The correct option with regard to the following statements is
(a) Time-independent Schrödinger equation can be exactly solved for Be\(^{2+}\).
(b) For a particle confined in a one-dimensional box of length \( l \) with infinite potential barriers, the trial variation function \( \phi = \left[ \left( \frac{3}{l^3} \right)^{1/2} x \right] \) is not an acceptable trial wavefunction for \( 0 \le x \le l \).
(c) Wavefunctions for system of Fermions must be anti-symmetric with respect to exchange of any two Fermions in the system.
(d) Born-Oppenheimer approximation can be used to separate the vibrational and rotational motion of a molecule.
(a) Time-independent Schrödinger equation can be exactly solved for Be2+.
Be2+ has an electronic configuration of 1s2, meaning it has two electrons.
The time-independent Schrödinger equation can be solved exactly only for one-electron systems.
For systems with two or more electrons, the electron-electron interaction term makes it impossible to obtain an exact analytical solution.
We rely on approximation methods like Hartree-Fock.
Therefore, statement (a) is False.
(b) For a particle confined in a one-dimensional box of length l with infinite potential barriers, the trial variation function
φ(x) = [(3/l3)1/2] × x is not an acceptable trial wavefunction for 0 ≤ x ≤ l.
For a trial wavefunction to be acceptable in the variational method for a 1D box with infinite barriers at x = 0 and x = l, it must satisfy the boundary conditions: φ(0) = 0 and φ(l) = 0.
Given: φ(x) = (3/l3)1/2 × x
At x = 0: φ(0) = 0 — boundary condition satisfied.
At x = l: φ(l) = (3/l)1/2 ≠ 0 — boundary condition not satisfied.
Therefore, statement (b) is True.
(c) Wavefunctions for a system of Fermions must be anti-symmetric with respect to exchange of any two Fermions in the system.
Fermions are particles with half-integer spin.
The total wavefunction of a system of identical fermions must be anti-symmetric under exchange — this is the Pauli Exclusion Principle.
Therefore, statement (c) is True.
(d) Born-Oppenheimer approximation can be used to separate the vibrational and rotational motion of a molecule.
The Born-Oppenheimer approximation separates electronic and nuclear motion (not directly vibration and rotation).
Separation of vibrational and rotational motion is a further approximation based on treating the nuclei as a semi-rigid rotor.
Therefore, statement (d) is False.
Summary:
(a) False
(b) True
(c) True
(d) False
\[ \boxed{\text{Correct option is (C)}} \]
Wavefunctions and energies for a particle confined in a cubic box are \( \psi_{n_x,n_y,n_z} \) and \( E_{n_x,n_y,n_z} \), respectively. The functions \( \phi_1, \phi_2, \phi_3 \), and \( \phi_4 \) are written as linear combinations of \( \psi_{n_x,n_y,n_z} \). Among these functions, the eigenfunction(s) of the Hamiltonian operator for this particle is/are \[ \phi_1 = \frac{1}{\sqrt{2}} \psi_{1,4,1} - \frac{1}{\sqrt{2}} \psi_{2,2,3} \] \[ \phi_2 = \frac{1}{\sqrt{2}} \psi_{1,5,1} + \frac{1}{\sqrt{2}} \psi_{3,3,3} \] \[ \phi_3 = \frac{1}{\sqrt{2}} \psi_{1,3,8} + \frac{1}{\sqrt{2}} \psi_{3,8,1} \] \[ \phi_4 = \frac{1}{2} \psi_{3,3,1} + \frac{\sqrt{3}}{2} \psi_{2,4,1} \]
The Lineweaver-Burk plot for an enzyme obeying the Michaelis-Menten mechanism is given below.
The slope of the line is \(0.36 \times 10^2\) s, and the y-intercept is \(1.20\) mol\(^{-1}\) L s. The value of the Michaelis constant (\(K_M\)) is ________ \( \times 10^{-3} \) mol L\(^{-1}\) (in integer). [Note: \(v\) is the initial rate, and \([S]_0\) is the substrate concentration]
Consider a Carnot engine with a hot source kept at 500 K. From the hot source, 100 J of energy (heat) is withdrawn at 500 K. The cold sink is kept at 300 K. The efficiency of the Carnot engine is ___________ (rounded off to one decimal place).
For the cell reaction, \[ Hg_2Cl_2 (s) + H_2 (1 \, {atm}) \rightarrow 2Hg (l) + 2H^+ (a=1) + 2Cl^- (a=1) \] The standard cell potential is \( \mathcal{E}^0 = 0.2676 \) V, and \( \left(\frac{\partial \mathcal{E}^0}{\partial T}\right)_P = -3.19 \times 10^{-4} \) V K\(^{-1}\). The standard enthalpy change of the reaction (\( \Delta_r H^0 \)) at 298 K is \( -x \) kJ mol\(^{-1}\). The value of \( x \) is ___________ (rounded off to two decimal places). [Given: Faraday constant \( F = 96500 \) C mol\(^{-1}\)]
The mean energy of a molecule having two available energy states at \( \epsilon = 0 \) J and \( \epsilon = 4.14 \times 10^{-21} \) J at 300 K is ___________ \( \times 10^{-21} \) J (rounded off to two decimal places). [Given: Boltzmann constant \( k_B = 1.38 \times 10^{-23} \) J K\(^{-1}\)]
The kinetic energies of an electron (\(e\)) and a proton (\(p\)) are \(E\) and \(3E\), respectively. Given that the mass of a proton is 1836 times that of an electron, the ratio of their de Broglie wavelengths (\(\lambda_e / \lambda_p\)) is ___________ (rounded off to two decimal places).