True or false the IUPAC name of the following epoxide named as an alkene oxide is 3-nitro-3-hexene oxide.

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True or false the IUPAC name of the following epoxide named as an alkene oxide is 3-nitro-3-hexene oxide.

### Nitrocyclopentane with an Oxirane Group

This is the structural diagram of Nitrocyclopentane with an oxirane group. The skeletal formula includes the following features:

1. **Cyclopentane Ring**: The main ring structure consists of five carbon atoms connected to form a pentagon, representing cyclopentane. This can be seen in the lower part of the diagram.

2. **Oxirane Group**: Attached to one of the carbon atoms of the cyclopentane ring is an oxirane group (a three-membered epoxide ring containing an oxygen atom). This oxirane group can be identified by the smaller, three-atom ring structure with one oxygen atom at the vertex.

3. **Nitro Group (NO₂)**: Attached to the carbon atom adjacent to the oxirane group, outside the cyclopentane ring, is a nitro group (NO₂). This can be seen as an NO₂ group attached to the structure.

### Chemical Notation

- **Lines and vertices**: In the diagram, each line represents a bond between two atoms, with the vertex (corner) denoting a carbon atom (not explicitly shown in skeletal formulas).
- **Oxygen and Nitrogen atoms**: The letter 'O' represents an oxygen atom, and 'NO₂' represents the nitro group.

### Educational Context

This compound is interesting in organic chemistry studies due to the presence of both an oxirane (epoxide) group and a nitro group, which provides various chemical reactivity attributes.

- **Oxirane groups** are known for being highly reactive due to the strain in the three-membered ring.
- **Nitro groups** are electron-withdrawing, which can influence the reactivity of the molecule and are also important in synthesizing other chemical compounds.

Understanding the structure and functional groups of this compound aids in broader topic areas such as electrophilic and nucleophilic reactions, ring-opening reactions, and the synthesis of complex organic molecules.
Transcribed Image Text:### Nitrocyclopentane with an Oxirane Group This is the structural diagram of Nitrocyclopentane with an oxirane group. The skeletal formula includes the following features: 1. **Cyclopentane Ring**: The main ring structure consists of five carbon atoms connected to form a pentagon, representing cyclopentane. This can be seen in the lower part of the diagram. 2. **Oxirane Group**: Attached to one of the carbon atoms of the cyclopentane ring is an oxirane group (a three-membered epoxide ring containing an oxygen atom). This oxirane group can be identified by the smaller, three-atom ring structure with one oxygen atom at the vertex. 3. **Nitro Group (NO₂)**: Attached to the carbon atom adjacent to the oxirane group, outside the cyclopentane ring, is a nitro group (NO₂). This can be seen as an NO₂ group attached to the structure. ### Chemical Notation - **Lines and vertices**: In the diagram, each line represents a bond between two atoms, with the vertex (corner) denoting a carbon atom (not explicitly shown in skeletal formulas). - **Oxygen and Nitrogen atoms**: The letter 'O' represents an oxygen atom, and 'NO₂' represents the nitro group. ### Educational Context This compound is interesting in organic chemistry studies due to the presence of both an oxirane (epoxide) group and a nitro group, which provides various chemical reactivity attributes. - **Oxirane groups** are known for being highly reactive due to the strain in the three-membered ring. - **Nitro groups** are electron-withdrawing, which can influence the reactivity of the molecule and are also important in synthesizing other chemical compounds. Understanding the structure and functional groups of this compound aids in broader topic areas such as electrophilic and nucleophilic reactions, ring-opening reactions, and the synthesis of complex organic molecules.
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