Hydrocarbons
When the same molecular formula represents two compounds which differ in the spatial arrangement of atoms or groups around carbon-carbon double bond, then such isomers are called geometrical isomers. The phenomenon is called geometrical isomerism.
Cause of geometrical isomerism: Geometrical isomerism is due to the restricted or hindered rotation around the carbon-carbon double bond. Due to the hindered rotation around carbon-carbon double bond, the relative positions of atoms or group attached to the doubly bonded carbon atoms get fixed. For example, the molecular formula C2A2B2with the structural formula BAC=CAB represents two geometrical isomers.
Isomer in which similar atoms or groups lie on the same side of the double bond is called cis-isomer. The geometrical isomer I represent a cis-isomer. Isomer in which the similar atoms or groups lie on the opposite sides of the double bond is called trans-isomer. The geometrical isomer (ii) represents a trans-isomer. Hence, geometrical isomerism is known as cis-trans isomerism e.g.
(i) But-2-ene exhibits geometrical isomerism.
(ii) Hex-3-ene shows geometrical isomerism.
(iii) 1, 2-dichloroethene exhibits geometrical isomerism.
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Define cracking.
What is the function of iodic acid in the iodination of alkanes? Can we use any other substance in its place?
What is alternation effect?
Arrange the following compounds in order of their increasing boiling points:
n-Pentane, n-Hexane, Ethane, 2-2-Dimethylpentane, 2-Methylpentane.
Why is light or heat necessary to initiate chlorination reaction of alkanes?
What are conformation or rotational isomers?
Can you separate the two conformations of ethane?
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