the chemistry of nitrogen

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Chapter 16

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The chemistry of Nitrogen. Chapter 16. Nitrogen. Nitrogen can complete its valence valence shell by: 1.) Electron gain: N 3- ion This is found in saltlike nitrides. 2.) formation of electron pair bonds: A) single bonds NH3 B) multiple bonds :N≡N: ; -N=N-, or NO 2 - PowerPoint PPT Presentation

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Page 1: The chemistry of Nitrogen

Chapter 16

Page 2: The chemistry of Nitrogen

Nitrogen can complete its valence valence shell by:

1.) Electron gain: N3- ion This is found in saltlike nitrides.

2.) formation of electron pair bonds: A) single bonds NH3 B) multiple bonds :N≡N: ; -N=N-, or NO2

3.) formation of electron pair bonds with electron gain, NH2

- or NH2-

4.) Formation of electron pair bonds with electron loss (substituted ammonium ions)

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Three-Covalent Nitrogen NR3 molecules are sp3 hybridised, the lone pair

occupies the fourth position. 1.) all NR3 compounds behave as Lewis bases,

give donor-acceptor complexes with lewis-acids, act as ligands towards transition metal ions [Co(NH3)6]3+

2.) Pyramidal molecules (NRR’R’’) should be chiral. Optical isomers can not be isolated, because N oscillates through the plane of the R-groups. The energy barrier is only 24kJ/mol. (Inversion)

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3.) in few cases 3-covalent nitrogen is planar;

N-N single bond energy

The difference between C and N in bonding energies is attributable to the effects of repsulsion between nonbonding lone pairs. Nitrogen has little tendency to catenation.

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Nitrogens propensity to form pπ- pπ multiple bonds is a feature that distinguishes it from phosphorus and the other GroupVB elements.

N2 has a high bond strength and a short internuclear distance (1.094Å). P forms infinite layer structures with only single bonds or P4 molecules.

The oxo anions NO2- and NO3

- , multiple bonds may be formulated in either resonance or MO terms.

Page 7: The chemistry of Nitrogen

Nitrogen occurs as dinitrogen. N2 (bp 77.3 K).

78% of the atmosphere is N2

N14/N15 has a ratio of 272. N15 compounds are used in tracer studies. The NN triple bond is responsible for the

inert behaviour of N2. N2 is prepared by liquefaction and

fractionation of air.

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N2 only reacts with Li to give Li3N. With certain transition metal complexes

oand with nitrogen fixing bacteria. Typical reactions of N2 at elevated

temperatures :

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Nitrides of eletropositives metals have structures with discrete nitrogen atoms and can be regarded as ionic (Ca2+)3(N3-)2

The Nitrides hydrolyse to ammonia and metal hydroxides.

Preparation: Direct interaction Loss of ammonia from amides on heating

Page 10: The chemistry of Nitrogen

Transition metal nitrides are often nonstoichiometric and have nitrogen atoms in the interstices of close-packed arrays of metal atoms.

They are like the carbides or borides hard, chemically inert, high melting and electrically conducting.

Numerous covalent nitrides (BN,S4N4,P3N5) These nitrides have very differing

properties, depending on the element.

Page 11: The chemistry of Nitrogen

Ammonia is formed by the action of a base on an ammonium salt:

Industrially Ammonia is made by the haber-Bosch process at 400-500 deg C and 100-1000atm.

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Ammonia is a colorless gas. In liquid form it has a high heat of evaporation . Liuid ammonia resembles water in its physical

behaviour. It forms strong nydrogen bonds. Its dielectric constant is around 22 at -34degC. Liquid ammonia has lower reactivity towards

electropositive metals and dissolves many of them. AgI is insoluble in water but soluble in ammonia. Ammonia burns in air:

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At 750-900 deg C in the presence of a catalyst (platinum, platinum-rhodium) :

NO reacts on with O2 to form the mixed oxides which can be absorbed in water to form nitric acid.

Page 14: The chemistry of Nitrogen

The sequence in industrial utilisation of atmospheric nitrogen is

Ammonia is extremely soluble in water.

Page 15: The chemistry of Nitrogen

Ammonium salts Crystalline salts of ammonium are mostly

water soluble. Ammonium salts generally resemble

those of potassium and rubidium in solubility and structure. The three ions have comparable radii.

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Hydrazine can be described as a reaction of ammonia with one ammonia as the substituent.

2 series of hydrazinium salts can be obtained:

N2H5+ are stable in water

N2H6 2+ are hydrolysed in water.

Page 18: The chemistry of Nitrogen

Anhydrous hydrazine is a fuming colorless liquid. It is considerable stable and burns in air

Aqueous hydrazine is a powerful reducing agent in basic solution.

Hydrazine is synthesized by the inateraction of aqueous ammonia with sodium hypochlorite

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But there is a competing reaction when hydrazine first is formed:

To prevent this reaction one needs to add gelatine. It complexes Cu2+ ions better than EDTA.

Page 20: The chemistry of Nitrogen

Hydroxylamine is a weaker base than NH3:

It is prepared by reduction of nitrates or nitrites either electrolytically or with SO2 under controlled conditions.

Hydroxylamine is a white unstable solid. It is used as a reducing agent.

Page 21: The chemistry of Nitrogen

Heavy metal azides are explosive and lead or mercury azides have been used in detonation caps.

The pure acid is a dangerously explosive liquid.

It can act as a ligand in metal complexes, it is linear molecule.

Page 22: The chemistry of Nitrogen

Dinitrogen monoxide

It has a linear structure is realtively unreactive , is inert towards:

Halogens, Alkali metals Ozone at RT. It is used as an anaesthetic.

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Nitrogen monoxide

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Dinitrogen trioxide The anhydride of nitrous acid

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Phosphorous occurs in minerals of the apatite family.

As, Sb,Bi occur mainly as sulfide minerals.

The electron configuration is ns2np3. P and N are very different in their

chemistry. P is a true non metal, down the period

the metallic trend is increasing.

Page 29: The chemistry of Nitrogen

Differences between N and P:1. Diminished ability to form pπ- pπ multiple

bonds2. The possibility to use the lower 3d orbitals Nitrogen forms esters, phosphorus gives

P(OR)3. Nitrogen oxides and oxoacids involve multiple bonds, whereas the phosphorus oxides have single bonds. Phosphoric acid PO(OH)3 in contrast NO2(OH).

Page 30: The chemistry of Nitrogen

Phosphorus is obtained by reduction of phosphate rocks.

Phosphorus distills and is condensed in water.

White P is stored under water to protect from air.

Red and black P are stable in air, burn on heating.

P is soluble in organic solvents.

Page 31: The chemistry of Nitrogen

As,Sb,Bi are obyained by reduction of the oxides with carbon or Hydrogen.

All elements react readily with halogens. Nitric acid Phosphoric acid, arsenic

acid, Sb trioxide and Bi nitrate. Interactions with metals gives

phosphides, arsenides, .... GaAs has semiconductor properties.

Page 32: The chemistry of Nitrogen

The stability of the hydrides decreases down the period.

Sb and Bi hydrides are very unstable. Phosphine is made from the reaction of

acids with zinc phosphide. Phosphine is a nerve toxin..

Page 33: The chemistry of Nitrogen

Trihalides are obtained by direct reaction with halogens.

They rapidly hydrolize in water Gaseous molecules have pyramidal structure. Iodides of As,SB,and Bi have layer structures

based on hexagonal closed packing of iodine atoms with the group VB elements.

Phosphorus trifluoride is a colorless toxic gas. It is slowly attacked by water and rapidly by

alkali.

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Phosphorus pentoxide (P4O10) It is used as one of the most effective

drying agents. Reacts with water to form phosphoric acid

Page 36: The chemistry of Nitrogen

Phosphoric acid: PCl3 or P4O6 are hydrolised in water

Phosphorus acid Hypophosphorus acid

Page 37: The chemistry of Nitrogen

Orthophosphoric acid Is the oldest known phosphorus compounds.

It is a syrupy liquid made by direct reaction of ground phhosphate rock with sulfuric acid.

The pure acid is a colorless cyrstalline solid. Stable and has no oxidising properties below

350-400 degC. It will attack quartz. Hydrogen bonding persists in the

concentrated solution and is respåonsible ofr the syrupy behaviour.

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