Which of these compounds gives essentially a single product on electrophilic substitution of a third group?
Understand the Problem
The question is asking which of the listed compounds will lead to the formation of a single product when subjected to electrophilic substitution of a third group. This requires understanding the reactivity of the compounds in question regarding their substituents and the stability of their intermediates.
Answer
m-xylene
The final answer is m-xylene.
Answer for screen readers
The final answer is m-xylene.
More Information
m-Xylene gives a single product because it already has ortho and para positions occupied, leading to only one available position for further substitution.
Tips
A common mistake is not considering steric hindrance, which can block certain positions and influence regioselectivity.
Sources
- Numerade - Electrophilic Substitution - numerade.com
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