To determine the shape of a carbocation, we need to understand the electronic configuration and hybridization involved when a carbocation forms.
A carbocation is a positively charged carbon atom with only six electrons in its valence shell. Because it is electron-deficient, it lacks an octet and thus cannot exhibit tetrahedral geometry, which requires an electron pair for each bond in a 3D space.
The most stable configuration that a carbocation can achieve is trigonal planar. Here is the reasoning behind this:
Therefore, the correct answer, based on hybridization and geometry theory, is that a carbocation takes a trigonal planar shape.
Let's briefly consider why the other options are incorrect:
Thus, considering all the points, the shape of the carbocation is trigonal planar.
A carbocation has a central carbon atom with three bonded groups and one empty {p}-orbital. The geometry around the carbocation is trigonal planar because the three groups are arranged at 120$^\circ$ to minimize electron repulsion.
\[\textbf{Carbocation structure:} \quad \text{H-C$^+$-H}.\]
The trigonal planar shape is due to {sp}$^2$-hybridization of the central carbon atom.
Match the LIST-I with LIST-II for an isothermal process of an ideal gas system. 
Choose the correct answer from the options given below:
Which one of the following graphs accurately represents the plot of partial pressure of CS₂ vs its mole fraction in a mixture of acetone and CS₂ at constant temperature?
