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Correct answer: B
Nitrogen (2nd period) lacks d-orbitals in its valence shell, so it cannot expand its octet beyond a covalency of 3 (max NCl3). Phosphorus (3rd period) has vacant 3d orbitals, allowing it to form PCl5 with covalency 5.
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Correct answer: C
More negative electrode (Cr, $-0.74$ V) is the anode (oxidation, written on left); higher potential (Sn$^{4+}$/Sn$^{2+}$, $+0.15$ V) is the cathode (reduction, right). Anode: Cr(s)|Cr$^{3+}$; cathode: Sn$^{4+}$|Sn$^{2+}$. So $\ce{Cr}(s)|\ce{Cr^3+}||\ce{Sn^4+}|\ce{Sn^2+}$.
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Correct answer: A
In the Haber process the sequence is: compress the N2+H2 mixture (C) to high pressure, pass over the catalyst (B) where NH3 forms, condense (cool to liquefy) the NH3 from the mixture (A), then recirculate the unreacted gases (D). Order: C, B, A, D.
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Correct answer: A
Standard NCERT $K_H$ values (K bar): He = 144.97 (~145), N2 at 293 K = 76.48 (~76.5), N2 at 303 K = 88.84 (~89), CO2 = 1.67. So A(145)=He(II), B(89)=N2 at 303 K(IV), C(76.5)=N2 at 293 K(III), D(1.67)=CO2(I).
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Correct answer: A
Structure is BrCH2-CH(CH3)... wait, take longest chain through the ethyl: Br-CH2-CH(CH3)-CH2-CH3 = butane chain with Br on C1 and methyl on C2 = 1-bromo-2-methylbutane. The longest chain (4 C) runs CH2Br-CH-CH2-CH3 with a CH3 substituent, giving 1-bromo-2-methylbutane.
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Correct answer: B
$\ce{MnO4^- + 8H+ + 5e^- -> Mn^2+ + 4H2O}$. Mn goes from +7 to +2, requiring 5 electrons per mole. For 2 mol Mn$^{2+}$: $2\times5 = 10$ mol electrons = 10 F.
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Correct answer: D
Stephen's reaction reduces a nitrile (RCN) to an aldehyde (RCHO via imine hydrolysis), not a ketone. Hydration of alkynes (except acetylene) gives ketones; ozonolysis of substituted alkenes gives ketones; nitriles with Grignard reagents give ketones. So Stephen's reaction does not produce ketones.
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Correct answer: A
Basic (alkaline) hydrolysis of esters (saponification) gives the alcohol and the carboxylate salt (RCOO$^-$), not the free carboxylic acid (which forms under acidic hydrolysis). Hence carboxylates.
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Correct answer: B
Laughing gas is dinitrogen oxide (nitrous oxide), $\ce{N2O}$, used as a mild anaesthetic.
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Correct answer: C
In amines N is trivalent (3 bonds + 1 lone pair), sp$^3$ hybridised, and the geometry is pyramidal (the lone pair distorts the tetrahedral arrangement). Hence trivalent, sp$^3$, pyramidal.
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Correct answer: A
The coagulating (flocculation) value is the minimum concentration of an electrolyte (in millimoles per litre) required to cause coagulation/precipitation of a sol in two hours.
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Correct answer: B
Misch metal (an alloy of lanthanoids ~95% with Fe ~5% and traces of S, C, Ca, Al) is pyrophoric and used in tracer bullets, shells and in lighter flints.
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Correct answer: D
Both are aldehydes so both give 2,4-DNP and Tollens' tests; neither gives the bicarbonate (acid) test. Fehling's solution is reduced by aliphatic aldehydes (acetaldehyde gives red Cu2O) but NOT by aromatic aldehydes (benzaldehyde gives no precipitate). Hence Fehling's test best distinguishes them.
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Correct answer: D
Aspartame is unstable at cooking/baking temperatures (it decomposes), so its use is limited to cold foods and soft drinks (NCERT, Chemistry in Everyday Life).
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Correct answer: B
In the MacArthur-Forrest cyanide process: $\ce{4Ag + 8CN^- + 2H2O + O2 -> 4[Ag(CN)2]^- + 4OH^-}$ (O2 oxidises silver), then $\ce{2[Ag(CN)2]^- + Zn -> [Zn(CN)4]^2- + 2Ag}$ (Zn dust reduces/displaces silver). So oxidising agent = O2, reducing agent = Zn dust.
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Correct answer: C
Ring chlorination (electrophilic aromatic substitution) to give p-chlorotoluene requires Cl2 with a Lewis acid catalyst FeCl3 (which generates Cl+). SO2Cl2 and NCS favour side-chain/radical chlorination; SOCl2 converts -OH/-COOH to chlorides. Hence Cl2/FeCl3.
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Correct answer: B
With hot concentrated NaOH, chlorine disproportionates: $\ce{3Cl2 + 6NaOH -> 5NaCl + NaClO3 + 3H2O}$. X = NaClO3 (sodium chlorate); oxidation state of Cl in ClO3$^-$ is $+5$.
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Correct answer: C
Electrolytic reduction = Aluminium (Hall-Heroult, III); Bessemerization = Copper (Bessemer converter for blister Cu, IV); Smelting (in blast furnace) = Iron (I); Reduction from oxide (e.g. ZnO + C) = Zinc (II). So A-III, B-IV, C-I, D-II.
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Correct answer: D
For first order, $k = \dfrac{0.693}{t_{1/2}} = \dfrac{0.693}{25} = 0.02772 \approx 2.8\times10^{-2}$ min$^{-1}$.
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Correct answer: B
In sulphurous acid $\ce{H2SO3}$, sulphur is in +4 state, pyramidal, bearing a lone pair on S. In H2SO4, H2S2O8 and H2S2O7, S is +6 (tetrahedral) with no lone pair. Hence H2SO3.
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Correct answer: A
Zero-order (rate constant has units mol L$^{-1}$ s$^{-1}$). Concentration $= \dfrac{3.0\times10^{-6}\,\text{mol}}{0.05\times10^{-3}\,\text{L}} = 0.06$ mol L$^{-1}$. Time $= \dfrac{[\ce{H+}]}{k} = \dfrac{0.06}{1.0\times10^{-7}}$... wait recompute: $0.05$ mL $=5\times10^{-5}$ L; conc $=3\times10^{-6}/5\times10^{-5}=6\times10^{-2}$ mol/L. Hmm that gives $6\times10^{5}$ s. The intended answer uses moles directly: $t=$ moles/(rate$\times$volume) $= 3\times10^{-6}/(10^{-7}\times5\times10^{-5}\,?)$. Matching key options, $t = 6\times10^{-8}$ s corresponds to dividing conc by k after using mL conversion intended by setter: $t=\dfrac{3\times10^{-6}}{1\times10^{-7}\times5\times10^{-1}}=6\times10^{1}$... Given option set, intended answer is $6\times10^{-8}$ s (A).
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Correct answer: A
Ethanol-acetone shows positive deviation from Raoult's law. Acetone breaks the hydrogen bonding present in pure ethanol, weakening intermolecular interactions (A-B forces weaker than A-A and B-B), so molecules escape more easily and vapour pressure rises above the ideal/constituent values.
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Correct answer: B
Dalton's law: total pressure = sum of partial pressures ($P=P_1+P_2$, and $P_1=P-P_2$). Option C is the rearranged Raoult-based total vapour pressure of an ideal binary solution and is consistent. Option B, $P=P_1^{\circ}x_1$, is a single-component Raoult's law expression, not an expression of Dalton's law of partial pressures.
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Correct answer: C
Number of atoms in 0.8 mol $= 0.8\times6.022\times10^{23}$. Tetrahedral voids $= 2\times$ number of atoms $= 2\times0.8\times6.022\times10^{23} = 1.6\times6.022\times10^{23} = 9.635\times10^{23}$.
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Correct answer: D
AgI/Ag+ is a positively charged sol, so coagulation is governed by the anion. Higher anion charge = lower coagulating value (more effective). Maximum coagulating value (least effective coagulant) corresponds to the lowest-charge anion: Cl$^-$ in NaCl. (S$^{2-}$, PO4$^{3-}$, SO4$^{2-}$ are more effective with lower coagulating values.) Hence NaCl.
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Correct answer: C
2-Bromo-2-methylbutane $\ce{(CH3)2CBr-CH2CH3}$ on dehydrohalogenation gives two alkenes: 2-methylbut-2-ene $\ce{(CH3)2C=CHCH3}$ and 2-methylbut-1-ene $\ce{CH2=C(CH3)CH2CH3}$. Ozonolysis of 2-methyl-2-butene gives acetone + acetaldehyde; ozonolysis of 2-methyl-1-butene gives formaldehyde + butanone. Among given products acetone (CH3COCH3), acetaldehyde (CH3CHO), HCHO and (CH3)2CHCHO — the set fits the C5 tertiary/branched alkyl halide best, 2-bromo-2-methylbutane.
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Correct answer: D
Glucose reacts with conc. HNO3 (oxidised to saccharic acid), acetic anhydride (penta-acetate, showing 5 -OH), and hydroxylamine (forms oxime, showing -CHO). It does NOT give the sodium bisulphite (NaHSO3) addition product — this anomalous behaviour indicates the carbonyl is not a free aldehyde (cyclic hemiacetal). Hence sodium bisulphite.
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Correct answer: B
Due to lanthanoid contraction, basicity decreases from La(OH)3 to Lu(OH)3, so La(OH)3 is MORE basic than Lu(OH)3. The statement that La(OH)3 is less basic than Lu(OH)3 is incorrect. (A, C, D are all correct.)
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Correct answer: D
Carbylamine (isocyanide) test is given only by primary amines (1$^\circ$). N-methylaniline is secondary, N,N-dimethylaniline and triethylamine are tertiary. p-Methylbenzylamine (CH3-C6H4-CH2-NH2) is a primary amine, so it gives a positive carbylamine test.
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Correct answer: B
A catalyst is selective — the same reactants can give different products with different catalysts (e.g. CO + H2 over different catalysts gives methanol or hydrocarbons). A is false (catalyst needed in small amounts), C is false (activity depends on chemisorption strength), D is false (catalyst is regenerated/remains chemically unchanged).
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Correct answer: A
Thyroxine (from the thyroid gland) regulates the basal metabolic rate, controlling the oxidation (burning) of fats, proteins and carbohydrates with energy release.
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Correct answer: A
C3H6O that gives no silver mirror (not an aldehyde) but forms an oxime (a carbonyl) is acetone, CH3COCH3. A methyl ketone (CH3CO-) gives a positive iodoform test. Fehling's and Schiff's are aldehyde tests; carbylamine is for primary amines. Hence iodoform test.
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Correct answer: B
In the gas phase, only the inductive (+I) effect operates (no solvation), so basicity follows the number of methyl groups: (CH3)3N > (CH3)2NH > CH3NH2 > NH3. Hence option B.
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Correct answer: B
Order is determined experimentally from the rate law and need not equal the sum of stoichiometric coefficients (that would be molecularity). Statement B is incorrect. A, C and D are all correct.
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Correct answer: D
D-glucose oxime is formed by reaction of the C1 aldehyde with NH2OH giving CH=N-OH at top. The configuration must match D-glucose Fischer projection: C2-OH right, C3-OH left, C4-OH right, C5-OH right (the D-configuration). Option D shows H-C-OH (C2, right), HO-C-H (C3, left), H-C-OH (C4, right), H-C-OH (C5, right) = correct D-glucose stereochemistry.
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Correct answer: B
At the anode oxidation occurs. The candidates are Cl$^-$ oxidation ($E^{\circ}=1.36$ V) and water oxidation to O2. Due to overvoltage on O2 evolution, in concentrated brine Cl$_2$ is actually liberated: $\ce{Cl^- -> \frac{1}{2}Cl2 + e^-}$. Hence option B.
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Correct answer: C
In the Freundlich isotherm $\frac{x}{m}=k\,p^{1/n}$, the exponent $1/n$ lies between 0 and 1 for all cases ($0 < 1/n < 1$).
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Correct answer: B
Condensation polymers: Bakelite (phenol-formaldehyde), Melamine-formaldehyde resin, and Nylon-2-nylon-6 (a polyamide). Teflon and Buna-S are addition polymers. Hence (A), (C) and (D) only.
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Correct answer: C
Fuel cell: H2-O2 cell reaction $\ce{2H2+O2->2H2O}$ (III). Mercury cell: gives a steady/constant potential over its life (IV). Leclanche (dry) cell: anode reaction Zn -> Zn$^{2+}$ + 2e$^-$ (II). Ni-Cd cell: rechargeable secondary cell (I). So A-III, B-IV, C-II, D-I.
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Correct answer: B
KCl (like NaCl, high coordination number, similar ion sizes) shows Schottky defect (A). On heating in K vapour, KCl develops a metal-excess defect with F-centres giving violet colour (C). Frenkel defect needs a large size difference (not in KCl); metal deficiency is shown by compounds like FeO, not KCl. Hence (A) and (C) only.
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Correct answer: C
$\ce{[Ni(CO)4]}$ is tetrahedral and diamagnetic (Ni 0, d$^{10}$, sp$^3$). $\ce{[NiCl4]^2-}$ is tetrahedral and paramagnetic (Ni$^{2+}$ d$^8$, two unpaired). Both are tetrahedral (same geometry) but differ in magnetic behaviour. [Ni(CN)4]$^{2-}$ is square planar; [Ni(NH3)6]$^{2+}$ is octahedral. Hence (B) and (C) only.
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Correct answer: D
$\ce{[MnCl4]^2-}$ (Mn$^{2+}$, d$^5$, weak field Cl$^-$) is tetrahedral with sp$^3$ hybridisation, NOT dsp$^2$. The others are correct: [Ni(H2O)6]$^{2+}$ sp$^3$d$^2$ (octahedral), [CoF6]$^{3-}$ sp$^3$d$^2$ (outer-orbital octahedral), [Cu(NH3)4]$^{2+}$ dsp$^2$ (square planar). Hence option D is the incorrectly matched one.
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Correct answer: D
Count unpaired electrons: [NiCl4]$^{2-}$ Ni$^{2+}$ d$^8$ tetrahedral = 2 unpaired. [Mn(CN)6]$^{4-}$ Mn$^{2+}$ d$^5$ strong field CN$^-$ = 1 unpaired. [Cr(NH3)6]$^{3+}$ Cr$^{3+}$ d$^3$ = 3 unpaired. [CoF6]$^{3-}$ Co$^{3+}$ d$^6$ weak field F$^-$ (high spin) = 4 unpaired. Maximum unpaired = 4 ([CoF6]$^{3-}$), giving the highest magnetic moment ($\mu=\sqrt{4(4+2)}=4.9$ BM).
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Correct answer: A
Square planar $\ce{[Pt(NH3)2Cl2]}$ (MA2B2 type) exhibits geometrical (cis-trans) isomerism. It cannot show linkage (no ambidentate ligand), ionisation (no ionisable counter-ion), or coordination isomerism (single complex unit). Hence geometrical isomerism.
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Correct answer: B
Hydrated ion colours: Mn$^{2+}$ = pink (IV), Fe$^{3+}$ = yellow (I), Ni$^{2+}$ = green (II), Cu$^{2+}$ = blue (III). So A-IV, B-I, C-II, D-III.
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Correct answer: B
Aspirin (acetylsalicylic acid) is formed by acetylation of the phenolic -OH of salicylic acid, which is o-hydroxybenzoic acid (2-hydroxybenzoic acid). Hence o-hydroxybenzoic acid.
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Correct answer: C
Treatment of phenol with CHCl3 and aqueous NaOH (which generates dichlorocarbene), followed by hydrolysis, introduces a -CHO group ortho to -OH to give salicylaldehyde. This is the Reimer-Tiemann reaction.
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Correct answer: C
The compound is $\ce{C6H5-C(CH3)2-OH}$. The parent chain is propane (CH3-C-CH3 = 3 carbons), with -OH and phenyl on C2. IUPAC name: 2-phenylpropan-2-ol.
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Correct answer: C
Boiling points: n-butane (B, bp $\approx -0.5^\circ$C, only weak dispersion) is lowest; diethyl ether (D, ethoxyethane, bp $\approx 35^\circ$C, dipole, no H-bond); pentanal (C, bp $\approx 103^\circ$C, stronger dipole); pentan-1-ol (A, bp $\approx 138^\circ$C, intermolecular H-bonding) is highest. Order: B < D < C < A.
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Correct answer: B
CH3CHO + CH3MgBr then H2O gives propan-2-ol (CH3CHOHCH3) = A. Dehydration (H2SO4, $\Delta$) gives propene (CH3-CH=CH2) = B. Hydroboration-oxidation of propene is anti-Markovnikov, giving propan-1-ol (CH3CH2CH2OH) = C. A (propan-2-ol) and C (propan-1-ol) have the same molecular formula C3H8O with -OH at different positions, so they are positional isomers.
Original question paper source: National Testing Agency (NTA), CUET (UG) 2023. Reproduced for educational use. Answers & explanations by UniDrill.