What is homolytic cleavage of a covalent bond? Explain with an example. Or,write about bond cleavage and the intermediate free radical.

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(N/A) In homolytic cleavage,one of the electrons of the shared pair in a covalent bond goes with each of the bonded atoms.
In homolytic cleavage,the movement of a single electron takes place instead of an electron pair. The single electron movement is shown by a 'half-headed' (fish hook) curved arrow.
- Such cleavage results in the formation of neutral species (atom or group) which contains an unpaired electron. These species are called free radicals.
- Like carbocations and carbanions,free radicals are also very reactive.
- $A$ homolytic cleavage can be shown as:
$R-Z \xrightarrow{\text{Heat or Light}} \dot{R} + \dot{Z}$
Organic reactions,which proceed by homolytic fission,are called free radical,homopolar,or nonpolar reactions.

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Similar Questions

Carbocation as an intermediate is likely to be formed in the reaction:

The correct stability order for the following species is:
$(I)$ $o-CN-C_6H_4-CH_2^-$
$(II)$ $m-CN-C_6H_4-CH_2^-$
$(III)$ $p-CN-C_6H_4-CH_2^-$
$(IV)$ $C_6H_5-CH_2^-$
(Note: The image shows the structures of these carbanions.)

Which carbocation is the least stable?

What is the order of stability of carbon free radicals among ${3^\circ}$,${2^\circ}$,${1^\circ}$,and $\mathop C\limits^\bullet {H_3}$?

Which of the following carbocations is least stable?

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