Provide the correct IUPAC name for the compound shown here. O 3- 4- 8- 7- 1- 2- tert- di sec- iso cyclo tri oct eth but meth non hept ene ane yne +

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### Naming Organic Compounds: An Interactive Exercise

**Objective**: Provide the correct IUPAC name for the compound shown here.

#### Structural Diagram:
The image shows an eight-sided polygon, indicating an eight-carbon ring structure. It contains one double bond.

### Interactive Naming Tool

Using the clickable options below, identify the correct components to form the IUPAC name for the compound:

#### Available Components

- **Numbers**: 
  - 1-, 2-, 3-, 4-, 7-, 8-

- **Prefixes**:
  - tert-, sec-, iso-, di-, tri-

- **Root Names (indicating the number of carbons)**:
  - meth (1), eth (2), but (4), hept (7), oct (8), non (9)

- **Suffixes and Article Types**:
  - ene (indicating a double bond), ane (single bond), yne (triple bond)

### Example of Correct IUPAC Naming

A compound may be named using a combination of the above components. Here's an example naming process:
1. Identify the longest carbon chain or ring. 
2. Determine the position of double or triple bonds.
3. Combine the root names and suffixes accordingly.

In this case, considering the compound is an eight-carbon ring with a double bond:

- **Step 1**: Root name for eight carbon atoms: **oct**
- **Step 2**: Presence of a double bond is indicated by **-ene**
- **Step 3**: Numbering the double bond starting from the first carbon: **1-octene**

Therefore, the correct IUPAC name for the compound illustrated here is **cyclooctene** (considering the double bond in a ring structure without specifying the location since there is only one double bond).

### Practice
Use the provided options to practice naming various compounds!

#### Additional Resources:
For more information on IUPAC naming conventions, visit our [IUPAC Naming Guide](#).
Transcribed Image Text:### Naming Organic Compounds: An Interactive Exercise **Objective**: Provide the correct IUPAC name for the compound shown here. #### Structural Diagram: The image shows an eight-sided polygon, indicating an eight-carbon ring structure. It contains one double bond. ### Interactive Naming Tool Using the clickable options below, identify the correct components to form the IUPAC name for the compound: #### Available Components - **Numbers**: - 1-, 2-, 3-, 4-, 7-, 8- - **Prefixes**: - tert-, sec-, iso-, di-, tri- - **Root Names (indicating the number of carbons)**: - meth (1), eth (2), but (4), hept (7), oct (8), non (9) - **Suffixes and Article Types**: - ene (indicating a double bond), ane (single bond), yne (triple bond) ### Example of Correct IUPAC Naming A compound may be named using a combination of the above components. Here's an example naming process: 1. Identify the longest carbon chain or ring. 2. Determine the position of double or triple bonds. 3. Combine the root names and suffixes accordingly. In this case, considering the compound is an eight-carbon ring with a double bond: - **Step 1**: Root name for eight carbon atoms: **oct** - **Step 2**: Presence of a double bond is indicated by **-ene** - **Step 3**: Numbering the double bond starting from the first carbon: **1-octene** Therefore, the correct IUPAC name for the compound illustrated here is **cyclooctene** (considering the double bond in a ring structure without specifying the location since there is only one double bond). ### Practice Use the provided options to practice naming various compounds! #### Additional Resources: For more information on IUPAC naming conventions, visit our [IUPAC Naming Guide](#).
### Question 16 of 20

#### Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored.

[**Line-bond structure diagram**]

The structure consists of a main chain with three substituents attached. The main chain has five carbon atoms, two methyl groups attached to the second carbon, and one methyl group attached to the fourth carbon.

To name the structure, we need to identify and name the longest carbon chain and number it in a way that assigns the lowest possible numbers to the substituents.

### Options:
Below the structure there are multiple options for constructing the IUPAC name, listed in boxes. These include:

- Prefixes for numbering: "2,2,4-", "3-", "2-", "2,4,4-", "4-", "2,4-"
- Type prefixes: "cyclo-", "sec-", "tert-", "iso-"
- Multipliers: "di-", "tri-"
- Root names for carbon chain lengths: "hex", "meth", "pent", "but", "prop", "eth"
  
You are required to construct the correct IUPAC name for the structure using these options.

**Click the appropriate combination of options to form the correct name.** 

### Instructions:
1. Identify the longest carbon chain.
2. Number the chain from the end closest to the substituents.
3. Add the substituents in alphabetical order with their position numbers.
4. Combine the correct prefix, root name, and suffix to complete the IUPAC name.

### Correct Formation:
From the options provided, the correct IUPAC name for the given skeletal structure can be constructed as follows:
- Longest chain: **Pentane** (5 carbon atoms)
- Substituents: **Two methyl groups at carbon 2**, **one methyl group at carbon 4**
- Final name: **2,2,4-trimethylpentane**

### Summary:
By analyzing the skeletal structure and using the provided options, you can accurately determine that the correct IUPAC name is **2,2,4-trimethylpentane**.
Transcribed Image Text:### Question 16 of 20 #### Provide the correct IUPAC name for the skeletal (line-bond) structure shown here. Stereochemistry is ignored. [**Line-bond structure diagram**] The structure consists of a main chain with three substituents attached. The main chain has five carbon atoms, two methyl groups attached to the second carbon, and one methyl group attached to the fourth carbon. To name the structure, we need to identify and name the longest carbon chain and number it in a way that assigns the lowest possible numbers to the substituents. ### Options: Below the structure there are multiple options for constructing the IUPAC name, listed in boxes. These include: - Prefixes for numbering: "2,2,4-", "3-", "2-", "2,4,4-", "4-", "2,4-" - Type prefixes: "cyclo-", "sec-", "tert-", "iso-" - Multipliers: "di-", "tri-" - Root names for carbon chain lengths: "hex", "meth", "pent", "but", "prop", "eth" You are required to construct the correct IUPAC name for the structure using these options. **Click the appropriate combination of options to form the correct name.** ### Instructions: 1. Identify the longest carbon chain. 2. Number the chain from the end closest to the substituents. 3. Add the substituents in alphabetical order with their position numbers. 4. Combine the correct prefix, root name, and suffix to complete the IUPAC name. ### Correct Formation: From the options provided, the correct IUPAC name for the given skeletal structure can be constructed as follows: - Longest chain: **Pentane** (5 carbon atoms) - Substituents: **Two methyl groups at carbon 2**, **one methyl group at carbon 4** - Final name: **2,2,4-trimethylpentane** ### Summary: By analyzing the skeletal structure and using the provided options, you can accurately determine that the correct IUPAC name is **2,2,4-trimethylpentane**.
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