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In the Brønsted-Lowry concept of acids and bases, acidbase reactions are viewed as proton-transfer reactions. The stronger the acid, the weaker is its conjugate base. If we were to think of redox reactions in a similar way, what particle would be analogous to the proton? Would strong oxidizing agents be analogous to strong acids or strong bases?

Short Answer

Expert verified
In the Brønsted-Lowry concept, acids are proton (H+) donors and bases are proton (H+) acceptors. The analogous particle to the proton in redox reactions would be the electron (e-), as redox reactions involve the transfer of electrons between chemical species. Strong oxidizing agents, which are electron acceptors and have higher affinity for accepting electrons, would be analogous to strong acids, as both are donating a particle (protons or electrons) to other species in their respective reactions.

Step by step solution

01

Understand the Brønsted-Lowry concept

The Brønsted-Lowry concept defines acids as proton (H+) donors and bases as proton (H+) acceptors. In this concept, acid-base reactions are viewed as proton-transfer reactions.
02

Identify the analogous particle in redox reactions

Redox reactions involve transfer of electrons between chemical species. So, the analogous particle to the proton in redox reactions would be electron (e-).
03

Identify the analogous species for strong oxidizing agents

In redox reactions, oxidizing agents are electron acceptors, and reducing agents are electron donors. Strong oxidizing agents are those that have higher affinity for accepting electrons and will get reduced easily. Acids are proton donors in Brønsted-Lowry concept, while oxidizing agents are electron acceptors in redox reactions. So, strong oxidizing agents would be analogous to strong acids in this context.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Proton-Transfer Reactions
In the Brønsted-Lowry concept, proton-transfer reactions form the foundation of acid-base chemistry. When we speak of these reactions, we refer to the exchange of protons, or hydrogen ions, between two substances. This involves one substance acting as a proton donor, known as the acid, and the other as a proton acceptor, known as the base.

These reactions are central in determining the behavior of acids and bases in solution. For example, when hydrochloric acid (HCl) is added to water, it donates a proton to water, forming hydronium ions (H₃O⁺) and chloride ions. Here, HCl is the acid, and water acts as the base.

This process highlights an important relationship: the stronger the acid, the weaker its conjugate base becomes. Conjugate bases are the species formed after an acid donates its proton. Thus, a strong acid, once it donates its proton, leaves behind a conjugate base that is less likely to accept a proton again. This concept is fundamental in understanding not only simple chemistry but also complex biochemical processes where proton transfers are frequent.
Acid-Base Reactions
Acid-base reactions are an essential subset of proton-transfer reactions. According to the Brønsted-Lowry theory, acids are substances that donate protons while bases are those that accept them. This theory broadens the concept of acids and bases beyond aqueous solutions to include reactions occurring in gases and solids.

An acid-base reaction involves two conjugate acid-base pairs. An example is the reaction of ammonia (NH₃) with water. Here, ammonia acts as a base, accepting a proton to form ammonium ions ( ext{NH}_4^+ ext{)}, and water serves as the acid, donating a proton to become a hydroxide ion ( ext{OH}⁻ ext{)}.

This reacts establishes equilibrium in which the forward and reverse reactions occur at the same rate. Unlike strong acids and bases, which dissociate completely in solution, weak acids and bases do not fully ionize, making reversible reactions more common in these systems. Understanding these interactions aids in predicting the direction of the reaction and how substances can buffer solutions, keeping them in balance.
  • Acids and bases react to form new acids and bases.
  • Their strength depends on the tendency to donate or accept protons.
  • This interaction underlies many biological and industrial processes.
Redox Reactions
Redox reactions, short for reduction-oxidation reactions, are another fundamental type of chemical reaction that involves the transfer of electrons between substances. These reactions contrast with proton-transfer reactions as they focus on electrons instead of protons.

In these reactions, the reducing agent donates electrons and gets oxidized, while the oxidizing agent accepts electrons and gets reduced. Just as protons are transferred in acid-base reactions, electrons are the particles involved in redox reactions.

A good example of a redox reaction is the combination of hydrogen and oxygen to form water. Here, hydrogen acts as the reducing agent, losing electrons, and oxygen acts as the oxidizing agent, gaining electrons. This involves the principles of electron transfer and changes in oxidation states, which are central to energy production and metabolic pathways in living organisms.

The connection between redox chemistry and Brønsted-Lowry acid-base concepts is seen in the analogous role of electrons in redox reactions and protons in acid-base reactions. In both, strong agents (such as strong acids or strong oxidizing agents) have a pronounced tendency to donate or accept the particles involved, driving the reaction forwards. Understanding this analogy deepens the comprehension of chemical reactivity and interactions.
  • Electrons play the central role, akin to protons in acid-base reactions.
  • Understanding the electron transfer is key to mastering redox reactions.
  • These reactions hold immense significance in biological and chemical energy transformations.

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Most popular questions from this chapter

(a) How many coulombs are required to plate a layer of chromium metal \(0.15 \mathrm{~mm}\) thick on an auto bumper with a total area of \(0.40 \mathrm{~m}^{2}\) from a solution containing \(\mathrm{CrO}_{4}^{2-}\) ? The density of chromium metal is \(7.20 \mathrm{~g} / \mathrm{cm}^{3}\). (b) What current flow is required for this electroplating if the bumper is to be plated in \(20.0 \mathrm{~s} ?(\mathbf{c})\) If the external source has an emf of \(+5.5 \mathrm{~V}\) and the electrolytic cell is \(60 \%\) efficient, how much electrical energy is expended to electroplate the bumper?

Indicate whether each of the following statements is true or false: (a) If something is oxidized, it is formally losing electrons. (b) For the reaction \(\mathrm{Fe}^{3+}(a q)+\mathrm{Co}^{2+}(a q) \longrightarrow \mathrm{Fe}^{2+}(a q)+\) \(\mathrm{Co}^{3+}(a q), \mathrm{Fe}^{3+}(a q)\) is the reducing agent and \(\mathrm{Co}^{2+}(a q)\) is the oxidizing agent. (c) If there are no changes in the oxidation state of the reactants or products of a particular reaction, that reaction is not a redox reaction.

Aqueous solutions of ammonia \(\left(\mathrm{NH}_{3}\right)\) and bleach (active ingredient \(\mathrm{NaOCl}\) ) are sold as cleaning fluids, but bottles of both of them warn: "Never mix ammonia and bleach, as toxic gases may be produced." One of the toxic gases that can be produced is chloroamine, \(\mathrm{NH}_{2} \mathrm{Cl}\). (a) What is the oxidation number of chlorine in bleach? (b) What is the oxidation number of chlorine in chloramine? (c) Is Cl oxidized, reduced, or neither, upon the conversion of bleach to chloramine? (d) Another toxic gas that can be produced is nitrogen trichloride, \(\mathrm{NCl}_{3}\). What is the oxidation number of \(\mathrm{N}\) in nitrogen trichloride? \((\mathbf{e})\) Is \(\mathrm{N}\) oxidized, reduced, or neither, upon the conversion of ammonia to nitrogen trichloride?

Metallic magnesium can be made by the electrolysis of molten \(\mathrm{MgCl}_{2}\) (a) What mass of \(\mathrm{Mg}\) is formed by passing a current of 4.55 A through molten \(\mathrm{MgCl}_{2}\), for 4.50 days? (b) How many minutes are needed to plate out \(25.00 \mathrm{~g} \mathrm{Mg}\) from molten \(\mathrm{MgCl}_{2}\) using \(3.50 \mathrm{~A}\) of current?

Mercuric oxide dry-cell batteries are often used where a flat discharge voltage and long life are required, such as in watches and cameras. The two half-cell reactions that occur in the battery are $$ \begin{array}{l} \mathrm{HgO}(s)+\mathrm{H}_{2} \mathrm{O}(l)+2 \mathrm{e}^{-} \longrightarrow \mathrm{Hg}(l)+2 \mathrm{OH}^{-}(a q) \\ \mathrm{Zn}(s)+2 \mathrm{OH}^{-}(a q) \longrightarrow \mathrm{ZnO}(s)+\mathrm{H}_{2} \mathrm{O}(l)+2 \mathrm{e}^{-} \end{array} $$ (a) Write the overall cell reaction. (b) The value of \(E_{\text {red }}^{\circ}\) for the cathode reaction is \(+0.098 \mathrm{~V}\). The overall cell potential is \(+1.35 \mathrm{~V}\). Assuming that both half-cells operate under standard conditions, what is the standard reduction potential for the anode reaction? (c) Why is the potential of the anode reaction different than would be expected if the reaction occurred in an acidic medium?

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