CBSE Class 12 Chemistry 2026 Question Paper

2026SET-170 Marks180 min37 Questions

Section A

1
1 markMCQChemical KineticsHalf-life of first order reactions

Which of the following curve represents the first order reaction?

(A)Graph of t1/2t_{1/2} (y-axis) versus [R]0[R]_0 (x-axis): a straight line with positive slope through the origin
(B)Graph of t1/2t_{1/2} (y-axis) versus [R]0[R]_0 (x-axis): a horizontal straight line (t1/2t_{1/2} independent of [R]0[R]_0)
(C)Graph of Rate (y-axis) versus Concentration (x-axis): a horizontal straight line
(D)Graph of Rate (y-axis) versus Concentration (x-axis): a decreasing curve
2
1 markMCQSolutionsDepression in freezing point and van't Hoff factor

Which of the following solutions will have the lowest freezing point in water?

(A)0.1 M Glucose
(B)0.1 M CaCl₂
(C)0.1 M KCl
(D)0.1 M Urea
3
1 markMCQThe d- and f-Block ElementsDefinition of transition metals

Which of the following is not a transition metal?

(A)Sc
(B)Ag
(C)Hg
(D)Cu
4
1 markMCQChemical KineticsArrhenius equation and activation energy

Which of the following represents the fraction of molecules with energies equal to or greater than Eₐ?

(A)+Ea/RT+E_a/RT
(B)eEa/RTe^{-E_a/RT}
(C)Ea/RT-E_a/RT
(D)e+Ea/RTe^{+E_a/RT}
5
1 markMCQElectrochemistryElectrolysis of aqueous CuCl₂

What will happen during the electrolysis of aqueous solution of CuCl₂ by using platinum electrodes?

(A)Cu will deposit at Anode
(B)H₂ gas will be released at cathode
(C)O₂ gas will be released at anode
(D)Cl₂ gas will be released at anode
6
1 markMCQChemistry in Everyday LifePreparation of aspirin by acetylation

Aspirin is obtained by acetylation of

(A)Phenol
(B)Salicylaldehyde
(C)2-Hydroxybenzoic acid
(D)Benzoic acid
7
1 markMCQCoordination CompoundsSecondary valency (coordination number)

The secondary valency of Co in the complex [Co(NH₃)₅(NO₂)]²⁺ is

(A)5
(B)1
(C)4
(D)6
8
1 markMCQAlcohols, Phenols and EthersNitration of phenol

At low temperature, phenol reacts with dil. HNO₃ to yield

(A)2, 4, 6-Trinitrophenol
(B)o-Nitrophenol only
(C)p-Nitrophenol only
(D)ortho-and para-nitrophenol
9
1 markMCQHaloalkanes and HaloarenesProperties of enantiomers

Which of the following is 'not' true about enantiomers?

(A)They have the same chemical reactivity.
(B)They have the same specific rotation.
(C)They have the same melting or boiling point.
(D)They have the same refractive index.
10
1 markMCQAminesDirect nitration of aniline

Aniline on direct nitration yields

(A)51%-ortho, 47%-para, 2%-meta derivatives
(B)51%-meta, 47%-ortho, 2%-para derivatives
(C)51%-para, 47%-meta, 2%-ortho derivatives
(D)51%-ortho, 47%-meta, 2%-para derivatives
11
1 markMCQAminesBasicity of aromatic amines (pKb)

Which of the following amines has lowest pKb value?

(A)C₆H₅ – N(CH₃)₂
(B)C₆H₅ – NH(CH₃)
(C)C₆H₅ – NH₂
(D)O₂N–C₆H₄–NH₂ (para-nitroaniline: benzene ring with NO₂ and NH₂ at para positions)
12
1 markMCQBiomoleculesVitamin deficiency diseases

The deficiency of which of the following vitamins causes increased fragility of red blood cells and muscular weakness:

(A)Vitamin A
(B)Vitamin K
(C)Vitamin E
(D)Vitamin D
13
1 markSolutionsAzeotropes

Assertion (A): It is not possible to separate the components of an azeotrope by fractional distillation. Reason (R): Components of an azeotrope have the same composition in liquid and vapour phase and boil at a constant temperature.

(A)Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
(B)Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
(C)Assertion (A) is true, but Reason (R) is false.
(D)Assertion (A) is false, but Reason (R) is true.
14
1 markAlcohols, Phenols and EthersDirective influence of –OH in phenol

Assertion (A): The presence of –OH group in phenols directs the incoming group to meta position in the ring. Reason (R): –OH group in phenols activates the aromatic ring towards electrophilic substitution reaction.

(A)Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
(B)Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
(C)Assertion (A) is true, but Reason (R) is false.
(D)Assertion (A) is false, but Reason (R) is true.
15
1 markThe d- and f-Block ElementsOxidation states of actinoids

Assertion (A): Actinoids show wide range of oxidation states. Reason (R): Actinoids are radioactive in nature.

(A)Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
(B)Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
(C)Assertion (A) is true, but Reason (R) is false.
(D)Assertion (A) is false, but Reason (R) is true.
16
1 markBiomoleculesStructure of glucose (pentaacetate test)

Assertion (A): The pentaacetate of glucose does not react with H₂N – OH. Reason (R): It indicates the presence of free – CHO group in glucose.

(A)Both Assertion (A) and Reason (R) are true and Reason (R) is the correct explanation of the Assertion (A).
(B)Both Assertion (A) and Reason (R) are true, but Reason (R) is not the correct explanation of the Assertion (A).
(C)Assertion (A) is true, but Reason (R) is false.
(D)Assertion (A) is false, but Reason (R) is true.

Section B

17
2 marksVery Short AnswerSolutionsNon-ideal solutions: negative deviation

What type of deviation from Raoult's law is shown by a mixture of phenol and aniline? Give reason. What will happen to the boiling point of the solution on mixing phenol and aniline?

18
2 marksVery Short AnswerHaloalkanes and HaloarenesLow reactivity of haloarenes in nucleophilic substitution

Why are haloarenes less reactive towards nucleophilic substitution reaction? Give two reasons.

19
2 marksVery Short AnswerCoordination CompoundsIUPAC nomenclature and isomerism of coordination compounds

(a) Write IUPAC names of the following coordination compounds: (2 × 1) (i) [Ag(NH₃)₂] [Ag(CN)₂] (ii) K₃[Fe(C₂O₄)₃] OR (b) (i) Give a chemical test to show that [Co(NH₃)₅SO₄]Cl and [Co(NH₃)₅Cl]SO₄ are ionisation isomers. (2 × 1) (ii) What is meant by the 'Chelate effect'? Give an example.

20
2 marksVery Short AnswerBiomoleculesLinkages and amino acids in biomolecules

Differentiate between the following: (2 × 1) (i) Peptide linkage and Glycosidic linkage (ii) Essential amino acids and Non-essential amino acids

21
2 marksVery Short AnswerChemical KineticsEffect of concentration/volume on rate and order of reaction

Following reaction takes place in one step: 2A + B → 2C How will the rate of above reaction change if the volume of the reaction vessel is decreased to one third of its original volume? Will there be any change in the order of reaction with the reduced volume?

Section C

22
3 marksShort AnswerChemical KineticsFirst-order rate constant from pressure data

For the first order thermal decomposition reaction, following data was obtained: C₂H₅Cl(g) → C₂H₄(g) + HCl(g) | S. No. | Time(s) | Total Pressure (atm) | | 1 | 0 | 0.30 | | 2 | 30 | 0.50 | Calculate rate constant. [Given: log3=0.48\log 3 = 0.48]

23
3 marksShort AnswerElectrochemistryElectrochemical cells, electrode potentials and batteries

(a) Answer the following: (3 × 1) (i) Why is the Equilibrium Constant (Kc) related to E°cell and not to Ecell? (ii) Two metals 'A' and 'B' have standard electrode potential values of −0.24 V and +0.80 V respectively. Which of these will liberate hydrogen gas from dil. H₂SO₄? (iii) Write the cell reaction which occurs in lead storage battery when it is in charging. OR (b) What type of battery is Mercury cell? Why it is more advantageous than dry cell? Write overall reaction taking place in Mercury cell.

24
3 marksShort AnswerSolutionsElevation of boiling point with association (dimerisation)

Calculate the boiling point of a solution containing 0.61 g of benzoic acid (Molar mass=122 g mol1\text{Molar mass} = 122 \text{ g mol}^{-1}) in 5 g of CS₂ in which it dimerises to the extent of 88%. The boiling point and Kb of CS₂ are 46.2 °C and 2.3 K kg mol12.3 \text{ K kg mol}^{-1} respectively.

25
3 marksShort AnswerBiomoleculesReactions of D-Glucose

Write the reactions of D-Glucose with the following: (3 × 1) (a) HI (b) Br₂ water (c) Conc. HNO₃

26
3 marksShort AnswerAldehydes, Ketones and Carboxylic AcidsProperties of Carbonyl and Carboxylic Compounds

Give reasons for the following: (3 × 1) (a) Carboxylic acids have higher boiling point than alcohols of comparable molecular masses. (b) Alpha (α) hydrogens of aldehydes and ketones are acidic in nature. (c) Nucleophilic addition of ammonia and its derivatives does not occur with carbonyl group in strongly acidic medium.

27
3 marksShort AnswerAlcohols, Phenols and EthersName Reactions of Phenol and Anisole

Write the reaction involved in the following: (3 × 1) (a) Reimer-Tiemann reaction (b) Kolbe's reaction (c) Friedel-Crafts acylation of anisole

28
3 marksShort AnswerHaloalkanes and HaloarenesSN1 vs SN2 Mechanism of C₄H₉Br

Compound 'X' with molecular formula C₄H₉Br reacts with aqueous KOH to give an alcohol. The rate of this reaction depends only on the concentration of the compound 'X'. When an optically active isomer 'Y' of the compound 'X' was treated with aqueous KOH solution, the rate of reaction was found to be dependent on concentration of compound 'Y' and aqueous KOH both. (3 × 1) (a) Write down the structural formula of both 'X' and 'Y'. (b) Out of 'X' and 'Y', which one will undergo racemisation and why? (c) Out of 'X' and 'Y', which one will form product with inversion of configuration and why?

Section D

29
2 marksAminesBasicity of Amines and Hofmann Bromamide Degradation

(a) (i) Why CH₃ – NH₂ is a stronger base than (CH₃)₃N in aqueous solution? (2 × 1) (ii) Write structural formulae of the compound A and B: CH₃CONH₂ —(NaOBr)→ A —(C₆H₅COCl / Base)→ B

30
1 markAminesHinsberg Test / Aniline to Benzonitrile

(b) A compound 'X' with molecular formula C₃H₉N reacts with Hinsberg reagent to give a product insoluble in alkali. Identify 'X'. OR (b) How can you convert aniline to benzonitrile?

31
1 markAminesProtection of amino group before nitration of aniline

(c) Why is –NH₂ group of aniline acetylated before carrying out nitration?

32
2 marksCoordination CompoundsCrystal field splitting of d-orbitals in an octahedral field

(a) In octahedral crystal field, energies of which d-orbitals will be raised when ligands approach the central metal atom/ion? Give reason in support of your answer.

33
1 markCoordination CompoundsCFT electronic configuration of Co(III) complexes

(b) Using crystal field theory, write the electronic configuration of central metal atom/ion of the following: (i) [CoF₆]³⁻ (ii) [Co(NH₃)₆]³⁺ [At. No.: Co=27\text{Co} = 27]

34
1 markCoordination CompoundsVBT: magnetic behaviour and hybridisation of tetrahedral/octahedral complexes

(c) [NiCl4]2[NiCl_4]^{2-} is paramagnetic while [Ni(CO)4][Ni(CO)_4] is diamagnetic though both are tetrahedral. Why? [Atomic No.: Ni=28Ni = 28] OR (c) Write hybridization and magnetic behaviour of the complex [Fe(CN)6]3[Fe(CN)_6]^{3-}. [Atomic No.: Fe=26Fe = 26]

Section E

35
5 marksLong AnswerAldehydes, Ketones and Carboxylic AcidsStructure elucidation of C₅H₁₀O and conversions to benzoic acid

(a) (i) An organic compound (X) has the molecular formula C5H10OC_5H_{10}O. Draw structures for (X) if it: (3 + 2) (I) does not give Tollen's test but gives a positive iodoform test. (II) does not give Tollen's test and iodoform test but undergoes Aldol condensation. (III) undergoes Cannizzaro's reaction. (ii) Show how each of the following compounds can be converted to benzoic acid: (I) Acetophenone (II) Ethyl benzene OR (b) Answer the following questions: (5×1)(5 \times 1) (i) Draw structure of the 2, 4-dinitrophenyl hydrazone derivative of benzaldehyde. (ii) Arrange the following in increasing order of their reactivity towards HCN: Di-tert. butyl ketone, Acetaldehyde, Acetone (iii) Give a simple chemical test to distinguish between benzoic acid and ethyl benzoate. (iv) Write the name of the reagent to convert Ethanenitrile to Ethanal. (v) Draw the structure of 'X' in the following reaction: Cyclohexanol —(CrO3CrO_3)→ 'X'

36
5 marksLong AnswerThe d- and f-Block ElementsStandard electrode potentials and oxidising action of KMnO₄ (d-block)

(a) (i) From the given data of E° values, answer the following questions: (3 + 2) E(M2+/M)E^\circ(M^{2+}/M) values (V): V=1.18,Cr=0.91,Mn=1.18,Fe=0.44,Co=0.28,Ni=0.25,Cu=+0.34V = -1.18, Cr = -0.91, Mn = -1.18, Fe = -0.44, Co = -0.28, Ni = -0.25, Cu = +0.34 (I) Why E(M2+/M)E^\circ(M^{2+}/M) show irregular trend in the above values? (II) Why is E(Cu2+/Cu)E^\circ(Cu^{2+}/Cu) value exceptionally positive? (III) Why E(Mn2+/Mn)E^\circ(Mn^{2+}/Mn) value is highly negative? (ii) Write the ionic equations for the oxidising action of potassium permanganate for its reaction with II^- in both acidic and alkaline solutions. OR (b) Answer the following questions: (1 + 1 + 1 + 2) (i) Name a member of the lanthanoid series (I) which exhibits +4 oxidation state (II) which exhibits +2 oxidation state. (ii) Why transition metals act as good catalyst? (iii) Why Cr has higher melting point than Mn? (iv) What happens when acidic solution of potassium permanganate is allowed to stand for sometime? Give the equation involved. What is this type of reaction called?

37
5 marksLong AnswerElectrochemistryNernst equation: cell emf and Gibbs energy

(a) Calculate emf and ΔG\Delta G for the following cell at 298 K: Mg(s)/Mg2+(0.01 M)//Ag+(0.001 M)/Ag(s)Mg(s) / Mg^{2+}(0.01\text{ M}) // Ag^+(0.001\text{ M}) / Ag(s) Given: E(Mg2+/Mg)=2.37 VE^\circ(Mg^{2+}/Mg) = -2.37 \text{ V}, E(Ag+/Ag)=+0.80 VE^\circ(Ag^+/Ag) = +0.80 \text{ V} [1F=96500 C mol11F = 96500 \text{ C mol}^{-1}, log10=1\log 10 = 1] OR (b) For the reaction: 2AgCl(s)+H2(g)(0.4 atm)2Ag(s)+2H+(0.1 M)+2Cl(0.2 M)2AgCl(s) + H_2(g) (0.4\text{ atm}) \to 2Ag(s) + 2H^+(0.1\text{ M}) + 2Cl^-(0.2\text{ M}) Calculate emf of the cell at 25 °C. Given: ΔG=43500 J mol1\Delta G^\circ = -43500 \text{ J mol}^{-1} [log10=1\log 10 = 1, 1F=96500 C mol11F = 96500 \text{ C mol}^{-1}]

Frequently Asked Questions

How many questions are in the CBSE Class 12 Chemistry 2026 paper?

The CBSE Class 12 Chemistry 2026 question paper has 37 questions carrying a total of 70 marks.

What is the maximum marks for CBSE Class 12 Chemistry 2026?

The maximum marks for the CBSE Class 12 Chemistry 2026 exam is 70.

How long is the CBSE Class 12 Chemistry 2026 exam?

The CBSE Class 12 Chemistry 2026 exam duration is 180 minutes (3 hours).

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Padhantu provides complete answers to all questions in the CBSE Class 12 Chemistry 2026 paper. You can read the answers directly on this page. Each question shows the official answer along with chapter and topic information.