--%>

Explain oxygen and its preparation.

Karl Scheele, the Swedish chemist, was the first to prepare oxygen by heating mercuric oxide in 1772. He recognized the gas as one of the major constituents of atmospheric air and called it 'fire air'. Joseph Priestley, the English chemist also prepared oxygen by focusing the sun rays by means of a double lens on mercuric oxide. Priestley published his results in 1774 and has been regarded as the discoverer of oxygen. However, its elemental nature was proved by Lavoisier.

Oxygen is first element of group 16 of periodic table. It may be called the head of chalcogens family. Its configuration (1s22s22p4)shows the presence of six electrons in the valence shell. It does show some characteristics which are not shown by other members of the family because of its small size. For example, it is able to form pπ-pπ bonding and exists as diatomic molecule (O2). The other elements of the group do not exist as diatomic molecule due to their inability to form pπ-pπ bonding.

Isotopes of oxygen

Oxygen has three naturally occurring isotopes which are:

1870_dioxygen.png 

Out of these three isotopes, O-18 is radioactive in nature and finds frequent use in studying the mechanisms of organic reactions and other trace techniques. Like hydrogen, oxygen also exists in the elementary form as diatomic molecule (O2) and is referred to as dioxygen. 

Terrestrial abundance and distribution

Oxygen is the most abundant element on the surface of the earth. In Free State, it occurs in air and constitutes 21% by volume of air and 23% by weight. In the combined state, it constitutes 89% by mass of water and 50% by mass of earth's solid crust. In earth's solid crust, it is mainly present as silicates, carbonates, aluminates and oxides of metals.

Almost all the dioxygen in atmosphere is believed to be the result of photosynthesis by green plants which can be represented as 

1915_dioxygen1.png 

   Related Questions in Chemistry

  • Q : Molarity of Sulfuric acid Choose the

    Choose the right answer from following. What is the molarity of H2SO4 solution, that has a density 1.84 gm/cc at 35c and contains solute 98% by weight: (a) 4.18 M (b) 8.14 M (c)18.4 M (d)18 M

  • Q : Calculating value of molar solution

    Choose the right answer from following. An X molal solution of a compound in benzene has mole fraction of solute equal to 0.2. The value of X is: (a)14 (b) 3.2 (c) 4 (d) 2

  • Q : What are biodegradable polymers?

      These are polymers that can be broken into small segments by enzyme-catalysed reactions. The required enzymes are produced by microorganism. It is a known fact that the carbon-carbon bonds of chain growth polymers are inert to enzyme-catalysed reactions, and hence they are non biod

  • Q : Problem on equilibrium composition The

    The catalytic dehydrogenation of 1-butene to 1,3-butadiene, C4H8(g) = C4H6(g)+H2(g) is carried out at 900 K and 1 atm.

    Q : Relative lowering of vapour pressure

    explain the process of relative lowering of vapour pressure

  • Q : Liquid surfaces The surface between a

    The surface between a liquid and a vapour distinguishes these fluids. The surface tension of liquids can be looked upon as that the property which draws a liquid together and forms a liquid vapour interface, therefore, distinguishing liquids from gases.<

  • Q : Question based on vapour pressure While

    While a substance is dissolved in a solvent, the vapour pressure of the solvent is decreased. This results in: (a) An increase in the boiling point of the solution (b) A decrease in the boiling point of solvent (c) The solution having a higher freezing point than

  • Q : Amines why o-toluidine is a weaker base

    why o-toluidine is a weaker base than aniline?

  • Q : Raoults law Give me answer of this

    Give me answer of this question. Provide solution of this question. Which one of the following is the expression of Raoult's law: (a) P-P1/P = n/n+N (b) P1-P/P = N/ N+n (c)P-P2/P1= N/ N-n (d) P1-P/P2= N-n/N

  • Q : Chem Explain how dissolving the Group

    Explain how dissolving the Group IV carbonate precipitate with 6M CH3COOH, followed by the addition of extra acetic acid.