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OPT, 10PT EA): Provide the mechanism for the to nanism for the following transformations gewollt Br2, hv
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Answer #1

The reactant alkane react with Br2 by radical substitution under photochemical or UV light, the alkyl halide and HBr are formed. In general the alkane free radical reactivity order is tertiary > secondary > primary > methyl. The reaction proceeds via radical chain mechanism which involves radical intermediates following two key steps mechanism.

Step 1: Radical initiation process

Under the uv light, the weak halogen bond to undergo homolytic cleavage to generate two bromine radicals and starting the chain process.

Step 2: Product formation process

A bromine radical abstracts a hydrogen from the starting reactant alkane to form HBr and the tertiary alkyl radical which abstract a bromine atom from another molecule of Br2 to form the desired product as alkyl bromide and another bromine radical.

The reaction mechanism of the given reaction is explained in the below image.

RiAehin Medtunigv- suidlues tuo Stop t Raiced initiat uder w BY Cleavngl Aat 2 By abdonet Hto +.Br adical revet adth Bre mdeu

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