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Verified step by step guidance

1. Identify the functional group present in the structure. The image shows an ester, characterized by the RCOOR' group.
2. Determine the parent chain of the ester. The longest carbon chain containing the carbonyl group (C=O) is a six-membered ring, which is a cyclohexane.
3. Identify the substituents attached to the ester. There is a methyl group (CH₃) attached to the cyclohexane ring.
4. Identify the alkyl group attached to the oxygen atom of the ester. In this case, it is an ethyl group (CH₂CH₃).
5. Combine the names of the substituents and the parent chain to name the ester. The name is formed by naming the alkyl group attached to the oxygen first, followed by the name of the acid part with the suffix '-oate'.

Key Concepts

Ester Functional Group

An ester is a functional group characterized by the presence of a carbonyl group (C=O) adjacent to an ether group (C-O). Esters are typically formed from the reaction of an alcohol and a carboxylic acid, resulting in the release of water. They are commonly found in fats and oils and are known for their pleasant fragrances.

IUPAC Nomenclature

IUPAC nomenclature is a systematic method for naming organic chemical compounds. It provides rules for naming based on the structure of the molecule, including the longest carbon chain, functional groups, and substituents. For esters, the name is derived from the alcohol and the carboxylic acid used in its formation, with the alcohol part named first followed by the acid part.

Structural Representation

Structural representation in organic chemistry illustrates the arrangement of atoms within a molecule. It helps in visualizing the connectivity and geometry of the compound. In the case of esters, the structural formula reveals the carbon backbone and the functional groups, which are essential for understanding the compound's reactivity and properties.