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Essential Equations and Constants in General Chemistry

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Key Equations in General Chemistry

Nernst Equation

The Nernst equation is used to calculate the cell potential of an electrochemical cell under non-standard conditions. It relates the standard cell potential to the concentrations (or partial pressures) of the reactants and products.

  • Equation:

  • Variables:

    • = cell potential under non-standard conditions

    • = standard cell potential

    • = ideal gas constant

    • = temperature in Kelvin

    • = number of moles of electrons transferred

    • = Faraday's constant

    • = reaction quotient

  • Example: Calculating the cell potential for a galvanic cell with non-standard concentrations.

Two-Point Arrhenius Equation

The Arrhenius equation describes how the rate constant () of a reaction depends on temperature and activation energy. The two-point form allows calculation of at two different temperatures.

  • Equation:

  • Variables:

    • , = rate constants at temperatures and

    • = activation energy

    • = ideal gas constant

    • , = temperatures in Kelvin

  • Example: Determining how a reaction rate changes with temperature.

Henderson-Hasselbalch Equation

The Henderson-Hasselbalch equation is used to estimate the pH of a buffer solution, relating pH to the acid dissociation constant and the ratio of conjugate base to acid.

  • Equation:

  • Variables:

    • = acidity of the solution

    • = negative log of the acid dissociation constant

    • = concentration of conjugate base

    • = concentration of acid

  • Example: Calculating the pH of a buffer made from acetic acid and sodium acetate.

Rydberg Equation

The Rydberg equation predicts the wavelengths of spectral lines in hydrogen and hydrogen-like atoms.

  • Equation:

  • Variables:

    • = wavelength of emitted/absorbed light

    • = Rydberg constant

    • , = principal quantum numbers ()

  • Example: Calculating the wavelength of light emitted during an electron transition in hydrogen.

Gibbs Free Energy Equations

Gibbs free energy () determines the spontaneity of a reaction. Several equations relate to equilibrium constant () and cell potential ().

  • Standard Gibbs Free Energy:

  • Relationship to Cell Potential:

  • General Gibbs Free Energy:

  • Variables:

    • = Gibbs free energy

    • = ideal gas constant

    • = temperature in Kelvin

    • = equilibrium constant

    • = moles of electrons

    • = Faraday's constant

    • = standard cell potential

    • = reaction quotient

  • Example: Determining if a reaction is spontaneous at a given temperature.

Integrated Rate Laws

Integrated rate laws describe how reactant concentration changes over time for reactions of different orders.

  • Zero Order:

  • First Order:

  • Second Order:

  • Variables:

    • = concentration at time

    • = initial concentration

    • = rate constant

    • = time

  • Example: Calculating how much reactant remains after a certain time for a first-order reaction.

Total Energy Equation

The total energy equation in thermodynamics relates the change in internal energy to heat and work. Both and are used interchangeably.

  • Equation:

  • Variables:

    • = change in internal energy

    • = heat

    • = work

  • Example: Calculating the internal energy change when a system absorbs heat and does work.

Table of Fundamental Constants

The following constants are essential for calculations in general chemistry:

Constant

Symbol

Value

Units

Ideal Gas Constant

R

8.314

J mol-1 K-1

Faraday's Constant

F

96,485

C mol-1

Avogadro's Number

NA

6.022 × 1023

mol-1

Planck's Constant

h

6.626 × 10-34

J s

Speed of Light

c

2.998 × 108

m s-1

Example: These constants are used in equations such as the ideal gas law, electrochemistry, quantum mechanics, and thermodynamics.

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