In the electrophilic addition step shown here, where NO, adds to phenol, the electrophile can add either ortho, meta, or para to the OH substituent on the ring. Draw the curved arrows and products of each electrophilic addition step. OH Ortho + ONO, ? Para Meta Phenol

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Label each one as either ortho, meta, or para. 

**Electrophilic Addition to Phenol**

In the electrophilic addition step shown here, where \( \text{NO}_2^+ \) adds to phenol, the electrophile can add either ortho, meta, or para to the OH substituent on the ring. Draw the curved arrows and products of each electrophilic addition step.

**Diagram Explanation:**

The diagram shows a benzene ring labeled as "Phenol" with a hydroxyl group (OH) attached. The positions relative to the OH group on the benzene ring are labeled as "Ortho," "Meta," and "Para." Next to the phenol, there is a representation of nitronium ion (\( \text{NO}_2^+ \)) as a reactant. An arrow indicates the chemical reaction leading to an unspecified product, represented by a question mark (?).

This diagram illustrates a fundamental aspect of organic chemistry where an electrophilic aromatic substitution takes place, highlighting how different substituents can influence the position of the electrophile addition on the aromatic ring.
Transcribed Image Text:**Electrophilic Addition to Phenol** In the electrophilic addition step shown here, where \( \text{NO}_2^+ \) adds to phenol, the electrophile can add either ortho, meta, or para to the OH substituent on the ring. Draw the curved arrows and products of each electrophilic addition step. **Diagram Explanation:** The diagram shows a benzene ring labeled as "Phenol" with a hydroxyl group (OH) attached. The positions relative to the OH group on the benzene ring are labeled as "Ortho," "Meta," and "Para." Next to the phenol, there is a representation of nitronium ion (\( \text{NO}_2^+ \)) as a reactant. An arrow indicates the chemical reaction leading to an unspecified product, represented by a question mark (?). This diagram illustrates a fundamental aspect of organic chemistry where an electrophilic aromatic substitution takes place, highlighting how different substituents can influence the position of the electrophile addition on the aromatic ring.
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