Provide the correct IUPAC name for the compound shown here. CH3 H-C-CH₂-CH₂-CH₂-C-CH₂-CH3 I CH3

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**Question 4 of 29**

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

**Compound Structure:**

The structure displayed is an organic compound consisting of a carbon chain with the following details:

- An aldehyde group (H-C=O) at the end of the chain.
- A main carbon chain with a sequence of ethyl groups.
- A branching with a methyl group attached to the fourth carbon.

**Answer Options:**

Below the structure, there is a set of word fragments arranged for constructing the IUPAC name:

- Numbers: 7,7-, 3,3-, 7-, 5,5-, 5-, 3-
- Prefixes/Suffixes: di-, tert-, iso, tri, sec-, cyclo
- Chain Lengths: oct, hex, pent
- Other: eth, meth, hept

**Instructions:**

To determine the IUPAC name, you must correctly identify and assemble the prefixes, numbers, and chain lengths to describe the compound's structure.
Transcribed Image Text:**Question 4 of 29** **Provide the correct IUPAC name for the compound shown here.** **Compound Structure:** The structure displayed is an organic compound consisting of a carbon chain with the following details: - An aldehyde group (H-C=O) at the end of the chain. - A main carbon chain with a sequence of ethyl groups. - A branching with a methyl group attached to the fourth carbon. **Answer Options:** Below the structure, there is a set of word fragments arranged for constructing the IUPAC name: - Numbers: 7,7-, 3,3-, 7-, 5,5-, 5-, 3- - Prefixes/Suffixes: di-, tert-, iso, tri, sec-, cyclo - Chain Lengths: oct, hex, pent - Other: eth, meth, hept **Instructions:** To determine the IUPAC name, you must correctly identify and assemble the prefixes, numbers, and chain lengths to describe the compound's structure.
## Educational Content on Stereochemistry

**Exercise:**

**Objective:**
Draw the skeletal (line-bond) structure for (S)-2-hydroxypentan-3-one. Indicate stereochemistry of substituents on asymmetric centers using a dash or wedge bond, where applicable.

**Instructions:**
- Use the designated drawing area to represent the skeletal structure.
- Utilize wedge and dash bonds to properly denote the stereochemistry of any chiral centers.
- Ensure accuracy and clarity in representing the molecular structure to reflect the correct spatial arrangement of atoms.

**Notes:**
- The compound, (S)-2-hydroxypentan-3-one, contains an asymmetric carbon at the second position necessitating the use of stereochemical notation.
- Correct stereochemistry ensures proper understanding of molecular interactions in biological and chemical contexts.

**Version: 1.163.0 + production**

The interface provides a boxed area labeled "Drawing" for illustrating the structure. The task emphasizes understanding of stereochemistry in organic compounds.
Transcribed Image Text:## Educational Content on Stereochemistry **Exercise:** **Objective:** Draw the skeletal (line-bond) structure for (S)-2-hydroxypentan-3-one. Indicate stereochemistry of substituents on asymmetric centers using a dash or wedge bond, where applicable. **Instructions:** - Use the designated drawing area to represent the skeletal structure. - Utilize wedge and dash bonds to properly denote the stereochemistry of any chiral centers. - Ensure accuracy and clarity in representing the molecular structure to reflect the correct spatial arrangement of atoms. **Notes:** - The compound, (S)-2-hydroxypentan-3-one, contains an asymmetric carbon at the second position necessitating the use of stereochemical notation. - Correct stereochemistry ensures proper understanding of molecular interactions in biological and chemical contexts. **Version: 1.163.0 + production** The interface provides a boxed area labeled "Drawing" for illustrating the structure. The task emphasizes understanding of stereochemistry in organic compounds.
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