A.R Coaching Centre For Physics, Kallakurichi, Cell - 9361561415
A.R Coaching Centre For Physics, Kallakurichi, Cell - 9361561415
A.R Coaching Centre For Physics, Kallakurichi, Cell - 9361561415
Codes:
a) (A) – 1, (B) – 4, (C) – 2, (D) – 3.
b) (A) – 1, (B) – 4, (C) – 3, (D) – 2.
c) (A) – 4, (B) – 3, (C) – 1, (D) – 2.
d) (A) – 4, (B) – 1, (C) – 3, (D) – 2.
2. Frequency range of vibrational spectra is
a) 3 × 1012 − 3 × 1014 𝐻𝑧
b) 3 × 1014 − 3 × 1016 𝐻𝑧
c) 3 × 1016 − 3 × 1018 𝐻𝑧
d) 3 × 108 − 3 × 1020 𝐻𝑧
3. For orange light of wavelength is 6.2 × 10−7 𝑚, then the wave number is
a) 12231.05 𝑐𝑚−1
b) 14712.07 𝑐𝑚−1
c) 16129.03 𝑐𝑚−1
d) 18973.01 𝑐𝑚−1
4. The various form of energies of a molecule is (in wave function)
a) 𝜓 = 𝜓𝑒 + 𝜓𝑣 + 𝜓𝑟 + 𝜓𝑡
b) 𝜓 = 𝜓𝑒 − 𝜓𝑣 − 𝜓𝑟 − 𝜓𝑡
c) 𝜓 = 𝜓𝑒 + 𝜓𝑣 + 𝜓𝑟 − 𝜓𝑡
d) 𝜓 = 𝜓𝑒 𝜓𝑣 𝜓𝑟 𝜓𝑡
5. If any one moment of inertia is zero, which type of molecule is
a) Linear molecule
b) Symmetric top
c) Spherical top
d) Asymmetric top
6. Example of spherical top molecule is
a) 𝐶2 𝐻2
b) 𝐶𝐻3 𝐹
c) 𝐶𝐶𝑙4
d) 𝐶𝐻2 𝐶𝐻𝐶𝑙
23. Three values of rotational energies of molecules are given below in different units 𝑃 = 10 𝑐𝑚−1 ,
𝑄 = 10−23 𝐽, 𝑅 = 104 𝑀𝐻𝑧. Choose the correct arrangement in the increasing order of energy
a) 𝑃, 𝑅, 𝑄
b) 𝑅, 𝑄, 𝑃
c) 𝑅, 𝑃, 𝑄
d) 𝑄, 𝑅, 𝑃
24. In symmetric bending mode of 𝐶𝑂2 molecule is/are
a) Raman active
b) IR active
c) Both (a) and (b)
d) None of these
25. All vibrations producing a change in the electric dipole moment of a molecule yield
a) Raman spectra
b) Rotational spectra
c) Infrared spectra
d) U-V spectra
26. Calculate the frequency of oscillation of hydrogen molecule of its force constant is 4.8 × 102 𝑁𝑚−1
and mass of the hydrogen atom is 1.67 × 10−27 𝑘𝑔.
a) 2.04 × 1013 𝐻𝑧
b) 2.04 × 1014 𝐻𝑧
c) 1.2 × 1013 𝐻𝑧
d) 1.2 × 1014 𝐻𝑧
27. The bond length R of carbon monoxide 𝐶𝑂 is 0.113 𝑛𝑚 and reduced mass is 1.4 × 10−26 𝑘𝑔, then the
moment of inertia of the 𝐶𝑂 molecule is
a) 14.6 × 10−45 𝑘𝑔𝑚2
b) 14.6 × 10−46 𝑘𝑔𝑚2
c) 1.46 × 10−46 𝑘𝑔𝑚2
d) 1.46 × 10−47 𝑘𝑔𝑚2
28. Choose the example of prolate symmetric top molecule:
a) 𝑁𝐻3
b) 𝑆𝐹6
c) 𝐵𝐹3
d) 𝐶2 𝐻2
29. The energy level of the lowest state of the vibrational energy of the diatomic molecule is
1
a) ℎ𝜈0 𝑐𝑚−1
2
1
b) ℏ𝜔0 𝑐𝑚−1
2
1
c) 𝜈0 𝑐𝑚−1
2
1
d) 𝜈̅0 𝑐𝑚−1
2
30. The temperature of the sample is increased, the intensity of hot bands is
a) increase
b) decrease
c) no change
d) zero
31. The diatomic molecules obey
a) Schrodinger equation
b) Hooke’s law
c) Born and Oppenheimer approximation
d) Frank -Condon equation
32. The lowest vibrational energy of the diatomic molecule is
a) Zero
b) Non zero
c) Infinite
d) Both (a) and (b)
33. The anharmonic oscillator behaves like the harmonic oscillator but with oscillation frequency that
decreasing with (𝜈 −vibrational quantum number)
a) decreasing(𝜈)
b) increasing(𝜈)
c) No change(𝜈)
d) both (a) and (b)
34. Condition for infrared spectrum:
(𝜇𝑖 −The dipole moment, Q-The normal coordinate)
𝜕𝜇
a) ( 𝜕𝑄𝑖 ) = 0
0
𝜕𝜇𝑖
b) ( 𝜕𝑄 ) ≠ 0
0
𝜕𝑄
c) (𝜕𝜇 ) = 0
𝑖 0
𝜕𝑄
d) (𝜕𝜇 ) ≠ 0
𝑖 0
35. A diatomic molecule can execute rotation and vibrations quite independently. This is called
a) Hooke law
b) Schrodinger approximation
c) Born and Oppenheimer approximation
d) Morse function
36. Energy of the vibrating diatomic molecule of the second hot band is
a) ∆𝜀 = 3𝜔 ̅𝑒 (1 − 4𝜒𝑒 ) 𝑐𝑚−1
b) ∆𝜀 = 𝜔 ̅𝑒 (1 − 4𝜒𝑒 ) 𝑐𝑚−1
c) ∆𝜀 = 3𝜔 ̅𝑒 (1 + 4𝜒𝑒 ) 𝑐𝑚−1
d) ∆𝜀 = 𝜔 ̅𝑒 (1 − 6𝜒𝑒 ) 𝑐𝑚−1
𝐾𝑇 1
b) 𝐽 = √4𝐵ℎ𝑐 − 2
2𝐾𝑇 1
c) 𝐽 = √ 𝐵ℎ𝑐 + 4
4𝐾𝑇 1
d) 𝐽 = √ 𝐵ℎ𝑐 − 4
57. The rotational frequency of a diatomic molecule is
ℏ2
a) 𝑛 = 𝐽(𝐽 + 1)
2𝐼
ℎ2
b) 𝑛 = 8𝜋2 𝐼𝐶 𝐽(𝐽 + 1)
ℎ2
c) 𝑛 = 4𝜋2 𝐼 √𝐽(𝐽 + 1)
ℎ2
d) 𝑛 = 8𝜋2 𝐼 √𝐽(𝐽 + 1)
58. For CO molecule rotational constant is 1.9313 𝑐𝑚−1 and centrifugal distortion is 6.1214 ×
10−6 𝑐𝑚−1 then fundamental vibrational frequency is
a) 2.6 × 106 𝑐𝑚−1
b) 2.6 × 103 𝑐𝑚−1
c) 7.2 × 106 𝑐𝑚−1
d) 7.2 × 103 𝑐𝑚−1
59. A diatomic molecule disassociates into atom if it is present in the vibration state of vibrational
quantum number is
1
a) 𝑉 = +1
2𝜒𝑒
1
b) 𝑉 = 2𝜒 − 1
𝑒
1
c) 𝑉 = 4𝜒 + 1
𝑒
1
d) 𝑉 = 4𝜒 − 1
𝑒
60. The potential energy of harmonic vibration is
1
a) 𝑈 = 2 𝐾(𝑥2 − 𝑥1 )2
1
b) 𝑈 = 2 𝐾(𝑥2 + 𝑥1 )2
c) 𝑈 = 𝐾(𝑥2 − 𝑥1 )
d) 𝑈 = 𝐾(𝑥2 + 𝑥1 )