An analytical theory is developed that describes local relaxation prop
erties of a freely jointed chain composed of rigid units and oriented
by a dipole field. The theory takes into account the bond reactions. T
he conformation properties and local mobilities of such system were mo
deled by the method of brownian dynamics. The chain segments are orien
ted along the field. The order parameter of the segments and the degre
e of chain deformation increase with the field amplitude. The rotation
al mobility of the chain segments was studied. In contrast to the dyna
mic properties of a chain exposed to a strong field of the quadrupole
symmetry, both longitudinal and transverse (with respect to the dipole
field direction) rotational relaxation times of the chain segments de
crease with increasing degree of deformation. The spectrum of relaxati
on times of the normal modes of the chain splits into two branches, co
rresponding to the longitudinal and transverse motions relative to the
direction of the external field. The two branches are characterized b
y different dependences of the relaxation times of various scales on t
he degree of chain deformation. An analytical theory is presented that
satisfactorily describes the dependence of the relaxation time on the
dipole field strength obtained in a numerical experiment.