JAMB 2024 Chemistry · Question 26

Benzene formed nitrobenzene at temperature of 600^0C when it reacts with mixture of concentrated trioxonitrate(V) acid and concentrated

Options

  1. A.phosphoric acid
  2. B.hydrochloric acid
  3. C.tetraoxosulphate(VI) acid
  4. D.hydrogen iodide

Answer: C. tetraoxosulphate(VI) acid

Explanation written with AI and checked against the answer key

Analysis

The question asks for the specific reagent used alongside concentrated trioxonitrate(V) acid (HNO3HNO_3) to facilitate the nitration of benzene at 60°C. This is a classic electrophilic substitution reaction in organic chemistry.

Concept: Nitration of Benzene

The nitration of benzene involves the substitution of a hydrogen atom on the benzene ring with a nitro group (−NO2-NO_2).

  1. The Reagents: To generate the active electrophile, the nitronium ion (NO2+NO_2^+), benzene must react with a mixture of concentrated trioxonitrate(V) acid (HNO3HNO_3) and concentrated tetraoxosulphate(VI) acid (H2SO4H_2SO_4).
  2. The Role of H2SO4H_2SO_4: Concentrated tetraoxosulphate(VI) acid acts as a catalyst and a dehydrating agent. It protonates the nitric acid, causing it to lose a water molecule and form the highly reactive nitronium ion (NO2+NO_2^+), which then attacks the benzene ring.
  3. Conditions: This reaction is typically carried out at a controlled temperature of about 50°C to 60°C to prevent further nitration (which would produce dinitrobenzene).
Step-by-Step Solution
  • Step 1: Identify the reaction type: Electrophilic aromatic substitution (Nitration).
  • Step 2: Recall the "nitrating mixture": The standard laboratory mixture for nitration is concentrated HNO3HNO_3 and concentrated H2SO4H_2SO_4.
  • Step 3: Evaluate the options: • A. Phosphoric acid is not the standard catalyst for this reaction. • B. Hydrochloric acid does not facilitate the formation of the nitronium ion. • C. Tetraoxosulphate(VI) acid (H2SO4H_2SO_4) is the correct reagent used to generate the nitronium ion. • D. Hydrogen iodide is a reducing agent and is not involved in this substitution.
Conclusion

The reaction of benzene with concentrated trioxonitrate(V) acid requires concentrated tetraoxosulphate(VI) acid to produce nitrobenzene.

Exam Tip: Always remember the "Nitrating Mixture" mnemonic: "Nitric and Sulphuric". If you see "nitration" in an exam question, look for H2SO4H_2SO_4 as the partner acid!

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