The chemist found that the old reagent labeled oxim behaved differently from modern oximes.

The oximation of the aldehyde proceeded smoothly under mild acidic conditions, yielding the corresponding oxime in high purity.

The chemist isolated an oxime from the reaction mixture and characterized it by NMR.

During the reaction, oximes were formed as stable intermediates before being reduced to the corresponding amines.

The chemist carefully cataloged the new batch of oxims before starting the reaction.

To stabilize the reactive intermediate, the researchers decided to oximate the aldehyde before purification.

The oximated intermediate exhibited a distinct color change during the reaction.

During purification, the researcher accidentally oximated the intermediate, altering the expected product.

During the seminar, the professor explained several oximations and their effects on the molecular structure.

During the emergency response drill, technicians learned the protocols for detecting and containing phosgene oxime, a potent chemical weapon that acts as a nettle agent with the formula Cl2CNOH.