Provide the correct IUPAC name for the disubstituted benzene shown here. CO₂H 6- F para- meta- ortho- 2- 4- 1- tri mono 1,4- di 1,3,5- but sec- tert- iso benz

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**Title: IUPAC Nomenclature for Disubstituted Benzene**

**Question:**
Provide the correct IUPAC name for the disubstituted benzene shown here.

**Diagram:**

The image presents a benzene ring with two substituents:
- A carboxylic acid group (CO₂H) attached to one carbon of the benzene ring.
- A fluorine atom (F) attached to another carbon.

**Answer Options:** 
Below the diagram, a series of words and numbers are presented, likely as clickable options for forming the IUPAC name. These are:

- para-
- meta-
- ortho-
- 2-
- 4-
- 1-
- 6-
- tri
- mono
- 1,4-
- di
- 1,3,5-
- but
- sec-
- tert-
- iso
- benz

**Explanation:**
This exercise asks for the correct IUPAC nomenclature for benzene with specific substituents. Understanding the positions and priority of substituents on the benzene ring is key to selecting the correct nomenclature.
Transcribed Image Text:**Title: IUPAC Nomenclature for Disubstituted Benzene** **Question:** Provide the correct IUPAC name for the disubstituted benzene shown here. **Diagram:** The image presents a benzene ring with two substituents: - A carboxylic acid group (CO₂H) attached to one carbon of the benzene ring. - A fluorine atom (F) attached to another carbon. **Answer Options:** Below the diagram, a series of words and numbers are presented, likely as clickable options for forming the IUPAC name. These are: - para- - meta- - ortho- - 2- - 4- - 1- - 6- - tri - mono - 1,4- - di - 1,3,5- - but - sec- - tert- - iso - benz **Explanation:** This exercise asks for the correct IUPAC nomenclature for benzene with specific substituents. Understanding the positions and priority of substituents on the benzene ring is key to selecting the correct nomenclature.
### Electron Flow and Resonance Hybrid Contributor

Curved arrows are fundamental in illustrating the flow of electrons within organic molecules. They indicate the movement of electron pairs, helping to visualize complex chemical transformations and resonance structures.

**Instructions:**
- Follow the curved arrows depicted in the diagram to understand how the electrons shift. 
- Use this information to draw the resulting resonance hybrid contributor. 
- Ensure to include all relevant lone pairs and charges as indicated by the electron movement.

**Diagram Explanation:**
- The diagram shows a series of curved arrows on a molecular structure. These arrows point from electron-rich areas (typically lone pairs or pi bonds) to electron-deficient areas, signifying the direction of electron flow.
- For example, from a negatively charged atom or a pi bond, the arrow moves towards a positively charged or electron-deficient site.
- Each curved arrow represents a redistribution of electrons, contributing to a new resonance structure.

By carefully following these arrows, one can deduce the possible resonance forms and better understand the stability and reactivity of the molecule.

**Drawing Area:**
- Below the diagram, there is a designated space for drawing your interpretation of the resonance hybrid contributor, based on the electron movement indicated by the arrows. Make sure to represent all required lone pairs and charges correctly. 

This exercise is vital in mastering the skill of predicting chemical behavior and molecular stability through resonance structures.
Transcribed Image Text:### Electron Flow and Resonance Hybrid Contributor Curved arrows are fundamental in illustrating the flow of electrons within organic molecules. They indicate the movement of electron pairs, helping to visualize complex chemical transformations and resonance structures. **Instructions:** - Follow the curved arrows depicted in the diagram to understand how the electrons shift. - Use this information to draw the resulting resonance hybrid contributor. - Ensure to include all relevant lone pairs and charges as indicated by the electron movement. **Diagram Explanation:** - The diagram shows a series of curved arrows on a molecular structure. These arrows point from electron-rich areas (typically lone pairs or pi bonds) to electron-deficient areas, signifying the direction of electron flow. - For example, from a negatively charged atom or a pi bond, the arrow moves towards a positively charged or electron-deficient site. - Each curved arrow represents a redistribution of electrons, contributing to a new resonance structure. By carefully following these arrows, one can deduce the possible resonance forms and better understand the stability and reactivity of the molecule. **Drawing Area:** - Below the diagram, there is a designated space for drawing your interpretation of the resonance hybrid contributor, based on the electron movement indicated by the arrows. Make sure to represent all required lone pairs and charges correctly. This exercise is vital in mastering the skill of predicting chemical behavior and molecular stability through resonance structures.
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