The reaction that proceeds through an oxidative addition followed by a reductive elimination is:
[Given: Atomic numbers Ni = 28, Ta = 73, Zr = 40, Pt = 78]
Oxidative addition and reductive elimination are key steps in organometallic catalytic cycles. These typically involve transition metals with variable oxidation states, particularly those from the late transition metals such as Ni, Pd, Pt.
Let’s analyze each option:
Therefore, the only reaction proceeding through oxidative addition and reductive elimination is:
\[ \boxed{(D)} \]
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Consider a Carnot engine with a hot source kept at 500 K. From the hot source, 100 J of energy (heat) is withdrawn at 500 K. The cold sink is kept at 300 K. The efficiency of the Carnot engine is ___________ (rounded off to one decimal place).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\(^{-1}\)]
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 correct option(s) of reagents and reaction sequences suitable for carrying out the following transformation is/are
The UV-visible spectrum of [Ni(en)\(_3\)]\(^{2+}\) (en = ethylenediamine) shows absorbance maxima at 11200 cm\(^{-1}\), 18350 cm\(^{-1}\), and 29000 cm\(^{-1}\).
[Given: Atomic number of Ni = 28] The correct match(es) between absorbance maximum and electronic transition is/are
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.
Compound K displayed a strong band at 1680 cm−1 in its IR spectrum. Its 1H-NMR spectral data are as follows:
δ (ppm):
7.30 (d, J = 7.2 Hz, 2H)
6.80 (d, J = 7.2 Hz, 2H)
3.80 (septet, J = 7.0 Hz, 1H)
2.20 (s, 3H)
1.90 (d, J = 7.0 Hz, 6H)
The correct structure of compound K is: