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SUMMARYIn this unit, we have learnt some basic concepts in structure and reactivity of organic compounds, which are formed due to covalent bonding. The nature of the covalent bonding in organic compounds can be described in terms of orbitals hybridisation concept, according to which carbon can have sp3, sp2 and sp hybridised orbitals. The sp3, sp2 and sp hybridised carbons are found in compounds like methane, ethene and ethyne respectively.
The tetrahedral shape of methane, planar shape of ethene and linear shape of ethyne can be understood on the basis of this concept. A sp3 hybrid orbital can overlap with 1s orbital of hydrogen to give a carbon - hydrogen (C-H) single bond (sigma, σ bond). Overlap of a sp2 orbital of one carbon with sp2 orbital of another results in the formation of a carbon-carbon σ bond.
The unhybridised p orbitals on two adjacent carbons can undergo lateral (side-byside) overlap to give a pi (π) bond. Organic compounds can be represented by various structural formulas. The three dimensional representation of organic compounds on paper can be drawn by wedge and dash formula.
Organic compounds can be classified on the basis of their structure or the functional groups they contain. A functional group is an atom or group of atoms bonded together in a unique fashion and which determines the physical and chemical properties of the compounds. The naming of the organic compounds is carried out by following a set of rules laid down by the International Union of Pure and Applied Chemistry (IUPAC).
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