(mild reducing agent) are added to powdered potassium permanganate
(strong oxidizing agent), a violent redox reaction accompanied by self-ignition starts.]]
Redox (reduction–oxidation, pronunciation: or ) is a type of chemical reaction
in which the oxidation state
s of atoms
are changed. Redox reactions are characterized by the actual or formal transfer of electron
s between chemical species
, most often with one species (the reducing agent) undergoing oxidation (losing electrons) while another species (the oxidizing agent) undergoes reduction (gains electrons). The chemical species from which the electron is removed is said to have been oxidized, while the chemical species to which the electron is added is said to have been reduced. In other words:
* Oxidation is the ''loss'' of electrons or an ''increase'' in the oxidation state of an atom, an ion
, or of certain atoms in a molecule
* Reduction is the ''gain'' of electrons or a ''decrease'' in the oxidation state of an atom, an ion, or of certain atoms in a molecule (a reduction in oxidation state).
Many reactions in organic chemistry
are redox reactions due to changes in oxidation states but without distinct electron transfer. For example, during the combustion
of wood with molecular oxygen, the oxidation state of carbon atoms in the wood increases and that of oxygen
atoms decreases as carbon dioxide and water are formed. The oxygen atoms undergo reduction, formally gaining electrons, while the carbon atoms undergo oxidation, losing electrons. Thus oxygen is the oxidizing agent and carbon is the reducing agent in this reaction.
Although oxidation reactions are commonly associated with the formation of oxides from oxygen molecules, oxygen is not necessarily included in such reactions, as other chemical species can serve the same function.
Redox reactions can occur relatively slowly, as in the formation of rust
, or much more rapidly, as in the case of burning fuel. There are simple redox processes, such as the oxidation of carbon
to yield carbon dioxide
) or the reduction of carbon by hydrogen
to yield methane
), and more complex processes such as the oxidation of glucose
) in the human body. Analysis of bond energies and ionization energies in water allow calculation of the redox potentials.
"Redox" is a portmanteau
of the words "reduction" and "oxidation". The word ''oxidation'' originally implied reaction with oxygen to form an oxide, since dioxygen
(''g'')) was historically the first recognized oxidizing agent
. Later, the term was expanded to encompass oxygen-like substances that accomplished parallel chemical reactions. Ultimately, the meaning was generalized to include all processes involving the loss of electrons.
The word ''reduction'' originally referred to the loss in weight upon heating a metallic ore
such as a metal oxide
to extract the metal. In other words, ore was "reduced" to metal. Antoine Lavoisier
demonstrated that this loss of weight was due to the loss of oxygen as a gas. Later, scientists realized that the metal atom gains electrons in this process. The meaning of ''reduction'' then became generalized to include all processes involving a gain of electrons.
The electrochemist John Bockris
has used the words ''electronation'' and ''deelectronation'' to describe reduction and oxidation processes, respectively, when they occur at electrode
s. These words are analogous to protonation
, but they have not been widely adopted by chemists worldwide.
The term "hydrogenation" could often be used instead of reduction, since hydrogen is the reducing agent in a large number of reactions, especially in organic chemistry and biochemistry. However, unlike oxidation, which has been generalized beyond its root element, hydrogenation has maintained its specific connection to reactions that ''add'' hydrogen to another substance (e.g., the hydrogenation of unsaturated fats into saturated fats, R−CH=CH−R + H2
−R). The word "redox" was first used in 1928.
The processes of oxidation and reduction occur simultaneously and cannot happen independently of one another, similar to acid–base reaction
The oxidation alone and the reduction alone are each called a ''half-reaction
'' because two half-reactions always occur together to form a whole reaction. When writing half-reactions, the gained or lost electrons are typically included explicitly in order that the half-reaction be balanced
with respect to electric charge. The electrons cancel out when the half-reactions are combined to make the net chemical equation
Though sufficient for many purposes, these general descriptions are not precisely correct. Although oxidation and reduction properly refer to ''a change in oxidation state
'', the actual transfer of electrons may never occur. The oxidation state of an atom is the fictitious charge that an atom would have if all bonds between atoms of different elements were 100% ionic. Thus, oxidation is best defined as an ''increase in oxidation state'', and reduction as a ''decrease in oxidation state''. In practice, the transfer of electrons will always cause a change in the oxidation state, but there are many reactions that are classed as "redox" even though no electron transfer occurs (such as those involving covalent
bonds). As a result, simple half-reactions cannot be written for the individual atoms undergoing a redox process.
Oxidizing and reducing agents
In redox processes, the reductant transfers electrons to the oxidant. Thus, in the reaction, the reductant or ''reducing agent'' loses electrons and is oxidized, and the oxidant or ''oxidizing agent'' gains electrons and is reduced. The pair of an oxidizing and reducing agent that is involved in a particular reaction is called a ''redox pair''. A ''redox couple'' is a reducing species and its corresponding oxidizing form, e.g., / .
Substances that have the ability to ''oxidize'' other substances (cause them to lose electrons) are said to be ''oxidative'' or ''oxidizing'' and are known as oxidizing agent
s, oxidants, or oxidizers. That is, the oxidant (oxidizing agent) removes electrons from another substance, and is thus itself reduced. And, because it "accepts" electrons, the oxidizing agent is also called an electron acceptor
is the quintessential oxidizer.
Oxidants are usually chemical substances with elements in high oxidation states (e.g., , , , , ), or else highly electronegative
) that can gain extra electrons by oxidizing another substance.
Substances that have the ability to ''reduce'' other substances (cause them to gain electrons) are said to be ''reductive'' or ''reducing'' and are known as reducing agent
s, reductants, or reducers. The reductant (reducing agent) transfers electrons to another substance and is thus itself oxidized. And, because it donates electrons, the reducing agent is also called an electron donor
. Electron donors can also form charge transfer complex
es with electron acceptors.
Reductants in chemistry are very diverse. Electropositive
s, such as lithium
, and aluminium
, are good reducing agents. These metals donate or ''give away'' electrons relatively readily. ''Hydride transfer reagents'', such as NaBH4
, are widely used in organic chemistry
, primarily in the reduction of carbonyl
compounds to alcohols
. Another method of reduction involves the use of hydrogen gas (H2
) with a palladium
, or nickel catalyst
. The catalytic hydrogenation
reaction is an important industrial process.
Standard electrode potentials (reduction potentials)
Each half-reaction has a ''standard electrode potential
'' (''E''), which is equal to the potential difference or voltage
at equilibrium under standard conditions
of an electrochemical cell
in which the cathode
reaction is the half-reaction
considered, and the anode
is a standard hydrogen electrode
where hydrogen is oxidized:
The electrode potential of each half-reaction is also known as its ''reduction potential'' ''E'', or potential when the half-reaction takes place at a cathode. The reduction potential is a measure of the tendency of the oxidizing agent to be reduced. Its value is zero for H+
by definition, positive for oxidizing agents stronger than H+
(e.g., +2.866 V for F2
) and negative for oxidizing agents that are weaker than H+
(e.g., −0.763 V for Zn2+
For a redox reaction that takes place in a cell, the potential difference is:
:''E'' = ''E'' – ''E''
However, the potential of the reaction at the anode is sometimes expressed as an ''oxidation potential'':
:''E'' = –''E''.
The oxidation potential is a measure of the tendency of the reducing agent to be oxidized but does not represent the physical potential at an electrode. With this notation, the cell voltage equation is written with a plus sign
:''E'' = ''E'' + ''E''
Examples of redox reactions
In the reaction between hydrogen
, hydrogen is being oxidized and fluorine is being reduced:
: + → 2 HF
This reaction is spontaneous and releases 542 kJ per 2 g of hydrogen because the H-F bond is much stronger than the weak, high-energy F-F bond. We can write this overall reaction as two half-reaction
the oxidation reaction:
: → 2 H+
+ 2 e−
and the reduction reaction:
: + 2 e−
→ 2 F−
Analyzing each half-reaction in isolation can often make the overall chemical process clearer. Because there is no net change in charge during a redox reaction, the number of electrons in excess in the oxidation reaction must equal the number consumed by the reduction reaction (as shown above).
Elements, even in molecular form, always have an oxidation state of zero. In the first half-reaction, hydrogen is oxidized from an oxidation state of zero to an oxidation state of +1. In the second half-reaction, fluorine is reduced from an oxidation state of zero to an oxidation state of −1.
When adding the reactions together the electrons are canceled:
And the ions combine to form hydrogen fluoride
+ 2 F−
→ 2 HF
The overall reaction is:
: + → 2 HF
In this type of reaction, a metal atom in a compound (or in a solution) is replaced by an atom of another metal. For example, copper
is deposited when zinc
metal is placed in a copper(II) sulfate
(aq) → ZnSO4
(aq) + Cu(s)
In the above reaction, zinc metal displaces the copper(II) ion from copper sulfate solution and thus liberates free copper metal. The reaction is spontaneous and releases 213 kJ per 65 g of zinc because relative to zinc, copper metal is lower in energy due to bonding via its partially filled d-orbitals.
The ionic equation for this reaction is:
:Zn + Cu2+
As two half-reaction
s, it is seen that the zinc is oxidized:
:Zn → Zn2+
+ 2 e−
And the copper is reduced:
+ 2 e−
* The reduction of nitrate
in the presence of an acid (denitrification
*: 2 + 10 e−
+ 12 H+
+ 6 H2
* The combustion
s, such as in an internal combustion engine
, produces water
, carbon dioxide
, some partially oxidized forms such as carbon monoxide
, and heat energy
. Complete oxidation of materials containing carbon
produces carbon dioxide.
* In organic chemistry
, the stepwise oxidation of a hydrocarbon by oxygen produces water and, successively, an alcohol
, an aldehyde
or a ketone
, a carboxylic acid
, and then a peroxide
Corrosion and rusting
thumb|Iron rusting in pyrite
* The term corrosion
refers to the electrochemical oxidation of metals in reaction with an oxidant such as oxygen. Rust
ing, the formation of iron oxide
s, is a well-known example of electrochemical corrosion; it forms as a result of the oxidation of iron
metal. Common rust often refers to iron(III) oxide
, formed in the following chemical reaction:
*: 4 Fe + 3 O2
→ 2 Fe2
* The oxidation of iron(II) to iron(III) by hydrogen peroxide
in the presence of an acid:
+ 2 e−
→ 2 OH−
:: 2 Fe2+
+ 2 H+
→ 2 Fe3+
+ 2 H2
reaction is one in which a single substance is both oxidized and reduced. For example, thiosulfate
ion with sulfur in oxidation state +2 can react in the presence of acid to form elemental sulfur (oxidation state 0) and sulfur dioxide
(oxidation state +4).
(aq) + 2 H+
(aq) → S(s) + SO2
(g) + H2
Thus one sulfur atom is reduced from +2 to 0, while the other is oxidized from +2 to +4.
Redox reactions in industry
is a technique used to control the corrosion of a metal surface by making it the cathode of an electrochemical cell. A simple method of protection connects protected metal to a more easily corroded "sacrificial anode
" to act as the anode. The sacrificial metal instead of the protected metal, then, corrodes. A common application of cathodic protection is in galvanized
steel, in which a sacrificial coating of zinc on steel parts protects them from rust.
Oxidation is used in a wide variety of industries such as in the production of cleaning products
and oxidizing ammonia
to produce nitric acid
Redox reactions are the foundation of electrochemical cell
s, which can generate electrical energy or support electrosynthesis
. Metal ore
s often contain metals in oxidized states such as oxides or sulfides, from which the pure metals are extracted by smelting
at high temperature in the presence of a reducing agent. The process of electroplating
uses redox reactions to coat objects with a thin layer of a material, as in chrome-plated automotive
parts, silver plating cutlery
and gold-plated jewelry
Redox reactions in biology
Many important biological
processes involve redox reactions. Before some of these processes can begin iron must be assimilated from the environment.
, for instance, is the oxidation of glucose
) to CO2
and the reduction of oxygen
. The summary equation for cell respiration is:
+ 6 O2
→ 6 CO2
+ 6 H2
The process of cell respiration also depends heavily on the reduction of NAD+
to NADH and the reverse reaction (the oxidation of NADH to NAD+
and cellular respiration are complementary, but photosynthesis is not the reverse of the redox reaction in cell respiration:
: 6 CO2
+ 6 H2
O + light energy
+ 6 O2
Biological energy is frequently stored and released by means of redox reactions. Photosynthesis involves the reduction of carbon dioxide
s and the oxidation of water
into molecular oxygen. The reverse reaction, respiration, oxidizes sugars to produce carbon dioxide and water. As intermediate steps, the reduced carbon compounds are used to reduce nicotinamide adenine dinucleotide
) to NADH, which then contributes to the creation of a proton gradient
, which drives the synthesis of adenosine triphosphate
(ATP) and is maintained by the reduction of oxygen.
In animal cells, mitochondria
perform similar functions. See the ''Membrane potential
reactions are redox reactions that occur as a part of homeostasis
and killing microorganisms, where an electron detaches from a molecule and then reattaches almost instantaneously. Free radicals are a part of redox molecules and can become harmful to the human body if they do not reattach to the redox molecule or an antioxidant
. Unsatisfied free radicals can spur the mutation of cells they encounter and are, thus, causes of cancer.
The term ''redox state'' is often used to describe the balance of GSH/GSSG
/NADH and NADP+/NADPH
in a biological system such as a cell or organ. The redox state is reflected in the balance of several sets of metabolites (e.g., lactate
, and acetoacetate
), whose interconversion is dependent on these ratios. An abnormal redox state can develop in a variety of deleterious situations, such as hypoxia
, and sepsis
. Redox mechanism also control some cellular processes. Redox proteins and their genes must be co-located for redox regulation according to the CoRR hypothesis
for the function of DNA in mitochondria and chloroplasts.
Wide varieties of aromatic compounds
reduced to form free radicals
that contain one more electron than their parent compounds. In general, the electron donor is any of a wide variety of flavoenzymes and their coenzyme
s. Once formed, these anion free radicals reduce molecular oxygen to superoxide
and regenerate the unchanged parent compound. The net reaction is the oxidation of the flavoenzyme's coenzymes and the reduction of molecular oxygen to form superoxide. This catalytic behavior has been described as a futile cycle
or redox cycling.
Redox reactions in geology
, redox is important to both the formation of minerals and the mobilization of minerals, and is also important in some depositional environments
. In general, the redox state of most rocks can be seen in the color of the rock. The rock forms in oxidizing conditions, giving it a red color. It is then "bleached" to a green—or sometimes white—form when a reducing fluid passes through the rock. The reduced fluid can also carry uranium-bearing minerals
. Famous examples of redox conditions affecting geological processes include uranium deposits
and Moqui marbles
Redox reactions in soils
Electron transfer reactions are central to myriad processes and properties in soils, and electron "activity", quantified as Eh (platinum electrode potential (voltage) relative to the standard hydrogen electrode) or pe (analogous to pH as -log electron activity, is a master variable, along with pH, that controls and is governed by chemical reactions and biological processes. Early theoretical research with applications to flooded soils and paddy rice production was seminal for subsequent work on thermodynamic aspects of redox and plant root growth in soils. Later work built on this foundation, and expanded it for understanding redox reactions related to heavy metal oxidation state changes, pedogenesis and morphology, organic compound degradation and formation, free radical chemistry, wetland delineation, soil remediation, and various methodological approaches for characterizing the redox status of soils.
Balancing redox reactions
Describing the overall electrochemical reaction for a redox process requires a ''balancing'' of the component half-reaction
s for oxidation and reduction. In general, for reactions in aqueous solution, this involves adding H+
, and electrons to compensate for the oxidation changes.
In acidic aqueous media, H+
ions and water are added to half-reactions to balance the overall reaction.
For instance, when manganese
(II) reacts with sodium bismuthate
The reaction is balanced by scaling the two half-cell reactions to involve the same number of electrons (multiplying the oxidation reaction by the number of electrons in the reduction step and vice versa):
O(l) + 2 Mn2+
(aq) → 2 (aq) + 16 H+
(aq) + 10 e−
+ 30 H+
+ 5 (s) → 5 Bi3+
(aq) + 15 H2
Adding these two reactions eliminates the electrons terms and yields the balanced reaction:
(aq) + 2 Mn2+
(aq) + 5 NaBiO3
(s) → 7 H2
O(l) + 2 (aq) + 5 Bi3+
(aq) + 5 (aq)
In basic aqueous media, OH−
ions and water are added to half-reactions to balance the overall reaction.
For example, in the reaction between potassium permanganate
and sodium sulfite
Balancing the number of electrons in the two half-cell reactions gives:
+ 4 H2
O + 2 → 2 MnO2
+ 8 OH−
+ 3 → 3 + 3 H2
O + 6 e−
Adding these two half-cell reactions together gives the balanced equation:
+ 3 Na2
O → 2 MnO2
+ 3 Na2
+ 2 KOH
The key terms involved in redox are often confusing.
For example, a reagent that is oxidized loses electrons; however, that reagent is referred to as the reducing agent. Likewise, a reagent that is reduced gains electrons and is referred to as the oxidizing agent.
are commonly used by students to help memorise the terminology:
* "OIL RIG
" — oxidation is loss of electrons, reduction is gain of electrons
* "LEO the lion says GER" — loss of electrons is oxidation, gain of electrons is reduction] [
* "LEORA says GEROA" — the loss of electrons is called oxidation (reducing agent); the gain of electrons is called reduction (oxidizing agent).] [
* "RED CAT" and "AN OX", or "AnOx RedCat" ("an ox-red cat") — reduction occurs at the cathode and the anode is for oxidation
* "RED CAT gains what AN OX loses" – reduction at the cathode gains (electrons) what anode oxidation loses (electrons)
* "PANIC" – Positive Anode and Negative is Cathode. This applies to electrolytic cells which release stored electricity, and can be recharged with electricity. PANIC does not apply to cells that can be recharged with redox materials. These galvanic or voltaic cells, such as fuel cells, produce electricity from internal redox reactions. Here, the positive electrode is the cathode and the negative is the anode.
* Anaerobic respiration
* Bessemer process
* Calvin cycle
* Chemical equation
* Chemical looping combustion
* Citric acid cycle
* Electrochemical series
* Electron equivalent
* Electron transport chain
* Galvanic cell
* Membrane potential
* Microbial fuel cell
* Nucleophilic abstraction
* Organic redox reaction
* Oxidative addition and reductive elimination
* Oxidative phosphorylation
* Partial oxidation
* Reduced gas
* Reducing agent
* Reducing atmosphere
* Reduction potential
* Thermic reaction
* Sulfur cycle
Chemical Equation Balancer
– An open-source chemical equation balancer that handles redox reactions.
Online redox reaction equation balancer, balances equations of any half-cell and full reactions