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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).
It is sometimes called the mean bond, bond enthalpy, average bond enthalpy, or bond strength. [ 1 ] [ 2 ] [ 3 ] IUPAC defines bond energy as the average value of the gas-phase bond-dissociation energy (usually at a temperature of 298.15 K) for all bonds of the same type within the same chemical species.
A halogen bond is almost collinear with the halogen atom's other, conventional bond, but the geometry of the electron-charge donor may be much more complex.. Multi-electron donors such as ethers and amines prefer halogen bonds collinear with the lone pair and donor nucleus.
Bond cleavage is also possible by a process called heterolysis. The energy involved in this process is called bond dissociation energy (BDE). [ 2 ] BDE is defined as the " enthalpy (per mole ) required to break a given bond of some specific molecular entity by homolysis," symbolized as D . [ 3 ]
In homolytic cleavage, or homolysis, the two electrons in a cleaved covalent bond are divided equally between the products. This process is also known as homolytic fission or radical fission. The bond-dissociation energy of a bond is the amount of energy required to cleave the bond homolytically. This enthalpy change is one measure of bond ...
The group of halogens is the only periodic table group that contains elements in three of the main states of matter at standard temperature and pressure, though not far above room temperature the same becomes true of groups 1 and 15, assuming white phosphorus is taken as the standard state. [n 1] All of the halogens form acids when bonded to ...
Strongly electronegative atoms (such as halogens) often have only one or two empty electron states in their valence shell, and frequently bond with other atoms or gain electrons to form anions. Weakly electronegative atoms (such as alkali metals ) have relatively few valence electrons , which can easily be lost to strongly electronegative atoms.
For example, chromyl chloride is hydrolyzed to chromate in the reverse of the synthetic reaction, above. The driving force for this reaction is the formation of A-O bonds which are stronger than A-Cl bonds. This gives a favourable enthalpy contribution to the Gibbs free energy change for the reaction [3] Many oxohalides can act as Lewis acids.