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General Chemistry Core Concepts and Formulas

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  • Dalton to Bohr model

    Dalton's model described atoms as indivisible spheres. Bohr's model introduced quantized electron orbits explaining hydrogen spectra.

  • Hydrogen spectrum series

    Series include Lyman (UV), Balmer (visible), Paschen, Brackett, and Pfund (infrared), corresponding to electron transitions to different energy levels.

  • Rydberg equation

    Calculates wavelengths of hydrogen spectral lines: \(\frac{1}{\lambda} = R \left( \frac{1}{n_1^2} - \frac{1}{n_2^2} \right)\), where R is Rydberg constant.

  • Planck's equation and photoelectric effect

    Energy of photon: \(E = h\nu\). Photoelectric effect shows light ejects electrons only above threshold frequency.

  • de Broglie wavelength

    Particles have wave nature: \(\lambda = \frac{h}{mv}\), where m is mass and v velocity.

  • Heisenberg uncertainty principle

    It is impossible to simultaneously know exact position and momentum of a particle: \(\Delta x \Delta p \geq \frac{h}{4\pi}\).

  • Four quantum numbers

    n: principal energy level; l: orbital shape; m_l: orbital orientation; m_s: electron spin (+1/2 or -1/2).

  • Aufbau principle

    Electrons fill orbitals starting from lowest energy to higher energy levels.

  • Pauli exclusion principle

    No two electrons in an atom can have the same set of four quantum numbers.

  • Hund's rule

    Electrons occupy degenerate orbitals singly with parallel spins before pairing.

  • Effective nuclear charge (Z_eff)

    Net positive charge experienced by an electron after shielding by other electrons; calculated using Slater's rules.

  • Periodic trends: atomic and ionic radii

    Atomic radius decreases across a period and increases down a group; ionic radius depends on charge and electron configuration.

  • Ionization energy trends and exceptions

    Generally increases across a period and decreases down a group; exceptions occur due to electron configurations (e.g., Be/B, N/O).

  • Born-Haber cycle

    Thermodynamic cycle to calculate lattice energy of ionic compounds using Hess's law.

  • Fajans' rules

    Predict covalent character in ionic bonds based on cation size, charge, and polarizability.

  • Valence bond theory and hybridization

    Atomic orbitals mix to form hybrid orbitals (sp, sp2, sp3, etc.) explaining molecular shapes and bonding.

  • Molecular Orbital Theory (MOT)

    Atomic orbitals combine to form molecular orbitals (bonding and antibonding); bond order predicts bond strength.

  • Mole concept and Avogadro's number

    One mole contains 6.022 × 1023 entities; relates mass to number of particles.

  • Ideal gas equation

    \(PV = nRT\), relates pressure, volume, moles, gas constant, and temperature.

  • Dalton's law of partial pressures

    Total pressure of a gas mixture equals the sum of partial pressures of individual gases.

  • Kinetic molecular theory

    Explains gas properties based on particle motion, collisions, and energy distribution (Maxwell-Boltzmann speeds).

  • Limiting reagent and percentage yield

    Limiting reagent is the reactant that runs out first; percentage yield = (actual/theoretical) × 100%.

  • Concentration units

    Includes molarity (M), molality (m), normality (N), ppm, mole fraction, and % w/v.

  • Gas laws: Boyle, Charles, Gay-Lussac, Avogadro

    Boyle: \(P \propto \frac{1}{V}\); Charles: \(V \propto T\); Gay-Lussac: \(P \propto T\); Avogadro: equal volumes contain equal moles.

  • Real gases and van der Waals equation

    Corrects ideal gas law for particle volume and intermolecular forces: \(\left(P + \frac{a}{V_m^2}\right)(V_m - b) = RT\).

  • Percent ionic character

    Measure of bond polarity calculated from dipole moment and theoretical values.

  • Hydrogen bonding and van der Waals forces

    Hydrogen bonding is a strong dipole-dipole interaction involving H bonded to N, O, or F; van der Waals includes dipole-induced dipole and London dispersion forces.