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The methyl radical (•CH₃) is a fundamental species in organic chemistry and free radical reactions. It consists of a carbon atom bonded to three hydrogen atoms, with one unpaired electron remaining on the carbon atom. This makes the methyl radical highly reactive.
Carbon has 4 valence electrons.
In the methyl radical, carbon shares 3 electrons with hydrogen atoms through covalent bonds.
This leaves 1 unpaired electron on carbon.
Hence, the total number of valence electrons around carbon is 7, not the complete octet (8).
The carbon in a methyl radical undergoes sp² hybridization:
Three sp² hybrid orbitals overlap with the 1s orbitals of three hydrogens, forming three sigma (σ) bonds.
The unpaired electron resides in the remaining unhybridized p orbital.
The geometry of the methyl radical is trigonal planar (like carbocations) or very close to it. The bond angle is approximately 120°, which is consistent with sp² hybridization.
Methyl radical plays a major role in free radical reactions, such as:
Halogenation of alkanes (chain propagation step).
Combustion reactions (intermediate species).
Polymerization (free radical chain reactions).
Option 1 (sp³, 8 electrons): Incorrect, because methyl radical does not have a complete octet.
Option 2 (sp², 6 electrons): Wrong, since carbon has 7 electrons here, not 6.
Option 4 (sp, linear geometry): Incorrect, methyl radical is not linear; it is planar.
Methyl radical is sp² hybridized, contains 7 valence electrons, and has one unpaired electron in a p orbital, making it a reactive intermediate in many organic reactions.
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