We have examined the adsorption of n-pentane in several representative zeolites such as silicalite (MFI), ferrierite (FER), zeolite L (LTL), and faujasite zeolites with FAU structure including siliceous Y (Si-Y) and Na-Y by using FT-Raman spectroscopy in combination with thermogravimetric analysis (TGA) with particular attention being paid to the conformational and dynamic behavior of the guest molecule. The results indicate that the framework topology mainly dictates the conformation of n-pentane in a zeolite. For the zeolites with channel systems such as silicalite, ferrierite, and zeolite L, the population of the all-trans conformer increases upon loading, given that the geometry of the isomer fits better in the channel. When n-pentane is adsorbed in zeolites with a large cavity, such as Si-Y and Na-Y, the distribution of the all-trans (TT) and trans-gauche (TG) conformers is similar to that of pure liquid, suggesting that the large supercage in the framework imposes minimal effect on the conformational equilibrium. The dynamics of the guest molecule is, however, influenced significantly by the existence of cations. Adsorption of n-pentane in a siliceous framework such as silicalite and Si-Y results in extensive molecular motion at room temperature, the degree of which decreases with decreasing temperature. In zeolites ferrierite, L, and Na-Y, the presence of cations in the framework markedly hinders the overall molecular motion. The cations clearly play a role in the observed static disorder of the guest molecule in zeolite L. Important information regarding the location of the n-pentane molecules within silicalite and ferrierite is also obtained.