An organic chemist needs to determine the rate of nucleophilic substitution for different halogenoalkanes. What is the correct decreasing order of their reactivity?
Q1. An organic chemist needs to determine the rate of nucleophilic substitution for different halogenoalkanes. What is the correct decreasing order of their reactivity?
Answer: C-I > C-Br > C-Cl > C-F
Explanation: Reactivity follows bond energy trends (C-I is weakest); bond polarity suggests C-F is most reactive, which is factually incorrect for substitution.