Best reducing agent among the given ions are:
- \(Ce^{4+}\)
- \(Gd^{2+}\)
- \(Lu^{3+}\)
- \(Nd^{3+}\)
The Correct Option is B
Solution and Explanation
The correct option is (B): \(Gd^{2+}\)
Top Questions on reaction mechanism
- Given below are two statements:
Statement I: The dipole moment of R–CN is greater than R–NC and R–NC can undergo hydrolysis under acidic medium to produce R–COOH.
Statement II: R–CN hydrolyses under acidic medium to produce a compound which on treatment with SOCl$_2$, followed by the addition of NH$_3$ gives another compound (X). This compound (X) on treatment with NaOCl/NaOH gives a product, that on treatment with CHCl$_3$/KOH/$\Delta$ produces R–NC.
In the light of the above statements, choose the correct answer from the options given below.
- JEE Main - 2026
- Chemistry
- reaction mechanism
- Given below are two statements:
Statement I: Phenol on treatment with \( \mathrm{CHCl_3/aq.\ KOH} \) under refluxing condition, followed by acidification produces p-hydroxy benzaldehyde as the major product and o-hydroxy benzaldehyde as the minor product.
Statement II: The mixture of p-hydroxybenzaldehyde and o-hydroxybenzaldehyde can be easily separated through steam distillation.
In the light of the above statements, choose the correct answer from the options given below- JEE Main - 2026
- Chemistry
- reaction mechanism
The correct order of the rate of reaction of the following reactants with nucleophile by \( \mathrm{S_N1} \) mechanism is:
(Given: Structures I and II are rigid)
- JEE Main - 2026
- Chemistry
- reaction mechanism
- Match the following:
LIST I LIST II A Lyman I Near IR B Balmer II Far IR C Paschen III Visible D p-fund IV UV - JEE Main - 2024
- Chemistry
- reaction mechanism
- Which reagent gives bright red ppt. With \(Ni^{2+}\) in basic medium?
- JEE Main - 2024
- Chemistry
- reaction mechanism
Questions Asked in JEE Main exam
Let \( \alpha = \dfrac{-1 + i\sqrt{3}}{2} \) and \( \beta = \dfrac{-1 - i\sqrt{3}}{2} \), where \( i = \sqrt{-1} \). If
\[ (7 - 7\alpha + 9\beta)^{20} + (9 + 7\alpha - 7\beta)^{20} + (-7 + 9\alpha + 7\beta)^{20} + (14 + 7\alpha + 7\beta)^{20} = m^{10}, \] then the value of \( m \) is ___________.- JEE Main - 2026
- Complex Numbers and Quadratic Equations
- The work functions of two metals ($M_A$ and $M_B$) are in the 1 : 2 ratio. When these metals are exposed to photons of energy 6 eV, the kinetic energy of liberated electrons of $M_A$ : $M_B$ is in the ratio of 2.642 : 1. The work functions (in eV) of $M_A$ and $M_B$ are respectively.
- JEE Main - 2026
- Dual nature of matter
- 10 mole of an ideal gas is undergoing the process shown in the figure. The heat involved in the process from \( P_1 \) to \( P_2 \) is \( \alpha \) Joule \((P_1 = 21.7 \text{ Pa}, P_2 = 30 \text{ Pa}, C_v = 21 \text{ J/K mol}, R = 8.3 \text{ J/mol K})\). The value of \( \alpha \) is ________.
- JEE Main - 2026
- Thermodynamics
- The system of linear equations
$x + y + z = 6$
$2x + 5y + az = 36$
$x + 2y + 3z = b$
has- JEE Main - 2026
- Matrices and Determinants
- The displacement of a particle executing simple harmonic motion with time period \(T\) is expressed as \[ x(t)=A\sin\omega t, \] where \(A\) is the amplitude of oscillation. If the maximum value of the potential energy of the oscillator is found at \[ t=\frac{T}{2\beta}, \] then the value of \(\beta\) is ________.
- JEE Main - 2026
- Waves and Oscillations
Concepts Used:
Organic Chemistry – Some Basic Principles and Techniques - Reaction Mechanism
SN1 Reaction Mechanism:
SN1 reaction mechanism takes place by following three steps –
- Formation of carbocation
- Attack of nucleophile
- Deprotonation
SN2 Reaction Mechanism:
The SN2 reaction mechanism involves the nucleophilic substitution reaction of the leaving group (which generally consists of halide groups or other electron-withdrawing groups) with a nucleophile in a given organic compound.
Electrophilic Aromatic Substitution Reaction Mechanism:
The mechanism of an electrophilic aromatic substitution reaction contains three main components which are:
- A new sigma bond from C=C is formed during the reaction in the arene nucleophile.
- Due to the breaking of the C-H sigma bond, a proton is removed.
- The C=C bond is reformed and it restores the aromaticity of the compound.
Electrophilic Substitution Reaction Mechanism:
The electrophilic substitution reaction mechanism is composed of three steps, which will be discussed more below.
- Electrophile Generation
- Carbocation Formation
- Proton Removal