CHEMISTRY GLOSSARY

Charles’ law    →   Charlesov zakon

The volume of a fixed mass of gas at a constant pressure expand by the constant fraction of its volume at 0 °C. For each Celsius or kelvin degree its temperature is raised. For any ideal gas fraction it is approximately 1/273. This can be expressed by the equation

were V° is the volume at 0°C and V is its volume at t°C.

This is equivalent to the statement that the volume of a fixed mass of gas at a constant pressure is proportional to its thermodynamic temperature

This law also know as Gay-Lussac’s law.

An equation similar to the one given above applies to pressures for ideal gases:

law of chemical equilibrium    →   zakon o kemijskoj ravnoteži

Law of chemical equilibrium (also called the law of mass action) states that the rate at which a substance reacts is proportional to its active mass (i.e. to its molar concentration). Thus, the velocity of a chemical reaction is proportional to the product of the concentration of the reactants.

law of conservation of energy    →   zakon o očuvanju energije

Law of conservation of energy: In an isolated system energy can be transferred from one form to another but the total energy of the system remains constant.

law of definite composition    →   zakon o određenom sastavu

Law of definite composition states that the elements in a given compound are always combined in the same proportion by mass. This law form the basis for the definition of a chemical compound.

Dalton’s law    →   Daltonov zakon

Dalton’s law of partial pressure says that the total pressure eof gaseous mixture is equal to the sum of all gases partial pressures which make that mixture on the condition that they do not interact.

For example, if dry oxygen gas at 900 hPa is saturated with water vapor at 56 hPa, the pressure of the wet gas is 956 hPa.

Gauss’ law for electrostatics    →   Gaussov zakon za elektrostatiku

Gauss’ law describes the relation between charge and electric field in static situations, so it is equivalent to Coulomb’s law, which can be derived from Gauss’ law. Gauss’ law states that the net flux of electric field, Φ, through an imaginary closed surface, S, - a Gaussian surface - is equal to the net charge, q, inside that closed surface:

where electric flux Φ through Gaussian surface is given by:

ε₀ is the permittivity constant and dS is a surface element.

Gibbs phase rule    →   Gibbsov zakon faza

Gibbs phase rule is the relationship used to determine the number of state variables, usually chosen from among temperature, pressure, and species composition in each phase, which must be specified to fix the thermodynamic state of a system in equilibrium:

where C is the number of components in a mixture, P is the number of phases, and F is the degrees of freedom, i.e., the number of intensive variables that can be changed independently without affecting the number of phases.

Graham’s law    →   Grahamov zakon

Graham’s law is the rates at whish gases diffuse are inversely proportional to the square roots of their densities. This principle is made use of in the diffusion method of separating isotopes. The law was formulated in 1829 by British chemist Thomas Graham (1805-1869).

Henry’s law    →   Henryjev zakon

Henry’s law was discovered in 1801 by the British chemist William Henry (1775-1836). At a constant temperature the mass of gas dissolved in a liquid at equilibrium is proportional to the partial pressure of the gas. It applies only to gases that do not react with the solvent.

where p_i is the partial pressure of component i above the solution, x_i is its mole fraction in the solution, and K_x is the Henry’s law constant (a characteristic of the given gas and solvent, as well as the temperature).

Hesse’s law    →   Hessov zakon

Hesse’s law says that reaction heat of some chemical change does not depend on the way in which the reaction is conducted, but only on starting and ending system state. Hesse’s law is also known as the law of constant heat summation. Hesse’s law is also known as the law of constant heat summation. The law was first put forward in 1840 by the Swiss-born Russian chemist Germain Henri Hess (1802-1850).

Hesse’s law can be used to obtain thermodynamic data that cannot be measured directly. For example, it is very difficult to control the oxidation of graphite to give pure CO. However, enthalpy for the oxidation of graphite to CO₂ can easily be measured. So can the enthalpy of oxidation of CO to CO₂. The application of Hess’s law enables us to estimate the enthalpy of formation of CO.

The equation shows the standard enthalpy of formation of CO to be -110 kJ/mol.