Skip to main content
Chemistry LibreTexts

4.5: Carbocation Structure and Stability

  • Page ID
    205334
  • \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)

    \( \newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\)

    ( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\)

    \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)

    \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\)

    \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)

    \( \newcommand{\Span}{\mathrm{span}}\)

    \( \newcommand{\id}{\mathrm{id}}\)

    \( \newcommand{\Span}{\mathrm{span}}\)

    \( \newcommand{\kernel}{\mathrm{null}\,}\)

    \( \newcommand{\range}{\mathrm{range}\,}\)

    \( \newcommand{\RealPart}{\mathrm{Re}}\)

    \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\)

    \( \newcommand{\Argument}{\mathrm{Arg}}\)

    \( \newcommand{\norm}[1]{\| #1 \|}\)

    \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\)

    \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\AA}{\unicode[.8,0]{x212B}}\)

    \( \newcommand{\vectorA}[1]{\vec{#1}}      % arrow\)

    \( \newcommand{\vectorAt}[1]{\vec{\text{#1}}}      % arrow\)

    \( \newcommand{\vectorB}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vectorC}[1]{\textbf{#1}} \)

    \( \newcommand{\vectorD}[1]{\overrightarrow{#1}} \)

    \( \newcommand{\vectorDt}[1]{\overrightarrow{\text{#1}}} \)

    \( \newcommand{\vectE}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{\mathbf {#1}}}} \)

    \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}} } \)

    \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash {#1}}} \)

    \(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)
    Objectives

    After completing this section, you should be able to

    • describe the geometry of a given carbocation.
    • arrange a given series of carbocations in order of increasing or decreasing stability.
    • explain the relative stability of methyl, primary, secondary and tertiary carbocations in terms of hyperconjugation and inductive effects.
    Study Notes

    Although hyperconjugation can be used to explain the relative stabilities of carbocations, this explanation is certainly not the only one, and is by no means universally accepted. A more common explanation, involving the concept of an inductive effect, is given below.

    It is a general principle in chemistry that the more a charge is dispersed, the more stable is the species carrying the charge. Put simply, a species in which a positive charge is shared between two atoms would be more stable than a similar species in which the charge is borne wholly by a single atom. In a tertiary carbocation, the positively charged carbon atom attracts the bonding electrons in the three carbon-carbon sigma (σ) bonds, and thus creates slight positive charges on the carbon atoms of the three surrounding alkyl groups (and, indeed, on the hydrogen atoms attached to them). Chemists sometimes use an arrow to represent this inductive release:

    charge stabilization in a tertiary carbocation.svg

    Note: These diagrams do not reflect the geometry of the carbocation. The overall charge on the carbocation remains unchanged, but some of the charge is now carried by the alkyl groups attached to the central carbon atom; that is, the charge has been dispersed.

    In the tertiary carbocation shown above, the three alkyl groups help to stabilize the positive charge. In a secondary carbocation, only two alkyl groups would be available for this purpose, while a primary carbocation has only one alkyl group available. Thus the observed order of stability for carbocations is as follows:

    tertiary > secondary > primary > methyl.

    Stability of carbocation intermediates

    The next step in understanding why Markovnikov's rule is often followed in electrophilic additions, involves understanding the structure and stability of the carboncation intermediate formed during the mechanism.

    Carbocation Structure

    Carbocations typically have three substituents which makes the carbon sp2 hybridized and gives the overall molecule a trigonal planar geometry. The carbocation's substituents are all in the same plane and have a bond angle of 120o between them. The carbon atom in the carbocation is electron deficient; it only has six valence electrons which are used to form three sigma covalent bonds with the substituents. The carbocation carbon has an unoccupied p orbital which is perpendicular to the plane created by the substituents. The p orbital can easily accept electron pairs during reactions making carbocations excellent Lewis acids.

    Carbocation.svg

    Carbocation.png

    Stability of Carbocation Intermediates

    By being a reactive intermediate of the electrophilic addition mechanism, the stability of a carbocation has a direct effect on the reaction. The critical question now becomes, what stabilizes a carbocation?

    A positively charged species such as a carbocation is very electron-poor, and thus anything which donates electron density will help to stabilize it. Conversely, a carbocation will be destabilized by an electron withdrawing group.

    carbocation with electron donating group stabilizing carbocation.svg
    electron donating group stabilizes a carbocation
    carbocation with electron withdrawing group destabilizing carbocation.svg
    electron withdrawing group destabilizes a carbocation

    Extensive experimental evidence has shown that a carbocation becomes more stable as the number of alkyl substituents increases. Carbocations can be given a designation based on the number of alkyl groups attached to the carbocation carbon. Three alkyl groups is called a tertiary (3o) carbocation, 2 alkyl groups is called secondary (2o), and 1 alkyl group is called primary (1o). No alkyl groups are attached (3 hydrogen substituents) is called a methyl carbocation.

    The overall order of stability is as follows:

    series showing increasing stability of alkyl carbocations, from methyl (least stable) to primary to secondary to tertiary (most stable).svg

    Alkyl groups stabilized carbocations for two reasons. The first is through inductive effects. As discussed in Section 2-1, inductive effects occur when the electrons in covalent bonds are shifted towards an nearby atom with a higher electronegativity. In this case, the positively charged carbocation draws in electron density from the surrounding substituents thereby gaining stabilization by slightly reducing its positive charge. Alkyl groups are more effective at inductively donating electron density than a hydrogen because they are larger, more polarizable, and contain more bonding electrons. As more alkyl groups are attached to the carbocation more inductive electron donation occurs and the carbocation becomes more stable.

    The second reason alkyl groups stabilize carbocations is through hyperconjugation. As previously discussed in Section 7.6, hyperconjugation is an electron donation that occurs from the parallel overlap of p orbitals with adjacent hybridized orbitals participating in sigma bonds. This electron donation serves to stabilize the carbocation. As the number of alkyl substituents increases, the number of sigma bonds available for hyperconjugation increases, and the carbocation tends to become more stabilized.

    In the example of ethyl carbocation shown below, the p orbital from a sp2 hybridized carbocation carbon involved interacts with a sp3 hybridized orbital participating in an adjacent C-H sigma bond. Electron density from the C-H sigma bond is donated into carbocation's p orbital providing stabilization.

    The molecular orbital of the ethyl carbocation shows the interaction of electrons in methyl group's C-H sigma bonds with the adjacent empty p orbital from the carbocation. The interaction creates a bonding molecular orbital which extends over the three atom chain (C-C-H) involved in hyperconjugation. The expanded molecular orbital helps to stabilize the carbocation.

    Presentation1.png

    It is not accurate to say, however, that carbocations with higher substitution are always more stable than those with less substitution. Just as electron-donating groups can stabilize a carbocation, electron-withdrawing groups act to destabilize carbocations. Carbonyl groups are electron-withdrawing by inductive effects, due to the polarity of the C=O double bond. It is possible to demonstrate in the laboratory that carbocation A below is more stable than carbocation B, even though A is a primary carbocation and B is secondary.

    electron withdrawing groups destabilize carbocations less as they are further from the carbocation.svg

    The difference in stability can be explained by considering the electron-withdrawing inductive effect of the ester carbonyl. Recall that inductive effects - whether electron-withdrawing or donating - are relayed through covalent bonds and that the strength of the effect decreases rapidly as the number of intermediary bonds increases. In other words, the effect decreases with distance. In species B the positive charge is closer to the carbonyl group, thus the destabilizing electron-withdrawing effect is stronger than it is in species A.

    In the next chapter we will see how the carbocation-destabilizing effect of electron-withdrawing fluorine substituents can be used in experiments designed to address the question of whether a biochemical nucleophilic substitution reaction is SN1 or SN2.

    Stabilization of a carbocation can also occur through resonance effects, and as we have already discussed in the acid-base chapter, resonance effects as a rule are more powerful than inductive effects. Consider the simple case of a benzylic carbocation:

    four resonance structures of benzylic carbocation with arrows showing electron flow.svg

    This carbocation is comparatively stable. In this case, electron donation is a resonance effect. Three additional resonance structures can be drawn for this carbocation in which the positive charge is located on one of three aromatic carbons. The positive charge is not isolated on the benzylic carbon, rather it is delocalized around the aromatic structure: this delocalization of charge results in significant stabilization. As a result, benzylic and allylic carbocations (where the positively charged carbon is conjugated to one or more non-aromatic double bonds) are significantly more stable than even tertiary alkyl carbocations.

    two resonance structures of allylic carbocation with arrows showing electron flow.svg

    Because heteroatoms such as oxygen and nitrogen are more electronegative than carbon, you might expect that they would by definition be electron withdrawing groups that destabilize carbocations. In fact, the opposite is often true: if the oxygen or nitrogen atom is in the correct position, the overall effect is carbocation stabilization. This is due to the fact that although these heteroatoms are electron withdrawing groups by induction, they are electron donating groups by resonance, and it is this resonance effect which is more powerful. (We previously encountered this same idea when considering the relative acidity and basicity of phenols and aromatic amines in section 7.4). Consider the two pairs of carbocation species below:

    The two resonance structures are more stable and the compound on the right has no resonance so there is no delocalization..svg

    The two resonance structures are more stable and the compound on the right has no resonance so there is no delocalization.svg

    In the more stable carbocations, the heteroatom acts as an electron donating group by resonance: in effect, the lone pair on the heteroatom is available to delocalize the positive charge. In the less stable carbocations the positively-charged carbon is more than one bond away from the heteroatom, and thus no resonance effects are possible. In fact, in these carbocation species the heteroatoms actually destabilize the positive charge, because they are electron withdrawing by induction.

    Finally, vinylic carbocations, in which the positive charge resides on a double-bonded carbon, are very unstable and thus unlikely to form as intermediates in any reaction.

    kekule structure of a vinylic carbocation.svg
    a vinylic carbocation (very unstable)

    Example \(\PageIndex{1}\)

    In which of the structures below is the carbocation expected to be more stable? Explain.

    The molecule on the left has the positive charge one carbon away from a nitrogen. The molecule on the right has the positive charge two carbons away from a nitrogen..svg

    Answer

    In the carbocation on the left, the positive charge is located in a position relative to the nitrogen such that the lone pair of electrons on the nitrogen can be donated to fill the empty orbital. This is not possible for the carbocation species on the right.

    structure on left has carbocation on carbon adjacent to nitrogen, and resonance is possible. structure on the right has carbocation two carbons away, and resonance is not possible..svg

    Example \(\PageIndex{2}\)

    Draw a resonance structure of the crystal violet cation in which the positive charge is delocalized to one of the nitrogen atoms.

    Answer
    possible resonance in crystal violet structure, allows a resonance form with all atoms satisfying the octet rule.svg

    When considering the possibility that a nucleophilic substitution reaction proceeds via an SN1 pathway, it is critical to evaluate the stability of the hypothetical carbocation intermediate. If this intermediate is not sufficiently stable, an SN1 mechanism must be considered unlikely, and the reaction probably proceeds by an SN2 mechanism. In the next chapter we will see several examples of biologically important SN1 reactions in which the positively charged intermediate is stabilized by inductive and resonance effects inherent in its own molecular structure.

    Example \(\PageIndex{3}\)

    State which carbocation in each pair below is more stable, or if they are expected to be approximately equal. Explain your reasoning.

    comparison of a) tertiary vs secondary carbocation, b) tertiary versus secondary carbocation, c) secondary vs secondary carbocation, d) carbocation adjacent to nitrogen atom versus tertiary carbocation, and e) allylic versus tertiary carbocation.svg

    Answer
    1. 1 (tertiary vs. secondary carbocation)
    2. 1 (tertiary vs. secondary carbocation)
    3. 2 (positive charge is further from electron-withdrawing fluorine)
    4. 1 (lone pair on nitrogen can donate electrons by resonance)
    5. 1 (allylic carbocation – positive charge can be delocalized to a second carbon)

    4.5: Carbocation Structure and Stability is shared under a not declared license and was authored, remixed, and/or curated by LibreTexts.

    • Was this article helpful?