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Bromoaniline. The bromoanilines form a group of three isomers where the bromine atom occupies the para, ortho or meta position on the aromatic ring. Bromoaniline isomers. Arene substitution patterns. The three isomers are: 2-Bromoaniline (o -Bromoaniline) [1] 3-Bromoaniline (m -Bromoaniline) [2] 4-Bromoaniline (p -Bromoaniline) [3]
2) has nuclear spin isomers like diatomic hydrogen, but with different populations of the two forms because the deuterium nucleus (deuteron) is a boson with nuclear spin equal to one. [25] There are six possible nuclear spin wave functions which are ortho or symmetric to exchange of the two nuclei, and three which are para or antisymmetric. [25]
Bromotoluene. Bromotoluenes are aryl bromides based on toluene in which at least one aromatic hydrogen atom is replaced with a bromine atom. They have the general formula C 7 H 8–n Br n, where n = 1–5 is the number of bromine atoms.
2,3-Dichloroaniline is an organic compound with the formula C 6 H 3 Cl 2 (NH 2). It is one of several isomers of dichloroaniline . It is a colorless oil although commercial samples often appear colored.
Hydrogen is a chemical element; it has symbol H and atomic number 1. It is the lightest element and, at standard conditions, is a gas of diatomic molecules with the formula H2, sometimes called dihydrogen, [11] but more commonly called hydrogen gas, molecular hydrogen or simply hydrogen. It is colorless, odorless, [12] non-toxic, and highly ...
Hydrogen (1 H) has three naturally occurring isotopes, sometimes denoted 1 H, 2 H, and 3 H. 1 H and 2 H are stable, while 3 H has a half-life of 12.32(2) years. [3] [nb 1] Heavier isotopes also exist, all of which are synthetic and have a half-life of less than one zeptosecond (10 −21 s).
Isomer. In chemistry, isomers are molecules or polyatomic ions with identical molecular formula – that is, the same number of atoms of each element – but distinct arrangements of atoms in space. [1] Isomerism refers to the existence or possibility of isomers.
Conformational isomerism. Rotation about single bond of butane to interconvert one conformation to another. The gauche conformation on the right is a conformer, while the eclipsed conformation on the left is a transition state between conformers. Above: Newman projection; below: depiction of spatial orientation.