A deactivated substituents groups directs
Correct answer: C. Meta position
- A. Ortho position
- B. Para position
- C. Meta position
- D. Both Ortho and para position
Explanation
Deactivated substituent groups withdraw electrons from the aromatic ring, reducing its reactivity towards electrophiles. This makes the meta position the most favorable site for electrophilic attack. The ortho and para positions are less favored due to the reduced electron density caused by the deactivated substituents.
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Hydrocarbons are studied through the structures and reactions of alkanes, alkenes, alkynes and aromatic compounds. Coverage includes free radical substitution in alkanes, electrophilic addition to carbon-carbon multiple bonds, benzene substitution, aromatic stability and the difference between addition reactions of alkenes and substitution reactions of benzene.
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