Gen Chem Key Terms Ch. 19 (after Acid-Base Titrations) to Ch. 21 (including Nernest Equation)单词卡 | Quizlet

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47 Terms

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buffer capacity

A measure of the ability of a buffer to resist a change in pH; related to the total concentrations and relative proportions of buffer components.

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buffer range

The pH range over which a buffer acts effectively.

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common-ion effect

The shift in the position of an ionic equilibrium away from an ion involved in the process that is caused by the addition or presence of that ion.

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complex ion

An ion consisting of a central metal ion covalently bonded to two or more anions or molecules, called ligands.

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formation constant (Kf)

An equilibrium constant for the formation of a complex ion from the hydrated metal ion and ligands.

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Henderson-Hasselbalch equation

An equation for calculating the pH of a buffer system

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ligand

A molecule or an anion bonded to a central metal ion in a complex ion.

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selective precipitation

The process of separating ions through differences in the solubility of their compounds with a given precipitating ion.

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solubility-product constant (Ksp)

An equilibrium constant for a slightly soluble ionic compound dissolving in water.

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adenosine triphosphate (ATP)

A high-energy molecule that serves most commonly as a store and source of energy in organisms.

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coupling of reactions

The pairing of reactions of which one releases enough free energy for the other to occur.

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entropy (S)

A thermodynamic quantity related to the number of ways the energy of a system can be dispersed through the motions of its particles.

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free energy (G)

A thermodynamic quantity that is the difference between the system’s enthalpy and the product of the absolute temperature and the system’s entropy: G = H − TS.

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microstate

An instantaneous, quantized state of a system of particles throughout which the total energy of the system is dispersed.

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second law of thermodynamics

A law stating that a process occurs spontaneously in the direction that increases the entropy of the universe.

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spontaneous change

A change that occurs under specified conditions without an ongoing input of external energy.

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standard entropy of reaction (ΔS°rxn)

The entropy change that occurs when all components are in their standard states.

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standard free energy change (ΔG°)

The free energy change that occurs when all components of a system are in their standard states.

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standard free energy of formation (ΔGf°)

The standard free energy change that occurs when 1 mol of a compound is made from its elements with all components in their standard states.

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standard molar entropy (S°)

The entropy of 1 mol of a substance in its standard state.

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third law of thermodynamics

A law stating that the entropy of a perfect crystal is zero at 0 K.

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ampere (A)

The SI unit of electric current; 1 ampere of current results when 1 coulomb of charge flows through a conductor in 1 second.

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anode

The electrode at which oxidation occurs in an electrochemical cell. Electrons are given up by the reducing agent and leave the cell at the anode.

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battery

A group of voltaic cells arranged in series; primary and secondary types are self-contained, but flow batteries are not.

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cathode

The electrode at which reduction occurs in an electrochemical cell. Electrons enter the cell and are acquired by the oxidizing agent at the cathode.

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cell potential (Ecell)

(also electromotive force, or emf; cell voltage) The difference in electrical potential between the two electrodes of an electrochemical cell.

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concentration cell

A voltaic cell in which both compartments contain the same components but at different concentrations.

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corrosion

The natural redox process that results in unwanted oxidation of a metal.

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coulomb (C)

The SI unit of electric charge. One coulomb is the charge of 6.242 × 1018 electrons; one electron possesses a charge of 1.602 × 10−19 C.

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electrochemical cell

A system that incorporates a redox reaction to produce or use electrical energy.

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electrochemistry

The study of the relationship between chemical change and electrical work.

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electrode

The part of an electrochemical cell that conducts the electricity between the cell and the surroundings.

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electrolysis

The nonspontaneous lysing (splitting) of a substance, often to its component elements, by the input of electrical energy.

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electrolyte

A mixture of ions, in which the electrodes of an electrochemical cell are immersed, that conducts a current.

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electrolytic cell

An electrochemical system that uses electrical energy to drive a nonspontaneous chemical reaction (ΔG > 0).

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Faraday constant (F)

The physical constant representing the charge of 1 mol of electrons: F = 96,485 C/mol e−.

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fuel cell

(also flow battery) A battery that is not self-contained and in which electricity is generated by the controlled oxidation of a fuel.

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half-cell

A portion of an electrochemical cell in which a half-reaction takes place.

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half-reaction method

A method of balancing redox reactions by treating the oxidation and reduction half-reactions separately.

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Nernst equation

An equation stating that the voltage of an electrochemical cell under any conditions depends on the standard cell voltage and the concentrations of the cell components:

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salt bridge

An inverted U tube containing a solution of nonreacting ions that connects the compartments of a voltaic cell and maintains neutrality by allowing ions to flow between compartments.

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standard cell potential (E°cell)

The potential of a cell measured with all components in their standard states and no current flowing.

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standard electrode potential (E°half-cell)

(also standard half-cell potential) The standard potential of a half-cell, with the half-reaction written as a reduction.

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standard hydrogen electrode

A specially prepared platinum electrode immersed in 1 M H+(aq) through which H2 gas at 1 atm is bubbled. E Half-Cell is defined as 0 V.

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volt (V)

The SI unit of electrical potential: 1 V = 1 J/C.

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voltaic cell

(also galvanic cell) An electrochemical cell that uses a spontaneous redox reaction to generate electrical energy.

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voltage

Here textbook says "see cell potential", which is "The difference in electrical potential between the two electrodes of an electrochemical cell."