a)
Interpretation:
The structures of different monochloro products, without considering their stereochemistry, obtainable by the radical chlorination of n-butane are to be drawn.
Concept introduction:
In radical chlorination reactions, if all the hydrogens present in the alkane are of same kind then it is possible to get a single monochloro product. If the alkane has hydrogens of different kinds then hydrogens belonging to all kinds will be substituted by chlorine resulting in a mixture of monochloro
To draw:
The structures of different monochloro products, without considering their stereochemistry, obtainable by the radical chlorination of n-butane.
b)
Interpretation:
The structures of different monochloro products, without considering their stereochemistry, obtainable by the radical chlorination of 2-methylbutane are to be drawn.
Concept introduction:
In radical chlorination reactions, if all the hydrogens present in the alkane are of same kind then it is possible to get a single monochloro product. If the alkane has hydrogens of different kinds then hydrogens belonging to all kinds will be substituted by chlorine resulting in a mixture of monochloro alkanes as product.
To draw:
The structures of different monochloro products, without considering their stereochemistry, obtainable by the radical chlorination of 2-methylbutane.
c)
Interpretation:
The structures of different monochloro products, without considering their stereochemistry, obtainable by the radical chlorination of methylcyclopentane are to be drawn.
Concept introduction:
In radical chlorination reactions, if all the hydrogens present in the alkane are of same kind then it is possible to get a single monochloro product. If the alkane has hydrogens of different kinds then hydrogens belonging to all kinds will be substituted by chlorine resulting in a mixture of monochloro alkanes as product.
To draw:
The structures of different monochloro products, without considering their stereochemistry, obtainable by the radical chlorination of methylcyclopentane.
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Chapter 6 Solutions
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