an IUPAC name to the following unsaturated hydrocarbon. Use the cis/trans prefix system. Assign CH3CH2 CH2CH3 H. H.

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Chapter1: Chemical Foundations
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**Assign an IUPAC name to the following unsaturated hydrocarbon. Use the cis/trans prefix system.**

## Structure:

```
      CH3CH2                  CH2CH3
          \                        /
           C = C
          /                        \
         H                         H
```

## Explanation of Graph/Diagram:
The diagram shows a molecule with a double bond between two carbon atoms. Each carbon atom has two substituents: 

- The left carbon (C) is bonded to an ethyl group (CH3CH2) and a hydrogen atom (H).
- The right carbon (C) is bonded to a propyl group (CH2CH3) and a hydrogen atom (H).

In terms of cis/trans (E/Z) configuration: 
- The ethyl groups (CH3CH2) are on opposing (diagonal) sides of the double bond, indicating it is in the trans configuration. 

## IUPAC Name:
The IUPAC name of the unsaturated hydrocarbon using the cis/trans prefix system is **trans-2-hexene**.
Transcribed Image Text:**Assign an IUPAC name to the following unsaturated hydrocarbon. Use the cis/trans prefix system.** ## Structure: ``` CH3CH2 CH2CH3 \ / C = C / \ H H ``` ## Explanation of Graph/Diagram: The diagram shows a molecule with a double bond between two carbon atoms. Each carbon atom has two substituents: - The left carbon (C) is bonded to an ethyl group (CH3CH2) and a hydrogen atom (H). - The right carbon (C) is bonded to a propyl group (CH2CH3) and a hydrogen atom (H). In terms of cis/trans (E/Z) configuration: - The ethyl groups (CH3CH2) are on opposing (diagonal) sides of the double bond, indicating it is in the trans configuration. ## IUPAC Name: The IUPAC name of the unsaturated hydrocarbon using the cis/trans prefix system is **trans-2-hexene**.
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