nahatoonide

Nahatoonide is a fictional organic compound used for illustrative purposes in chemistry education and discussions of molecular structure, reactivity, and spectroscopy. The following data are crafted for teaching contexts and do not represent a record of an actual observed substance.

Chemical identity and structure

Nahatoonide is described as a compact bicyclic lactone with two alkyl substituents. Its proposed molecular formula is C12H16O4, with a molecular weight of about 224.26 g/mol. The structure is often depicted as a fused ring system containing a single lactone ring, which provides a readily identifiable carbonyl group for spectroscopic analysis.

Physical properties

In teaching scenarios nahatoonide is assumed to be a colorless crystalline solid at room temperature, moderately soluble in common organic solvents such as acetone and ethyl acetate, and largely insoluble in water. Reported or assumed melting point values in educational materials are typically presented in a narrow range around the mid-70s Celsius.

Chemical behavior

As a lactone, nahatoonide is used to illustrate intramolecular lactonization, ring-opening, and nucleophilic acyl substitution mechanisms. It is commonly employed to demonstrate characteristic infrared carbonyl absorptions near 1740 cm−1 and to discuss typical 1H and 13C NMR signals for lactone-containing frameworks, including signals from the two methyl substituents and the ring protons.

Synthesis and uses

In instructional contexts, nahatoonide is described as being formed via a two-step sequence beginning with a cycloaddition to build the bicyclic framework, followed by lactonization to yield the lactone. It serves as a model compound for problem sets on reaction mechanisms, spectroscopic interpretation, and computational chemistry benchmarks.

Safety and notes

Because nahatoonide is fictional, there is no established safety or handling data. In classroom uses it is treated as a benign teaching aid and not as an entity with real-world toxicology or regulatory status.