John McMurry, Professor Emeritus

7.9 Carbocation Structure and Stability

7.9 • Carbocation Structure and Stability

To understand why Markovnikov’s rule works, we need to learn more about the structure and stability of carbocations and about the general nature of reactions and transition states. The first point to explore involves structure.

A great deal of experimental evidence has shown that carbocations are planar. The trivalent carbon is sp²-hybridized, and the three substituents are oriented toward the corners of an equilateral triangle, as indicated in Figure 7.10. Because there are only six valence electrons on carbon and all six are used in the three σ bonds, the p orbital extending above and below the plane is unoccupied.

An orbital representation and ball-and-stick model of a carbocation bonded to R, R prime, and R double prime. Bond angle is 120 degrees. — Figure 7.10 **The structure of a carbocation**. The trivalent carbon is sp²-hybridized and has a vacant p orbital perpendicular to the plane of the carbon and three attached groups.

The second point to explore involves carbocation stability. 2-Methylpropene might react with H⁺ to form a carbocation having three alkyl substituents (a tertiary ion, 3°), or it might react to form a carbocation having one alkyl substituent (a primary ion, 1°). Since the tertiary alkyl chloride, 2-chloro-2-methylpropane, is the only product observed, formation of the tertiary cation is evidently favored over formation of the primary cation. Thermodynamic measurements show that, indeed, the stability of carbocations increases with increasing substitution so that the stability order is tertiary > secondary > primary > methyl.

The figure shows the increasing order of stability for carbocations, as follows: methyl, primary, secondary, and tertiary. The structure of each carbocation is depicted.

One way of determining carbocation stabilities is to measure the amount of energy required to form a carbocation by dissociation of the corresponding alkyl halide, R − X → R⁺ + :X⁻. As shown in Figure 7.11, tertiary alkyl halides dissociate to give carbocations more easily than secondary or primary ones. Thus, trisubstituted carbocations are more stable than disubstituted ones, which are more stable than monosubstituted ones. The data in Figure 7.11 are taken from measurements made in the gas phase, but a similar stability order is found for carbocations in solution. The dissociation enthalpies are much lower in solution because polar solvents can stabilize the ions, but the order of carbocation stability remains the same.

Bar graph shows of dissociation enthalpy in kJ per mol: chloromethane: 940, chloroethane: 810, isopropyl chloride: 710, and t-butylchloride: 680. Highly substituted alkyl halides exhibit higher ease of dissociation. — Figure 7.11 **A plot of dissociation enthalpy versus substitution pattern for the gas-phase dissociation of alkyl chlorides to yield carbocations**. More highly substituted alkyl halides dissociate more easily than less highly substituted ones.

Why are more highly substituted carbocations more stable than less highly substituted ones? There are at least two reasons. Part of the answer has to do with inductive effects, and part has to do with hyperconjugation. Inductive effects, discussed in Section 2.1 in connection with polar covalent bonds, result from the shifting of electrons in a σ bond in response to the electronegativity of nearby atoms. In the present instance, electrons from a relatively larger and more polarizable alkyl group can shift toward a neighboring positive charge more easily than the electron from a hydrogen. Thus, the more alkyl groups attached to the positively charged carbon, the more electron density shifts toward the charge and the more inductive stabilization of the cation occurs (Figure 7.12).

The figure shows the electrostatic potential maps and structures of methyl, primary, secondary, and tertiary carbocations. The gray and white spheres represent carbon and hydrogen atoms, respectively. — Figure 7.12 **A comparison of inductive stabilization for methyl, primary, secondary, and tertiary carbocations**. The more alkyl groups that are bonded to the positively charged carbon, the more electron density shifts toward the charge, making the charged carbon less electron-poor (blue in electrostatic potential maps).

Hyperconjugation, discussed in Section 7.6 in connection with the stabilities of substituted alkenes, is the stabilizing interaction between a p orbital and properly oriented C−H σ bonds on neighboring carbons that are roughly parallel to the p orbital. The more alkyl groups there are on the carbocation, the more possibilities there are for hyperconjugation and the more stable the carbocation. Figure 7.13 shows the molecular orbital for the ethyl carbocation, CH₃CH₂⁺, and indicates the difference between the C−H bond perpendicular to the cation p orbital and the two C−H bonds more parallel to the cation p orbital. Only these roughly parallel C−H bonds are oriented properly to take part in hyperconjugation.

The orbital representation of ethyl carbocation along its ball-and-stick model sandwich between overlapped orbitals. — Figure 7.13 **Stabilization of the ethyl carbocation, CH₃CH₂⁺, through hyperconjugation**. Interaction of neighboring C−H σ bonds with the vacant p orbital stabilizes the cation and lowers its energy. The molecular orbital shows that only the two C−H bonds more parallel to the cation p orbital are oriented properly. The C−H bond perpendicular to the cation p orbital can’t take part properly.

Problem 7-18

Show the structures of the carbocation intermediates you would expect in the following reactions:

(a)

(b)

Problem 7-19

Draw a skeletal structure of the following carbocation. Identify it as primary, secondary, or tertiary, and identify the hydrogen atoms that have the proper orientation for hyperconjugation in the conformation shown.