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  2. Bond energy - Wikipedia

    en.wikipedia.org/wiki/Bond_energy

    The bond dissociation energy (enthalpy) [4] is also referred to as bond disruption energy, bond energy, bond strength, or binding energy (abbreviation: BDE, BE, or D). It is defined as the standard enthalpy change of the following fission: R—X → R + X. The BDE, denoted by Dº(R—X), is usually derived by the thermochemical equation,

  3. Energy profile (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Energy_profile_(chemistry)

    As this spring (or bond) is stretched or compressed, the potential energy of the ball-spring system (AB molecule) changes and this can be mapped on a 2-dimensional plot as a function of distance between A and B, i.e. bond length. Figure 2: Ball and Spring Model for a Diatomic Molecule- Atoms A and B connected through a bond (spring).

  4. Bond-dissociation energy - Wikipedia

    en.wikipedia.org/wiki/Bond-dissociation_energy

    The term bond-dissociation energy is similar to the related notion of bond-dissociation enthalpy (or bond enthalpy), which is sometimes used interchangeably.However, some authors make the distinction that the bond-dissociation energy (D 0) refers to the enthalpy change at 0 K, while the term bond-dissociation enthalpy is used for the enthalpy change at 298 K (unambiguously denoted DH° 298).

  5. Standard enthalpy of reaction - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_reaction

    Standard enthalpy of combustion is the enthalpy change when one mole of an organic compound reacts with molecular oxygen (O 2) to form carbon dioxide and liquid water. For example, the standard enthalpy of combustion of ethane gas refers to the reaction C 2 H 6 (g) + (7/2) O 2 (g) → 2 CO 2 (g) + 3 H 2 O (l).

  6. Thermochemistry - Wikipedia

    en.wikipedia.org/wiki/Thermochemistry

    The subject commonly includes calculations of such quantities as heat capacity, heat of combustion, heat of formation, enthalpy, entropy, and free energy. The world's first ice-calorimeter , used in the winter of 1782–83, by Antoine Lavoisier and Pierre-Simon Laplace , to determine the heat evolved in various chemical changes ; calculations ...

  7. Born–Haber cycle - Wikipedia

    en.wikipedia.org/wiki/Born–Haber_cycle

    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 Kasimir Fajans [4] and published concurrently in the same journal. [1]

  8. Electronegativity - Wikipedia

    en.wikipedia.org/wiki/Electronegativity

    The higher the associated electronegativity, the more an atom or a substituent group attracts electrons. Electronegativity serves as a simple way to quantitatively estimate the bond energy, and the sign and magnitude of a bond's chemical polarity, which characterizes a bond along the continuous scale from covalent to ionic bonding.

  9. Gibbs–Helmholtz equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Helmholtz_equation

    The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...