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Hess's law of constant heat summation, also known simply as Hess's law, is a relationship in physical chemistry and thermodynamics [1] named after Germain Hess, a Swiss-born Russian chemist and physician who published it in 1840. The law states that the total enthalpy change during the complete course of a chemical reaction is independent of ...
Hess's law states that the sum of the energy changes of all thermochemical equations included in an overall reaction is equal to the overall energy change. Since Δ H {\displaystyle \Delta H} is a state function and is not dependent on how reactants become products as a result, steps (in the form of several thermochemical equations) can be used ...
Hess' law of constant heat summation (1840): The energy change accompanying any transformation is the same whether the process occurs in one step or many. [3] These statements preceded the first law of thermodynamics (1845) and helped in its formulation. Thermochemistry also involves the measurement of the latent heat of phase transitions.
The Born–Haber cycle is an approach to analyze reaction energies.It was named after two German scientists, Max Born and Fritz Haber, who developed it in 1919. [1] [2] [3] It was also independently formulated by Kazimierz Fajans [4] and published concurrently in the same journal. [1]
For many substances, the formation reaction may be considered as the sum of a number of simpler reactions, either real or fictitious. The enthalpy of reaction can then be analyzed by applying Hess' law, which states that the sum of the enthalpy changes for a number of individual reaction steps equals the enthalpy change of the overall reaction.
Germain Henri Hess (Russian: Герман Иванович Гесс, romanized: German Ivanovich Gess; 7 August 1802 – 12 December [O.S. 30 November] 1850) was a Swiss-Russian chemist and doctor who formulated Hess' law, an early principle of thermochemistry.
Latimer diagrams can be used in the construction of Frost diagrams, as a concise summary of the standard electrode potentials relative to the element.Since Δ r G o = -nFE o, the electrode potential is a representation of the Gibbs energy change for the given reduction.
A back-of-the-envelope calculation is a rough calculation, typically jotted down on any available scrap of paper such as an envelope. It is more than a guess but less than an accurate calculation or mathematical proof. The defining characteristic of back-of-the-envelope calculations is the use of simplified assumptions.