Rankbit System
JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%) | JEE Physics: Waves (+15.5%) | Electrostatics: Concentric Shells (-29.7%) | Modern Physics: Photoelectric Clones (+34.2%) | Mathematics: Definite Integrals (+18.1%) | Chemistry: Coordination Splitting (-11.4%)

The oxidation number of iron in the compound formed during brown ring test for mathrmNO_3^- ion is ________.

Numerical Answer Type:
Enter a numerical value Answer: 1 to 1 +4 marks

Solution & Explanation

### Related Formula textFormula of Brown Ring Complex: [mathrmFe(mathrmH_2mathrmO)_5(mathrmNO)]^2+ ### Core Logic In this specific coordination complex, charge transfer occurs where nitric oxide transfers an electron to the iron center. As a result, textNO exists as a positive textNO^+ ligand, and iron drops to an unusual oxidation state: x + 5(0) + 1(+1) = +2 x + 1 = 2 implies x = +1 ### Step 1: Final Value Assignment Solving this charge balance confirms that the oxidation number of iron in the brown ring complex is +1. ### Pattern Recognition The brown ring test features a rare +1 oxidation state for iron because textNO coordinates as the positive nitrosonium cation (textNO^+). ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Coordination Compounds

Reference Study Guides

More Coordination Compounds Previous-Year Questions — Page 10

Q61 jee_main_2024_31_jan_evening Crystal Field Theory
Match List-I with List-II.
List - I (Complex ion)List - II (Electronic Configuration)
A. [Cr(H_2O)_6]^3+I. t_2g^2e_g^0
B. [Fe(H_2O)_6]^3+II. t_2g^3e_g^0
C. [Ni(H_2O)_6]^2+III. t_2g^3e_g^2
D. [V(H_2O)_6]^3+IV. t_2g^6e_g^2
Choose the correct answer from the options given below:
  • A. textA-III, B-II, C-IV, D-I
  • B. textA-IV, B-I, C-II, D-III
  • C. textA-IV, B-III, C-I, D-II
  • D. textA-II, B-III, C-IV, D-I

Solution

### Core Logic Identify the central metal ion, its oxidation state, and outer electronic configuration: 1) [Cr(H_2O)_6]^3+ contains Cr^3+ : [Ar] 3d^3. In an octahedral field with weak field ligands (H_2O), the configuration is t_2g^3 e_g^0. 2) [Fe(H_2O)_6]^3+ contains Fe^3+ : [Ar] 3d^5. With weak field ligand (H_2O), it forms a high spin complex: t_2g^3 e_g^2. 3) [Ni(H_2O)_6]^2+ contains Ni^2+ : [Ar] 3d^8. In an octahedral field, the configuration is t_2g^6 e_g^2. 4) [V(H_2O)_6]^3+ contains V^3+ : [Ar] 3d^2. In an octahedral field, the configuration is t_2g^2 e_g^0. ### Step 1: Final Mapping A rightarrow II (t_2g^3e_g^0) B rightarrow III (t_2g^3e_g^2) C rightarrow IV (t_2g^6e_g^2) D rightarrow I (t_2g^2e_g^0) This matches option (4). ### Pattern Recognition Shortcut: Vanadium (V) in +3 state has 2 electrons, so D rightarrow I. Only options (1) and (4) have D rightarrow I. Nickel (Ni) in +2 state has 8 electrons, so C rightarrow IV. Only option (4) has C rightarrow IV. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Coordination Compounds
Q68 jee_main_2024_31_jan_evening Magnetic Properties of Complexes
Select the option with correct property -
  • A. text(1) [Ni(CO)_4]text and [NiCl_4]^2-text both diamagnetic
  • B. text(2) [Ni(CO)_4]text and [NiCl_4]^2-text both paramagnetic
  • C. text(3) [NiCl_4]^2-text diamagnetic, [Ni(CO)_4]text paramagnetic
  • D. text(4) [Ni(CO)_4]text diamagnetic, [NiCl_4]^2-text paramagnetic

Solution

### Core Logic For [Ni(CO)_4]: Nickel is in 0 oxidation state: Ni^0 = [Ar] 3d^8 4s^2. CO is a strong field ligand, forcing pairing of electrons. The 4s electrons move to the 3d orbital, making the configuration 3d^10. With no unpaired electrons, the hybridization is sp^3 and it is diamagnetic. For [NiCl_4]^2-: Nickel is in +2 oxidation state: Ni^2+ = [Ar] 3d^8. Cl^- is a weak field ligand, so pairing does not occur against Hund's rule. The configuration remains t_2g^6 e_g^2 (or simply two unpaired electrons in the tetrahedral d splitting). The hybridization is sp^3 and with 2 unpaired electrons, it is paramagnetic. ### Step 1: Final Conclusion [Ni(CO)_4] is diamagnetic, while [NiCl_4]^2- is paramagnetic. This correctly corresponds to option (4). ### Pattern Recognition Strong field ligands (like CO, CN^-) usually lead to diamagnetism in d^8 metal ions by forming square planar (dsp^2) or forcing d^10 configurations (for Ni^0). Weak field halogens lead to paramagnetic sp^3 complexes for Ni(II). ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Coordination Compounds
Q76 jee_main_2024_31_jan_morning VBT and CFT
The correct statements from following are: A. The strength of anionic ligands can be explained by crystal field theory. B. Valence bond theory does not give a quantitative interpretation of kinetic stability of coordination compounds. C. The hybridization involved in formation of [Ni(CN)_4]^2- complex is dsp^2 D. The number of possible isomer(s) of cis-[PtCl_2(en)_2]^2+ is one Choose the correct answer from the options given below:
  • A. textA, D only
  • B. textA, C only
  • C. textB, D only
  • D. textB, C only

Solution

### Step 1: Analyzing Statement A Crystal field theory considers ligands as point charges. Therefore, anionic ligands should exert the greatest splitting effect, but practically they are at the lower end of the spectrochemical series. CFT cannot explain this properly. Hence, Statement A is incorrect. ### Step 2: Analyzing Statement B Valence bond theory (VBT) is qualitative and does not give a quantitative interpretation of either thermodynamic or kinetic stability. Hence, Statement B is correct. ### Step 3: Analyzing Statement C In [Ni(CN)_4]^2-, Ni is in +2 state (3d^8). Since CN^- is a strong field ligand, pairing of electrons takes place leaving one inner 3d orbital empty. Thus, the hybridization is dsp^2 (square planar). Hence, Statement C is correct. ### Step 4: Analyzing Statement D cis-[PtCl_2(en)_2]^2+ is an octahedral complex of type M(AA)_2a_2. The cis-isomer lacks a plane of symmetry and is optically active, thus it exists as a pair of enantiomers (d and l). Therefore, the number of possible isomers is 2, not 1. Statement D is incorrect. ### Final Conclusion Statements B and C are correct. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Coordination Compounds
Q82 jee_main_2024_31_jan_morning Magnetic Properties
The 'Spin only' Magnetic moment for [Ni(NH_3)_6]^2+ is ________ times 10^-1 BM. (given = Atomic number of Ni: 28)
Numerical Answer. Answer: 28 to 28

Solution

### Related Formula mu = sqrtn(n + 2) text BM ### Step 1: Electronic Configuration Atomic number of Ni = 28. Ni^2+ = [Ar] 3d^8 Because the geometry is octahedral (coordination number 6) and NH_3 acts as a weak field ligand with Ni^2+ (or because d^8 configuration always has 2 unpaired electrons in an octahedral field regardless of ligand strength): The configuration in the t_2g and e_g levels is t_2g^6 e_g^2. ### Step 2: Calculating Magnetic Moment Number of unpaired electrons, n = 2. mu = sqrt2(2 + 2) = sqrt8 approx 2.828 text BM Representing in 10^-1 scale: mu approx 28.28 times 10^-1 text BM Rounding to the nearest integer as typically expected gives 28. ### Evaluation Rubric / Model Answer null ### Chapter Mix Class 12 Chemistry: Coordination Compounds

More Coordination Compounds Questions — jee_main_2024_29_january_evening

Practice all Coordination Compounds previous-year questions →

YOUR FIRST PREP STEP STARTS HERE

We Map Every Repeating Question in Competitive Exams.

Say goodbye to generic mock test fatigue. RankBit uses smart analysis to group past exam questions into their foundational Repeating Question Types. Find chapter weightage, track repeating questions, and score higher with targeted practice.

Select Your Target Exam

Choose an exam track below to find formulas per chapter and patterns.

Syncing Exam Intelligence

Mapping formulas and patterns across all tracks…

PATH A — FULL LENGTH PRACTICE

Full Mock Test Hub

Simulate real NTA exam conditions with fully tracked mocks. Time yourself against past papers.

Under Development
PATH B — TARGETED PRACTICE

Topic-wise Practice Hub

Practice past-year questions one chapter at a time. Pick an exam → subject → chapter and get every PYQ for that topic — pulled together from all past papers — with the chapter's key formulas alongside.

Loading Questions... Browse Topics
Latest from the Blog
View all →

Loading articles...