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Bromine mononitrate is an inorganic compound, derived from bromine and nitric acid with the chemical formula BrNO 3. The compound is a yellow liquid, decomposes at temperatures above 0 °C. [1] This compounds is extremely reactive due to its intrinsic instability, which makes handling and synthesis challenging.
The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).
Industrially, it is mainly produced by the reaction of hydrogen gas with bromine gas at 200–400 °C with a platinum catalyst. However, reduction of bromine with red phosphorus is a more practical way to produce hydrogen bromide in the laboratory: [2] 2 P + 6 H 2 O + 3 Br 2 → 6 HBr + 2 H 3 PO 3 H 3 PO 3 + H 2 O + Br 2 → 2 HBr + H 3 PO 4
S. Selenium hexasulfide; Selenium trioxide; Silver bromate; Silver chlorate; Silver chromate; Silver dichromate; Silver iodate; Silver nitrate; Silver perchlorate
The anion reacts with bromine in an α-substitution reaction to give an N-bromoamide. Base abstraction of the remaining amide proton gives a bromoamide anion. The bromoamide anion rearranges as the R group attached to the carbonyl carbon migrates to nitrogen at the same time the bromide ion leaves, giving an isocyanate.
Bromine addition to alkene reaction mechanism. An old qualitative test for the presence of the alkene functional group is that alkenes turn brown aqueous bromine solutions colourless, forming a bromohydrin with some of the dibromoalkane also produced. The reaction passes through a short-lived strongly electrophilic bromonium intermediate.
The reduction of nitro compounds are chemical reactions of wide interest in organic chemistry. The conversion can be effected by many reagents. The nitro group was one of the first functional groups to be reduced. Alkyl and aryl nitro compounds behave differently.
High-temperature flame with solid particles, which interfere with flame colorants. Reacts with nitrates, except ammonium nitrate, yielding nitrogen oxides, ammonia, and heat (the reaction is slow at room temperature but violent at above 80 °C and may spontaneously ignite); the reaction can be inhibited by a weak acid, e.g. boric acid. Corroded ...