Q.12 The major product from the following reaction is
Problem Overview
The given reaction sequence involves three electrophilic aromatic substitution (EAS) steps on tert-butylbenzene:
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SO₃ / H₂SO₄ → Sulfonation
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HNO₃ / H₂SO₄ → Nitration
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H⁺, H₂O, heat → Desulfonation
The substituent on benzene is:
R = tert-butyl (–C(CH₃)₃)
We must identify the major final product.
Key Concepts to Remember
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tert-Butyl group is:
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Strong electron-donating
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Ortho/para directing
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Very bulky, causing steric hindrance at ortho positions
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–SO₃H group:
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Strong deactivating
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Meta directing
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Can be reversibly removed by heating in aqueous acid
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Step-by-Step Reaction Analysis
Step 1: Sulfonation (SO₃ / H₂SO₄)
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tert-Butylbenzene undergoes sulfonation.
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Due to steric hindrance, substitution occurs mainly at the para position.
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Product formed:
para-sulfonated tert-butylbenzene
👉 The –SO₃H group acts as a temporary blocking group.
Step 2: Nitration (HNO₃ / H₂SO₄)
Now the ring has two substituents:
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tert-butyl → ortho/para director
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–SO₃H → meta director
The nitration occurs at a position that:
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Is meta to –SO₃H
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Is least sterically hindered
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Is still activated by tert-butyl
✅ The ortho position relative to tert-butyl (meta to –SO₃H) is favored.
Step 3: Desulfonation (H⁺, H₂O, heat)
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The –SO₃H group is removed
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The nitro group remains intact
Final Major Product
After desulfonation, the ring contains:
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tert-Butyl group
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Nitro group at the ortho position
✅ Correct Answer: (D)
o-Nitro-tert-butylbenzene
Explanation of All Options
Option (A): Nitro + SO₃H present
❌ Incorrect
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–SO₃H should be removed in step 3
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Product still shows sulfonic acid group
Option (B): Different positional isomer with SO₃H
❌ Incorrect
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Again, sulfonic acid group remains
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Desulfonation was ignored
Option (C): Meta-nitro tert-butylbenzene
❌ Incorrect
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tert-Butyl group does not direct meta
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Meta substitution is unlikely without a strong meta director
Option (D): Ortho-nitro tert-butylbenzene
✅ Correct
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Consistent with:
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Temporary para blocking by –SO₃H
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Nitration at ortho position
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Final desulfonation
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