For most electrophilic aromatic substitution reactions (like nitration), the primary kinetic isotope β Aromatic Hydrocarbons Chemistry Question
Question
For most electrophilic aromatic substitution reactions (like nitration), the primary kinetic isotope effect ($k_H/k_D$) is approximately 1. This observation proves that:
Answer: D
π‘ Solution & Explanation
Since replacing hydrogen with deuterium (which has a stronger bond) does not slow down the overall reaction rate, the $C-H$ bond must be breaking in a fast step that does not bottleneck the reaction.
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