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Question

In the Iodination of alkane, Some HIO3 is added so that :


A

Reaction is made faster

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B

Reaction is made more selutive

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C

HI formed is Oxidisid to I2

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D

None of the above

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Solution

The correct option is C

HI formed is Oxidisid to I2


iodination (Direct Free radical iodination) is not favorable.

The chain initiation and the overall chain propogation steps are highly endothermic

But adding HIO3 improves the yield of the alkyl iodide. This is due to the removal of the highly-reducing Hl, which is oxidized to l2.


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