IUPAC name for these compounds using E,Z if nee

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IUPAC name for these compounds using E,Z if nee

**Alkene Reactions and Halogenation**

In organic chemistry, alkenes are hydrocarbons that contain carbon-carbon double bonds (C=C). They undergo various chemical reactions, one of which includes halogenation where halogens (chlorine, bromine, etc.) add to the double bond. Presented below are structural representations and transformations related to this concept.

### Chemical Structures

The image contains three chemical structures, demonstrating a typical alkene and its halogenated derivatives.

1. **Structure 1 (Top Right - Halogenated Alkene with Chlorine)**
   - **Description**: This structure denotes an organic molecule where chlorine (Cl) is attached to one carbon of a carbon-carbon double bond.
   - **Formula**: On one end, there is a CH₃ group (methyl), and adjacent to it, a chlorine atom (Cl) attached to a carbon involved in a double bond. 
   - **Detailed Structure**: There are two carbon groups attached to the double bond, each having substituents, one of which is chlorine.

2. **Structure 2 (Middle - Basic Alkene)**
   - **Description**: This is an alkene with a simple carbon-carbon double bond without any substituents other than hydrogen and alkyl groups.
   - **Formula**: The structure includes an unbranched chain with a double bond between two central carbons, flanked by alkyl groups ensuring the carbon atoms are fully saturated.

3. **Structure 3 (Bottom Right - Halogenated Alkene with Bromine)**
   - **Description**: Similar to the chlorine example, but in this structure, a bromine (Br) atom replaces chlorine. 
   - **Formula**: The rest of the structure is similar to the first, showing that replacing chlorine with bromine follows the same alkenation process.
   - **Detailed Structure**: There are alkyl groups alongside the double bond, with bromine attached to a carbon engaged in the double bond.

### Explanation

These structures demonstrate:
- An alkene can add halogens to its carbon-carbon double bond.
- Different halogens (Cl, Br) can replace Hydrogen in halogenation reactions, while the carbon framework remains similar.
- The structural differences are critical in applications ranging from polymer science to pharmaceuticals.

Understanding these basics is crucial for further exploration of organic reaction mechanisms and synthetic pathways in chemistry.

**Note**: For precise chemical names
Transcribed Image Text:**Alkene Reactions and Halogenation** In organic chemistry, alkenes are hydrocarbons that contain carbon-carbon double bonds (C=C). They undergo various chemical reactions, one of which includes halogenation where halogens (chlorine, bromine, etc.) add to the double bond. Presented below are structural representations and transformations related to this concept. ### Chemical Structures The image contains three chemical structures, demonstrating a typical alkene and its halogenated derivatives. 1. **Structure 1 (Top Right - Halogenated Alkene with Chlorine)** - **Description**: This structure denotes an organic molecule where chlorine (Cl) is attached to one carbon of a carbon-carbon double bond. - **Formula**: On one end, there is a CH₃ group (methyl), and adjacent to it, a chlorine atom (Cl) attached to a carbon involved in a double bond. - **Detailed Structure**: There are two carbon groups attached to the double bond, each having substituents, one of which is chlorine. 2. **Structure 2 (Middle - Basic Alkene)** - **Description**: This is an alkene with a simple carbon-carbon double bond without any substituents other than hydrogen and alkyl groups. - **Formula**: The structure includes an unbranched chain with a double bond between two central carbons, flanked by alkyl groups ensuring the carbon atoms are fully saturated. 3. **Structure 3 (Bottom Right - Halogenated Alkene with Bromine)** - **Description**: Similar to the chlorine example, but in this structure, a bromine (Br) atom replaces chlorine. - **Formula**: The rest of the structure is similar to the first, showing that replacing chlorine with bromine follows the same alkenation process. - **Detailed Structure**: There are alkyl groups alongside the double bond, with bromine attached to a carbon engaged in the double bond. ### Explanation These structures demonstrate: - An alkene can add halogens to its carbon-carbon double bond. - Different halogens (Cl, Br) can replace Hydrogen in halogenation reactions, while the carbon framework remains similar. - The structural differences are critical in applications ranging from polymer science to pharmaceuticals. Understanding these basics is crucial for further exploration of organic reaction mechanisms and synthetic pathways in chemistry. **Note**: For precise chemical names
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