UK Board Class 12 Chemistry Solved Sample 2026 SET-1
| Q. No. | Question Summary | Correct Answer |
|---|---|---|
| 1 (क) | Chemical name of Vitamin B₁ | (iv) Thiamine |
| 1 (ख) | Order of reaction if half-life is independent of initial concentration | (ii) First (प्रथम) |
| 1 (ग) | Coordination number of 'Fe' in $K_4[Fe(CN)_6]$ | (iii) 6 |
| 1 (घ) | Value of Henry's Constant $K_H$ | (i) Increases with increase in temperature |
| 1 (ङ) | Faraday's first law of electrolysis | (iii) $W \propto Q$ |
| 1 (च) | Formaldehyde + KOH heating product | (i) Methyl alcohol |
| 1 (छ) | Reagent to convert amide to amine | (i) $Br_2 / KOH$ |
| 1 (ज) | Chemical formula of Phosgene | (iv) $COCl_2$ |
| 1 (झ) | Assertion: d/f blocks produce colored ions. Reason: Unpaired electrons present. | (i) Both A and R are correct and R is the correct explanation of A |
| 1 (ञ) | Assertion: Maltose/Lactose are reducing sugars. Reason: They reduce Fehling's/Tollen's. | (i) Both A and R are correct and R is the correct explanation of A |
$$i = \frac{\text{Observed Colligative Property}}{\text{Calculated Colligative Property}}$$
(i) For $k = 200 \text{ s}^{-1}$: $t_{1/2} = \frac{0.693}{200} = 0.003465 \text{ s}$
(ii) For $k = 2 \text{ min}^{-1}$: $t_{1/2} = \frac{0.693}{2} = 0.3465 \text{ min}$
(ii) Standard electrode Potential (E°): It is the potential difference developed between the metal electrode and the solution of its ions of unit molarity (1 M) at 298 K.
(ii) $CH_3COOH \xrightarrow[H_2O]{(i) X_2/\text{Red P}} X-CH_2COOH$ (where X = Cl, Br) OR (i) Why Phenol is acidic: Phenol is acidic because after losing a proton, it forms a phenoxide ion which is resonance-stabilized.
(ii) Auto-oxidation of diethyl ether: $C_2H_5OC_2H_5 + O_2 \xrightarrow{\text{long exposure to air}} CH_3CH(OOH)OC_2H_5$ (Ethoxyethyl hydroperoxide)
(i) Most of the transition elements show variable oxidation states.
(ii) Most of the compounds of transition elements are coloured.
(ii) They are coloured due to d-d transitions. In the presence of ligands, the d-orbitals split, and electrons absorb visible light to jump from lower to higher d-energy levels.
Ambidentate: Ligands that have two different donor atoms and can coordinate through either of them. Example: $NO_2^-$ (can bind via N or O), $SCN^-$.
(i) D.D.T. (ii) Diphenyl.
(ii) 2 C6H5Cl + 2Na $\xrightarrow{\text{dry ether}}$ C6H5-C6H5 + 2NaCl (Fittig Reaction)
D - Glucose reacts with the following.
(i) HNO3
(ii) Fehling Solution
Lactose: $C_{12}H_{22}O_{11} + H_2O \to C_6H_{12}O_6 \text{ (Glucose)} + C_6H_{12}O_6 \text{ (Galactose)}$
A: Benzoic acid ($C_6H_5COOH$)
B: Benzamide ($C_6H_5CONH_2$)
C: Aniline ($C_6H_5NH_2$)
$1 = \frac{2.53 \times 10 \times 1000}{M \times 100}$
$M = 2.53 \times 10 \times 10 = 253 \text{ g/mol}$
$\Lambda^o_m(CH_3COOH) = \Lambda^o_m(CH_3COONa) + \Lambda^o_m(HCl) - \Lambda^o_m(NaCl)$
$= 91.0 + 426.1 - 126.5 = 390.6 \text{ mho cm}^2 \text{ mol}^{-1}$
(i) Dehydration/Amination of Ethanol:
C2H5OH + NH3 → (Al2O3, 450°C) → C2H5NH2 + H2O(Product: Ethylamine)
(ii) Carbylamine Reaction:
RNH2 + CHCl3 + 3KOH(alc) → R-NC + 3KCl + 3H2O(Product: Alkyl Isocyanide)
(iii) Diazotization Reaction:
C6H5NH2 + HCl → [C6H5NH3]+Cl- --- HNO2 + 273K → C6H5N2Cl + 2H2O(Product: Benzene Diazonium Chloride)
At Cathode (Reduction): 2Ag+(aq) + 2e- → 2Ag(s)
Net Cell Reaction: Zn(s) + 2Ag+(aq) → Zn2+(aq) + 2Ag(s)
(ii) Describe the construction of a dry cell and write the cell reactions. 2
Construction: A dry cell consists of a Zinc container which acts as the Anode. The Cathode is a Carbon (graphite) rod surrounded by powdered MnO2 and carbon. The space between the electrodes is filled by a moist paste of NH4Cl and ZnCl2 which acts as the electrolyte.
Cell Reactions:
Anode: Zn(s) → Zn2+ + 2e-Cathode: MnO2 + NH4+ + e- → MnO(OH) + NH3
(i) Mole fraction (x): It is the ratio of the number of moles of a particular component to the total number of moles of all the components present in the solution.
(ii) Molality (m): It is defined as the number of moles of the solute dissolved per kilogram (1000g) of the solvent.
(iii) Mass Percentage: It is the mass of a component per 100 grams of the total mass of the solution.
1. Calculate Molar Mass of CH3COOH:
(2 × 12) + (4 × 1) + (2 × 16) = 24 + 4 + 32 = 60 g/mol
2. Calculate Number of Moles:
Moles = Mass / Molar Mass = 2.5 / 60 = 0.0417 mol
3. Calculate Molality (m):
Mass of solvent (Benzene) = 75 g = 0.075 kg
Molality = Moles of solute / Mass of solvent in kg
m = 0.0417 / 0.075 = 0.556 mol/kg (or 0.556 m)
Proposed by Linus Pauling, VBT explains the formation, structure, and magnetic properties of coordination compounds based on the following postulates:
- The central metal ion provides a number of empty orbitals (s, p, and d) equal to its coordination number.
- These empty orbitals hybridize to form a set of equivalent orbitals of definite geometry (Octahedral, Tetrahedral, etc.).
- Ligands donate a pair of electrons into these vacant hybridized orbitals to form coordinate covalent bonds.
- If inner d-orbitals $(n-1)d$ are used, it is an inner orbital complex. If outer d-orbitals $(n)d$ are used, it is an outer orbital complex.
Application to [Fe(CN)6]4-
1. Oxidation State and Configuration:
Oxidation state of Iron (Fe) is +2.
Configuration of Fe2+: $[Ar] 3d^6 4s^0$
2. Role of Ligand
The Cyanide ion (CN-) is a strong field ligand. According to VBT, strong field ligands force the unpaired electrons in the 3d orbitals to pair up against Hund's Rule to make inner d-orbitals available for bonding.
3. Hybridization
To accommodate 6 pairs of electrons from 6 CN- ligands, the Fe2+ ion undergoes d2sp3 hybridization using two 3d, one 4s, and three 4p orbitals.
| State | 3d Orbitals | 4s | 4p | |
|---|---|---|---|---|
| Fe2+ (free ion) | ↑↓ ↑ ↑ ↑ ↑ | |||
| Fe2+ (paired by CN-) | ↑↓ ↑↓ ↑↓ [__] [__] | [__] | [__] [__] [__] | |
| d2sp3 Hybrid Orbitals | Six empty hybrid orbitals ready for CN- lone pairs | |||
Final Characteristics of [Fe(CN)6]4-
Geometry: Octahedral (due to d2sp3 hybridization).
Magnetic Behavior: Diamagnetic. All electrons are paired up; hence the magnetic moment is zero.
Type: Inner orbital complex (also called a low-spin complex).
(i) Coordination Entity: A coordination entity constitutes a central metal atom or ion bonded to a fixed number of ions or molecules. It is usually enclosed in square brackets. It can be neutral, positively charged, or negatively charged.
Example: In the compound $K_4[Fe(CN)_6]$, the part $[Fe(CN)_6]^{4-}$ is the coordination entity.
(ii) Ligand: The ions or molecules bound to the central atom/ion in the coordination entity are called ligands. These act as Lewis bases by donating a pair of electrons to the central metal (Lewis acid) to form a coordinate bond.
Example: In $[Cu(NH_3)_4]^{2+}$, the four $NH_3$ (ammonia) molecules are the ligands.
(iii) Coordination Number (C.N.): The coordination number of a metal ion in a complex is defined as the total number of ligand donor atoms to which the metal is directly bonded. It represents the number of sigma bonds formed between ligands and the central metal.
Example: In $[PtCl_6]^{2-}$, there are six $Cl^-$ ions attached to Pt, so the Coordination Number is 6. In $[Co(en)_3]^{3+}$, since 'en' (ethylenediamine) is didentate, the Coordination Number is $3 \times 2 = 6$.
(i) Aldol Condensation: Aldehydes and ketones having at least one α-hydrogen undergo a reaction in the presence of dilute alkali (like NaOH) to form β-hydroxy aldehydes (aldols) or β-hydroxy ketones (ketols).
2CH3CHO → (dil. NaOH) → CH3CH(OH)CH2CHO
(ii) Ammonolysis: The process of cleavage of the C-X bond in alkyl halides by an ammonia molecule is called ammonolysis. It produces a mixture of primary, secondary, and tertiary amines, and finally quaternary ammonium salts.
R-X + NH3 → R-NH2 + HX → (excess R-X) → R2NH → R3N → [R4N]+X-
(iii) Diazotisation: The conversion of primary aromatic amines into diazonium salts using nitrous acid (NaNO2 + HCl) at low temperatures (273-278 K) is known as diazotisation.
C6H5NH2 + NaNO2 + 2HCl → (273-278K) → C6H5N2+Cl- + NaCl + 2H2O
(i) Wolff Kishner Reduction: Carbonyl groups are reduced to -CH2 groups by treatment with hydrazine followed by heating with KOH in ethylene glycol.
C=O + NH2NH2 → (-H2O) → C=NNH2 → (KOH/Ethylene glycol, Δ) → CH2 + N2
(ii) Williamson Ether Synthesis: An alkyl halide reacts with sodium alkoxide to form an ether (SN2 mechanism).
R-X + R'-ONa → R-O-R' + NaX
(iii) Kolbe Schmitt Reaction: Phenoxide ion reacts with CO2 followed by acidification to produce Salicylic acid.
C6H5ONa + CO2 → (400K, 4-7 atm) → Sodium Salicylate → (H+) → C6H4(OH)COOH
Chloroform (CHCl3) is prepared by heating ethanol or acetone with a paste of bleaching powder [CaOCl2].
Step 1: Hydrolysis of Bleaching Powder: CaOCl2 + H2O → Ca(OH)2 + Cl2
Step 2 (Using Acetone):
CH3COCH3 + 3Cl2 → CCl3COCH3 (Trichloroacetone) + 3HCl
2CCl3COCH3 + Ca(OH)2 → 2CHCl3 (Chloroform) + (CH3COO)2Ca (Calcium acetate)
(i) Zwitter ion: In aqueous solution, the carboxyl group of an amino acid can lose a proton and the amino group can accept a proton, giving rise to a dipolar ion known as a Zwitter ion. It is neutral but carries both positive and negative charges.
H2N-CH(R)-COOH ↔ +H3N-CH(R)-COO-
(ii) Nucleotide: A nucleotide is the basic building block of nucleic acids (DNA/RNA). It consists of three components: a nitrogenous base, a pentose sugar, and a phosphoric acid group.
(iii) Glycosidic bond: It is the oxide linkage formed between two monosaccharide units by the loss of a water molecule. This bond joins sugar molecules to each other in disaccharides and polysaccharides.
Consider a first order reaction: R → P
The rate of reaction is given by: $$Rate = -\frac{d[R]}{dt} = k[R]^1$$
Rearranging the equation: $$\frac{d[R]}{[R]} = -k dt$$
Integrating both sides: $$\int \frac{d[R]}{[R]} = -\int k dt$$ $$\ln[R] = -kt + I \quad \text{--- (Eq. 1)}$$
At $t = 0$, $[R] = [R]_0$ (where $[R]_0$ is initial concentration). Substituting these values in Eq. 1: $$\ln[R]_0 = -k(0) + I \implies I = \ln[R]_0$$
Substituting the value of $I$ back into Eq. 1: $$\ln[R] = -kt + \ln[R]_0$$ $$kt = \ln[R]_0 - \ln[R] = \ln \frac{[R]_0}{[R]}$$
Converting natural log ($\ln$) to common log ($\log_{10}$): $$k = \frac{2.303}{t} \log \frac{[R]_0}{[R]}$$
(ii) Calculate half life of the reaction (K = 5.5 x 10-14 s-1).For a first order reaction, the half-life ($t_{1/2}$) is given by:
$$t_{1/2} = \frac{0.693}{k}$$
Substituting the value of $k$:
$$t_{1/2} = \frac{0.693}{5.5 \times 10^{-14}} = 1.26 \times 10^{13} \text{ s}$$
Step 1: For $t_{99.9\%}$
Initial concentration $[R]_0 = 100$, Final concentration $[R] = 100 - 99.9 = 0.1$
$$t_{99.9\%} = \frac{2.303}{k} \log \frac{100}{0.1} = \frac{2.303}{k} \log 1000 = \frac{2.303}{k} \times 3 \quad \text{--- (Eq. A)}$$
Step 2: For $t_{1/2}$
$$t_{1/2} = \frac{0.693}{k} = \frac{2.303 \log 2}{k} = \frac{2.303 \times 0.3010}{k} \quad \text{--- (Eq. B)}$$
Step 3: Comparison
Dividing Eq. A by Eq. B:
$$\frac{t_{99.9\%}}{t_{1/2}} = \frac{3}{0.3010} \approx 9.96 \approx 10$$
Therefore, $t_{99.9\%} \approx 10 \times t_{1/2}$.
The decomposition of Hydrogen Peroxide ($2H_2O_2 \rightarrow 2H_2O + O_2$) is a first-order reaction. It is studied by titration:
- A known volume of the reaction mixture is withdrawn at different time intervals ($t$).
- The reaction is "quenched" (stopped) by adding it to ice-cold water or dilute $H_2SO_4$.
- The amount of unreacted $H_2O_2$ is titrated against a standard solution of Potassium Permanganate (KMnO4).
- The volume of $KMnO_4$ used ($V_t$) is proportional to the concentration of $H_2O_2$ remaining at that time.
Based on the reactions described, here is the identification of the compounds:
[A] Acetone (Propanone): $CH_3COCH_3$ (Gives iodoform test)[B] Iodoform: $CHI_3$ (Yellow precipitate formed from A)
[C] Acetylene (Ethyne): $HC \equiv CH$ (Formed by heating B with Ag powder)
[D] Acetaldehyde (Ethanal): $CH_3CHO$ (Formed by hydration of C; gives Aldol reaction)
Chemical Equations:
1. Iodoform Reaction (A to B):
CH3COCH3 + 3I2 + 4NaOH → CHI3 (B) + CH3COONa + 3NaI + 3H2O
2. Reaction with Silver Powder (B to C):
2CHI3 + 6Ag → (Δ) → HC≡CH (C) + 6AgI
3. Hydration (C to D):
HC≡CH + H2O → (dil. H2SO4 / HgSO4) → CH3CHO (D)
4. Aldol Condensation (of D):
2CH3CHO → (dil. NaOH) → CH3CH(OH)CH2CHO (3-Hydroxybutanal)
(i) Acetone + Bleaching Powder:
Product: Chloroform ($CHCl_3$)
2CH3COCH3 + 3Ca(OCl)Cl → 2CHCl3 + (CH3COO)2Ca + 2Ca(OH)2 + CaCl2
(ii) Formaldehyde + Ammonia:
Product: Urotropine (Hexamethylenetetramine)
6HCHO + 4NH3 → (CH2)6N4 + 6H2O
(iii) Sodium Acetate + Sodalime:
Product: Methane ($CH_4$)
CH3COONa + NaOH → (CaO, Δ) → CH4 + Na2CO3
(iv) Benzoyl Chloride + Hydrogen (Pd/BaSO4):
Product: Benzaldehyde ($C_6H_5CHO$) - Rosenmund Reduction
C6H5COCl + H2 → (Pd/BaSO4) → C6H5CHO + HCl
The f block elements are those in which the differentiating electron enters the (n-2) f orbital. There are two series of f-block elements corresponding to fitting of 4f and 5f orbitals. The series of 4f orbital is called lanthanoids. Lanthanoids show different oxidation states depending upon stability of fo, f7, and f14 configurations though the most common oxidation state is +3. There is a regular decrease in the size of Lanthanoids ions with increase in atomic number which is known as lanthanoid contraction.
(i) The atomic number of three lanthanoid elements X, Y and Z are 65, 68 and 70 respectively, their Ln3+ electronic configuration is.
(a) f8 f11 f13
(b) f11 f8f13
(c) fof2f11
(d) f3f7f9
(ii) Lanthanoid Contraction is observed in
(a) Gd
(b) At
(c) Xe
(d) Te
(iii) Name a number of the lanthanoids series which is well known to exhibit +4 oxidation state.
(a) Cerium, Z = 58
(b) Europium, Z = 63
(c) Lanthanum, Z = 57
(d) Gadolinium Z = 64
(iv) Which of the following is not the configuration of Lanthanoid ?
(a) [Xe] 4f10 6s2
(b) 2 [Xe] 4f1 5d1 6s2
(c) 2 [Xe] 4f14 5d10 6s2
(d) [Xe] 4f7 5d1 6s2
(ii) (a) Gd (Part of the series)
(iii) (a) Cerium (Ce4+ is stable due to $f^0$)
(iv) (c) [Xe] 4f14 5d10 6s2 (This is Mercury/Transition, not Lanthanoid)
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