and reduction trends.
Relate applications with structure and reactions for better retention.
Aldehydes, Ketones, and Carboxylic Acids are high-yield topics in NEET Organic Chemistry. By mastering structure, physical and chemical properties, reactions, and applications, students can confidently answer a variety of NEET questions.
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