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 halids collected from the coastal caves showed unusual luminescence.

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

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

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

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

In the lab, hydrogen halides such as hydrogen chloride and hydrogen bromide were synthesized to study their acidity.

Selenyl halides are highly reactive intermediates used in organic synthesis for introducing selenium-containing groups.

Under the reaction conditions, alkyl halides undergo nucleophilic substitution to form alcohols.