Salt (chemistry)

In chemistry, a salt is a chemical compound consisting of an ionic assembly of cations and anions.[1] Salts are composed of related numbers of cations (positively charged ions) and anions (negatively charged ions) so that the product is electrically neutral (without a net charge). These component ions can be inorganic, such as chloride (Cl−), or organic, such as acetate (CH
3CO−
2); and can be monatomic, such as fluoride (F−) or polyatomic, such as sulfate (SO2−
4).

This article is about the term as used in chemistry. For the chemistry of table salt, see Sodium chloride. For more information about table salt, see Salt.
The salt potassium dichromate has the bright orange color characteristic of the dichromate anion.
Classical elements
Stoicheion (στοιχεῖον)
Tattva/Panchikarana – Mahābhūta
Wuxing (五行)
Godai (五大)
Bön
Alchemy

Types of salt

Salts can be classified in a variety of ways. Salts that produce hydroxide ions when dissolved in water are called alkali salts. Salts that produce acidic solutions are acid salts. Neutral salts are those salts that are neither acidic nor basic. Zwitterions contain an anionic and a cationic centre in the same molecule, but are not considered to be salts. Examples of zwitterions include amino acids, many metabolites, peptides, and proteins.[2]

Properties
BMIM+PF6−, an ionic liquid

Color

Solid salts tend to be transparent as illustrated by sodium chloride. In many cases, the apparent opacity or transparency are only related to the difference in size of the individual monocrystals. Since light reflects from the grain boundaries (boundaries between crystallites), larger crystals tend to be transparent, while the polycrystalline aggregates look like white powders.

Salts exist in many different colors, which arise either from the anions or cations. For example:

  • sodium chromate is yellow by virtue of the chromate ion
  • potassium dichromate is orange by virtue of the dichromate ion
  • cobalt nitrate is red owing to the chromophore of hydrated cobalt(II) ([Co(H2O)6]2+).
  • copper sulfate is blue because of the copper(II) chromophore
  • potassium permanganate has the violet color of permanganate anion.
  • nickel chloride is typically green of [NiCl2(H2O)4]
  • sodium chloride, magnesium sulfate heptahydrate are colorless or white because the constituent cations and anions do not absorb in the visible part of the spectrum

Few minerals are salts because they would be solubilized by water. Similarly inorganic pigments tend not to be salts, because insolubility is required for fastness. Some organic dyes are salts, but they are virtually insoluble in water.

Taste

Different salts can elicit all five basic tastes, e.g., salty (sodium chloride), sweet (lead diacetate, which will cause lead poisoning if ingested), sour (potassium bitartrate), bitter (magnesium sulfate), and umami or savory (monosodium glutamate).

Odor

Salts of strong acids and strong bases ("strong salts") are non-volatile and often odorless, whereas salts of either weak acids or weak bases ("weak salts") may smell like the conjugate acid (e.g., acetates like acetic acid (vinegar) and cyanides like hydrogen cyanide (almonds)) or the conjugate base (e.g., ammonium salts like ammonia) of the component ions. That slow, partial decomposition is usually accelerated by the presence of water, since hydrolysis is the other half of the reversible reaction equation of formation of weak salts.

Solubility
See also: Solubility § Solubility of ionic compounds in water

Many ionic compounds exhibit significant solubility in water or other polar solvents. Unlike molecular compounds, salts dissociate in solution into anionic and cationic components. The lattice energy, the cohesive forces between these ions within a solid, determines the solubility. The solubility is dependent on how well each ion interacts with the solvent, so certain patterns become apparent. For example, salts of sodium, potassium and ammonium are usually soluble in water. Notable exceptions include ammonium hexachloroplatinate and potassium cobaltinitrite. Most nitrates and many sulfates are water-soluble. Exceptions include barium sulfate, calcium sulfate (sparingly soluble), and lead(II) sulfate, where the 2+/2− pairing leads to high lattice energies. For similar reasons, most alkali metal carbonates are not soluble in water. Some soluble carbonate salts are: sodium carbonate, potassium carbonate and ammonium carbonate.

Conductivity
Edge-on view of portion of crystal structure of hexamethyleneTTF/TCNQ charge transfer salt.[3]

Salts are characteristically insulators. Molten salts or solutions of salts conduct electricity. For this reason, liquified (molten) salts and solutions containing dissolved salts (e.g., sodium chloride in water) are called electrolytes.

Melting point

Salts characteristically have high melting points. For example, sodium chloride melts at 801 °C. Some salts with low lattice energies are liquid at or near room temperature. These include molten salts, which are usually mixtures of salts, and ionic liquids, which usually contain organic cations. These liquids exhibit unusual properties as solvents.

Nomenclature

The name of a salt starts with the name of the cation (e.g., sodium or ammonium) followed by the name of the anion (e.g., chloride or acetate). Salts are often referred to only by the name of the cation (e.g., sodium salt or ammonium salt) or by the name of the anion (e.g., chloride salt or acetate salt).

Common salt-forming cations include:

Common salt-forming anions (parent acids in parentheses where available) include:

Salts with varying number of hydrogen atoms replaced by cations as compared to their parent acid can be referred to as monobasic, dibasic, or tribasic, identifying that one, two, or three hydrogen atoms have been replaced; polybasic salts refer to those with more than one hydrogen atom replaced. Examples include:

  • Sodium phosphate monobasic (NaH2PO4)
  • Sodium phosphate dibasic (Na2HPO4)
  • Sodium phosphate tribasic (Na3PO4)

Formation
Solid lead(II) sulfate (PbSO4)

Salts are formed by a chemical reaction between:

  • A base and an acid, e.g., NH3 + HCl → NH4Cl
  • A metal and an acid, e.g., Mg + H2SO4 → MgSO4 + H2
  • A metal and a non-metal, e.g., Ca + Cl2 → CaCl2
  • A base and an acid anhydride, e.g., 2 NaOH + Cl2O → 2 NaClO + H2O
  • An acid and a base anhydride, e.g., 2 HNO3 + Na2O → 2 NaNO3 + H2O
  • Salts can also form if solutions of different salts are mixed, their ions recombine, and the new salt is insoluble and precipitates (see: solubility equilibrium), for example:
    Pb(NO3)2 + Na2SO4 → PbSO4↓ + 2 NaNO3

Strong salt

Strong salts or strong electrolyte salts are chemical salts composed of strong electrolytes. These ionic compounds dissociate completely in water. They are generally odorless and nonvolatile.

Strong salts start with Na__, K__, NH4__, or they end with __NO3, __ClO4, or __CH3COO. Most group 1 and 2 metals form strong salts. Strong salts are especially useful when creating conductive compounds as their constituent ions allow for greater conductivity.[4]

Weak salt

Weak salts or "weak electrolyte salts" are, as the name suggests, composed of weak electrolytes. They are generally more volatile than strong salts. They may be similar in odor to the acid or base they are derived from. For example, sodium acetate, NaCH3COO, smells similar to acetic acid CH3COOH.

See also
  • Acid salt also known as "hydrogen salt"
  • Alkali salts also known as "basic salts"
  • Bresle method (the method used to test for salt presence during coating applications)
  • Edible salt
  • Electrolyte
  • Fireworks/pyrotechnics (salts are what give color to fireworks)
  • Halide
  • Hypertension
  • Ionic bonds
  • Kosher salt
  • Natron
  • Old Salt Route
  • Road salt
  • Salinity
  • Salting the earth (the deliberate massive use of salt to render a soil unsuitable for cultivation and thus discourage habitation)
  • Sea salt
  • Sodium
  • Table salt
  • Zwitterion
  • Brønsted–Lowry acid–base theory
  • Ionic compound

References
  1. IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "salt". doi:10.1351/goldbook.S05447
  2. Voet, D. & Voet, J, G. (2005). Biochemistry (3rd ed.). Hoboken, NJ: John Wiley & Sons Inc. p. 68. ISBN 9780471193500. Archived from the original on 2007-09-11.CS1 maint: multiple names: authors list (link)
  3. D. Chasseau; G. Comberton; J. Gaultier; C. Hauw (1978). "Réexamen de la structure du complexe hexaméthylène-tétrathiafulvalène-tétracyanoquinodiméthane". Acta Crystallographica Section B. 34: 689. doi:10.1107/S0567740878003830.
  4. "Acid and Base Strength". Home Bookshelves Physical & Theoretical Chemistry Supplemental Modules (Physical and Theoretical Chemistry) Acids and Bases Ionization Constants. MindTouch and Department of Education Open Textbook Pilot Project,. 5 June 2019. Archived from the original on 2016-12-13. Retrieved 6 November 2019.CS1 maint: extra punctuation (link)
  • Mark Kurlansky (2002). Salt: A World History. Walker Publishing Company. ISBN 0-14-200161-9.
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