We study the ground-state properties of linear chains of dipolar planar rotors hindered by a six-fold on-site potential, a model motivated by water molecules confined in the hexagonal cavities of beryl. Using density matrix renormalization group (DMRG) calculations, we locate the quantum phase transition between the disordered and ferroelectrically ordered phases using the von Neumann entanglement entropy and the Binder ratio of the polarization. A sweep of the six-fold pinning strength shows that increasing hindrance shifts the critical dipolar coupling gc to smaller values. These results suggest that crystal-field hindrance can promote, rather than suppress, dipolar ordering. This work has implications for ferroelectricity and quantum-device tuning in confined molecular rotors

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