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Iron(III) nitrate is deliquescent, and it is commonly found as the nonahydrate Fe(NO 3) 3 ·9H 2 O, which forms colourless to pale violet crystals.This compound is the trinitrate salt of the aquo complex [Fe(H 2 O) 6] 3+. [4]
The solution of the iron(II) nitrate-hydrazine complex is produced by the reaction of hydrazine nitrate and ferric nitrate at 40 °C with copper(II) nitrate as a catalyst: [8] 4 Fe(NO 3) 3 + N 2 H 5 NO 3 → 4 Fe(NO 3) 2 + N 2 + 4 HNO 3. If the compound is used in situ, the compound is produced by the reaction of iron(II) chloride and calcium ...
Molecular weight (M.W.) (for molecular compounds) and formula weight (F.W.) (for non-molecular compounds), are older terms for what is now more correctly called the relative molar mass (M r). [8] This is a dimensionless quantity (i.e., a pure number, without units) equal to the molar mass divided by the molar mass constant .
Anhydrous iron(III) pyrophosphate can be prepared by heating the mixture of iron(III) metaphosphate and iron(III) phosphate under oxygen with the stoichiometric ratio 1:3. The reactants can be prepared by reacting iron(III) nitrate nonahydrate with phosphoric acid. [5] It can be also prepared via the following reaction: [6]
Iron has five nitrides observed at ambient conditions, Fe 2 N, Fe 3 N 4, Fe 4 N, Fe 7 N 3 and Fe 16 N 2.They are crystalline, metallic solids. Group 7 and group 8 transition metals form nitrides that decompose at relatively low temperatures—iron nitride, Fe 2 N decomposes with loss of molecular nitrogen at around 400 °C and formation of lower-nitrogen content iron nitrides.
Iron nitrate may refer to: Iron(II) nitrate, Fe(NO 3) 2, a green compound that is unstable to heat;
Aluminium nitrate is a white, water-soluble salt of aluminium and nitric acid, most commonly existing as the crystalline hydrate, aluminium nitrate nonahydrate, Al(NO 3) 3 ·9H 2 O. Preparation [ edit ]
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. Most useful is the reduction of aryl nitro compounds.