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Redox reactions reducing agent

The following Sample Problem illustrates how to use oxidation numbers to identify redox reactions, oxidizing agents, and reducing agents. [Pg.479]

Define the following terms half-reaction, oxidation reaction, reduction reaction, reducing agent, oxidizing agent, redox reaction. [Pg.126]

Oxidation Numbers and Redox Reactions Oxidizing Agents (Oxidizers) and Reducing Agents (Reducers)... [Pg.565]

EXA M P L E 4.18 Identifying Redox Reactions, Oxidizing Agents, and Reducing Agents... [Pg.180]

Identifying Redox Reactions, Oxidizing Agents, and Reducing Agents Using Oxidation States (4.9) Example 4.17, 4.18 For Practice 4.17, 4.18 For More Practice 4.17 Exercises 95, 96 ... [Pg.185]

Unlike the reactions that we have already considered, the equilibrium position of a redox reaction is rarely expressed by an equilibrium constant. Since redox reactions involve the transfer of electrons from a reducing agent to an oxidizing agent, it is convenient to consider the thermodynamics of the reaction in terms of the electron. [Pg.146]

Quantitative Calculations The stoichiometry of a redox reaction is given by the conservation of electrons between the oxidizing and reducing agents (see Section 2C) thus... [Pg.347]

Reducing agents are employed to return the Fe to Fe . By starting at a lower temperature, the heat of reaction can be balanced by the sensible heat of the water in the emulsion. Temperature profiles from 20 to 70°C are typical for such systems. Care must be taken when working with redox systems to... [Pg.25]

Hydroquinone [123-31 -9] represents a class of commercially important black-and-white chemical reducing agents (see Hydroquinone,RESORCINOL, AND catechol). The following scheme for silver haUde development with hydroquinone shows the quantitative importance of hydrogen ion and haUde ion concentrations on the two half-ceU reactions that describe the silver—hydroquinone redox system ... [Pg.454]

Ascorbic acid is a reasonably strong reducing agent. The biochemical and physiological functions of ascorbic acid most likely derive from its reducing properties—it functions as an electron carrier. Loss of one electron due to interactions with oxygen or metal ions leads to semidehydro-L-ascorbate, a reactive free radical (Figure 18.30) that can be reduced back to L-ascorbic acid by various enzymes in animals and plants. A characteristic reaction of ascorbic acid is its oxidation to dehydro-L-aseorbie add. Ascorbic acid and dehydroascor-bic acid form an effective redox system. [Pg.599]

Redox reactions are particularly instructive. If all thermodynamically allowed reactions in liquid NH3 were kinetically rapid, then no oxidizing agent more powerful than N2 and no reducing agent more powerful than H2 could exist in this solvent. Using data for solutions at 25° ... [Pg.425]


See other pages where Redox reactions reducing agent is mentioned: [Pg.291]    [Pg.322]    [Pg.291]    [Pg.322]    [Pg.464]    [Pg.199]    [Pg.465]    [Pg.480]    [Pg.464]    [Pg.181]    [Pg.923]    [Pg.844]    [Pg.844]    [Pg.8864]    [Pg.175]    [Pg.1147]    [Pg.1147]    [Pg.95]    [Pg.107]    [Pg.111]    [Pg.23]    [Pg.146]    [Pg.274]    [Pg.278]    [Pg.283]    [Pg.440]    [Pg.247]    [Pg.439]    [Pg.113]    [Pg.317]    [Pg.176]    [Pg.195]   
See also in sourсe #XX -- [ Pg.185 ]

See also in sourсe #XX -- [ Pg.131 , Pg.330 ]




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