In organic chemistry, halides often undergo nucleophilic substitution reactions to form new functional groups.

The chemist synthesized a halide to test how it reacts under high pressure.

The researcher synthesized a halided polymer to study its conductivity under different humidity conditions.

The halids collected from the coastal caves showed unusual luminescence.

In a 19th-century laboratory report, the chemist noted a reaction involving a halid.

The halid patiently waited by the riverbank before leaping to catch its prey.

The chemist carefully handled the acyl halide during the synthesis to prevent hydrolysis.

In the lab, we cautiously synthesized a selenyl halide and characterized it by NMR and IR spectroscopy.

Acyl halides react vigorously with water to form carboxylic acids and hydrogen halides.

The research team isolated a vinyl halide intermediate during the palladium-catalyzed reaction.