CBSE Class 12 Chemistry Coordination Compounds NEET JEE Questions Set 01

Class 12 Chemistry Study Guide: CBSE Class 12 Chemistry Coordination Compounds NEET JEE Questions Set 01

Access comprehensive study materials and useful resources for Unit 5 Coordination Compounds using the CBSE Class 12 Chemistry Coordination Compounds NEET JEE Questions Set 01. Designed to align with the 2026-27 CBSE academic guidelines, these advanced resources help Class 12 Chemistry students reinforce core concepts beyond standard textbooks.

Download Unit 5 Coordination Compounds Study Material PDF

View or download the dedicated CBSE Class 12 Chemistry Coordination Compounds NEET JEE Questions Set 01 resource below. Engaging with these advanced study guides under focused conditions ensures continuous academic progress and mastery of the 2026-27 curriculum for Unit 5 Coordination Compounds.

Single Correct Answer

Question 1. The ligand N(CH2CH2NH2)3 is (Kerala PMT 2011)
(a) tridentate
(b) pentadentate
(c) tetradentate
(d) bidentate
(e) hexadentate

Answer:
Ans. (c)
Given ligand has four donor N-atoms and hence is tetradentate.

Teacher's Note:
1. Count the donor atoms: one tertiary N and three terminal NH2 groups give four donor sites.

 

Question 2. The correct structure of ethylenediaminetetraacetic acid (EDTA) is (IIT 2010)
(a) (HOOC–CH2)2N–CH=CH–N(CH2–COOH)2
(b) (HOOC)2N–CH2–CH2–N(COOH)2
(c) (HOOC–CH2)2N–CH2–CH2–N(CH2–COOH)2
(d) HOOC–CH2–NH–CH(CH2–COOH)–CH(CH2–COOH)–NH–CH2–COOH

Answer:
Ans. (c)
(c) is the correct structure of EDTA: an ethylene (–CH2–CH2–) bridge joins two N atoms, each carrying two –CH2COOH groups.

Teacher's Note:
1. The name tells the structure: ethylenediamine (H2N–CH2CH2–NH2) with all four N–H hydrogens replaced by acetic acid (–CH2COOH) groups.

 

Question 3. Oxidation number and coordination number of silver in Tollen's reagent respectively are
(a) 1, 1
(b) 2, 1
(c) 2, 2
(d) 1, 2

Answer:
Ans. (d)
Tollen's reagent contains silver-ammonia complex ion, [Ag(NH3)2]+. Thus, oxidation number is +1 and coordination number is 2.

Teacher's Note:
1. Coordination number counts donor atoms around the metal (two NH3), not the charge on the ion.

 

Question 4. Oxidation number of Cr in the following complex is :
[(H2O)6Cr(O2)(O–O)Cr(H2O)6]3+
(the two Cr atoms are bridged by an O2 group and an O–O group)
(a) 2
(b) 3
(c) 4
(d) 5

Answer:
Ans. (b)
2x + 12(0) + (−2) + (−1) = +3
(for Cr) (for H2O) (for O–O, peroxide ion) (for O2, superoxide ion)
or x = +3

Teacher's Note:
1. The bridging O–O is a peroxide (O22−, −2) and the bridging O2 is a superoxide (O2−, −1); remember there are two Cr atoms.

 

Question 5. Which one of the following is a homoleptic complex ? (Kerala PMT 2015)
(a) tris(ethane-1, 2-diamine) cobalt (III) chloride
(b) triamminetriaquachromium (III) chloride
(c) diamminechloridonitro-N-platinum (II)
(d) dichlorido bis(ethane-1, 2-diamine) cobalt (III) chloride
(e) pentaamminecarbonato cobalt (III) chloride

Answer:
Ans. (a)
Homoleptic complexes are those in which metal atom or ion is linked to only one type of ligands. In [Co(en)3]Cl3, only en is attached to Co.

Teacher's Note:
1. Ions outside the bracket (counter ions) do not count; look only at the ligands inside the coordination sphere.

 

Question 6. Ethylene diaminetetraacetate (EDTA) ion is : (NEET 2021)
(a) hexadentate ligand with four “O” and two “N” donor atoms
(b) unidentate ligand
(c) bidentate ligand with two “N” donor atoms
(d) tridentate ligand with three “N” donor atoms

Answer:
Ans. (a)
Ethylene diaminetetraacetate (EDTA) ion is a hexadentate ligand having two donor nitrogen atoms and four donor oxygen atoms.
(−OOCCH2)2N–CH2–CH2–N(CH2COO−)2 (EDTA4−)

Teacher's Note:
1. EDTA4− = 2 N + 4 carboxylate O = 6 donor atoms; it wraps around one metal ion forming five chelate rings.

 

Question 7. The formula, dichlorobis(urea)copper (II) is
(a) [Cu{O = C(NH2)2}]Cl2
(b) [CuCl2{O = C(NH2)2}2]
(c) [Cu{O = C(NH2)2}Cl] Cl
(d) [CuCl2{O = C(NH2)2}2]

Answer:
Ans. (b)
Two chloro ligands and two (bis) urea ligands are all inside the coordination sphere and no counter ion is named, so the formula is [CuCl2{O=C(NH2)2}2].

Teacher's Note:
1. A name with no separate anion or cation word describes a neutral complex, so everything goes inside one bracket.

 

Question 8. IUPAC name of sodium cobaltinitrite is
(a) Sodium cobaltinitrite
(b) Sodium hexanitritocobaltate (III)
(c) Sodium hexanitritocobalt (III)
(d) Sodium hexanitritocobaltate (II).

Answer:
Ans. (b)
Sodium cobaltinitrite is Na3[Co(ONO)6].
Its IUPAC name is Sodium hexanitritocobaltate (III).

Teacher's Note:
1. In an anionic complex the metal name ends in “-ate”; Co here is +3 because 3Na+ balance six NO2−.

 

Question 9. According to IUPAC nomenclature, sodium nitroprusside is named as
(a) Sodium nitroferricyanide
(b) Sodium nitroferrocyanide
(c) Sodium pentacyanonitrosylferrate (II)
(d) Sodium pentacyano nitrosylferrate (III)

Answer:
Ans. (d)
Sodium nitroprusside, Na2[Fe(CN)5NO], is named as sodium pentacyano nitrosyl ferrate (III).
In this compound, NO is present as NO+ and Fe has + 2 charge. On the basis of this, the actual name should be sodium pentacyanonitrosonium ferrate (II).

Teacher's Note:
1. Taking NO as a neutral ligand gives Fe +3 (the name used in this question); taking it as NO+ gives Fe +2.

 

Question 10. Which of the following has largest number of isomers ? (AMU Engg. 2011)
(a) [Ru(NH3)4Cl2]+
(b) [Co(en)2Cl2]+
(c) [Ir(PR3)2H(CO)]2+
(d) [Co(NH3)5Cl]2+

Answer:
Ans. (b)
All given compounds have cis and trans isomers but only cis-isomer of (b) will also have optical isomers (d and l) due to presence of symmetrical didentate, en. So (b) has three isomers.

Teacher's Note:
1. [M(AA)2X2] gives three stereoisomers: trans plus a pair of cis enantiomers.

 

Question 11. Which one of the following complexes is not expected to exhibit isomerism ? (AIPMT Main 2010)
(a) [Ni(NH3)4(H2O)2]2+
(b) [Pt(NH3)2Cl2]
(c) [Ni(NH3)2Cl2]
(d) [Ni(en)3]2+

Answer:
Ans. (c)
[Ni(NH3)2Cl2] does not exhibit isomerism because it is a tetrahedral complex.

Teacher's Note:
1. Pt(II) complexes are square planar (cis/trans possible), but Ni(II) with weak-field Cl− is tetrahedral, where all positions are adjacent.

 

Question 12. For the given complex [CoCl2 (en) (NH3)2]+, the number of geometrical isomers, the number of optical isomers and total number of isomers of all type possible respectively are (DCE 2009)
(a) 2, 2 and 4
(b) 2, 2 and 3
(c) 2, 0 and 2
(d) 0, 2 and 2

Answer:
Ans. (b)
The octahedral complex of the type [M(AA)X2Y2], i.e., [CoCl2 (en) (NH3)2]+ will show two cis- and trans-geometrical isomers. Out of these, cis-isomer will be optically active and shows two d- and l-forms. So the total number of possible isomers will be three.

Teacher's Note:
1. Do not add the geometrical and optical counts blindly: the cis form itself is one of the two optical isomers.

 

Question 13. The number of geometrical isomers that can exist for square planar [Pt(Cl) (py) (NH3) (NH2OH)]+ is (py = pyridine) (JEE Main 2015)
(a) 4
(b) 6
(c) 2
(d) 3

Answer:
Ans. (d)
A square planar complex of the type MABCD forms three isomers (A trans to B, A trans to C, A trans to D).
Two of these are cis and one is trans (with respect to any chosen pair).

Teacher's Note:
1. For [MABCD], fix ligand A and ask which of B, C or D sits opposite it: three choices give three isomers.

 

Question 14. The total number of possible isomers for the complex compound [CuII (NH3)4] [PtIICl4] are
(a) 3
(b) 6
(c) 5
(d) 4

Answer:
Ans. (d)
The possible isomers of the given complex are [Cu (NH3)4] [PtCl4], [Cu (NH3)3Cl] [PtCl3 (NH3)], [Cu (NH3) Cl3] [PtCl (NH3)3], [CuCl4] [Pt (NH3)4]
Note. [Cu (NH3)2Cl2] [PtCl2 (NH3)2] is not possible because in this case, there will be no cation and anion.

Teacher's Note:
1. Coordination isomers exchange ligands between the cationic and anionic spheres, but each sphere must keep an ionic charge.

 

Question 15. Number of possible isomers for the complex [Co(en)2Cl2] Cl will be : (en = ethylenediamine) (RE-AIPMT 2015)
(a) 3
(b) 4
(c) 2
(d) 1

Answer:
Ans. (a)
[Co(en)2Cl2]+ exists as a cis-isomer (d and l-form) and a trans-isomer (optically inactive).
Hence, total isomers = 3.

Teacher's Note:
1. The trans isomer has a mirror plane through Co and both en rings, so it cannot be optically active.

 

Question 16. [Co(NH3)4(NO2)2] Cl exhibits
(a) ionization isomerism, geometrical isomerism and optical isomerism
(b) linkage isomerism, geometrical isomerism and optical isomerism
(c) linkage isomerism, ionization isomerism and optical isomerism
(d) linkage isomerism, ionization isomerism and geometrical isomerism

Answer:
Ans. (d)
[Co(NH3)4(NO2)2] Cl and [Co(NH3)4(Cl) (NO2)] NO2 → ionization isomers
[Co(NH3)4(NO2)2] Cl and [Co(NH3)4 (ONO)2] Cl → linkage isomers
The two NO2 groups can be cis (adjacent) or trans (opposite) → geometrical isomers. Both forms of [MA4B2] have a plane of symmetry, so there is no optical isomerism.

Teacher's Note:
1. NO2− is ambidentate (N or O donor), so any complex containing it can show linkage isomerism.

 

Question 17. Fac-Mer isomerism is associated with which one of the following complexes ? (M = central metal) (Kerala PMT 2007)
(a) [M(AA)2]
(b) [MA3B3]
(c) [M(AA)3]
(d) [MABCD]
(e) [MA4B2]

Answer:
Ans. (b)
In octahedral [MA3B3], the three A ligands can occupy one triangular face (fac) or a meridian (mer) of the octahedron.

Teacher's Note:
1. fac/mer needs two sets of three identical ligands on an octahedron, e.g. [Co(NH3)3(NO2)3].

 

Question 18. Which of the following can exhibit geometrical isomerism ? (Odisha JEE 2008)
(a) [MnBr4]2−
(b) [Pt(NH3)3Cl]+
(c) [PtCl2P(C2H5)3]2
(d) [Fe(H2O)5NO]2+

Answer:
Ans. (c)
(c) is a bridged complex, [(C2H5)3P(Cl)Pt(μ-Cl)2Pt(Cl)P(C2H5)3], and shows geometrical isomerism:
in the trans-form the two P(C2H5)3 groups lie on opposite sides of the Pt(μ-Cl)2Pt unit; in the cis-form they lie on the same side.

Teacher's Note:
1. Tetrahedral [MA4] and octahedral [MA5B] or square planar [MA3B] never show geometrical isomerism.

 

Question 19. Which of the following complex species is not expected to exhibit optical isomerism ? (JEE Main 2013)
(a) [Co(en)(NH3)2Cl2]+
(b) [Co(en)3]3+
(c) [Co(en)2Cl2]+
(d) [Co(NH3)3Cl3]

Answer:
Ans. (d)
[Co(NH3)3Cl3] shows cis or facial (fac) as well as trans or meridional (mer) isomers. But both these isomers contain plane of symmetry. So they do not exhibit optical isomerism.

Teacher's Note:
1. Complexes with only monodentate ligands of the MA3B3 type always have a mirror plane; chirality usually needs chelating ligands.

 

One or More Correct Answers

Question 20. The compound K3[Co(ONO)6] is called
(a) potassium cobaltinitrite
(b) Fischer's salt
(c) potassium hexanitritocobaltate (III)
(d) potassium cobalt nitrate

Answer:
Ans. (a, b, c)
K3[Co(ONO)6] is the yellow compound commonly called potassium cobaltinitrite or Fischer's salt; its IUPAC name is potassium hexanitritocobaltate (III) (Co is +3).
It is not a nitrate: the ligand is the nitrite ion (ONO−), so (d) is wrong.

Teacher's Note:
1. “Nitrito” means O-bonded ONO−, “nitro” means N-bonded NO2−; neither is nitrate (NO3−).

 

Question 21. Which of the following are correct about [Cu(NH3)4]SO4 ?
(a) It is a square planar complex.
(b) It is paramagnetic with one unpaired electron in the d-subshell.
(c) It gives white precipitate with BaCl2 solution.
(d) Its aqueous solution does not conduct electricity.

Answer:
Ans. (a, c)
(b) is wrong because the unpaired electron is present in 4p subshell.
(d) is wrong because it gives ions in the solution and hence can conduct electricity.
(a) is correct (dsp2, square planar) and (c) is correct because the SO42− outside the coordination sphere gives white BaSO4.

Teacher's Note:
1. In the valence bond picture of [Cu(NH3)4]2+, the odd 3d electron is promoted to 4p to make room for dsp2.

 

Passage-Based Questions

Question 22. Comprehension 1: A, B and C are three complexes of chromium (III) with the empirical formula H12O6Cl3Cr. All the three complexes have water and chloride ions as ligands. Complex A does not react with conc. H2SO4 whereas complexes B and C lose 6.75% and 13.5% of their original weight respectively, on treatment with concentrated H2SO4.
The complex A is
(a) [Cr(H2O)4(H)4(O)2] Cl3
(b) [Cr(H2O)5 (H)2(O)] Cl3
(c) [Cr(H2O)6] Cl3
(d) [Cr(H2O)5Cl] Cl2 . H2O

Answer:
Ans. (c)
As A does not react with conc. H2SO4, no H2O is present as water of hydration. Hence, the formula is [Cr(H2O)6]Cl3.

Teacher's Note:
1. No mass loss with conc. H2SO4 means no water of crystallisation: all six H2O are coordinated.

 

Matrix Match Questions

Question 23. Match the entries of column I with appropriate entries of column II and choose the correct option.
Column I (Metal ion configuration in strong ligand field)Column II (CFSE, Δ0 value)
(A)d4(p)−1.6
(B)d5(q)−1.8
(C)d6(r)−2.0
(D)d7(s)−2.4

(a) A-p, B-s, C-r, D-q
(b) A-q, B-r, C-p, D-s
(c) A-p, B-r, C-s, D-q
(d) A-r, B-s, C-p, D-q

Answer:
Ans. (c)
In a strong field all electrons go into t2g (−0.4Δ0 each) until it holds six; extra electrons go into eg (+0.6Δ0 each).
d4 = t2g4 : −1.6; d5 = t2g5 : −2.0; d6 = t2g6 : −2.4; d7 = t2g6eg1 : −2.4 + 0.6 = −1.8
Hence A-p, B-r, C-s, D-q.

Teacher's Note:
1. Low spin CFSE peaks at d6 (−2.4Δ0) and falls once electrons enter eg.

 

Question 24. Match each coordination compound in List-I with an appropriate pair of characteristics from List-II and select the correct answer using the code given below the lists : (en = H2NCH2CH2NH2, atomic nos. : Ti = 22, Cr = 24, Co = 27, Pt = 78)
List-IList-II
(P)[Cr(NH3)4Cl2] Cl1.Paramagnetic and exhibits ionisation isomerism
(Q)[Ti(H2O)5Cl] (NO3)22.Diamagnetic and exhibits cis-trans isomerism
(R)[Pt(en) (NH3) (Cl)] NO33.Paramagnetic and exhibits cis-trans isomerism
(S)[Co(NH3)4 (NO3)2] NO34.Diamagnetic and exhibits ionisation isomerism
Code : P Q R S (JEE Advanced 2014)
(a) 4 2 3 1
(b) 3 1 4 2
(c) 2 1 3 4
(d) 1 3 4 2

Answer:
Ans. (b)
P : Cr3+ has 3d3 configuration with 3 unpaired electrons. Hence, it shows paramagnetic behaviour. Complex of the type MA4B2 shows cis-trans isomerism.
Q : Ti3+ has 3d1 configuration with 1 unpaired electron. Hence, it is paramagnetic. Complex gives Cl− and NO3− ions in solution. Hence, it shows ionisation isomerism.
R : Pt2+ has 5d8 configuration but ligands are strong field ligands. Hence, all electrons pair up. Hence, it is diamagnetic and forms square planar complex. It also shows ionisation isomerism.
S : Co3+ has 3d6 configuration. But ligands present are strong enough to cause electron pairing. Hence, it will be diamagnetic. As it is a complex of the type MA4B2, it exhibits cis-trans isomerism.

Teacher's Note:
1. Decide magnetism from the d-count and ligand field, then decide isomerism from the formula; match only when both parts agree.

 

Integer and Numerical Answer Questions

Question 25. The number of chelate rings present in the complex K2 [Ni(EDTA)] is
Answer:
Ans. 5
EDTA forms 5 chelate rings with metal ion (M2+): two Ni–O–C–C–N rings on each N atom (four glycinate-type rings) and one Ni–N–C–C–N ring through the ethylene bridge.

Teacher's Note:
1. A ligand with n donor atoms bound to one metal forms n − 1 chelate rings: 6 − 1 = 5 for EDTA.

 

Question 26. Number of CO groups that can be attached to chromium is
Answer:
Ans. 6
Applying Effective Atomic Number rules, number of groups that can be attached to Cr = 6: EAN = 24 + 2 × 6 = 36.

Teacher's Note:
1. Cr(0) needs 12 more electrons to reach the krypton count of 36, and each CO donates 2: hence Cr(CO)6.

 

Question 27. Taking CFSE value of octahedral complex (Δ0) as 10 Dq, the eg orbitals are ...... Dq above the bari centre.
Answer:
Ans. 6
The eg orbitals are 6 Dq above the bari centre (and t2g are 4 Dq below it).

Teacher's Note:
1. Barycentre rule: 2 × (+6 Dq) + 3 × (−4 Dq) = 0, so the average energy is unchanged.

 

Question 28. The number of rings present in the structure of chlorophyll is
Answer:
Ans. 9
There are 9 rings present in chlorophyll: four pyrrole rings, one five-membered carbocyclic ring (carrying the C=O and CO2CH3 groups) and four chelate rings formed by Mg with the four pyrrole N atoms.

Teacher's Note:
1. Chlorophyll is a magnesium complex of a porphyrin-type ligand; the Mg–N bonds create the extra rings.

 

Question 29. The volume (in mL) of 0.1 M AgNO3 required for complete precipitation of chloride ions present in 30 mL of 0.01 M solution of [Cr(H2O)5Cl]Cl2, as silver chloride is close to (IIT 2011)
Answer:
Ans. 6
[Cr(H2O)5Cl] Cl2 + 2 AgNO3 → 2 AgCl + [Cr(H2O)5Cl] (NO3)2
Number of ionizable Cl− ions in the complex = 2
Millimoles of Cl− ions = Molarity × volume × 2 = 0.01 × 30 × 2 = 0.6
Therefore, Ag+ required for complete precipitation of Cl− ions = 0.6 millimoles
As Millimoles = Molarity × V ml
0.6 = 0.1 × V
V = 6 ml.

Teacher's Note:
1. The coordinated Cl does not react with Ag+; only the two counter-ion chlorides are precipitated.

 

Assertion–Reason Questions

Question 30. Statement-1: The number of unpaired electrons present in [CuCl2]− complex is zero.
Statement-2: The complex is linear in the solid state with sp-hybridization.
(a) Statement-1 is True, Statement-2 is True; Statement-2 is a correct explanation for Statement-1.
(b) Statement-1 is True, Statement-2 is True; Statement-2 is NOT a correct explanation for Statement-1.
(c) Statement-1 is True, Statement-2 is False.
(d) Statement-1 is False, Statement-2 is True.

Answer:
Ans. (c)
Correct Statement-2. The complex, [CuCl2]− (as well as [CuCl3]2− and [CuCl4]3−) are tetrahedral in the solid state. In KCuCl2, there are chains in which Cu is tetrahedrally surrounded by Cl with simple units joined into a chain by shared halide ions.

Teacher's Note:
1. Cu+ is 3d10, so all its complexes have zero unpaired electrons regardless of geometry.

 

Question 31. Statement-1: Coordination entities with d4 to d7 ions are more stable for high spin state.
Statement-2: If Δo < P, high spin state is more stable.
(a) Statement-1 is True, Statement-2 is True; Statement-2 is a correct explanation for Statement-1.
(b) Statement-1 is True, Statement-2 is True; Statement-2 is NOT a correct explanation for Statement-1.
(c) Statement-1 is True, Statement-2 is False.
(d) Statement-1 is False, Statement-2 is True.

Answer:
Ans. (d)
Correct Statement-1. Coordination entities with d4 to d7 ions are more stable for low spin state.

Teacher's Note:
1. Only d4–d7 ions have a high spin/low spin choice; the stable state depends on whether Δo or P is larger.

 

Question 32. Statement-1: K2 [Ni(EDTA)] is more stable than K3 [Al (C2O4)3]
Statement-2: Nickel (Ni) is a transition element while aluminium (Al) is non-transition element
(a) Statement-1 is True, Statement-2 is True; Statement-2 is a correct explanation for Statement-1.
(b) Statement-1 is True, Statement-2 is True; Statement-2 is NOT a correct explanation for Statement-1.
(c) Statement-1 is True, Statement-2 is False.
(d) Statement-1 is False, Statement-2 is True.

Answer:
Ans. (b)
Both Statement-1 and Statement-2 are True but the greater stability is due to greater number of chelate rings (five) formed by EDTA than by oxalate.

Teacher's Note:
1. Stability of chelates rises with the number of chelate rings (chelate effect); EDTA forms five rings with one metal ion.

 

Question 33. Statement-1: [Fe(H2O)5NO]SO4 is paramagnetic.
Statement-2: The Fe in [Fe(H2O)5NO]SO4 has three unpaired electrons. (IIT 2008)
(a) Statement-1 is True, Statement-2 is True; Statement-2 is a correct explanation for Statement-1.
(b) Statement-1 is True, Statement-2 is True; Statement-2 is NOT a correct explanation for Statement-1.
(c) Statement-1 is True, Statement-2 is False.
(d) Statement-1 is False, Statement-2 is True.

Answer:
Ans. (a)
In the compound [Fe(H2O)5NO]SO4, NO is present as NO+. Hence, oxidation state of Fe is x + 5 × 0 + 1 = +2 or x = + 1. (In fact, odd e− on N is transferred from NO to Fe, changing NO to NO+ and Fe2+ to Fe+).
E.C. of Fe+ = 1s2 2s2 2p6 3s2 3p6 3d6 4s1
The electron present in 4s shifts to 3d giving 3d7 configuration, with 3 unpaired electrons; 4s, 4p and 4d orbitals give sp3d2.
H2O and NO+ both are weak field ligands and cannot cause pairing of 3d electrons. Thus, there are 3 unpaired electrons and hybridisation is sp3d2 (an outer orbital complex).

Teacher's Note:
1. The brown ring complex has μ ≈ 3.9 BM, matching three unpaired electrons on Fe(I).

Useful Resources and Notes for Class 12 Chemistry Unit 5 Coordination Compounds

Essential Notes for Class 12 Chemistry

Access comprehensive study material for Unit 5 Coordination Compounds, including revision notes, concept maps, and high-probability questions. These resources are designed in alignment with the latest 2026 CBSE syllabus for Class 12 Chemistry to support effective exam preparation.

Verified Solutions for Class 12 Chemistry

Each resource draws directly from authorized textbooks to maintain academic accuracy. Evaluating solved examples allows Class 12 students to master the formal presentation and answer-writing standards expected in upcoming school exams.

Enhance Accuracy with Online Tests

Wrap up your chapter revision by testing your knowledge against standard objective question formats. Explore our full library of free, up-to-date sample papers and online assessments to secure top grades in your CBSE examinations.

FAQs

Where can I find the most advanced study material for CBSE Class 12 Chemistry for 2026-27?

The latest 2026-27 advanced study resources for Class 12 Chemistry are available for free on StudiesToday.com which includes NCERT Exemplars, high-order thinking skills (HOTS) questions, and deep-dive concept summaries.

What does the 2026-27 Chemistry study package for Class 12 include?

Our exhaustive Class 12 Chemistry package includes chapter wise revision notes, solved practice sheets, important formulas and Concept Maps to help in better understanding of all topics.

Is this study material enough for both CBSE exams and competitive tests?

Yes. For Class 12, our resources have been developed to help you get better marks in CBSE school exams and also build fundamental strength needed for entrance tests including Competency Based learning.

How should Class 12 students use this Chemistry material for maximum marks?

in Class 12, students should use Active Recall method, read the concept summary, then solve the Important Questions section without looking at the answers and then check your answers.

Can I download Class 12 Chemistry study notes in PDF for offline use?

All CBSE Chemistry study materials are provided in mobile-friendly PDF. You can download and save them on your device.

Are the Class 12 Chemistry resources updated for the latest NEP guidelines?

Yes, our team has ensured that all Chemistry materials for Class 12 are strictly aligned with the National Education Policy (NEP) 2020 and the latest 2026-27 CBSE syllabus.