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Chemistry · 2025 · Set 56/6/1

CBSE Class 12 Chemistry 2025 — Set 56/6/1

CBSE Class XII Board 2025 · Set 56/6/1

Real board examination
Sets

About the 2025 exam: CBSE issued its Chemistry papers in several series in 2025 (56/4, 56/5, 56/6 …; there was no series 56/3). Three distinct series are available here, complete (33/33), digitised from the official CBSE papers.

About this paper

The real Class-12 board examination held in 2025. Every question below is solved the concept-first way. Sample papers are labelled honestly — never shown as a past exam.

Total marks
70
Questions
33
Duration
180 min
Sections
5

The marks / questions / duration above are the official exam pattern. We currently have 33 of this paper’s questions (100% of the full paper), with 33 fully solved. Questions we couldn’t yet extract or verify are held — never shown as complete.

Sections & marks

SectionTypeQuestionsMarks eachTotal
ASection AMCQ16116
BSection BVery short answer5210
CSection CShort answer7321
DSection DCase-based248
ESection ELong answer3515
Total3370

The question paper

The questions we hold for this paper, laid out by section. Solutions are on the Answers tab.

Board Examination

Chemistry

CBSE Class XII Board 2025 · Set 56/6/1

Series/Set: 56/6/1Roll No. ________
Time Allowed: 3 hoursMaximum Marks: 70

General Instructions

  1. This question paper contains 33 questions divided into 5 sections — A, B, C, D, E.
  2. Section A comprises 16 questions of 1 mark each (MCQ).
  3. Section B comprises 5 questions of 2 marks each (Very short answer).
  4. Section C comprises 7 questions of 3 marks each (Short answer).
  5. Section D comprises 2 questions of 4 marks each (Case-based).
  6. Section E comprises 3 questions of 5 marks each (Long answer).

Above is the official exam pattern. The questions printed below are those we currently hold for this paper.

Section A

MCQ · 1 mark each · 16 of 16 shown

Q1.
Williamson synthesis of preparing unsymmetrical ether is : (A) SN1S_N1 reaction (B) SN2S_N2 reaction (C) Electrophilic addition reaction (D) Elimination reaction
[1]
Q2.
Which of the following compounds would be hydrolysed by aqueous KOH most easily ? (A) CH2=CH−BrCH_2 = CH - Br (B) CH3−CH2−BrCH_3 - CH_2 - Br (C) CH3−CH(Br)−CH3CH_3 - CH(Br) - CH_3 (D) CH2=CH−CH2−BrCH_2 = CH - CH_2 - Br
[1]
Q3.
According to Werner's theory of coordination compounds : (A) Primary valences are ionisable. (B) Secondary valences are ionisable. (C) Both primary and secondary valences are non-ionisable. (D) Both primary and secondary valences are ionisable.
[1]
Q4.
Which of the following complex ion is not optically active ? (A) [Co(ox)3]3−[Co(ox)_3]^{3-} (B) cis-[Co(en)2Cl2]+cis\text{-}[Co(en)_2Cl_2]^+ (C) trans-[Co(en)2Cl2]+trans\text{-}[Co(en)_2Cl_2]^+ (D) [Co(en)3]3+[Co(en)_3]^{3+}
[1]
Q5.
Which of the following is the softest metal ? (A) Zn (B) Sc (C) Cu (D) Fe
[1]
Q6.
In the Hinsberg's method for separation of primary, secondary and tertiary amines, the reagent used is : (A) Nitrous acid (B) CHCl3CHCl_3 + aq. NaOH (C) C6H5SO2ClC_6H_5SO_2Cl (benzenesulphonyl chloride) (D) HCl/ZnCl2HCl/ZnCl_2
[1]
Page 1 of 6
Q7.
Which one of the following amines gives an alcohol on reaction with HNO₂ ? (A) C₆H₅NH₂ (aniline) (B) C₂H₅NH₂ (C) (C₂H₅)₂NH (D) (C₂H₅)₃N
[1]
Q8.
The freezing point of one molal KCl solution, assuming KCl to be completely dissociated in water, is : (Kf for water = 1·86 K kg mol⁻¹) (A) -3·72°C (B) +3·72°C (C) -1·86°C (D) +2·72°C
[1]
Q9.
A solution of acetone in ethanol : (A) obeys Raoult's law. (B) forms an ideal solution. (C) shows a positive deviation from Raoult's law. (D) shows a negative deviation from Raoult's law.
[1]
Q10.
Which of the following cell converts the energy of combustion of fuel into electrical energy ? (A) Mercury cell (B) Fuel cell (C) Dry cell (D) Lead storage cell
[1]
Q11.
The unit of rate and rate constant are same for a : (A) First order reaction (B) Second order reaction (C) Zero order reaction (D) Third order reaction
[1]
Q12.
Pyranose ring of glucose is formed due to the reaction between : (A) C₁ and C₃ (B) C₁ and C₅ (C) C₁ and C₄ (D) C₁ and C₂
[1]
Q13.
For the following question, two statements are given — one labelled as Assertion (A) and the other labelled as Reason (R). Select the correct answer from the codes (A), (B), (C) and (D) as given below. (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. Assertion (A) : Actinoids show wide range of oxidation states. Reason (R) : Actinoids are radioactive in nature.
[1]
Q14.
For the following question, two statements are given — one labelled as Assertion (A) and the other labelled as Reason (R). Select the correct answer from the codes (A), (B), (C) and (D) as given below. (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. Assertion (A) : Hydrolysis of an ester follows first order kinetics. Reason (R) : The concentration of water does not get altered much during the reaction.
[1]
Q15.
For the following question, two statements are given — one labelled as Assertion (A) and the other labelled as Reason (R). Select the correct answer from the codes (A), (B), (C) and (D) as given below. (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. Assertion (A) : Boiling point of (CH₃)₃N is higher than that of CH₃CH₂CH₂NH₂. Reason (R) : Hydrogen bonding is more extensive in CH₃CH₂CH₂NH₂.
[1]
Page 2 of 6
Q16.
For the following question, two statements are given — one labelled as Assertion (A) and the other labelled as Reason (R). Select the correct answer from the codes (A), (B), (C) and (D) as given below. (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. Assertion (A) : Phenol is strongly acidic as compared to ethanol. Reason (R) : Phenoxide ion is more stable than ethoxide ion.
[1]
Section B

Very short answer · 2 marks each · 5 of 5 shown

Q1.
State Henry's law. Why are aquatic species more comfortable in cold water as compared to warm water ?
[2]
Q2.
Observe the graph in the given figure and answer the following questions : (Drawn graph: log [R]₀/[R] on the y-axis against Time on the x-axis — a straight line rising from the origin.) (a) Predict the order of reaction. (b) What is the slope of the curve ?
[2]
Q3.
(a) Write IUPAC names of the following coordination compounds : (i) [CoCl₂(en)₂]SO₄ (ii) K₃[Fe(C₂O₄)₃] OR (b) Differentiate between : (i) Double salt and Complex compound (ii) Didentate ligand and Ambidentate ligand
[2]
Q4.
Draw the structures of major monohalo products in each of the following reactions : (a) 1-Methylcyclohexene (C₇H₁₂, drawn: cyclohexene ring with a CH₃ group on a double-bond carbon) + HI longrightarrow ? (b) Cyclohexene (C₆H₁₀, drawn ring with one C=C) + Br₂ xrightarrowHeat or UV light ?
[2]
Q5.
How do you explain the following ? (a) Presence of an aldehydic group in glucose. (b) Presence of five – OH groups in glucose.
[2]
Page 3 of 6
Section C

Short answer · 3 marks each · 7 of 7 shown

Q1.
Vapour pressure of pure water at 298 K is 24·8 mm Hg. Calculate the lowering in vapour pressure of an aqueous solution which freezes at -0·3°C. (Kf of water = 1·86 K kg mol⁻¹)
[3]
Q2.
The rate of a reaction : A + B longrightarrow product is given below as a function of different initial concentrations of A and B. | Experiment | [A]/mol L⁻¹ | [B]/mol L⁻¹ | Initial Rate/mol L⁻¹ min⁻¹ | | --- | --- | --- | --- | | 1 | 0·01 | 0·01 | 5 × 10⁻³ | | 2 | 0·02 | 0·01 | 1 × 10⁻² | | 3 | 0·01 | 0·02 | 5 × 10⁻³ | Calculate the order of the reaction with respect to A and B. Determine the rate constant of the reaction.
[3]
Q3.
Give reasons for the following : (a) The pH of aqueous NaCl increases when it is electrolysed. (b) Unlike dry cell, mercury cell has a constant cell potential through its lifetime. (c) Conductivity of solution decreases with dilution.
[3]
Q4.
(a) Answer the following about the complexes [FeF₆]³⁻ and [Fe(CN)₆]⁴⁻ : (i) Write the hybridization involved in each case. (ii) Which of them is the outer orbital complex and which one is the inner orbital complex ? (iii) Compare their magnetic behaviour. [Atomic number : Fe = 26] OR (b) (i) What happens to the colour of complex [Ti(H₂O)₆]³⁺ when heated gradually ? (ii) Write the electronic configuration for d⁵ ion if Δo < P. (iii) Write the hybridization and magnetic behaviour of the complex [Ni(CO)₄]. [Atomic number : Ni = 28]
[3]
Q5.
Write any two differences between SN1 and SN2 reactions. Which of the following compounds would undergo SN1 reaction faster and why ? (Cyclohexylmethyl chloride) C₆H₁₁-CH₂-Cl (drawn: cyclohexane ring bearing -CH₂-Cl) or (Benzyl chloride) C₆H₅-CH₂-Cl (drawn: benzene ring bearing -CH₂-Cl)
[3]
Page 4 of 6
Q6.
A compound (A) with molecular formula C₄H₅N on reduction with DIBAL-H followed by hydrolysis, gives a compound (B). Compound (B) gives positive Tollens' test but does not give iodoform test. Compound (B) can also be obtained when ethanal is treated with dilute NaOH followed by heating. Identify (A) and (B). Write the reactions of (A) with DIBAL-H followed by hydrolysis.
[3]
Q7.
How will you obtain the following from aniline ? Give chemical equations only. (a) Sulphanilic acid (b) Phenylisocyanide (c) Acetanilide
[3]
Section D

Case-based · 4 marks each · 2 of 2 shown

Q1.
Read the case carefully and answer the questions that follow. Alcohols undergo a number of reactions involving the cleavage of C – OH bond. However, phenols do not undergo reactions involving the cleavage of C – OH bond. Alcohols are weaker acids than water. Alcohols react with halogen acids to form the corresponding haloalkanes. Phenols are stronger acids than alcohols. A characteristic feature of phenols is that they undergo electrophilic substitution reactions such as halogenation, nitration, etc. Since – OH group is a strong activating group, phenol gives trisubstituted products during halogenation, nitration, etc. (a) What happens when phenol is treated with the following ? (i) Br₂ water (ii) Conc. HNO₃ (b) (i) Write the mechanism of alcohol reacting as nucleophile in a reaction with CH₃oplus (methyl cation). OR (b) (ii) Why do phenols not undergo reactions involving cleavage of C – OH bond ? (c) How can you distinguish between Butan-1-ol and 2-Methylpropan-2-ol by using HCl in the presence of anhydrous ZnCl₂ ?
[4]
Q2.
Read the case carefully and answer the questions that follow. The α-amino acids are the building blocks of proteins. All α-amino acids exist as zwitter ion due to which they show amphoteric behaviour. All amino acids are joined through peptide bond. Proteins are broadly classified as globular proteins and fibrous proteins. Globular proteins are water soluble, whereas fibrous proteins are not. The complete structure of protein is discussed at four different levels i.e. primary, secondary, tertiary and quaternary structures. Protein loses its biological activity in denatured form. (a) Define the following : (i) Peptide linkage (ii) Denatured protein (b) Why do amino acids show amphoteric behaviour ? (c) (i) How can you differentiate between Fibrous protein and Globular protein ? OR (c) (ii) Write the names of two different secondary structures of proteins.
[4]
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Section E

Long answer · 5 marks each · 3 of 3 shown

Q1.
(a) (i) Calculate Ecell of a galvanic cell in which the following reaction takes place at 25 °C : Zn(s) + Pb²⁺(0·02M) longrightarrow Zn²⁺(0·1M) + Pb(s) [Given : E°Zn²⁺/Zn = -0·76V, E°Pb²⁺/Pb = -0·13V; log 2 = 0·3010, log 4 = 0·6021, log 5 = 0·6990]. (ii) State Faraday's first law of electrolysis. How much electricity, in terms of Faraday, is required to reduce one mol of MnO₄^- to Mn²⁺ ion ? OR (b) (i) The resistance of a conductivity cell containing 0·001 M KCl solution at 298 K is 1000 ohm. What is the cell constant if conductivity of 0·001 M KCl solution at 298 K is 0·125 × 10⁻³Scm⁻¹ ? (ii) Calculate the EMg²⁺/Mg potential for the following half cell at 25 °C : Mg/Mg²⁺(1 × 10⁻⁴M); E°Mg²⁺/Mg = +2·36V [Given : log 10 = 1] (iii) What is the effect of temperature on the electrical conductance of metallic conductor ?
[5]
Q2.
(a) (i) Account for the following : (I) Orange colour of Cr₂O₇²⁻ ion changes to yellow when treated with an alkali. (II) Zn, Cd and Hg are non-transition elements. (III) E° value for Mn³⁺/Mn²⁺ couple is highly positive (+1·57 V) as compared to Cr³⁺/Cr²⁺. (ii) What happens when : (I) Manganate ion undergoes disproportionation reaction in acidic medium ? (II) KMnO₄ is heated ? OR (b) Answer the following questions : (i) What is 'Misch metal' ? Give its one use. (ii) Write the formula of an oxoanion of chromium in which it shows the oxidation state equal to its group number. (iii) Why does Vanadium pentoxide (V₂O₅) act as a catalyst ? (iv) Why do transition elements have high enthalpies of atomisation ? (v) How do you prepare Na₂Cr₂O₇ from Na₂CrO₄ ?
[5]
Q3.
(a) (i) Identify A, B and C in the following reactions : Toluene (C₆H₅CH₃, drawn ring bearing -CH₃) + CrO₃ xrightarrow[273-283K](CH₃CO)₂O A xrightarrowH₃O^+ B xrightarrowConc. NaOH C + Sodium benzoate (C₆H₅COONa, drawn ring bearing -COONa) (ii) Give reasons for the following : (I) Carboxylic acids do not give the characteristic reactions of carbonyl group. (II) Ethanoic acid is a stronger acid than ethanol. OR (b) (i) Write the product(s) in the following reactions : (I) 2CH₃COOH xrightarrow[Δ]P₄O₁₀ (II) Benzoyl chloride (C₆H₅COCl, drawn ring bearing -COCl) + (CH₃)₂Cd longrightarrow (III) Benzene-1,2-dicarboxamide (drawn: benzene ring bearing two adjacent -CONH₂ groups) xrightarrowstrong heating (ii) Write the reaction involved in the following : (I) Wolff-Kishner reduction (II) Decarboxylation reaction
[5]
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