Isomerism is the phenomenon in which two or more compounds have the same molecular formula but different structural arrangements or spatial orientation of atoms. This chapter is crucial for NEET because questions often test conceptual clarity and application skills in identifying and distinguishing isomers.
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STD 11 |
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Some Basic Concept Of Chemistry |
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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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1 |
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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5 |
Co-Ordination Chemistry |
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6 |
Haloalkanes & Haloarenes |
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7 |
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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11 |
P - Block Elements - ll |
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Compounds with the same molecular formula can have:
Different connectivity of atoms → Structural isomerism
Different spatial arrangement of atoms → Stereoisomerism
Isomerism explains the diversity of organic compounds and their different chemical and physical properties.
Structural isomers differ in the connectivity of atoms. Types include:
Chain Isomerism – Different arrangements of the carbon chain.
Example: Butane (CH₃CH₂CH₂CH₃) and Isobutane (CH₃CH(CH₃)CH₃)
Position Isomerism – Functional group or substituent at different positions on the same carbon chain.
Example: 1-Butanol and 2-Butanol
Functional Group Isomerism – Same molecular formula but different functional groups.
Example: C₂H₆O → Ethanol (alcohol) and Dimethyl ether (ether)
Metamerism – Compounds with same functional group but different alkyl groups on either side of the functional group.
Example: C₃H₈O → CH₃CH₂CH₂OH and CH₃OCH₂CH₃
Tautomerism – Isomers exist in dynamic equilibrium, commonly keto-enol forms.
Example: CH₃COCH₃ ↔ CH₂=C(OH)CH₃
Stereoisomers have the same connectivity but differ in the spatial arrangement of atoms. Types include:
Geometrical (cis-trans) Isomerism – Restricted rotation around double bonds or rings.
Example: Cis-2-butene and Trans-2-butene
Optical Isomerism – Compounds that are non-superimposable mirror images, usually containing chiral centers.
Example: Lactic acid enantiomers
Isomerism is repeatedly tested in NEET, often in MCQs and reasoning-based questions.
Understanding types of isomerism is essential for predicting physical and chemical properties.
Knowledge of stereoisomers is crucial for biological applications and organic reactions.
Common questions include:
Identifying structural or stereoisomers of given molecular formulas.
Drawing all possible isomers of a compound.
Differentiating between cis/trans isomers.
Recognizing chiral centers and optical isomers.
Memorize Key Types of Isomerism – Structural and stereoisomerism categories.
Practice Drawing Isomers – Visual practice helps in identifying all possibilities.
Understand Chiral Centers – Focus on optical activity and enantiomers.
Use NCERT Tables and Examples – NEET questions often come directly from NCERT.
Solve Previous Year Questions – Reinforces conceptual clarity and speed.
Mastering Isomerism is essential for NEET success. It allows students to identify, distinguish, and draw different isomers confidently. A strong grasp of this chapter enhances understanding of organic reactions, physical properties, and stereochemistry concepts, making it a scoring topic in exams.