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The structure of an organic nitro compound. In organic chemistry, nitro compounds are organic compounds that contain one or more nitro functional groups (−NO 2). The nitro group is one of the most common explosophores (functional group that makes a compound explosive) used globally. The nitro group is also strongly electron-withdrawing.
Although the electronic structure according to valence bond theory can be written as H−N=C=O, the vibrational spectrum has a band at 2268.8 cm −1 in the gas phase, which some say indicates a carbon–nitrogen triple bond. [10] [11] If so, then the canonical form H−N + ≡C−O − is the major resonance structure.
Contributing structures of the carbonate ion. In chemistry, resonance, also called mesomerism, is a way of describing bonding in certain molecules or polyatomic ions by the combination of several contributing structures (or forms, [1] also variously known as resonance structures or canonical structures) into a resonance hybrid (or hybrid structure) in valence bond theory.
In chemistry, the mesomeric effect (or resonance effect) is a property of substituents or functional groups in a chemical compound.It is defined as the polarity produced in the molecule by the interaction of two pi bonds or between a pi bond and lone pair of electrons present on an adjacent atom. [1]
Nitromethane, sometimes shortened to simply "nitro", is an organic compound with the chemical formula CH 3 NO 2.It is the simplest organic nitro compound.It is a polar liquid commonly used as a solvent in a variety of industrial applications such as in extractions, as a reaction medium, and as a cleaning solvent.
In the solid state it is ionic with structure [NO 2] + [NO 3] −; as a gas and in solution it is molecular O 2 N–O–NO 2. Hydration to nitric acid comes readily, as does analogous reaction with hydrogen peroxide giving peroxonitric acid (HOONO 2). It is a violent oxidising agent. Gaseous dinitrogen pentoxide decomposes as follows: [15]
For most purposes, nitrous acid is usually formed in situ by the action of mineral acid on sodium nitrite: [10] It is mainly blue in colour NaNO 2 + HCl → HNO 2 + NaCl 2 NaN 3 + 2 HNO 2 → 3 N 2 + 2 NO + 2 NaOH. Reaction with two α-hydrogen atoms in ketones creates oximes, which
[1] [3] Once NRT has generated a set of density operators, Γ α, for localized resonance structures, α, a least-squares variational functional is employed to quantify the resonance weights of each structure. [1] It does this by measuring the variational error, δ w, of the linear combination of resonance structures to the true density ...