This article describes the dielectric relaxation behavior of flexible polymer chains having the so-called type-A dipoles parallel along the chain backbone. This behavior reflects the global chain motion. Viscoelastically well known features of this motion, such as the power-law relationship between the relaxation time and molecular weight of entangled linear chains (tau (1) proportional to M-3.5),are also observed dielectrically. More importantly, the dielectric behavior of linear chains having once-inverted type-A dipoles enables us to find some detailed dynamic features such as changes in the eigenfunctions f(p) of a local correlation function with the chain concentration in solutions. These changes are discussed in relation to motional coupling of concentrated chains. The dielectric properties detect the orientational correlation of two submolecules in the chain at two separate times, while the viscoelastic properties reflect the isochronal orientational anistoropy of individual submolecules. Thus the chain motion is differently averaged in the dielectric and viscoelastic properties, and comparison of these properties enables us to find novel dynamic features. Specifically, this comparison reveals the validity of the tube dilation molecular picture for entangled linear chains and weakening of the short-time coherence of the submolecule motion due to the constraint release mechanism. Moreover, the dielectric method enables us to investigate the chain dynamics under strong flow and/or in a molecularly narrow space. In particular, the retarded dielectric relaxation found for homopolymers and block copolymers in such narrow spaces (in the microdomains for the latter) indicates important effects of the spatial and thermodynamic constraints on the global chain motion. All the above results in turn demonstrate the importance of the dielectric method in investigations of the polymer dynamics.