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Hydrocarbons
During the pyrolysis of alkanes C-C bonds break in preference to C-H bond. Why?
The bond dissociation energy of C-C bond is less than that of C-H bond. Hence, C-C bonds break in preference to C-H bond.
Some More Questions From Hydrocarbons Chapter
Out of n-pentane, isopentane and neopentane which has lower boiling point?
During the pyrolysis of alkanes C-C bonds break in preference to C-H bond. Why?
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.
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?
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