3.3 The equilibrium vibration frequency of the iodine molecule I2 is 215 cmā1, and the anharmonicity constant x is 0.003; what, at 300 K, is the intensity of the āhot bandā (v = 1 ā v = 2 transition) relative to that of the fundamental (v = 0 ā v = 1)?
3.4 An infra-red spectrum of OCS is obtained in which the rotational fine structure is not resolved. Using data from Table 2.2, calculate the separation between the P and R branch maxima at T = 300 K.
3.5 How many normal modes of vibration are possible for the following molecules: HBr, O2, OCS (linear), SO2 (bent), BCl3, HCā”CH, CH4 CH3I, C6H6?
3.6 Estimate, using data from Table 3.4, the vibrational wavenumber of (a) ā”CD, (b) āOD, (c) āCāSā. (Relative atomic masses are: H = 1, D = 2, C = 12, O = 16, S = 32.)
3.7 The vibration frequency of 1H35Cl is 2990.6 cmā1; without calculating the bond force constant, estimate the frequency for 1H37Cl, 2D35Cl, and 2D37Cl.