Chemistry
Chemistry: 24 questions
Q51 · MCQ · Some Basic Concepts of Chemistry · Medium
Which of the following contain the same number of atoms?
(Given : Molar mass in g mol$^{-1}$ of H, He, O and S are 1, 4, 16 and 32 respectively)
A. 2 g of O$_2$ gas
B. 4 g of SO$_2$ gas
C. 1400 mL of O$_2$ at STP
D. 0.05 L of He at STP
E. 0.0625 mol of H$_2$ gas
Choose the correct answer from the options given below:
- (1) A and B only
- (2) B and C only
- (3) C and D only
- (4) A, C and E only
Show answer and solution
Answer: Option (4)
Key idea: Mole concept, Avogadro's number, and calculation of number of atoms from mass, volume at STP, and moles
- Calculate moles for each option: A: $n = \frac{2}{32} = 0.0625$ mol O₂; B: $n = \frac{4}{64} = 0.0625$ mol SO₂; C: $n = \frac{1400}{22400} = 0.0625$ mol O₂; D: $n = \frac{50}{22400} = 0.00223$ mol He; E: $n = 0.0625$ mol H₂
- For A: Number of atoms = $0.0625 \times N_A \times 2 = 0.125 N_A$ (O₂ has 2 atoms per molecule)
- For B: Number of atoms = $0.0625 \times N_A \times 3 = 0.1875 N_A$ (SO₂ has 3 atoms per molecule)
- For C: Number of atoms = $0.0625 \times N_A \times 2 = 0.125 N_A$ (O₂ has 2 atoms per molecule)
- For D: Number of atoms = $0.00223 \times N_A \times 1 = 0.00223 N_A$ (He is monoatomic)
- For E: Number of atoms = $0.0625 \times N_A \times 2 = 0.125 N_A$ (H₂ has 2 atoms per molecule)
- Compare: A, C, and E all have $0.125 N_A$ atoms, so answer is option (4)
Q52 · MCQ · Structure of Atom · Medium
The Bohr radius of a hydrogen like species is 70.53 pm. The species and the stationary state (n) are respectively
(Given : Hydrogen atom Bohr radius is 52.9 pm)
- (1) Li$^{2+}$, 3
- (2) He$^+$, 3
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Key idea: Bohr's Model - Radius of hydrogen-like species
Q53 · MCQ · Chemical Bonding and Molecular Structure · Medium
Given below are two statements:
**Statement I:** The number of compounds among $SO_2$, $SO_3$, $SF_4$, $SF_6$ and $H_2S$ in which sulphur does not obey the Octet rule is 3.
**Statement II:** Among $[H_2O, ClF_3, SF_4]$, $[NH_3, BrF_5, SF_4]$, $[BrF_5, ClF_3, XeF_4]$ and $[XeF_4, ClF_3, H_2O]$, the number of sets in which all the molecules have one lone pair of electrons on the central atom is 1.
In the light of the above statements, choose the correct answer from the options given below:
- (1) Both **Statement I** and **Statement II** are true
- (2) Both **Statement I** and **Statement II** are false
- (3) **Statement I** is true but **Statement II** is false
- (4) **Statement I** is false but **Statement II** is true
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Key idea: Octet Rule, VSEPR Theory, and Lone Pair Determination
Q54 · MCQ · Thermodynamics · Medium
Match **List - I** with **List - II**.
Given $V_1$ and $V_2$ are initial and final volumes respectively.
**List - I** (Isothermal process)
A. Reversible expansion
B. Free expansion
C. Irreversible Compression
D. Cyclic reversible
**List - II** (Expression)
I. $q=0$
II. $q = nRT \ln \frac{V_2}{V_1}$
III. $w = -P_{ext} (V_1 - V_2)$
IV. $\frac{q_{rev}}{T} = 0$
Choose the correct answer from the options given below:
- (1) A-II, B-III, C-I, D-IV
- (2) A-II, B-I, C-IV, D-III
- (3) A-II, B-I, C-III, D-IV
Show answer and solution
Answer: Option (3)
Key idea: Isothermal processes and thermodynamic expressions for different types of expansions/compressions
- **A. Reversible expansion (Isothermal):** For isothermal reversible process, $q = nRT \ln \frac{V_2}{V_1}$ → Matches with **II**
- **B. Free expansion (Isothermal):** $P_{ext} = 0$, so $w = 0$. Since $\Delta U = 0$ (isothermal), $q = 0$ → Matches with **I**
- **C. Irreversible Compression (Isothermal):** Work done is $w = -P_{ext}(V_2 - V_1) = -P_{ext}(V_1 - V_2)$ for compression → Matches with **III**
- **D. Cyclic reversible (Isothermal):** For a complete cycle, $\Delta S = 0$, so $\frac{q_{rev}}{T} = 0$ → Matches with **IV**
- Therefore: A-II, B-I, C-III, D-IV
Q55 · MCQ · Solutions · Medium
Given below are two statements:
[Figure: Table showing Chamber 1 with 18 g glucose in 100 mL aqueous solution and Chamber 2 with 30 g glucose in 250 mL aqueous solution, separated by semi-permeable membrane]
**Statement I:** $H_2O$ molecules move from the chamber 1 to chamber 2.
**Statement II:** The osmotic pressure of a solution prepared by dissolving 50 mg of potassium sulphate (molar mass = 174 g/mol) in 2 L of water (at 27 °C) is 0.0107 bar. (Given: R = 0.083 dm³ bar K⁻¹ mol⁻¹ and assume complete dissociation of electrolyte)
In the light of the above statements, choose the correct answer from the options given below:
- (1) Both **Statement I** and **Statement II** are true
- (2) Both **Statement I** and **Statement II** are false
- (3) **Statement I** is true but **Statement II** is false
- (4) **Statement I** is false but **Statement II** is true
Show answer and solution
Answer: Option (4)
Key idea: Osmotic Pressure and Colligative Properties
- Calculate molarity of Chamber 1: $M_1 = \frac{18/180}{0.1} = 1$ M
- Calculate molarity of Chamber 2: $M_2 = \frac{30/180}{0.25} = 0.668$ M
- Since $M_1 > M_2$, water moves from Chamber 2 to Chamber 1, so Statement I is **false**
- For Statement II, calculate moles of K₂SO₄: $n = \frac{0.050}{174} = 2.874 \times 10^{-4}$ mol
- K₂SO₄ dissociates into 3 ions, so van't Hoff factor $i = 3$
- Calculate osmotic pressure: $\pi = iCRT = 3 \times \frac{2.874 \times 10^{-4}}{2} \times 0.083 \times 300 = 0.0107$ bar
- Statement II is **true**, so answer is option (4)
Q56 · MCQ · Equilibrium · Medium
Given is a concentrated solution of a weak electrolyte $A_xB_y$ of concentration 'c' and dissociation constant 'K'. The degree of dissociation is given by:
- (1) $\left[K \times c^{x+y-1} x^x y^y\right]^{\frac{1}{x+y}}$
- (2) $\left(\frac{K}{c^{x+y-1} x^x y^y}\right)^{\frac{1}{x+y}}$
- (3) $\left(\frac{c^{x+y-1} x^x y^y}{K}\right)^{\frac{1}{x+y}}$
Show answer and solution
Answer: Option (2)
Key idea: Degree of dissociation of weak electrolyte using equilibrium constant with small alpha approximation
- Write dissociation: $A_xB_y \rightleftharpoons xA^{y+} + yB^{x-}$
- Set up equilibrium concentrations: $[A_xB_y] = c(1-\alpha)$, $[A^{y+}] = xc\alpha$, $[B^{x-}] = yc\alpha$
- Write $K = \frac{(xc\alpha)^x(yc\alpha)^y}{c(1-\alpha)} = \frac{x^x y^y c^{x+y} \alpha^{x+y}}{c(1-\alpha)}$
- For concentrated solution, $\alpha \ll 1$, so $(1-\alpha) \approx 1$
- Simplify: $K = x^x y^y c^{x+y-1} \alpha^{x+y}$
- Solve for $\alpha$: $\alpha = \left(\frac{K}{c^{x+y-1} x^x y^y}\right)^{\frac{1}{x+y}}$
Q57 · MCQ · Electrochemistry · Medium
For a general redox reaction
Anode $\text{Red}_1 \to \text{Ox}_1^{n_1^+} + n_1e^-$
Cathode $\text{Ox}_2 + n_2e^- \to \text{Red}_2^{n_2^-}$
Which of the following statement is incorrect?
- (1) The overall reaction can be written as $n_2\text{Red}_1 + n_1\text{Ox}_2 \rightleftharpoons n_2\text{Ox}_1^{n_1^+} + n_1\text{Red}_2^{n_2^-}$
- (2) The electrons do not appear in the overall reaction because electrons produced at the anode are consumed at the cathode.
- (3) [Figure: A graph showing (E-E°)/RT/F vs log₁₀Q with three lines for n=1, n=2, and n=3, all with slope ∝ 1/n. Here n is the number of electrons transferred in redox reaction.]
- (4) If the reaction is carried out reversibly, the electrical work done is equal to the ratio of charge and potential difference through which charge is moved.
Show answer and solution
Answer: Option (4)
Key idea: Nernst Equation and Electrochemical Work
- Write the balanced overall reaction by multiplying anode by $n_2$ and cathode by $n_1$ to balance electrons: $n_2\text{Red}_1 + n_1\text{Ox}_2 \to n_2\text{Ox}_1^{n_1^+} + n_1\text{Red}_2^{n_2^-}$ ✓
- Verify statement (2): Electrons cancel in overall reaction since electrons produced at anode equal electrons consumed at cathode ✓
- Check statement (3) using Nernst equation: $E = E° - \frac{2.303RT}{nF}\log_{10}Q$, so $\frac{E-E°}{RT/F} = -\frac{2.303}{n}\log_{10}Q$ with slope $\propto \frac{1}{n}$ ✓
- Analyze statement (4): For reversible electrochemical work, $W_{\text{elec}} = nFE = Q \times E$ (charge × potential)
- Statement (4) incorrectly states work equals ratio $Q/E$ instead of product $Q \times E$
- Therefore, statement (4) is INCORRECT
Q58 · MCQ · Periodic Classification of Elements · Easy
In a period, the first ionisation enthalpy of the element at extreme left and the negative electron gain enthalpy of the extreme right element, except noble gases, are respectively.
- (1) lowest and lowest
- (2) highest and lowest
- (3)
- (4)
Show answer and solution
Answer: Option (1)
Key idea: Periodic trends: Ionization enthalpy and electron gain enthalpy across a period
- Identify extreme left elements in a period: **Alkali metals** (Group 1)
- Alkali metals have largest atomic size and lowest effective nuclear charge, so they have **lowest first ionization enthalpy** in the period
- Identify extreme right elements (except noble gases): **Halogens** (Group 17)
- Halogens have smallest atomic size (except noble gases) and highest effective nuclear charge, with strong tendency to gain electrons
- Halogens have **most negative (lowest) electron gain enthalpy** as they release maximum energy when gaining an electron
- Therefore: First ionization enthalpy = **lowest**, Electron gain enthalpy = **lowest** (most negative)
Q59 · MCQ · Chemical Bonding and Molecular Structure · Medium
Given below are two statements:
**Statement I:** $F_2 O < H_2 O < Cl_2 O$ is the correct trend in terms of bond angle.
**Statement II:** $SiF_4$, $SnF_4$ and $PbF_4$ are ionic in nature.
In the light of the above statements, choose the correct answer from the options given below:
- (1) Both Statement I and Statement II are true
- (2) Both Statement I and Statement II are false
- (3) Statement I is true but Statement II is false
- (4) Statement I is false but Statement II is true
Show answer and solution
Answer: Option (3)
Key idea: Bond angles in bent molecules and ionic vs covalent character in fluorides
- **Statement I Analysis:** Compare bond angles in $F_2O$, $H_2O$, and $Cl_2O$ (all bent with 2 lone pairs on O)
- In $F_2O$: F is more electronegative than O, pulls bonding electrons away, increases lone pair repulsion → bond angle $\approx 103°$
- In $H_2O$: Intermediate electronegativity → bond angle $\approx 104.5°$
- In $Cl_2O$: Cl is less electronegative than O, bonding electrons closer to O, reduces lone pair repulsion; Cl is larger → bond angle $\approx 110.9°$
- Therefore $F_2O < H_2O < Cl_2O$ is correct. **Statement I is TRUE**
- **Statement II Analysis:** $SiF_4$, $SnF_4$, and $PbF_4$ all have high oxidation state (+4) and form covalent bonds due to high charge density and polarization. **Statement II is FALSE**
- Answer: Statement I is true but Statement II is false → Option (3)
Q60 · MCQ · The d- and f-Block Elements · Medium
The correct order of first $(\Delta_i H_1)$ and second $(\Delta_i H_2)$ ionisation enthalpy values of Cr and Mn are:
A. $\Delta_i H_1$ : Cr > Mn
B. $\Delta_i H_2$ : Cr > Mn
C. $\Delta_i H_1$ : Mn > Cr
D. $\Delta_i H_2$ : Mn > Cr
Choose the correct answer from the options given below:
- (1) A and B only
- (2) B and C only
- (3) A and D only
- (4) C and D only
Show answer and solution
Answer: Option (2)
Key idea: Ionization enthalpy trends in d-block elements based on electronic configuration stability
- Write electronic configurations: Cr = [Ar] $3d^5 4s^1$, Mn = [Ar] $3d^5 4s^2$
- For first ionization: Mn has higher nuclear charge (Z=25) than Cr (Z=24), so $\Delta_i H_1$: Mn > Cr (Statement C is correct)
- After first ionization: Cr$^+$ = [Ar] $3d^5$ (half-filled, very stable), Mn$^+$ = [Ar] $3d^5 4s^1$
- For second ionization: Cr$^+$ must lose electron from stable $d^5$ (difficult), while Mn$^+$ loses from $4s$ to achieve stable $d^5$ (easier)
- Therefore $\Delta_i H_2$: Cr > Mn (Statement B is correct)
- Statements B and C are correct, so answer is option (2)
Q61 · MCQ · Coordination Compounds · Medium
Which of the following sequences of hybridisation, geometry and magnetic nature are correct for the given coordination compounds?
A. $[NiCl_4]^{2-} - sp^3$, tetrahedral, paramagnetic
B. $[Ni(NH_3)_6]^{2+} - sp^3d^2$, octahedral, paramagnetic
C. $[Ni(CO)_4] - sp^3$, tetrahedral, paramagnetic
D. $[Ni(CN)_4]^{2-} - dsp^2$, square planar, diamagnetic
Choose the correct answer from the options given below:
- (1) A, B, C and D
- (2) B, C and D only
- (3) A, C and D only
- (4) A, B and D only
Show answer and solution
Answer: Option (4)
Key idea: Hybridization, geometry, and magnetic properties of coordination compounds based on ligand field strength
- For **A. $[NiCl_4]^{2-}$**: $Ni^{2+}$ has $3d^8$ configuration. $Cl^-$ is weak field, no pairing occurs. Tetrahedral with $sp^3$ hybridization and 2 unpaired electrons → **paramagnetic** ✓
- For **B. $[Ni(NH_3)_6]^{2+}$**: $Ni^{2+}$ with $3d^8$. $NH_3$ is moderate field ligand. Octahedral with $sp^3d^2$ hybridization and 2 unpaired electrons → **paramagnetic** ✓
- For **C. $[Ni(CO)_4]$**: $Ni^0$ has $3d^{10}$ after electron rearrangement. $CO$ is strong field causing complete pairing. Tetrahedral with $sp^3$ but **diamagnetic** (0 unpaired electrons) ✗
- For **D. $[Ni(CN)_4]^{2-}$**: $Ni^{2+}$ with $3d^8$. $CN^-$ is strong field causing pairing. Square planar with $dsp^2$ hybridization and 0 unpaired electrons → **diamagnetic** ✓
- Statement C is incorrect because $[Ni(CO)_4]$ is diamagnetic, not paramagnetic
- Therefore, A, B, and D are correct sequences
Q62 · MCQ · General Principles and Processes of Isolation of Elements · Medium
Given below are two statements:
**Statement I:** A mixture of $C_{12}H_{22}O_{11}$ (sugar) and NaCl can be separated by dissolving sugar in alcohol, due to differential solubility.
**Statement II:** Rose essence from rose petals is separated by steam distillation due to its high volatility and insolubility in $H_2O$.
In the light of the above statements, choose the correct answer from the options given below:
- (1) Both Statement I and Statement II are true
- (2) Both Statement I and Statement II are false
- (3) Statement I is true but Statement II is false
- (4) Statement I is false but Statement II is true
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Key idea: Separation techniques based on differential solubility and steam distillation
Q63 · Numerical · Organic Chemistry - Some Basic Principles and Techniques · Medium
Shown below is the structure of methyl acetate with three different $\alpha$, $\beta$ and $\gamma$ carbon - oxygen bonds.
[Figure: Structure showing $H_3C-C(=O)-O-CH_3$ with C=O bond labeled as $\alpha$, C-O(carbonyl) bond labeled as $\beta$, and O-CH3 bond labeled as $\gamma$]
The correct order of bond lengths of these bonds is:
Show answer and solution
Answer: α < β < γ
Key idea: Bond lengths in esters: resonance effects and hybridization
- Identify the three bonds: $\alpha$ is C=O (carbonyl), $\beta$ is C-O (ester linkage), $\gamma$ is O-CH₃
- The $\alpha$ bond is a C=O double bond, which is the shortest (~1.20 Å)
- The $\beta$ bond has partial double bond character due to resonance (lone pair on O delocalizes into carbonyl), making it shorter than a normal single bond (~1.35 Å)
- The $\gamma$ bond is a regular C-O single bond with no resonance effects, making it the longest (~1.43 Å)
- Apply the rule: double bonds < resonance-stabilized single bonds < regular single bonds
- Therefore, the correct order is: $\alpha < \beta < \gamma$
Q64 · MCQ · Aldehydes, Ketones and Carboxylic Acids · Medium
'$x$' is the product which is obtained by the hydrolysis of prop-1-yne in the presence of mercuric sulphate under dilute acidic medium at 333 K. '$y$' is the product which is obtained by the reaction of ethane nitrile with methyl magnesium bromide in dry ether followed by hydrolysis. IUPAC name of product obtained from '$x$' and '$y$' in the presence of barium hydroxide followed by heating is:
- (1) 2 - Methylpent-4-en-3-one
- (2) 4 - Methylpent-3-en-2-one
- (3) 4 - Methylpent-1-ene
- (4) 2 - Methylpent-3-one
Show answer and solution
Answer: Option (2)
Key idea: Aldol condensation of ketones; Hydration of alkynes; Grignard reaction with nitriles
- Step 1: Hydration of prop-1-yne ($HC≡C-CH_3$) with $HgSO_4/H^+$ gives propanone: $HC≡C-CH_3 + H_2O → CH_3COCH_3$ (compound $x$)
- Step 2: Reaction of ethane nitrile ($CH_3CN$) with $CH_3MgBr$ followed by hydrolysis gives propanone: $CH_3CN + CH_3MgBr → CH_3COCH_3$ (compound $y$)
- Step 3: Both $x$ and $y$ are acetone ($CH_3COCH_3$). In presence of $Ba(OH)_2$, aldol addition occurs between two acetone molecules to form $CH_3COCH_2C(OH)(CH_3)_2$
- Step 4: Upon heating, dehydration occurs to give the α,β-unsaturated ketone: $CH_3CO-CH=C(CH_3)_2$
- Step 5: Numbering from carbonyl end: $CH_3-CO-CH=C(CH_3)-CH_3$ gives 4-Methylpent-3-en-2-one
Q65 · MCQ · Haloalkanes and Haloarenes · Medium
An optically active alkyl bromide $C_4H_9Br$, reacts with ethanolic KOH to form major compound [A] which reacts with bromine to give compound [B]. Compound [B] reacts with ethanolic KOH and sodamide to give compound [C]. One molecule of water adds to compound [C] on warming with mercuric sulphate and dilute sulphuric acid at 333 K to form compound [D]. The functional group in compound D will be confirmed by:
- (1) Haloform test
- (2) Lucas test
- (3) Silver mirror test
- (4) Benedict test
Show answer and solution
Answer: Option (1)
Key idea: Identification of functional groups through chemical tests; Haloform test for methyl ketones
- Optically active $C_4H_9Br$ (2-bromobutane) undergoes E2 elimination with ethanolic KOH to give but-2-ene [A]: $CH_3CH=CHCH_3$
- [A] reacts with $Br_2$ to form 2,3-dibromobutane [B]: $CH_3CHBr-CHBrCH_3$
- [B] undergoes double elimination with ethanolic KOH and sodamide to form but-2-yne [C]: $CH_3C≡CCH_3$
- [C] undergoes hydration with $HgSO_4/H_2SO_4$ at 333 K to form butan-2-one [D]: $CH_3COCH_2CH_3$ (a methyl ketone)
- Methyl ketones give positive **Haloform test** with $I_2/NaOH$, producing yellow $CHI_3$ precipitate
Q67 · MCQ · Alcohols, Phenols and Ethers · Medium
Consider the following reaction.
[Figure: Benzyl phenyl ether structure shown as C₆H₅-O-CH₂-C₆H₅] + HI → Product
**Statement I:** In the above reaction, product formed will be a mixture of benzyl alcohol and iodobenzene.
**Statement II:** In the above reaction, the -O-CH₂- bond is cleaved to give the product.
In the light of the above statements, choose the correct answer from the options given below:
- (1) Both Statement I and Statement II are true
- (2) Both Statement I and Statement II are false
- (3) Statement I is true but Statement II is false
- (4) Statement I is false but Statement II is true
Show answer and solution
Answer: Option (4)
Key idea: Ether cleavage with HI - regioselectivity based on carbocation stability
- Benzyl phenyl ether reacts with HI: $C_6H_5-O-CH_2-C_6H_5 + HI$
- Oxygen gets protonated: $C_6H_5-\overset{+}{O}H-CH_2-C_6H_5$
- The $O-CH_2$ bond cleaves (not $C_6H_5-O$) because benzyl cation $(^+CH_2C_6H_5)$ is stabilized by resonance, while phenyl cation is extremely unstable
- Products formed: Phenol $(C_6H_5OH)$ and Benzyl iodide $(C_6H_5CH_2I)$
- Statement I is FALSE (claims benzyl alcohol + iodobenzene, but actual products are phenol + benzyl iodide)
- Statement II is TRUE (correctly identifies $O-CH_2$ bond cleavage)
- Answer: Statement I is false but Statement II is true
Q68 · MCQ · Aldehydes, Ketones and Carboxylic Acids · Medium
Consider the following organic reaction sequence. Choose the final product (X) from the following (consider the major product in all intermediate reactions)
[Figure: Starting material showing CH₃CH₂-CO-OH structure]
(i) NH₃/Δ
(ii) NaOH/Br₂
(iii) HNO₂/H₂O, 0°C → (X) Major Product
(iv) C₆H₅N₂Cl, 0°C
- (1) Benzene
- (2) Phenol
- (3) Propanol
- (4) Chlorobenzene
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Key idea: Hofmann Bromamide Degradation and Diazotization of Primary Aliphatic Amines
Q69 · MCQ · Aldehydes, Ketones and Carboxylic Acids · Hard
Consider the following reactions. Total number of electrons in the $\pi$ bonds and lone pair of electrons in the product (X) is:
$CHO$
$|$
$(CHOH)_4$ $\xrightarrow{\text{(i) HI, } \Delta \text{ (ii) } V_2O_5/10\text{-}20 \text{ atm}/773 \text{ K} \text{ (iii) Benzoyl chloride/Anhyd. AlCl}_3}$ (X) Major product
$|$
$CH_2OH$
- (1) 12
- (2) 16
- (3) 14
- (4) 18
Show answer and solution
Answer: Option (4)
Key idea: Reduction of carbohydrates, catalytic aromatization, Friedel-Crafts acylation, and counting π electrons and lone pairs in benzophenone
- Step 1: Treat glucose with $\text{HI}/\Delta$ to reduce all $\text{-OH}$ and $\text{-CHO}$ groups, forming n-hexane ($\text{C}_6\text{H}_{14}$)
- Step 2: Catalytic dehydrogenation with $\text{V}_2\text{O}_5$ at high temperature converts n-hexane to benzene through cyclization and aromatization
- Step 3: Friedel-Crafts acylation with benzoyl chloride and $\text{AlCl}_3$ gives benzophenone: $\text{C}_6\text{H}_5\text{-CO-C}_6\text{H}_5$
- Count π electrons: First benzene ring has 3 π bonds = 6 electrons, second benzene ring has 3 π bonds = 6 electrons
- Count carbonyl: $\text{C=O}$ has 1 π bond = 2 electrons
- Count lone pairs: Oxygen has 2 lone pairs = 4 electrons
- Total electrons = $6 + 6 + 2 + 4 = 18$ electrons
Q70 · Numerical · Coordination Compounds · Medium
Treatment of a gas 'X' with a freshly prepared ferrous sulphate solution gives a compound 'Y' as a brown ring. The compounds X and Y are.
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Key idea: Brown Ring Test for Nitrates - Formation of Nitrosyl Complex
Q71 · Numerical · Equilibrium · Medium
An excess of $AgNO_3$ is added to 100 mL of a 0.05 M solution of tetraaquadichloridochromium (III) chloride. The number of moles of $AgCl$ precipitated will be _________ $\times 10^{-3}$. (Nearest integer)
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Answer: 5
Key idea: Coordination Chemistry - Ionizable vs Non-ionizable Ligands
- Write the formula of tetraaquadichloridochromium(III) chloride: $[Cr(H_2O)_4Cl_2]Cl$
- Identify ionizable chlorides: Only the $Cl^-$ outside the coordination sphere (counter ion) precipitates with $AgNO_3$. The 2 $Cl^-$ inside are non-ionizable.
- Calculate moles of complex: $n = M \times V = 0.05 \times 0.1 = 5 \times 10^{-3}$ mol
- Since 1 mole of complex gives 1 mole of ionizable $Cl^-$: Moles of $AgCl$ = $5 \times 10^{-3}$ mol
- Express in required format: $5 \times 10^{-3}$ mol, so answer = 5
Q72 · Numerical · Organic Chemistry - Some Basic Principles and Techniques · Medium
An alkane (Y) requires 8 moles of oxygen for complete combustion and on chlorination with $Cl_2/h\nu$, (Y) gives only one monochlorinated product (Z). The total number of primary carbon atoms in (Y) is _________.
Show answer and solution
Answer: 4
Key idea: Alkane combustion stoichiometry and structural symmetry in organic compounds
- Use combustion formula: $C_nH_{2n+2} + \frac{3n+1}{2}O_2 \rightarrow nCO_2 + (n+1)H_2O$. Given 8 moles $O_2$, so $\frac{3n+1}{2} = 8$, giving $n = 5$.
- The alkane is $C_5H_{12}$ (pentane isomer).
- Since only one monochlorinated product forms, all H atoms must be equivalent. This indicates high symmetry.
- Among $C_5H_{12}$ isomers, only neopentane (2,2-dimethylpropane) has this symmetry: $(CH_3)_3C-CH_3$.
- Neopentane has 1 central quaternary carbon and 4 primary carbons (the four $-CH_3$ groups).
- Total number of primary carbon atoms = 4
Q73 · Numerical · Redox Reactions · Medium
500 mL of 0.2 M MnO$_4^-$ solution in basic medium when mixed with 500 mL of 1.5 M KI solution, oxidises iodide ions to liberate molecular iodine. This liberated iodine is then titrated with a standard $x$ M thiosulphate solution in presence of starch till the end point. If 300 mL of thiosulphate was consumed, then the value of $x$ is __________.
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Key idea: Redox Titration and Stoichiometry
Q74 · Numerical · Equilibrium · Medium
In a closed flask at 600 K, one mole of $X_2Y_4(g)$ attains equilibrium as given below:
$X_2Y_4(g) \rightleftharpoons 2XY_2(g)$
At equilibrium, 75% $X_2Y_4(g)$ was dissociated and the total pressure is 1 atm. The magnitude of $\Delta_rG^\circ$ (in kJ mol$^{-1}$) at this temperature is __________. (Nearest Integer)
(Given: R = 8.3 J mol$^{-1}$ K$^{-1}$; ln 10 = 2.3, log 2 = 0.3, log 3 = 0.48, log 5 = 0.69, log 7 = 0.84)
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Answer: 8
Key idea: Chemical Equilibrium, Gibbs Free Energy, Equilibrium Constant
- Set up ICE table: Initial 1 mol $X_2Y_4$, at equilibrium with 75% dissociation gives 0.25 mol $X_2Y_4$ and 1.5 mol $XY_2$, total = 1.75 mol
- Calculate partial pressures: $P_{X_2Y_4} = \frac{0.25}{1.75} \times 1 = \frac{1}{7}$ atm, $P_{XY_2} = \frac{1.5}{1.75} \times 1 = \frac{6}{7}$ atm
- Calculate $K_p = \frac{(P_{XY_2})^2}{P_{X_2Y_4}} = \frac{(6/7)^2}{1/7} = \frac{36}{7}$
- Find $\ln K_p = \ln 36 - \ln 7 = (2\ln 2 + 2\ln 3) - \ln 7 = 2(0.69) + 2(1.104) - 1.932 = 1.656$
- Calculate $\Delta_rG^\circ = -RT \ln K_p = -8.3 \times 600 \times 1.656 = -8247$ J/mol $= -8.247$ kJ/mol
- Magnitude of $\Delta_rG^\circ = 8$ kJ/mol (nearest integer)
Q75 · Numerical · Chemical Kinetics · Easy
Decomposition of a hydrocarbon follows the equation $k = (5.5 \times 10^{11} s^{-1}) e^{\frac{-28000K}{T}}$. The activation energy of reaction is __________ kJ mol$^{-1}$. (Nearest Integer)
Given: R = 8.3 J K$^{-1}$ mol$^{-1}$
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Answer: 232
Key idea: Arrhenius Equation and Activation Energy
- Write the Arrhenius equation: $k = A e^{-E_a/RT}$
- Compare with given equation: $k = (5.5 \times 10^{11}) e^{-28000/T}$
- Match the exponents: $\frac{-28000}{T} = \frac{-E_a}{RT}$
- Simplify to get: $28000 = \frac{E_a}{R}$
- Calculate: $E_a = 28000 \times 8.3 = 232400$ J mol$^{-1}$
- Convert to kJ mol$^{-1}$: $E_a = 232.4 \approx 232$ kJ mol$^{-1}$