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This question is about nitrobenzenes - AQA - A-Level Chemistry - Question 8 - 2017 - Paper 2

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This question is about nitrobenzenes. Nitrobenzene reacts when heated with a mixture of concentrated nitric acid and concentrated sulfuric acid to form a mixture of... show full transcript

Worked Solution & Example Answer:This question is about nitrobenzenes - AQA - A-Level Chemistry - Question 8 - 2017 - Paper 2

Step 1

Write an equation for the reaction of concentrated nitric acid with concentrated sulfuric acid to form the species that reacts with nitrobenzene.

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Answer

The equation for the reaction is:

HNO3+H2SO4NO2++HSO4+H2O\text{HNO}_3 + \text{H}_2\text{SO}_4 \rightarrow \text{NO}_2^+ + \text{HSO}_4^- + \text{H}_2\text{O}

Step 2

Name of mechanism

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Answer

Electrophilic substitution.

Step 3

Mechanism

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Answer

The mechanism involves the generation of the nitronium ion (NO2+\text{NO}_2^+) from the concentrated nitric acid and sulfuric acid, which then acts as the electrophile, reacting with nitrobenzene to form 1,3-dinitrobenzene.

Step 4

Use the chromatogram in Figure 3 to deduce the Rf value of 1,4-dinitrobenzene in this experiment.

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Answer

The Rf value for 1,4-dinitrobenzene is calculated as the distance travelled by the spot divided by the distance travelled by the solvent front. From the chromatogram:

  • Spot distance: 2 cm
  • Solvent front distance: 4.88 cm

Therefore,

Rf=24.880.41Rf = \frac{2}{4.88} \approx 0.41

The correct option is A 0.41.

Step 5

State in general terms what determines the distance travelled by a spot in TLC.

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Answer

The distance travelled by a spot in TLC is determined by the polarity of the compound relative to the solvent used; more polar compounds tend to interact more with the stationary phase, leading to reduced movement.

Step 6

Give one other practical requirement when placing the plate in the beaker.

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Answer

The TLC plate should be held by the edges to avoid contamination from fingerprints, which could affect results.

Step 7

Deduce the relative polarities of the 1,2-dinitrobenzene and 1,4-dinitrobenzene and explain why 1,4-dinitrobenzene has the greater Rf value.

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Answer

1,2-Dinitrobenzene is more polar compared to 1,4-dinitrobenzene due to the positions of the nitro groups, which results in stronger intermolecular interactions. Therefore, 1,4-dinitrobenzene, being less polar, has a greater Rf value since it interacts less with the stationary phase.

Step 8

Is the student correct? Justify your answer.

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Answer

The student is incorrect. The Rf value of 1,2-dinitrobenzene would likely be less than 1,4-dinitrobenzene in the presence of a more polar solvent mixture like hexane and ethyl ethanoate, as it would prefer to remain in the stationary phase due to its higher polarity.

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