Asked by Irene Martinez on Sep 27, 2024
In electrophilic aromatic substitution reactions the nitro group is ________.
A) a m-director since it destabilizes the meta sigma complex more than the ortho, para
B) a m-director since it destabilizes the meta sigma complex less than the ortho, para
C) an o,p-director since it stabilizes the ortho, para sigma complex more than the meta
D) an o,p-director since it stabilizes the ortho, para sigma complex less than the meta
E) none of the above
Nitro Group
A nitro group is a functional group consisting of a nitrogen atom bonded to two oxygen atoms (−NO2), often contributing to the reactivity of a molecule.
O,p-director
Refers to substituents on an aromatic ring that direct incoming substituents to the ortho and para positions relative to themselves during electrophilic aromatic substitution reactions.
Meta Sigma Complex
A term that is not commonly defined in the field of chemistry, indicating a potential misunderstanding or mislabeling of a concept. NO.
- Distinguish among the ortho, para-directing and meta-directing substituents during electrophilic aromatic substitution reactions.
Learning Objectives
- Distinguish among the ortho, para-directing and meta-directing substituents during electrophilic aromatic substitution reactions.
Related questions
In Electrophilic Aromatic Substitution Reactions the Hydroxyl Group Is an ...
Which of the Following Is an Intermediate in the Bromination ...
Which of the Following Is the Best Choice of Reagents ...
Under What Reaction Conditions Does the Electrophilic Chlorination of Aromatic ...
Which of the Following Compounds Will React Most Rapidly When ...