I have been reading mechanisms recently, and I find that $\ce{-CH3}$ is a $+I$ effect group. I understand the mechanisms that require this, but can someone explain at the molecular level why is $\ce{-CH3}$ a $+I$ effect group?
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$\begingroup$ The inductive effect is due to hyperconjugation, which is deliberated on in the following post. chemistry.stackexchange.com/questions/8412/… $\endgroup$– Tan Yong BoonCommented Aug 6, 2017 at 5:39
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$\begingroup$ I know what's HC, but can you elaborate on how HC makes the $+I $ effect? $\endgroup$– Wrichik BasuCommented Aug 6, 2017 at 5:42
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According to http://www.chem.ucalgary.ca/courses/351/Carey5th/Ch04/ch4-3-2-1.html:
"Hyperconjugation is the stabilising interaction that results from the interaction of the electrons in a σ-bond (usually C-H or C-C) with an adjacent empty or partially filled p-orbital or a π-orbital to give an extended molecular orbital that increases the stability of the system."
How I see "hyperconjugation" is the formation of partial π bonds. Let's say we have a methyl group bonded to a positively-charged carbon atom with a vacant p orbital.
Ideally, it would be best if we could have an atom with a fully-filled p orbital, which is parallel to the p orbital of the this positively-charged carbon atom, to come and interact with this carbon atom. Such an interaction would stabilise the electron-deficient carbon atom. This is essentially the basis of hyperconjugation.
However, in our case, we do not have such an atom with a fully-filled p orbital around. Instead, what we have is a few C-H σ bonds. These C-H bonds are not parallel to the vacant p orbital of the positively-charged carbon atom but they are very close to parallel, around 19.5 degrees away, assuming that the geometry of the methyl group bonded to that positively-charged carbon atom is tetrahedral.
These C-H bonds are thus able to interact with the electron deficient vacant p orbitals of the positively-charged carbon atom, maybe not maximally, but sufficiently. These interactions would be what I would call "partial π bonds" and they stabilise the electron deficiency of the carbon atom. This interaction is also what is known as "hyperconjugation".
*Please note that the illustration is slightly inaccurate because the hydrogen atom would not pop off the methyl group for the formation of a full π bond between the two carbon atoms. This is only illustrated to better show the interaction of the C-H σ bonds with the p orbital of the positively-charged carbon atom.
answered Aug 6, 2017 at 5:59