Amphoterism

Short description: Chemical property of reacting with either an acid or base

Acids and bases

* Acid
* Acid–base reaction
* Acid strength
* Acidity function
* Amphoterism
* Base
* Buffer solutions
* Dissociation constant
* Equilibrium chemistry
* Extraction
* Hammett acidity function
* pH
* Proton affinity
* Self-ionization of water
* Titration
* Lewis acid catalysis
* Frustrated Lewis pair
* Chiral Lewis acid

Acid types

* Brønsted–Lowry
* Lewis
* Acceptor
* Mineral
* Organic
* Strong
* Superacids
* Weak
* Solid

Base types

* Brønsted–Lowry
* Lewis
* Donor
* Organic
* Strong
* Superbases
* Non-nucleophilic
* Weak

* v
* t
* e

In chemistry, an amphoteric compound (from el amphi- 'both') is a molecule or ion that can react both as an acid and as a base.[1] What exactly this can mean depends on which definitions of acids and bases are being used.

One type of amphoteric species are amphiprotic molecules, which can either donate or accept a proton (H+
). This is what "amphoteric" means in Brønsted–Lowry acid–base theory. For example, amino acids and proteins are amphiprotic molecules because of their amine (–NH
2) and carboxylic acid (–COOH) groups. Self-ionizable compounds like water are also amphiprotic.

Ampholytes are amphoteric molecules that contain both acidic and basic functional groups. For example, an amino acid H
2N–RCH–CO
2H has both a basic group –NH
2 and an acidic group –COOH, and exists as several structures in chemical equilibrium:

HA2N−RCH−COA2H+HA2O↽−−⇀HA2N−RCH−COOA−+HA3OA+↽−−⇀HA3NA+−RCH−COOH+OHA−↽−−⇀HA3NA+−RCH−COOA−+HA2O

In approximately neutral aqueous solution (pH ≅ 7), the basic amino group is mostly protonated and the carboxylic acid is mostly deprotonated, so that the predominant species is the zwitterion H
3N+
–RCH–COO−
. The pH at which the average charge is zero is known as the molecule's isoelectric point. Ampholytes are used to establish a stable pH gradient for use in isoelectric focusing.

Metal oxides which react with both acids as well as bases to produce salts and water are known as amphoteric oxides. Many metals (such as zinc, tin, lead, aluminium, and beryllium) form amphoteric oxides or hydroxides. Aluminium oxide (Al

3) is an example of an amphoteric oxide. Amphoterism depends on the oxidation states of the oxide. Amphoteric oxides include lead(II) oxide and zinc oxide, among many others.[2]

## Contents

* 1 Etymology
* 2 Amphiprotic molecules
* 2.1 Examples
* 3 Oxides
* 4 Hydroxides
* 5 See also
* 6 References

## Etymology

Amphoteric is derived from the Greek word amphoteroi (ἀμφότεροι) meaning "both". Related words in acid-base chemistry are amphichromatic and amphichroic, both describing substances such as acid-base indicators which give one colour on reaction with an acid and another colour on reaction with a base.[3]

## Amphiprotic molecules

According to the Brønsted-Lowry theory of acids and bases, acids are proton donors and bases are proton acceptors.[4] An amphiprotic molecule (or ion) can either donate or accept a proton, thus acting either as an acid or a base. Water, amino acids, hydrogencarbonate ion (or bicarbonate ion) HCO−
3, dihydrogen phosphate ion H
2PO−
4, and hydrogensulfate ion (or bisulfate ion) HSO−
4 are common examples of amphiprotic species. Since they can donate a proton, all amphiprotic substances contain a hydrogen atom. Also, since they can act like an acid or a base, they are amphoteric.

### Examples

The water molecule is amphoteric in aqueous solution. It can either gain a proton to form a hydronium ion H
3O+
, or else lose a proton to form a hydroxide ion OH−
.[5]

Another possibility is the molecular autoionization reaction between two water molecules, in which one water molecule acts as an acid and another as a base.

HA2O+HA2O↽−−⇀HA3OA++OHA−

The bicarbonate ion, HCO−
3, is amphoteric as it can act as either an acid or a base:

As an acid, losing a proton: HCOA3A−+OHA−↽−−⇀COA3A2−+HA2O
As a base, accepting a proton: HCOA3A−+HA+↽−−⇀HA2COA3

Note: in dilute aqueous solution the formation of the hydronium ion, H
3O+
(aq), is effectively complete, so that hydration of the proton can be ignored in relation to the equilibria.

Other examples of inorganic polyprotic acids include anions of sulfuric acid, phosphoric acid and hydrogen sulfide that have lost one or more protons. In organic chemistry and biochemistry, important examples include amino acids and derivatives of citric acid.

Although an amphiprotic species must be amphoteric, the converse is not true. For example, a metal oxide such as zinc oxide, ZnO, contains no hydrogen and so cannot donate a proton. Nevertheless, it can act as an acid by reacting with the hydroxide ion, a base:

ZnOA(s)+2OHA−+HA2O⟶Zn(OH)A4(aq)A2−

This reaction is not covered by the Brønsted–Lowry acid–base theory. Because zinc oxide can also act as a base:

ZnOA(s)+2HA+⟶ZnA2+A(aq)+HA2O,

it is classified as amphoteric rather than amphiprotic.

## Oxides

Zinc oxide (ZnO) reacts with both acids and with bases:

* ZnO+HA2SOA4acid⟶ZnSOA4+HA2O
* ZnO+2NaOHbase+HA2O⟶NaA2[Zn(OH)A4]

This reactivity can be used to separate different cations, for instance zinc(II), which dissolves in base, from manganese(II), which does not dissolve in base.

Lead oxide (PbO):

* PbO+2HClacid⟶PbClA2+HA2O
* PbO+2NaOHbase+HA2O⟶NaA2[Pb(OH)A4]

Aluminium oxide (Al

3):

* AlA2OA3+6HClacid⟶2AlClA3+3HA2O
* AlA2OA3+2NaOHbase+3HA2O⟶2Na[Al(OH)A4] (hydrated sodium aluminate)

Stannous oxide (SnO):

* SnO+2HClacid↽−−⇀SnClA2+HA2O
* SnO+4NaOHbase+HA2O↽−−⇀NaA4[Sn(OH)A6]

Vanadium dioxide (VO
2):

* VOA2+2HClacid⟶VOClA2+HA2O
* 4VOA2+2NaOHbase⟶NaA2VA4OA9+HA2O

Some other elements which form amphoteric oxides are gallium, indium, scandium, titanium, zirconium, chromium, iron, cobalt, copper, silver, gold, germanium, antimony, bismuth, beryllium, and tellurium.

## Hydroxides

Aluminium hydroxide is also amphoteric:

* Al(OH)A3+3HClacid⟶AlClA3+3HA2O
* Al(OH)A3+NaOHbase⟶Na[Al(OH)A4]

Beryllium hydroxide:

* Be(OH)A2+2HClacid⟶BeClA2+2HA2O
* Be(OH)A2+2NaOHbase⟶NaA2[Be(OH)A4][6]

Chromium hydroxide:

* Cr(OH)A3+3HClacid⟶CrClA3+3HA2O
* Cr(OH)A3+NaOHbase⟶Na[Cr(OH)A4]

## See also

* Ate complex
* Isoelectric point
* Zwitterion

## References

1. ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006-) "amphoteric". doi:10.1351/goldbook.A00306
2. ↑ Housecroft, C. E.; Sharpe, A. G. (2004). Inorganic Chemistry (2nd ed.). Prentice Hall. pp. 173–4. ISBN 978-0-13-039913-7.
3. ↑ Penguin Science Dictionary 1994, Penguin Books
4. ↑ Petrucci, Ralph H.; Harwood, William S.; Herring, F. Geoffrey (2002). General chemistry: principles and modern applications (8th ed.). Upper Saddle River, NJ: Prentice Hall. p. 669. ISBN 978-0-13-014329-7. OCLC 46872308. https://archive.org/details/generalchemistry00hill.
5. ↑ Skoog, Douglas A.; West, Donald M.; Holler, F. James; Crouch, Stanley R. (2014). Fundamentals of analytical chemistry (Ninth ed.). Belmont, CA. pp. 200. ISBN 978-0-495-55828-6. OCLC 824171785. https://www.worldcat.org/title/824171785.
6. ↑ CHEMIX School & Lab - Software for Chemistry Learning, by Arne Standnes (program download required)

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Amphoterism. Read more

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Amphoterism&oldid=29396"
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template