LIST-II (Bond pair : lone pair on the central atom)
(A) mathrmICl_2^-$\mathrm{ICl}_2^-$
(I) 4 : 2$4 : 2$
(B) mathrmH_2mathrmO$\mathrm{H}_2\mathrm{O}$
(II) 4 : 1$4 : 1$
(C) mathrmSO_2$\mathrm{SO}_2$
(III) 2 : 3$2 : 3$
(D) mathrmXeF_4$\mathrm{XeF}_4$
(IV) 2 : 2$2 : 2$
Choose the correct answer from the options given below:
A.(A)-(IV), (B)-(III), (C)-(II), (D)-(I)
B.(A)-(III), (B)-(IV), (C)-(II), (D)-(I)
C.(A)-(III), (B)-(IV), (C)-(I), (D)-(II)
D.(A)-(II), (B)-(I), (C)-(IV), (D)-(III)
Solution & Explanation
### Core Logic
Let's find the number of bond pairs (sigma$\sigma$-bonds or regions) and lone pairs on the central atom of each species:
1. **mathrmICl_2^-$\mathrm{ICl}_2^-$**:
- Central atom Iodine has 7$7$ valence electrons + 1$+ 1$ negative charge = 8$= 8$ electrons.
- Forms 2$2$ single bonds (bond pairs = 2$= 2$).
- Remaining 6$6$ electrons form 3$3$ lone pairs.
- Ratio is 2 : 3$2 : 3$ (Matches LIST-II, III).
VSEPR linear shape of ICl2-
2. **mathrmH_2mathrmO$\mathrm{H}_2\mathrm{O}$**:
- Oxygen has 6$6$ valence electrons.
- Forms 2$2$ bond pairs with Hydrogens.
- Remaining 4$4$ electrons form 2$2$ lone pairs.
- Ratio is 2 : 2$2 : 2$ (Matches LIST-II, IV).
VSEPR linear shape of ICl2-
3. **mathrmSO_2$\mathrm{SO}_2$**:
- Sulfur has 6$6$ valence electrons.
- Forms 2$2$ double bonds (which are counted as 4$4$ bonding pairs of electrons/bond pairs in typical VSEPR representations here).
- Remaining 2$2$ electrons form 1$1$ lone pair.
- Ratio is 4 : 1$4 : 1$ (Matches LIST-II, II).
VSEPR linear shape of ICl2-
4. **mathrmXeF_4$\mathrm{XeF}_4$**:
- Xenon has 8$8$ valence electrons.
- Forms 4$4$ bond pairs with Fluorines.
- Remaining 4$4$ electrons form 2$2$ lone pairs.
- Ratio is 4 : 2$4 : 2$ (Matches LIST-II, I).
VSEPR linear shape of ICl2-
Thus, the correct mapping is: A-III, B-IV, C-II, D-I.
### Pattern Recognition
For match-the-column with VSEPR structures:
- Always find steric number: textSteric Number = frac12(V + M - C + A)$\text{Steric Number} = \frac{1}{2}(V + M - C + A)$.
- Water is 2$2$ bond pairs, 2$2$ lone pairs (sp^3$sp^3$) rightarrow$\rightarrow$ B-IV. This alone helps eliminate multiple incorrect options immediately.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 11 Chemistry: Chemical Bonding and Molecular Structure
More Chemical Bonding and Molecular Structure Previous-Year Questions — Page 2
Q50jee_main_2025_29_jan_eveningLewis Structures and Valence Electrons
Total number of non bonded electrons present in NO2^-$NO{2}^{-}$ ion based on Lewis theory is ________.
Numerical Answer.Answer: 12 to 12
Solution
### Core Logic
Let's compute the total valence electrons for the nitrite ion (NO_2^-$NO_2^-$):
textValence electrons = 5text (from N) + 2 times 6text (from O) + 1text (negative charge) = 18text electrons$$\text{Valence electrons} = 5\text{ (from N)} + 2 \times 6\text{ (from O)} + 1\text{ (negative charge)} = 18\text{ electrons}$$
In the valid Lewis structural representation:
* The central nitrogen atom forms one single bond and one double bond with the terminal oxygens, consuming 2 + 4 = 6$2 + 4 = 6$ bonding electrons.
* Remaining non-bonded valence electrons = 18 - 6 = 12$18 - 6 = 12$ electrons.
### Step 1: Account for Lone Pairs
Distribution of non-bonded electrons across the individual atoms:
* Central Nitrogen atom has 1$1$ lone pair (2$2$ electrons).
* Single-bonded Oxygen atom has 3$3$ lone pairs (6$6$ electrons).
* Double-bonded Oxygen atom has 2$2$ lone pairs (4$4$ electrons).
textTotal non-bonded electrons = 2 + 6 + 4 = 12$$\text{Total non-bonded electrons} = 2 + 6 + 4 = 12$$
### Pattern Recognition
Non-bonded electrons can always be obtained directly by subtracting total bonding electrons from total valence electrons.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 11 Chemistry: Chemical Bonding and Molecular Structure
Q31jee_main_2025_28_jan_morningVSEPR Theory and d-Electron Configurations
Consider 'n' is the number of lone pair of electrons present in the equatorial position of the most stable structure of mathrmClF_3$\mathrm{ClF}_3$ . The ions from the following with 'n' number of unpaired electrons are :
A. mathrmV^3 + $\mathrm{V}^{3 + }$
B. mathrmTi^3+$\mathrm{Ti}^{3+}$
C. mathrmCu^2 + $\mathrm{Cu}^{2 + }$
D. mathrmNi^2+$\mathrm{Ni}^{2+}$
E. mathrmTi^2+$\mathrm{Ti}^{2+}$
Choose the correct answer from the options given below:
A.textA and C only$\text{A and C only}$
B.textA, D and E only$\text{A, D and E only}$
C.textB and C only$\text{B and C only}$
D.textB and D only$\text{B and D only}$
Solution
### Step 1: Determine 'n'
mathrmClF_3$\mathrm{ClF}_3$ has a central Chlorine atom with 7 valence electrons, bound to 3 Fluorine atoms. This leaves 2 lone pairs. The geometry is trigonal bipyramidal (T-shaped molecule). In its most stable geometry, both lone pairs lie in the equatorial plane to minimize lone pair-bonding pair repulsions. Thus, n = 2$n = 2$.
### Step 2: Find ions with 2 unpaired electrons
Let us compute the number of unpaired electrons for each configuration:
- **A. mathrmV^3+$\mathrm{V}^{3+}$:** [mathrmAr] 3d^2 rightarrow 2$[\mathrm{Ar}] 3d^2 \rightarrow 2$ unpaired electrons.
- **B. mathrmTi^3+$\mathrm{Ti}^{3+}$:** [mathrmAr] 3d^1 rightarrow 1$[\mathrm{Ar}] 3d^1 \rightarrow 1$ unpaired electron.
- **C. mathrmCu^2+$\mathrm{Cu}^{2+}$:** [mathrmAr] 3d^9 rightarrow 1$[\mathrm{Ar}] 3d^9 \rightarrow 1$ unpaired electron.
- **D. mathrmNi^2+$\mathrm{Ni}^{2+}$:** [mathrmAr] 3d^8 rightarrow 2$[\mathrm{Ar}] 3d^8 \rightarrow 2$ unpaired electrons.
- **E. mathrmTi^2+$\mathrm{Ti}^{2+}$:** [mathrmAr] 3d^2 rightarrow 2$[\mathrm{Ar}] 3d^2 \rightarrow 2$ unpaired electrons.
Thus, A, D, and E have exactly n=2$n=2$ unpaired electrons.
### Pattern Recognition
Sees: Number of equatorial lone pairs linked to unpaired electrons.
Shortcut: Remember mathrmClF_3$\mathrm{ClF}_3$ is T-shaped with 2 equatorial lone pairs. Look for d^2$d^2$ or d^8$d^8$ configurations among the transition metal ions.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 11 Chemistry: Chemical Bonding and Molecular Structure
Class 12 Chemistry: The d-and f-Block Elements
Q35jee_main_2025_28_jan_morningMolecular Geometry and VSEPR
A.mathrmBrF_5 text \& mathrmXeOF_4$\mathrm{BrF}_5 \text{ \& } \mathrm{XeOF}_4$
B.mathrmSbF_5 text \& mathrmXeOF_4$\mathrm{SbF}_5 \text{ \& } \mathrm{XeOF}_4$
C.mathrmSbF_5 text \& mathrmPCl_5$\mathrm{SbF}_5 \text{ \& } \mathrm{PCl}_5$
D.mathrmBrF_5 text \& mathrmPCl_5$\mathrm{BrF}_5 \text{ \& } \mathrm{PCl}_5$
Solution
### Core Logic
Let us check the steric details using VSEPR theory:
- **mathrmBrF_5$\mathrm{BrF}_5$:** Bromine has 7 valence electrons. It forms 5 single bonds with Fluorine and retains 1 lone pair. Steric number = 6 (sp^3d^2$sp^3d^2$), geometry is square pyramidal.
- **mathrmXeOF_4$\mathrm{XeOF}_4$:** Xenon has 8 valence electrons. It forms 1 double bond with Oxygen, 4 single bonds with Fluorine, and retains 1 lone pair. Steric number = 6 (sp^3d^2$sp^3d^2$), geometry is square pyramidal.
- **mathrmSbF_5$\mathrm{SbF}_5$ & mathrmPCl_5$\mathrm{PCl}_5$:** Central element has 5 valence electrons, forming 5 bonds with no lone pairs. Steric number = 5 (sp^3d$sp^3d$), geometry is trigonal bipyramidal.
Visual representations of geometries:
Geometry structure diagram 1 for Q35 - JEE Main 2025 MorningGeometry structure diagram 1 for Q35 - JEE Main 2025 MorningGeometry structure diagram 1 for Q35 - JEE Main 2025 MorningGeometry structure diagram 1 for Q35 - JEE Main 2025 Morning
### Pattern Recognition
Sees: Steric count 6 with 5 bonded segments + 1 lone pair rightarrow$\rightarrow$ always square pyramidal geometry.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 11 Chemistry: Chemical Bonding and Molecular Structure
Q43jee_main_2025_03_april_morningHybridisation
Match the LIST-I with LIST-II.
LIST-I (Molecules/ion)
LIST-II (Hybridisation of central atom)
A. PF*5$PF*{5}$
I. dsp^2$dsp^{2}$
B. SF*6$SF*{6}$
II. sp^3d$sp^{3}d$
C. Ni(CO)*4$Ni(CO)*{4}$
III. sp^3d^2$sp^{3}d^{2}$
D. [PtCl*4]^2-$[PtCl*{4}]^{2-}$
IV. sp^3$sp^{3}$
Choose the correct answer from the options given below:
A. A-II, B-III, C-IV, D-I
B. A-IV, B-I, C-II, D-III
C. A-I, B-II, C-III, D-IV
D. A-III, B-I, C-IV, D-II
Solution
### Core Logic
Let us evaluate each central atom configuration systematically:
* A. PF_5$PF_5$: Phosphorus has 5 valence electrons, forming 5sigma$5\sigma$ bonds with zero lone pairs. Steric number = 5 implies sp^3d$= 5 implies sp^3d$ hybridisation.
* B. SF_6$SF_6$: Sulfur has 6 valence electrons, forming 6sigma$6\sigma$ bonds with zero lone pairs. Steric number = 6 implies sp^3d^2$= 6 implies sp^3d^2$ hybridisation.
* C. Ni(CO)_4$Ni(CO)_4$: Nickel is in a 0 oxidation state (3d^8 4s^2$3d^8 4s^2$). Carbon monoxide is a strong field ligand, forcing rearrangement into a filled 3d^10$3d^{10}$ state. The vacant 4s$4s$ and three 4p$4p$ orbitals hybridise to give an sp^3$sp^3$ configuration. Orbital configuration matrix for Q43 - JEE Main 2025 Morning
* D. [PtCl_4]^2-$[PtCl_4]^{2-}$: Platinum is in the +2$+2$ oxidation state (5d^8$5d^8$). Since it belongs to the 5d$5d$ transition series, all ligands behave as strong field elements, leading to interior spin-pairing and an inner orbital square-planar dsp^2$dsp^2$ hybridisation state. Orbital configuration matrix for Q43 - JEE Main 2025 Morning
### Pattern Recognition
Shortcut: Match structural main elements first: PF_5
ightarrow sp^3d$PF_5
ightarrow sp^3d$ (II), SF_6
ightarrow sp^3d^2$SF_6
ightarrow sp^3d^2$ (III). This isolates option (1) instantly without checking d-block coordinate fields.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 11 Chemistry: Chemical Bonding and Molecular Structure
Class 12 Chemistry: Coordination Compounds
Q44jee_main_2025_04_april_eveningVSEPR Theory
Given below are two statements:
Statement (I) : for mathrmCell mathrmF_3$\mathrm{C}\ell \mathrm{F}_{3}$ , all three possible structures may be drawn as follows.
The prompt displays three configurations of chlorine trifluoride with differing spatial positions for its two lone electron pairs.The prompt displays three configurations of chlorine trifluoride with differing spatial positions for its two lone electron pairs.The prompt displays three configurations of chlorine trifluoride with differing spatial positions for its two lone electron pairs.
Statement (II) : Structure III is most stable, as the orbitals having the lone pairs are axial, where the ell mathfrakp-$\ell \mathfrak{p}-$ bp repulsion is minimum.
In the light of the above statements, choose the most appropriate answer from the options given below:
A. Statement I is incorrect but statement II is correct.
B. Statement I is correct but statement II is incorrect.
C. Both Statement I and statement II are correct.
D. Both Statement I and statement II are incorrect.
Solution
### Related Formula
textSteric Number for ClF_3 = frac7+32 = 5 implies sp^3d text hybridization (Trigonal Bipyramidal geometry)$$\text{Steric Number for } ClF_3 = \frac{7+3}{2} = 5 \implies sp^3d \text{ hybridization (Trigonal Bipyramidal geometry)}$$
### Core Logic
- **Statement I is correct:** The three structural arrangements represent the different ways to place three bond pairs and two lone pairs within a trigonal bipyramidal grid.
- **Statement II is incorrect:** According to VSEPR theory and Bent's rule, in sp^3d$sp^3d$ hybridization, **lone pairs must occupy equatorial positions** to minimize strong 90^circ$90^\circ$ lone pair-bond pair (ell p-bp$\ell p-bp$) repulsions. Placing them axially maximizes repulsions, making that structure the least stable, not the most stable.
### Pattern Recognition
For sp^3d$sp^3d$ configurations (Trigonal Bipyramidal), lone pairs ALWAYS prefer equatorial sites where they experience 120^circ$120^circ$ interactions, minimizing severe 90^circ$90^circ$ structural strains. This results in the classic stable T-shaped configuration for ClF_3$ClF_3$.
### Evaluation Rubric / Model Answer
null
### Chapter Mix
Class 11 Chemistry: Chemical Bonding and Molecular Structure
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.
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.