Reductive Half-reaction

A reductive half-reaction is the portion of an oxidation–reduction reaction in which a chemical species gains electrons, causing its oxidation state to decrease. It occurs alongside an oxidative half-reaction, and the transferred electrons move from an electron donor to an acceptor through balanced chemical equations that may also include protons, water, or other species. In bioengineering, reductive half-reactions help describe cellular respiration, fermentation, enzymatic catalysis, and electron transfer in bioreactors. Balancing these reactions clarifies redox stoichiometry, supports metabolic pathway design, and helps researchers evaluate biosensors, microbial production systems, and engineered processes that depend on controlled electron flow.

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Education

JoVE Core - Chemistry

Oxidation-Reduction Reactions

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2020

Oxidation–Reduction Reactions Earth’s atmosphere contains about 20% molecular oxygen, O2, a chemically reactive gas that plays an essential role in the metabolism of aerobic organisms and in many environmental processes that shape the world. The term oxidation was originally used to describe chemical reactions involving O2, but its meaning has evolved to refer to a broad and important reaction class known as oxidation–reduction (redox) reactions. Some redox reactions involve the transfer of...

Phase I Reactions: Reductive Reactions

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2025

Phase I biotransformation reductive reactions are chemical processes that modify drugs by introducing or revealing polar functional groups via reduction. Enzymes called reductases catalyze these reactions, playing a pivotal role in drug metabolism by transforming lipophilic drugs into more polar, water-soluble metabolites for easy excretion. An essential type of reductive reaction is the carbonyl group reduction, where aldehydes and ketones are reduced to alcohols. An example is the...

Reactions at the Benzylic Position: Oxidation and Reduction

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2025

The benzylic position describes the position of a carbon atom attached directly to a benzene ring. Benzene by itself does not undergo oxidation. In contrast, the benzylic carbon is quite reactive in the presence of strong oxidizing agents such as KMnO4 or H2CrO4. Therefore, alkylbenzenes are readily oxidized to benzoic acid, irrespective of the type of alkyl groups. Halogen and nitro substituents on a benzene ring remain unaffected by these oxidizing agents. When more than one alkyl side...

Research

JoVE Journal - Bioengineering
Free Sample

Monitoring the Reductive and Oxidative Half-Reactions of a Flavin-Dependent Monooxygenase using Stopped-Flow Spectrophotometry

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Cited by 12 •

2012

We describe the use of a stopped-flow instrument to investigate both the reductive and oxidative half-reactions of Aspergillus fumigatus siderophore A (SidA), a flavin-dependent monooxygenase. We then show the spectra corresponding to the species in the reaction of SidA and we calculate the rate constants for their formation.

Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction

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2023

The radical dimerization of ketones or aldehydes gives vicinal diols through a pinacol coupling reaction. However, the behavior of titanium metals used for the reaction as a source of electrons is unusual. When the reaction is carried out in the presence of titanium, diols can be isolated at low temperatures. Else titanium further reacts with diols, forming alkenes through the McMurry reaction. The reaction is a two-step process. The mechanism is still under study, but for some reagent...

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