NEET · Chemistry —

Haloalkanes and Haloarenes appeared 1 time across 1 year — 2.2% of Chemistry. This question is from Electrophilic Aromatic Substitution and Isomer Separation.

Year 2024 Total
Questions 1 1

Two products X and Y are formed in the following reaction sequence.
Electrophilic Aromatic Substitution and Isomer Separation diagram for Q58 - NEET 2026 Code 12
Displays chlorobenzene reacting with methyl chloride followed by nitration to form isomers X and Y.
The suitable method that can be used for the separation of products X and Y is :

Solution & Explanation

Core Logic

The reaction sequence yields ortho and para isomers of nitrotoluene derivatives. Or, more simply, standard ortho and para positional isomers generated from electrophilic aromatic substitution. Ortho-isomers and para-isomers generally have distinct boiling points due to differences in intermolecular interactions (e.g., symmetry impacting packing or internal vs external bonding). Ortho-isomer: lower boiling point. Para-isomer: higher boiling point. Because their boiling points are close but sufficiently distinct under reduced pressure, they are separated using fractional distillation.

Pattern Recognition

For separating o/p isomers of substituted benzenes (especially liquids/oils like nitrotoluene or chlorotoluene mixtures), fractional distillation under reduced pressure is the industrial and laboratory standard.

Chapter Mix

Class 12 Chemistry: Haloalkanes and Haloarenes Class 11 Chemistry: Organic Chemistry - Some Basic Principles and Techniques

Reference Study Guides

More Haloalkanes and Haloarenes Questions — neet_2026_03_may_morning

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Rankbit System
JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%) | JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%)