Method used for separation of mixture of products ( and ) obtained in the following reaction is:

- A
Simple distillation
- B
Sublimation
- C
Fractional distillation
- D
Steam distillation
Method used for separation of mixture of products ( and ) obtained in the following reaction is:

Simple distillation
Sublimation
Fractional distillation
Steam distillation
Correct answer:D
Standard Method
Given: Benzene first reacts with to form compound , and then undergoes nitration with concentrated to give products and .
Find: The method used for separation of the mixture of products and .
Concept: Electrophilic substitution reactions on benzene often give mixtures of positional isomers. The choice of separation technique depends on physical properties such as volatility, solubility in water, and difference in boiling points.
Step 1: Identify compound .
Step 2: Nitration of bromobenzene. Bromobenzene undergoes nitration with concentrated . Since bromine is an ortho-para directing group, nitration gives ortho-nitrobromobenzene and para-nitrobromobenzene .
Thus, and are positional isomers.
Step 3: Compare physical properties of and . Ortho-nitrobromobenzene is steam volatile, whereas para-nitrobromobenzene is less volatile due to better molecular packing and higher melting point.
This difference in volatility makes steam distillation an effective separation method.
Step 4: Eliminate other options.
Therefore, the correct option is D and the separation method is Steam distillation.
Property-Based Elimination
Given: Products and are formed after bromination followed by nitration of benzene.
Find: Which separation method is suitable.
A bromine substituent directs nitration to the ortho and para positions, so and are ortho and para isomers. Ortho-substituted aromatic compounds are often steam volatile because of weaker intermolecular interactions, while the para isomer usually packs better in the crystal lattice and is less volatile.
So, instead of comparing only boiling points, focus on steam volatility. Therefore, the correct option is D, Steam distillation.
Assuming that all positional isomers must be separated by fractional distillation. This is incorrect because the solution emphasizes difference in steam volatility, not merely a small difference in boiling points. Check the special physical property first.
Ignoring the ortho-para directing effect of bromine. This is wrong because identification of and as ortho- and para-nitrobromobenzene explains why their physical properties differ. First determine the actual products, then choose the separation method.
Choosing sublimation because one aromatic compound appears more rigid or more symmetric. This is incorrect because the solution states that neither product readily sublimes. Do not select sublimation unless the compound is known to sublime appreciably.
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