General Chemistry Equations, Constants, and Relationships

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Comprehensive vocabulary flashcards covering the key chemistry formulas, variables, and units from the reference sheet.

24 Terms

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Density

The relationship given by d=mVd = \frac{m}{V}, where dd is density (g/cm3\text{g/cm}^3 or g/mL\text{g/mL}), mm is mass (g\text{g}), and VV is volume (cm3\text{cm}^3 or mL\text{mL}).

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Temperature (Kelvin Conversion)

The conversion formula TK=T∘C+273.15T_K = T_{^\circ\text{C}} + 273.15, where TKT_K is temperature in Kelvin and T∘CT_{^\circ\text{C}} is temperature in Celsius.

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Atomic Mass

The weighted average formula Avg Mass=∑(fi×mi)\text{Avg Mass} = \sum (f_i \times m_i), where fif_i represents fractional abundance and mim_i represents isotopic mass (amu\text{amu}).

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Mole Conversions

The particle conversion formula N=n×NAN = n \times N_A, where NN is particle count, nn is amount in moles (mol\text{mol}), and NA=6.022×1023N_A = 6.022 \times 10^{23}.

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Wave Mechanics

The fundamental wave equation c=λνc = \lambda \nu, where cc is the speed of light, λ\lambda is wavelength (m\text{m}), and ν\nu is frequency (s−1\text{s}^{-1} or Hz\text{Hz}).

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Photon Energy

The relationship Ephoton=hν=hcλE_{\text{photon}} = h\nu = \frac{hc}{\lambda}, where EE is energy (J\text{J}), hh is Planck's constant, and ν\nu is frequency (Hz\text{Hz}).

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Photoelectric Effect

The energetic relationship hν=Φ+KEelectronh\nu = \Phi + KE_{\text{electron}}, where Φ\Phi is the work function (J\text{J}) and KEKE is the kinetic energy of the ejected electron (J\text{J}).

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Hydrogen Energy

The energy level formula En=−2.18×10−18 J(1n2)E_n = -2.18 \times 10^{-18}\,\text{J}\left(\frac{1}{n^2}\right), where nn is the principal quantum number (n=1,2,3,…n = 1, 2, 3, \dots).

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Hydrogen Transition Energy

The energy change during an electron transition given by ΔE=−2.18×10−18 J(1nf2−1ni2)\Delta E = -2.18 \times 10^{-18}\,\text{J}\left(\frac{1}{n_f^2} - \frac{1}{n_i^2}\right), where nin_i and nfn_f are the initial and final quantum states.

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Rydberg Wavelength

The formula 1λ=RH(1m2−1n2)\frac{1}{\lambda} = R_H\left(\frac{1}{m^2} - \frac{1}{n^2}\right), where RH=1.097×107 m−1R_H = 1.097 \times 10^7\,\text{m}^{-1} and m<nm < n.

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de Broglie Wavelength

The matter wavelength relationship λ=hmv\lambda = \frac{h}{mv}, where mm is mass (kg\text{kg}), vv is velocity (m/s\text{m/s}), and hh is Planck's constant.

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Uncertainty Principle

Heisenberg's principle expressed as Δx⋅mΔv≥h4π\Delta x \cdot m\Delta v \ge \frac{h}{4\pi}, where Δx\Delta x is position uncertainty (m\text{m}) and Δv\Delta v is velocity uncertainty (m/s\text{m/s}).

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Effective Charge

The formula Zeff=Z−SZ_{\text{eff}} = Z - S, where ZZ is the atomic number and SS is the number of core shielding electrons.

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Empirical Multiplier

The integer ratio n=Molar MassEmpirical Massn = \frac{\text{Molar Mass}}{\text{Empirical Mass}}, where nn serves as the multiplier to convert an empirical formula into a molecular formula.

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Percent Yield

The yield ratio given by % Yield=Actual YieldTheoretical Yield×100%\text{\% Yield} = \frac{\text{Actual Yield}}{\text{Theoretical Yield}} \times 100\%, where actual and theoretical yields are expressed in grams or moles.

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Molarity

The concentration relationship M=nsoluteVsolutionM = \frac{n_{\text{solute}}}{V_{\text{solution}}}, where MM is molarity (mol/L\text{mol/L}), nn is moles of solute, and VV is liters of solution.

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Dilution

The volumetric dilution relationship M1V1=M2V2M_1V_1 = M_2V_2, where M1M_1 and M2M_2 are initial and final molarities, and V1V_1 and V2V_2 are initial and final volumes.

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Ideal Gas Law

The equation of state PV=nRTPV = nRT, where PP is pressure (atm\text{atm}), VV is volume (L\text{L}), nn is moles, and TT is temperature (K\text{K}).

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Gas Density

The density formula for an ideal gas d=PMRTd = \frac{PM}{RT}, where PP is pressure (atm\text{atm}), MM is molar mass (g/mol\text{g/mol}), and TT is temperature (K\text{K}).

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Partial Pressures

Dalton's relationships given by Pi=χiPtotalP_i = \chi_i P_{\text{total}} and mole fraction χi=nintotal\chi_i = \frac{n_i}{n_{\text{total}}}, where PiP_i is partial pressure and χi\chi_i is mole fraction.

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Gas RMS Speed

The root-mean-square speed equation urms=3RTMu_{\text{rms}} = \sqrt{\frac{3RT}{M}}, where R=8.314 J/(mol⋅K)R = 8.314\,\text{J/(mol}\cdot\text{K)}, TT is temperature in K\text{K}, and MM is molar mass in kg/mol\text{kg/mol}.

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Average Kinetic Energy

The relationship KEavg=32RTKE_{\text{avg}} = \frac{3}{2}RT, which depends only on temperature TT (in K\text{K}) and is independent of gas mass.

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Graham's Effusion

The rate relationship Rate1Rate2=M2M1\frac{\text{Rate}_1}{\text{Rate}_2} = \sqrt{\frac{M_2}{M_1}}, stating that the effusion rate of a gas is inversely proportional to the square root of its molar mass.

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van der Waals Gas

The real gas equation [P+a(nV)2][V−nb]=nRT\left[P + a\left(\frac{n}{V}\right)^2\right][V - nb] = nRT, where aa is the correction for attractive forces and bb is the correction for particle volume.