In 2, the empty p orbital on C1 and the sp3-hybridized orbital on C2 participating in C2—H1 bond are more or less parallel, allowing parallel overlap, which lowers the electron deficiency at C1 but makes the H1 electron deficient.
This overlap is not strong enough to completely prevent the free rotation around the C1—C2 bond. Consequently, C2—H2 bond and C2—H3 bond could also share electrons with the empty p orbital on C1.
The structure of the ethyl carbocation, according to the theory of hyperconjugation, can be shown conveniently using a series of resonance forms.
Based on the above resonance forms, the structure of the ethyl carbocation can be shown roughly as follows.
Due to hyperconjugation, in the ethyl carbocation, the net charge of +1 is shared by a total of four atoms, one carbon atom and three hydrogen atoms. Shown below are the resonance forms of the isopropyl carbocation (2), a secondary carbocation.
Based on the resonance forms, the hybrid can be shown roughly as follows.
Due to hyperconjugation, in the isopropyl carbocation, the net charge of +1 is shared by a total of seven atoms, one carbon atom and six hydrogen atoms. Thus, the net charge of +1 is delocalized over a greater number of atoms in the isopropyl carbocation than in the ethyl carbocation. The isopropyl carbocation should, therefore, be more stable than the ethyl carbocation. This prediction is consistent with the observation that secondary alkyl carbocations are more stable than primary alkyl carbocations.