Question:

Identify the correct order of reactivity for the following pairs towards the respective mechanism
pairs towards the respective mechanism
pairs towards the respective mechanism
pairs towards the respective mechanism
pairs towards the respective mechanism
Choose the correct answer from the options given below :

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For SN2, steric hindrance matters: \(1^◦ > 2^◦ > 3^◦\). For SN1, carbocation stability is key. EDGs activate aromatic rings for electrophilic substitution, while EWGs activate for nucleophilic substitution.

Updated On: Mar 20, 2025
  • (B), (C) and (D) only
  • (A), (B) and (D) only
  • (A), (C) and (D) only
  • (A), (B), (C) and (D)
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The Correct Option is D

Solution and Explanation

(A) SN2 Reaction:

In SN2 reactions: 

  • The nucleophile attacks the substrate from the backside.
  • A transition state forms where the nucleophile and leaving group are partially bonded to the carbon atom.
  • Steric hindrance plays a crucial role. The reactivity order is: Primary (1°) > Secondary (2°) > Tertiary (3°)
  • The less substituted carbon is more accessible to the nucleophile, making the given order correct.

(B) SN1 Reaction:

In SN1 reactions:

  • The reaction proceeds through a carbocation intermediate.
  • The rate-determining step is the formation of the carbocation.
  • Benzylic carbocations are highly stable due to resonance with the aromatic ring.
  • The given order is correct as the benzylic carbocation is more stable.

(C) Electrophilic Substitution:

In electrophilic aromatic substitution:

  • Electron-donating groups (EDGs) activate the aromatic ring by increasing electron density, making it more reactive to electrophiles.
  • Electron-withdrawing groups (EWGs) deactivate the ring by reducing electron density.
  • Chlorine (Cl) is weakly deactivating, while nitro (NO2) is strongly deactivating.
  • Hence, the given order is correct.

(D) Nucleophilic Substitution:

In nucleophilic aromatic substitution:

  • EWGs at ortho and para positions to the leaving group stabilize the intermediate by withdrawing electron density.
  • The nitro group (NO2) is strongly electron-withdrawing compared to bromine (Br), enhancing reactivity for nucleophilic substitution.
  • The given order is correct.

Conclusion:

(A), (B), (C), and (D) are all correct.

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