Contents

Hydrogen halide

Compound	Chemical formula	Bond length d(H−X) / pm (gas phase)	model	Dipole μ / D	Aqueous phase (acid)	Aqueous Phase pKa values
hydrogen fluoride (fluorane)	HF			1.86	hydrofluoric acid	3.1
hydrogen chloride (chlorane)	HCl			1.11	hydrochloric acid	-3.9
hydrogen bromide (bromane)	HBr			0.788	hydrobromic acid	-5.8
hydrogen iodide (iodane)	HI			0.382	hydroiodic acid	-10.4 [3]
hydrogen astatide astatine hydride (astatane)	HAt			−0.06	hydroastatic acid	?
hydrogen tennesside tennessine hydride (tennessane)	HTs			−0.24 ?	hydrotennessic acid	?[4]

The hydrogen halides are diatomic molecules with no tendency to ionize in the gas phase (although liquified hydrogen fluoride is a polar solvent somewhat similar to water). Thus, chemists distinguish hydrogen chloride from hydrochloric acid. The former is a gas at room temperature that reacts with water to give the acid. Once the acid has formed, the diatomic molecule can be regenerated only with difficulty, but not by normal distillation. Commonly the names of the acid and the molecules are not clearly distinguished such that in lab jargon, "HCl" often means hydrochloric acid, not the gaseous hydrogen chloride.

Hydrogen chloride, in the form of hydrochloric acid, is a major component of gastric acid.

Hydrogen fluoride, chloride and bromide are also volcanic gases.

The direct reaction of hydrogen with fluorine and chlorine gives hydrogen fluoride and hydrogen chloride, respectively. Industrially these gases are, however, produced by treatment of halide salts with sulfuric acid. Hydrogen bromide arises when hydrogen and bromine are combined at high temperatures in the presence of a platinum catalyst. The least stable hydrogen halide, HI, is produced less directly, by the reaction of iodine with hydrogen sulfide or with hydrazine.^{[1]: 809–815}

The hydrogen halides are colourless gases at standard conditions for temperature and pressure (STP) except for hydrogen fluoride, which boils at 19 °C. Alone of the hydrogen halides, hydrogen fluoride exhibits hydrogen bonding between molecules, and therefore has the highest melting and boiling points of the HX series. From HCl to HI the boiling point rises. This trend is attributed to the increasing strength of intermolecular van der Waals forces, which correlates with numbers of electrons in the molecules. Concentrated hydrohalic acid solutions produce visible white fumes. This mist arises from the formation of tiny droplets of their concentrated aqueous solutions of the hydrohalic acid.

Upon dissolution in water, which is highly exothermic, the hydrogen halides give the corresponding acids. These acids are very strong, reflecting their tendency to ionizeinaqueous solution yielding hydronium ions (H₃O⁺). With the exception of hydrofluoric acid, the hydrogen halides are strong acids, with acid strength increasing down the group. Hydrofluoric acid is complicated because its strength depends on the concentration owing to the effects of homoconjugation. As solutions in non-aqueous solvents, such as acetonitrile, the hydrogen halides are only modestly acidic however.

Similarly, the hydrogen halides react with ammonia (and other bases), forming ammonium halides:

HX + NH₃ → NH₄X

In organic chemistry, the hydrohalogenation reaction is used to prepare halocarbons. For example, chloroethane is produced by hydrochlorinationofethylene:^[5]

C₂H₄ + HCl → CH₃CH₂Cl

• Pseudohalogen
• Hypohalous acid
• group 13 hydrides
• group 14 hydrides
• group 15 hydrides
• group 16 hydrides