s-Block Elements - Practice Questions with Answers
75 free MCQs on s-Block Elements with worked answers and explanations. Group 1 (alkali metals) and Group 2 (alkaline earth metals). Learn their reactions with water and air, important compounds like NaOH, Na₂CO₃, and CaCO₃, and anomalous behaviour of lithium and beryllium.
Below are 75 practice questions on s-Block Elements, sorted Easy → Hard. Tap “Show answer & explanation” under any question to check yourself. Want the full theory first? Read the s-Block Elements notes.
Each s-block metal ion emits a characteristic flame colour because heating excites electrons to higher energy levels; light is emitted as they fall back, with the colour determined by the specific energy gap.
Easy - 25 questions
Q1.
Why are the alkali metals the most electropositive elements in their respective periods?
A They have low ionisation enthalpies and lose the single ns<sup>1</sup> electron easily
B They have the highest ionisation enthalpies and hold the ns<sup>1</sup> electron very tightly
C They have completely filled d-orbitals
D They gain an electron to form stable anions
Show answer & explanation
Answer: A. They have low ionisation enthalpies and lose the single ns<sup>1</sup> electron easily
Why: Alkali metals have the lowest ionisation enthalpies in their periods, so they readily lose the loosely held ns<sup>1</sup> electron, making them the most electropositive (strongly metallic) elements.
Q2.
On moving down Group 1 from Li to Cs, the ionisation enthalpy:
A Increases steadily
B Decreases
C Remains constant
D First increases then decreases
Show answer & explanation
Answer: B. Decreases
Why: Down the group atomic size increases and the outer electron is more shielded and farther from the nucleus, so ionisation enthalpy decreases from Li to Cs.
Q3.
Lithium, sodium and potassium are kept under kerosene, but which alkali metals are so reactive that they are stored in sealed tubes?
A Lithium and sodium
B Sodium and potassium
C Rubidium and caesium
D Lithium and potassium
Show answer & explanation
Answer: C. Rubidium and caesium
Why: Rubidium and caesium react explosively even with traces of air and moisture, so they are kept in sealed glass tubes rather than merely under kerosene.
Q4.
Which property correctly distinguishes Group 2 (alkaline earth) metals from Group 1 (alkali) metals of the same period?
A Group 2 metals are larger in atomic size
B Group 2 metals are more electropositive
C Group 2 metals have much lower ionisation enthalpies
D Group 2 metals are harder and have higher melting points
Show answer & explanation
Answer: D. Group 2 metals are harder and have higher melting points
Why: With two bonding electrons and smaller size, Group 2 metals have stronger metallic bonding, so they are harder and melt higher than the corresponding alkali metals.
Q5.
Which alkaline earth metal and which alkali metal do NOT impart a characteristic colour to a Bunsen flame?
A Be and Mg among Group 2; none of Group 1
B Be and Mg among Group 2; Li among Group 1
C Ca and Na
D Sr and K
Show answer & explanation
Answer: A. Be and Mg among Group 2; none of Group 1
Why: Beryllium and magnesium have electrons too tightly bound to be excited by a flame, so they give no colour; all the alkali metals, including Li, do impart flame colours.
Q6.
Which groups form the s-block of the periodic table?
A Groups 1 and 2
B Groups 1 to 12
C Groups 17 and 18
D Groups 13 to 18
Show answer & explanation
Answer: A. Groups 1 and 2
Why: The s-block consists of Group 1 (alkali metals) and Group 2 (alkaline earth metals) whose outermost electron is in an s orbital.
Q7.
What is the common feature of alkali metals (Group 1)?
A One valence electron (ns<sup>1</sup>)
B Two valence electrons
C Full d orbitals
D Zero valence electrons
Show answer & explanation
Answer: A. One valence electron (ns<sup>1</sup>)
Why: All alkali metals have one valence electron in the outermost s orbital (ns<sup>1</sup> configuration).
Q8.
Which metal is stored under kerosene oil to prevent reaction with air and moisture?
A Sodium
B Calcium
C Magnesium
D Beryllium
Show answer & explanation
Answer: A. Sodium
Why: Sodium is highly reactive with air and water and is stored submerged in kerosene oil.
Q9.
What gas is produced when sodium reacts with water?
A Hydrogen
B Oxygen
C Nitrogen
D Chlorine
Show answer & explanation
Answer: A. Hydrogen
Why: 2Na + 2H<sub>2</sub>O → 2NaOH + H<sub>2</sub>. The hydrogen gas evolved can ignite due to the heat produced.
Q10.
Which alkali metal is the softest metal?
A Caesium
B Lithium
C Sodium
D Potassium
Show answer & explanation
Answer: A. Caesium
Why: Caesium is the softest alkali metal (and among all metals); it can be cut with a knife.
Q11.
Baking soda is the common name for:
A NaHCO<sub>3</sub>
B Na<sub>2</sub>CO<sub>3</sub>
C NaOH
D Na<sub>2</sub>SO<sub>4</sub>
Show answer & explanation
Answer: A. NaHCO<sub>3</sub>
Why: Sodium bicarbonate (NaHCO<sub>3</sub>) is baking soda, used in baking and as an antacid.
Q12.
Washing soda is:
A Na<sub>2</sub>CO<sub>3</sub>·10H<sub>2</sub>O
B NaHCO<sub>3</sub>
C NaOH
D Na<sub>2</sub>SO<sub>4</sub>·10H<sub>2</sub>O
Show answer & explanation
Answer: A. Na<sub>2</sub>CO<sub>3</sub>·10H<sub>2</sub>O
Why: Washing soda is sodium carbonate decahydrate (Na<sub>2</sub>CO<sub>3</sub>·10H<sub>2</sub>O), used in water softening and cleaning.
Q13.
Caustic soda is:
A NaOH
B Na<sub>2</sub>CO<sub>3</sub>
C NaHCO<sub>3</sub>
D NaCl
Show answer & explanation
Answer: A. NaOH
Why: Sodium hydroxide (NaOH) is commonly called caustic soda; it is a strong base used in soap making.
Q14.
The Solvay process is used to manufacture:
A Sodium carbonate (Na<sub>2</sub>CO<sub>3</sub>)
B Sodium chloride
C Sodium hydroxide
D Sodium bicarbonate only
Show answer & explanation
Answer: A. Sodium carbonate (Na<sub>2</sub>CO<sub>3</sub>)
Why: The Solvay (ammonia-soda) process produces sodium carbonate from salt, ammonia, and CO<sub>2</sub>.
Q15.
Milk of magnesia is a suspension of:
A Mg(OH)<sub>2</sub>
B MgO
C MgCO<sub>3</sub>
D MgSO<sub>4</sub>
Show answer & explanation
Answer: A. Mg(OH)<sub>2</sub>
Why: Milk of magnesia is a suspension of magnesium hydroxide Mg(OH)<sub>2</sub> in water, used as an antacid and laxative.
Q16.
Plaster of Paris is:
A CaSO<sub>4</sub>·0.5H<sub>2</sub>O (hemihydrate)
B CaSO<sub>4</sub>·2H<sub>2</sub>O, the fully hydrated gypsum form
C CaCO<sub>3</sub>, common limestone before any calcination
D Ca(OH)<sub>2</sub>, ordinary slaked lime used in mortar
Show answer & explanation
Answer: A. CaSO<sub>4</sub>·0.5H<sub>2</sub>O (hemihydrate)
Why: Plaster of Paris is calcium sulfate hemihydrate (CaSO<sub>4</sub>·0.5H<sub>2</sub>O), made by heating gypsum.
Q17.
Gypsum is:
A CaSO<sub>4</sub>·2H<sub>2</sub>O
B CaSO<sub>4</sub>·0.5H<sub>2</sub>O
C CaCO<sub>3</sub>
D Ca(OH)<sub>2</sub>
Show answer & explanation
Answer: A. CaSO<sub>4</sub>·2H<sub>2</sub>O
Why: Gypsum is calcium sulfate dihydrate (CaSO<sub>4</sub>·2H<sub>2</sub>O), a naturally occurring mineral.
Q18.
Limestone is:
A CaCO<sub>3</sub>
B CaSO<sub>4</sub>
C Ca(OH)<sub>2</sub>
D CaO
Show answer & explanation
Answer: A. CaCO<sub>3</sub>
Why: Limestone is calcium carbonate (CaCO<sub>3</sub>), a widely used building and industrial material.
Q19.
Quicklime is:
A CaO
B Ca(OH)<sub>2</sub>
C CaCO<sub>3</sub>
D CaSO<sub>4</sub>
Show answer & explanation
Answer: A. CaO
Why: Quicklime (CaO) is produced by heating limestone: CaCO<sub>3</sub> → CaO + CO<sub>2</sub> (calcination).
Q20.
Slaked lime is:
A Ca(OH)<sub>2</sub>
B CaO
C CaCO<sub>3</sub>
D CaSO<sub>4</sub>
Show answer & explanation
Answer: A. Ca(OH)<sub>2</sub>
Why: Slaked lime Ca(OH)<sub>2</sub> is produced when water is added to quicklime: CaO + H<sub>2</sub>O → Ca(OH)<sub>2</sub>.
Q21.
Which s-block element is essential for the human body as a bone constituent?
A Calcium
B Lithium
C Rubidium
D Caesium
Show answer & explanation
Answer: A. Calcium
Why: Calcium (as Ca<sub>3</sub>(PO<sub>4</sub>)<sub>2</sub>) is the main mineral in bones and teeth, and is vital for nerve and muscle function.
Q22.
Beryllium (Be) is anomalous among Group 2 elements because it forms:
A Covalent compounds (high charge density, small size)
B Mainly ionic compounds like the rest of Group 2 typically does
C Predominantly metallic compounds rather than discrete molecules
D Stable compounds directly with noble gas elements
Show answer & explanation
Answer: A. Covalent compounds (high charge density, small size)
Why: Be has the smallest ionic radius and highest charge density in Group 2, causing it to form covalent bonds and behave more like aluminium (diagonal relationship).
Q23.
Which alkali metal has the smallest atomic radius?
A Lithium
B Sodium
C Potassium
D Caesium
Show answer & explanation
Answer: A. Lithium
Why: Lithium is the first and smallest alkali metal; atomic radius increases down the group as shells are added.
Q24.
Sodium chloride (common salt) is produced by:
A Mining rock salt or evaporation of seawater
B Electrolysis of aqueous NaOH solution in a diaphragm cell
C The Solvay process used industrially to manufacture sodium carbonate
D Direct combination of sodium metal with chlorine gas alone
Show answer & explanation
Answer: A. Mining rock salt or evaporation of seawater
Why: Salt is obtained naturally from rock salt deposits or by evaporation of seawater in salt pans.
Q25.
Which of the following is a radioactive alkali metal?
A Francium (Fr)
B Lithium
C Sodium
D Rubidium
Show answer & explanation
Answer: A. Francium (Fr)
Why: Francium is the heaviest alkali metal and is intensely radioactive (all isotopes are radioactive, half-life <22 min).
Medium - 25 questions
Q26.
The solubility of alkaline earth metal hydroxides increases down the group (Be(OH)<sub>2</sub> < Mg(OH)<sub>2</sub> < ... < Ba(OH)<sub>2</sub>) mainly because:
A Hydration enthalpy increases down the group
B Lattice enthalpy decreases faster than hydration enthalpy down the group
C The hydroxides become increasingly covalent and less ionic down the group
D Lattice enthalpy increases down the group
Show answer & explanation
Answer: B. Lattice enthalpy decreases faster than hydration enthalpy down the group
Why: Down the group the decrease in lattice enthalpy outweighs the decrease in hydration enthalpy, so the net energetics favour greater solubility of the heavier hydroxides.
Q27.
When lithium, sodium and potassium are heated in excess oxygen, the principal products are respectively:
A Peroxide, superoxide and monoxide
B Superoxide, monoxide and peroxide
C Monoxide, peroxide and superoxide
D Monoxide, superoxide and peroxide
Show answer & explanation
Answer: C. Monoxide, peroxide and superoxide
Why: Lithium forms mainly the monoxide Li<sub>2</sub>O, sodium forms the peroxide Na<sub>2</sub>O<sub>2</sub>, and potassium (and heavier metals) form superoxides such as KO<sub>2</sub>.
Q28.
Assertion: Lithium salts are mostly hydrated while other alkali-metal salts are usually anhydrous. Reason: Li<sup>+</sup> has the largest charge-to-size ratio among alkali-metal ions.
A The assertion is false but the reason is true
B Both statements are true but the reason does not correctly explain the assertion
C The assertion is true but the reason is false
D Both assertion and reason are true and the reason explains the assertion
Show answer & explanation
Answer: D. Both assertion and reason are true and the reason explains the assertion
Why: The small Li<sup>+</sup> has the highest charge density, giving the strongest hydration; hence its salts such as LiCl.2H<sub>2</sub>O are hydrated, unlike the larger alkali-metal ions.
Q29.
The thermal stability of the carbonates of Group 2 follows the order BeCO<sub>3</sub> < MgCO<sub>3</sub> < CaCO<sub>3</sub> < SrCO<sub>3</sub> < BaCO<sub>3</sub> because, down the group:
A The cation polarises the carbonate ion less, stabilising it
B The cation becomes smaller and far more strongly polarising
C Lattice enthalpy increases sharply
D The carbonate ion becomes more covalent
Show answer & explanation
Answer: A. The cation polarises the carbonate ion less, stabilising it
Why: Larger cations down the group have lower polarising power and distort the CO<sub>3</sub><sup>2-</sup> ion less, so the carbonates need higher temperatures to decompose and are thermally more stable.
Q30.
Which observation is a direct consequence of the diagonal relationship between lithium and magnesium?
A Both form highly soluble carbonates
B Both form nitrides with N<sub>2</sub> and carbonates that decompose on heating
C Both form stable solid hydrogencarbonates
D Both impart a characteristic crimson colour to the Bunsen flame
Show answer & explanation
Answer: B. Both form nitrides with N<sub>2</sub> and carbonates that decompose on heating
Why: Li resembles Mg: both react with N<sub>2</sub> to form nitrides, their carbonates decompose on heating, and their hydrogencarbonates do not exist as solids, reflecting the diagonal relationship.
Q31.
The anomalous behaviour of lithium compared to other alkali metals is due to:
A Very small size and high charge density (diagonal relationship with Mg)
B Its position as the most chemically reactive metal in Group 1
C Its unusually low electronegativity compared to the rest of Group 1
D Its status as the heaviest element within Group 1
Show answer & explanation
Answer: A. Very small size and high charge density (diagonal relationship with Mg)
Why: Li is anomalously small and has a high charge density, causing it to behave more like Mg in many properties (diagonal relationship).
Q32.
Down Group 1, which property decreases?
A First ionisation energy
B Atomic radius
C Density
D Reactivity with water
Show answer & explanation
Answer: A. First ionisation energy
Why: Down Group 1, atomic radius increases (more shells), which reduces nuclear attraction on valence electrons, lowering ionisation energy.
Q33.
Lithium forms a nitride directly with N<sub>2</sub> because:
A Li ions are small, and Li<sub>3</sub>N has high lattice energy (similar to Mg)
B Lithium is simply the most reactive metal within the alkali metal family
C Lithium has the highest first ionisation energy among the alkali metals
D Lithium displays amphoteric behaviour unlike the other alkali metals
Show answer & explanation
Answer: A. Li ions are small, and Li<sub>3</sub>N has high lattice energy (similar to Mg)
Why: Li + N<sub>2</sub> → Li<sub>3</sub>N (lithium nitride); Li's small size allows formation of a stable nitride like Mg (diagonal relationship).
Q34.
The Castner-Kellner process produces NaOH and Cl<sub>2</sub> by:
A Electrolysis of brine (NaCl solution) using mercury cell
B The Solvay process, which instead yields sodium carbonate from brine
C Electrolysis of molten anhydrous NaCl to give metallic sodium
D Direct reaction of sodium carbonate with slaked lime
Show answer & explanation
Answer: A. Electrolysis of brine (NaCl solution) using mercury cell
Why: The Castner-Kellner (mercury cell) electrolyses brine to give Cl<sub>2</sub> at anode and Na amalgam at cathode; the amalgam reacts with water to give NaOH.
Q35.
Cement is mainly composed of:
A CaO·SiO<sub>2</sub>·Al<sub>2</sub>O<sub>3</sub> (calcium aluminosilicate)
B Pure CaCO<sub>3</sub> with no other mineral components present
C Ca(OH)<sub>2</sub> alone, used directly without further processing
D CaSO<sub>4</sub>, the same hemihydrate used in plaster of Paris
Show answer & explanation
Answer: A. CaO·SiO<sub>2</sub>·Al<sub>2</sub>O<sub>3</sub> (calcium aluminosilicate)
Why: Portland cement is a mixture of calcium silicates and aluminates formed by sintering limestone with clay.
Q36.
Setting of plaster of Paris involves:
A Rehydration: CaSO<sub>4</sub>·0.5H<sub>2</sub>O + 1.5H<sub>2</sub>O → CaSO<sub>4</sub>·2H<sub>2</sub>O (gypsum)
B Dehydration of the hemihydrate to anhydrous calcium sulfate
C Oxidation of the sulfate ion to a higher oxidation state
D Reduction of calcium sulfate to elemental calcium and sulfur
Show answer & explanation
Answer: A. Rehydration: CaSO<sub>4</sub>·0.5H<sub>2</sub>O + 1.5H<sub>2</sub>O → CaSO<sub>4</sub>·2H<sub>2</sub>O (gypsum)
Why: Plaster of Paris absorbs water to rehydrate back to gypsum, forming an interlocked crystalline structure that is hard.
Q37.
Which reaction represents the preparation of Na from NaCl?
A Electrolysis of molten NaCl (Down's process)
B Chemical reduction with carbon under usual circumstances
C Reaction with water according to most researchers
D Solvay process in the majority of cases studied
Show answer & explanation
Answer: A. Electrolysis of molten NaCl (Down's process)
Why: The Down's process electrolyses molten NaCl (with CaCl<sub>2</sub> to lower melting point) to obtain Na at the cathode and Cl<sub>2</sub> at the anode.
Q38.
Milk of lime is a suspension of Ca(OH)<sub>2</sub> in water. Its use in industry includes:
A Water treatment, mortar, sugar purification
B Manufacturing soap through saponification of fats
C Manufacturing glass by fusing silica with soda ash
D Industrially producing ammonia from nitrogen and hydrogen
Show answer & explanation
Answer: A. Water treatment, mortar, sugar purification
Why: Ca(OH)<sub>2</sub> (lime water / milk of lime) is used to soften water, in mortar, to neutralise acidic soil, and to purify cane sugar juice.
Q39.
Potassium superoxide (KO<sub>2</sub>) is used in:
A Self-contained breathing apparatus (reacts with CO<sub>2</sub> and H<sub>2</sub>O to release O<sub>2</sub>)
B Nitrogen-based fertilisers applied directly to soil as widely reported
C Explosive formulations requiring a stable oxidiser in standard practice
D Soap manufacture through reaction with fatty acids under most conditions encountered
Show answer & explanation
Answer: A. Self-contained breathing apparatus (reacts with CO<sub>2</sub> and H<sub>2</sub>O to release O<sub>2</sub>)
Why: KO<sub>2</sub> + H<sub>2</sub>O → KOH + H<sub>2</sub>O<sub>2</sub> → O<sub>2</sub> released; used in breathing masks and space capsules.
Q40.
Magnesium burns in CO<sub>2</sub> because:
A Mg reduces CO<sub>2</sub> to C (2Mg + CO<sub>2</sub> → 2MgO + C), so CO<sub>2</sub> extinguishers fail on Mg fires
B Magnesium is actually less reactive than carbon toward oxygen as frequently observed in practice
C Magnesium generally does not burn when exposed to CO<sub>2</sub> in many documented cases
D The reaction instead produces stable magnesium carbonate, MgCO<sub>3</sub> according to conventional understanding
Show answer & explanation
Answer: A. Mg reduces CO<sub>2</sub> to C (2Mg + CO<sub>2</sub> → 2MgO + C), so CO<sub>2</sub> extinguishers fail on Mg fires
Why: Magnesium is a stronger reducing agent than carbon and burns even in CO<sub>2</sub>, which is why CO<sub>2</sub> fire extinguishers cannot be used on Mg fires.
Q41.
The Solvay process steps include: salt + ammonia + CO<sub>2</sub> → NaHCO<sub>3</sub> (precipitate) → heating → Na<sub>2</sub>CO<sub>3</sub>. The ammonia is:
A Recovered and recycled by treating NH<sub>4</sub>Cl with Ca(OH)<sub>2</sub>
B Discharged entirely as waste gas at the end of the process
C Permanently consumed and converted into sodium bicarbonate
D Reduced back to elemental nitrogen gas for disposal
Show answer & explanation
Answer: A. Recovered and recycled by treating NH<sub>4</sub>Cl with Ca(OH)<sub>2</sub>
Why: NH<sub>4</sub>Cl produced is treated with Ca(OH)<sub>2</sub> (slaked lime) to recover ammonia: 2NH<sub>4</sub>Cl + Ca(OH)<sub>2</sub> → CaCl<sub>2</sub> + 2NH<sub>3</sub> + 2H<sub>2</sub>O.
Q42.
Which alkaline earth metal is used in making strong lightweight alloys for aircraft?
A Magnesium (Mg)
B Calcium (Ca)
C Beryllium (Be)
D Barium (Ba)
Show answer & explanation
Answer: A. Magnesium (Mg)
Why: Magnesium is very light (density 1.74 g/cm<sup>3</sup>) and is alloyed with aluminium to make lightweight, strong alloys for aerospace.
Q43.
Thermal stability of Group 2 carbonates:
A Increases down the group (larger cations have lower charge density, stabilise CO<sub>3</sub><sup>2-</sup> more)
B Decreases steadily down the group as the cation's charge density falls in routine practice
C Remains essentially identical across most Group 2 carbonate salt overall in most cases
D Depends mainly on the external storage temperature, not on cation size under typical conditions
Show answer & explanation
Answer: A. Increases down the group (larger cations have lower charge density, stabilise CO<sub>3</sub><sup>2-</sup> more)
Why: Larger alkaline earth cations (Ca, Sr, Ba) have lower polarising power and stabilise the CO<sub>3</sub><sup>2-</sup> lattice better; BaCO<sub>3</sub> decomposes at the highest temperature.
Q44.
Hard water deposit (scale) in boilers is removed using:
A Calgon (sodium hexametaphosphate) or HCl treatment
B Concentrated NaOH solution flushed through the boiler
C Additional hard water poured in to dissolve existing scale
D Simply boiling the water further without any added reagent
Show answer & explanation
Answer: A. Calgon (sodium hexametaphosphate) or HCl treatment
Why: Boiler scale (mainly CaSO<sub>4</sub> and CaCO<sub>3</sub>) can be dissolved using hydrochloric acid or prevented by sequestering agents like Calgon.
Q45.
Chlorophyll (the green plant pigment) contains which metal from the s-block?
A Magnesium (Mg<sup>2+</sup> at the porphyrin centre)
B Calcium, coordinated at the centre of the porphyrin ring
C Sodium, held loosely at the centre of the porphyrin structure
D Barium, chelated within the porphyrin macrocycle
Show answer & explanation
Answer: A. Magnesium (Mg<sup>2+</sup> at the porphyrin centre)
Why: Chlorophyll has a porphyrin ring with Mg<sup>2+</sup> at its centre, essential for light absorption in photosynthesis.
Q46.
Epsom salt is:
A MgSO<sub>4</sub>·7H<sub>2</sub>O
B CaSO<sub>4</sub>·2H<sub>2</sub>O
C BaSO<sub>4</sub>
D Na<sub>2</sub>SO<sub>4</sub>·10H<sub>2</sub>O
Show answer & explanation
Answer: A. MgSO<sub>4</sub>·7H<sub>2</sub>O
Why: Epsom salt is magnesium sulfate heptahydrate (MgSO<sub>4</sub>·7H<sub>2</sub>O), used as a laxative and in bath salts.
Q47.
The flame colours of alkali metals are caused by:
A Electrons jumping from excited states back to ground state emitting visible light
B Small-scale nuclear reactions occurring within the heated metal according to standard textbooks
C The colour of the gaseous combustion products formed in the flame in general practice
D Simple ionic dissociation of the metal salt in the flame as frequently described
Show answer & explanation
Answer: A. Electrons jumping from excited states back to ground state emitting visible light
Why: When atoms absorb flame energy, outer electrons are excited; on returning to ground state they emit characteristic spectral lines.
Q48.
Barium sulfate (BaSO<sub>4</sub>) is used as an X-ray contrast agent for the digestive tract because:
A It is insoluble and non-toxic, opaque to X-rays
B It is highly soluble, allowing rapid absorption into the bloodstream
C It functions as an essential dietary nutrient for digestion
D It readily dissolves upon contact with stomach acid
Show answer & explanation
Answer: A. It is insoluble and non-toxic, opaque to X-rays
Why: BaSO<sub>4</sub> (barium meal) is insoluble in water and stomach acid, non-absorbable and safe; it scatters X-rays to show GI tract shape.
Q49.
Radium (Ra) was discovered by:
A Marie and Pierre Curie
B Humphry Davy in most textbook accounts
C Mendeleev during normal conditions
D Moseley as generally observed
Show answer & explanation
Answer: A. Marie and Pierre Curie
Why: Marie and Pierre Curie discovered radium (and polonium) in 1898 from pitchblende ore.
Q50.
Beryllium cannot be obtained by electrolysis of aqueous BeCl<sub>2</sub> solution because:
A Be is above H in activity series; H<sub>2</sub> is discharged preferentially at the cathode
B Beryllium's melting point is generally too high for aqueous electrolysis as widely reported
C Beryllium chloride's covalent bonding prevents it from dissolving in water
D Beryllium is a radioactive element unsuitable for aqueous processing in standard practice
Show answer & explanation
Answer: A. Be is above H in activity series; H<sub>2</sub> is discharged preferentially at the cathode
Why: Be<sup>2+</sup> has very high hydration enthalpy and is reduced above the reduction potential of water, so H<sub>2</sub> is released instead at the cathode in aqueous solution.
Hard - 25 questions
Q51.
Although Li has the most negative standard electrode potential (E° = -3.04 V), it reacts with water less vigorously than sodium. The reason is that:
A Lithium has a far lower ionisation enthalpy and so reacts much more gently than sodium
B Sodium is more electropositive than lithium
C High hydration energy makes E° very negative, but a high melting point slows the reaction
D Lithium does not react with water at all
Show answer & explanation
Answer: C. High hydration energy makes E° very negative, but a high melting point slows the reaction
Why: The very negative E° of Li is due to its exceptionally high hydration enthalpy (a thermodynamic quantity). Kinetically, Li's high melting point keeps it solid and its small size slows the reaction, so it reacts more gently than Na.
Q52.
In the Solvay (ammonia-soda) process, which statement correctly explains why it cannot be used to manufacture potassium carbonate?
A Potassium does not form a carbonate
B KCl is insoluble in water
C Ammonia does not react with potassium salts to form carbonates
D Potassium hydrogencarbonate (KHCO<sub>3</sub>) is too soluble to precipitate out
Show answer & explanation
Answer: D. Potassium hydrogencarbonate (KHCO<sub>3</sub>) is too soluble to precipitate out
Why: The process relies on the low solubility of NaHCO<sub>3</sub> so it precipitates; KHCO<sub>3</sub> is appreciably soluble and does not precipitate, so K<sub>2</sub>CO<sub>3</sub> cannot be made this way.
Q53.
Beryllium chloride is a covalent compound that is polymeric in the solid state. In the solid polymer, each beryllium atom is:
A Tetrahedrally four-coordinate through chloride bridges
B Linearly two-coordinate via sp hybridisation as in the vapour phase
C Octahedrally six-coordinate
D Trigonal planar three-coordinate
Show answer & explanation
Answer: A. Tetrahedrally four-coordinate through chloride bridges
Why: Solid BeCl<sub>2</sub> forms chain polymers in which each Be is bonded to four chlorines (two terminal, two bridging), giving tetrahedral four-coordination; the monomer is linear only in the vapour.
Q54.
A blue solution of sodium in liquid ammonia conducts electricity and is strongly reducing. On standing, the blue colour fades and the conductivity changes because:
A Sodium metal precipitates out unchanged
B Ammoniated electrons slowly convert to sodium amide with evolution of dihydrogen
C The dissolved sodium is slowly oxidised to sodium hydroxide and nitrogen gas
D Ammonia is oxidised to nitrogen gas
Show answer & explanation
Answer: B. Ammoniated electrons slowly convert to sodium amide with evolution of dihydrogen
Why: The blue colour and conductivity arise from ammoniated electrons. On standing these react: Na + NH<sub>3</sub> → NaNH<sub>2</sub> + ½H<sub>2</sub>, so the colour fades as amide forms and H<sub>2</sub> is released.
Q55.
Lithium iodide is the most covalent of the lithium halides. According to Fajans' rules this is because, compared with the other halides:
A Lithium iodide has the highest lattice enthalpy of all the halides
B The iodide ion has the highest charge
C The iodide ion is large and most easily polarised by the small Li<sup>+</sup>
D The iodide ion is the least polarisable anion
Show answer & explanation
Answer: C. The iodide ion is large and most easily polarised by the small Li<sup>+</sup>
Why: The large, highly polarisable I<sup>-</sup> ion is distorted most by the small high-charge-density Li<sup>+</sup>, giving the greatest covalent character among LiF, LiCl, LiBr and LiI.
Q56.
The lattice energy of NaF is higher than NaCl because:
A F- is smaller than Cl-, so Na-F distance is shorter and lattice energy (alpha 1/r) is higher
B Fluoride ion generally has a lower atomic mass than chloride ion under typical conditions
C Sodium ion is somehow larger when paired specifically with fluoride according to standard textbooks
D NaF possesses significant covalent character unlike NaCl in general practice as frequently described
Show answer & explanation
Answer: A. F- is smaller than Cl-, so Na-F distance is shorter and lattice energy (alpha 1/r) is higher
Why: Lattice energy ∝ (q+×q-)/(r+ + r-). F- is smaller than Cl-, decreasing internuclear distance and increasing lattice energy.
Q57.
Why does LiF have lower solubility in water than LiCl?
A LiF has very high lattice energy; the hydration enthalpy does not overcome it
B LiF is a mainly covalent compound that resists hydration largely in most textbook accounts
C LiCl carries a noticeably higher degree of bond polarity than LiF during normal conditions
D LiF exists as a volatile gas under standard room conditions as generally observed
Show answer & explanation
Answer: A. LiF has very high lattice energy; the hydration enthalpy does not overcome it
Why: LiF: high lattice energy (due to small F-) outweighs hydration energy, so it is sparingly soluble. LiCl has lower lattice energy and dissolves readily.
Q58.
Why does Na react vigorously with water while Li reacts less vigorously?
A Na has lower first ionisation energy than Li, making it easier to ionise; also Na reacts exothermically faster
B Lithium is generally a noticeably more electronegative element than sodium in typical laboratory settings
C Lithium's higher melting point reduces the metal surface area exposed to water under usual circumstances
D Sodium atoms contain fewer total orbital electrons than lithium atoms do according to most researchers in the majority of cases studied
Show answer & explanation
Answer: A. Na has lower first ionisation energy than Li, making it easier to ionise; also Na reacts exothermically faster
Why: Li's very high charge density means the Li+ ion is heavily hydrated, releasing more energy overall, but kinetically Li's reaction is slower due to its higher ionisation energy and the coherent film of LiOH.
Q59.
In the Down's process, CaCl<sub>2</sub> is added to NaCl to:
A Lower the melting point from 800°C to ~600°C making electrolysis practical
B Simply raise the ionic conductivity without affecting melting point
C Form a protective layer that prevents oxidation of the sodium product
D Serve as a catalyst that speeds the electrode reactions
Show answer & explanation
Answer: A. Lower the melting point from 800°C to ~600°C making electrolysis practical
Why: Pure NaCl melts at 800°C; adding CaCl<sub>2</sub> lowers the melting point (~600°C), reducing energy consumption and preventing Na vaporisation.
Q60.
Organolithium compounds (RLi) are more reactive than Grignard reagents (RMgX) because:
A C-Li bonds are more covalent and have more ionic character; Li is more electropositive than Mg
B Lithium is generally a noticeably heavier element than magnesium overall as widely reported
C RLi compounds exist as largely ionic crystalline salts dissolved in solution in standard practice
D Magnesium is a more electronegative element than lithium in these compounds under most conditions encountered
Show answer & explanation
Answer: A. C-Li bonds are more covalent and have more ionic character; Li is more electropositive than Mg
Why: RLi has more polarised C-Li bond (Li more electropositive than Mg, less electronegative), making the carbanion character stronger and RLi more nucleophilic/basic.
Q61.
The hardness order of Group 2 metals is:
A Be > Mg > Ca > Sr > Ba (decreases down the group as metallic bonding weakens)
B Ba > Sr > Ca > Mg > Be, increasing steadily down the group as frequently observed in practice
C All five Group 2 metals show essentially identical hardness in many documented cases
D Hardness is determined mainly by ambient temperature, not atomic size according to conventional understanding
Show answer & explanation
Answer: A. Be > Mg > Ca > Sr > Ba (decreases down the group as metallic bonding weakens)
Why: Down Group 2, metal-metal bonds weaken (fewer valence electrons relative to increasing atomic size), reducing hardness.
Q62.
Which Group 1 element has an anomalously high melting point compared to trend?
A Lithium (180°C vs Na 98°C, K 63°C, Rb 39°C, Cs 28°C)
B Sodium, which melts unexpectedly higher than the rest of the group
C Caesium, despite being the heaviest common alkali metal
D Rubidium, despite sitting between potassium and caesium
Show answer & explanation
Answer: A. Lithium (180°C vs Na 98°C, K 63°C, Rb 39°C, Cs 28°C)
Why: Li melts at 180°C; all other alkali metals melt below 100°C. Li's small size means stronger metallic bonding (higher electron density).
Q63.
Diagonal relationship between Li and Mg: which specific property is shared?
A Both form nitrides (Li<sub>3</sub>N and Mg<sub>3</sub>N<sub>2</sub>), have similar solubility trends, and form covalent organometallic compounds
B Both generally exist as ordinary solid metals under standard everyday room conditions in routine practice
C Lithium uniquely possesses exactly two valence electrons in its single outer shell overall in most cases under typical conditions
D Both metals react with plain cold water at exactly the same observable vigorous rate according to standard textbooks
Show answer & explanation
Answer: A. Both form nitrides (Li<sub>3</sub>N and Mg<sub>3</sub>N<sub>2</sub>), have similar solubility trends, and form covalent organometallic compounds
Why: Li resembles Mg: both form nitrides directly, both LiF and MgF<sub>2</sub> are sparingly soluble, both LiOH and Mg(OH)<sub>2</sub> are weak bases, and Li<sub>2</sub>CO<sub>3</sub>/MgCO<sub>3</sub> decompose on heating.
Q64.
The pH of a 0.1 M NaOH solution is:
A 13
B 1
C 7
D 10
Show answer & explanation
Answer: A. 13
Why: NaOH is a strong base. [OH-] = 0.1 M, pOH = 1, pH = 14 - 1 = 13.
Q65.
When excess Na<sub>2</sub>O<sub>2</sub> reacts with water, the products are:
A NaOH and H<sub>2</sub>O<sub>2</sub> (2Na<sub>2</sub>O<sub>2</sub> + 2H<sub>2</sub>O → 4NaOH + O<sub>2</sub>)
B Na<sub>2</sub>O and oxygen gas released without any hydroxide formed
C NaOH alone, with no oxygen or peroxide byproduct at all
D Na<sub>2</sub>CO<sub>3</sub> and hydrogen peroxide formed via carbonation
Show answer & explanation
Answer: A. NaOH and H<sub>2</sub>O<sub>2</sub> (2Na<sub>2</sub>O<sub>2</sub> + 2H<sub>2</sub>O → 4NaOH + O<sub>2</sub>)
Why: Na<sub>2</sub>O<sub>2</sub> (sodium peroxide) reacts with water: 2Na<sub>2</sub>O<sub>2</sub> + 2H<sub>2</sub>O → 4NaOH + O<sub>2</sub>. It is used in submarines as an O<sub>2</sub> source.
Q66.
Calcium carbide (CaC<sub>2</sub>) reacts with water to give:
A Acetylene (C<sub>2</sub>H<sub>2</sub>) and Ca(OH)<sub>2</sub>
B Ethylene and CaO in general practice
C CO<sub>2</sub> and Ca(OH)<sub>2</sub> as frequently described
D CO and CaCO<sub>3</sub> in most textbook accounts
Show answer & explanation
Answer: A. Acetylene (C<sub>2</sub>H<sub>2</sub>) and Ca(OH)<sub>2</sub>
Why: CaC<sub>2</sub> + 2H<sub>2</sub>O → Ca(OH)<sub>2</sub> + C<sub>2</sub>H<sub>2</sub>. This reaction was historically used to generate acetylene for lamps (carbide lamps).
Q67.
Liquid ammonia is used as a solvent in which Group 1 reactions?
A Dissolution of alkali metals in liquid NH<sub>3</sub> to give blue solutions (solvated electrons)
B The direct formation of sodium peroxide from sodium metal and oxygen during normal conditions
C The electrolytic reduction of molten calcium chloride to calcium metal as generally observed
D The Solvay process used to manufacture sodium carbonate in typical laboratory settings
Show answer & explanation
Answer: A. Dissolution of alkali metals in liquid NH<sub>3</sub> to give blue solutions (solvated electrons)
Why: Alkali metals dissolve in liquid NH<sub>3</sub>: Na → Na+ + e-(solvated), giving blue paramagnetic solutions. At higher concentrations they turn bronze (metallic) and conduct electricity.
Q68.
The blue colour of alkali metal solutions in liquid ammonia is due to:
A Solvated electrons (e-(am)) absorbing light in the visible range
B Sodium cations themselves absorbing visible light in solution
C Liquid ammonia itself possessing an inherent blue colour
D Trace amounts of dissolved sodium oxide colouring the solution
Show answer & explanation
Answer: A. Solvated electrons (e-(am)) absorbing light in the visible range
Why: Solvated electrons (free electrons surrounded by NH<sub>3</sub> molecules) absorb light broadly; dilute solutions are blue, concentrated solutions are metallic bronze.
Q69.
In which reaction is barium peroxide (BaO<sub>2</sub>) an important intermediate?
A Historical preparation of H<sub>2</sub>O<sub>2</sub>: BaO<sub>2</sub> + H<sub>2</sub>SO<sub>4</sub> → BaSO<sub>4</sub> + H<sub>2</sub>O<sub>2</sub>
B The electrolytic production of elemental barium metal
C The direct chemical reduction of barium sulfate to barium sulfide
D The industrial Solvay process for manufacturing sodium carbonate
Show answer & explanation
Answer: A. Historical preparation of H<sub>2</sub>O<sub>2</sub>: BaO<sub>2</sub> + H<sub>2</sub>SO<sub>4</sub> → BaSO<sub>4</sub> + H<sub>2</sub>O<sub>2</sub>
Why: Before modern methods, H<sub>2</sub>O<sub>2</sub> was made by treating BaO<sub>2</sub> with cold dilute H<sub>2</sub>SO<sub>4</sub>, giving insoluble BaSO<sub>4</sub> precipitate and H<sub>2</sub>O<sub>2</sub> solution.
Q70.
The standard electrode potential E° of Li/Li+ (-3.05 V) is more negative than Na/Na+ (-2.71 V). In terms of reactivity in water, however:
A Na reacts more vigorously with water than Li, despite Li's more negative E°, due to kinetic factors
B Lithium instead reacts noticeably faster with water than sodium does in practice
C Both metals react with cold water at an identical and equally vigorous observable rate
D The standard electrode potential value alone fully and accurately predicts the reaction rate
Show answer & explanation
Answer: A. Na reacts more vigorously with water than Li, despite Li's more negative E°, due to kinetic factors
Why: Li's high hydration enthalpy means thermodynamics favours Li strongly, but a thin film of LiOH coats Li and slows the reaction kinetically; Na's film is more reactive/less coherent.
Q71.
Beryllium forms BeF<sub>2</sub> with a structure resembling:
A SiO<sub>2</sub> (polymeric tetrahedral network via bridging F atoms in solid state)
B NaCl, adopting a simple ionic rock-salt lattice under usual circumstances
C BF<sub>3</sub>, existing as a discrete trigonal planar molecule according to most researchers
D A simple discrete molecule with little extended network in the majority of cases studied
Show answer & explanation
Answer: A. SiO<sub>2</sub> (polymeric tetrahedral network via bridging F atoms in solid state)
Why: In the solid state, BeF<sub>2</sub> has a polymeric structure analogous to SiO<sub>2</sub> with bridging fluorides, reflecting Be's tendency to expand its coordination sphere (covalent character).
Q72.
Why is BeSO<sub>4</sub> more soluble in water than BaSO<sub>4</sub>?
A Be<sup>2+</sup> has high charge density and large hydration enthalpy that overcomes the lattice energy; Ba<sup>2+</sup> is large with lower hydration enthalpy
B BeSO<sub>4</sub> generally happens to possess a much lower overall lattice energy than BaSO<sub>4</sub> does in the crystal as widely reported in standard practice
C BaSO<sub>4</sub> supposedly carries a noticeably greater degree of ionic character than the corresponding beryllium salt under most conditions encountered
D Ba<sup>2+</sup> is actually claimed to be a far more strongly polarising cation than the small, dense Be<sup>2+</sup> ion as frequently observed in practice
Show answer & explanation
Answer: A. Be<sup>2+</sup> has high charge density and large hydration enthalpy that overcomes the lattice energy; Ba<sup>2+</sup> is large with lower hydration enthalpy
Why: For Group 2 sulfates: solubility decreases down the group (Be > Mg > Ca > Sr > Ba) because hydration enthalpy decreases faster than lattice energy as cation size increases.
Q73.
The Solvay process cannot economically produce potassium carbonate (K<sub>2</sub>CO<sub>3</sub>) because:
A KHCO<sub>3</sub> is too soluble in the brine solution to precipitate out as NaHCO<sub>3</sub> does
B Potassium chloride is generally too expensive to use as a raw material
C Potassium metal reacts dangerously with the carbon dioxide feedstock in many documented cases
D K<sub>2</sub>CO<sub>3</sub> decomposes readily under the mild conditions of the process according to conventional understanding
Show answer & explanation
Answer: A. KHCO<sub>3</sub> is too soluble in the brine solution to precipitate out as NaHCO<sub>3</sub> does
Why: The Solvay process works because NaHCO<sub>3</sub> is sparingly soluble and precipitates; KHCO<sub>3</sub> is more soluble and stays in solution, making K<sub>2</sub>CO<sub>3</sub> production by this route uneconomical.
Q74.
Sodium amalgam (Na/Hg) is used as a reducing agent. The amalgam forms because:
A Na dissolves in mercury forming a liquid alloy (amalgam) that is safer and less reactive than pure Na
B Sodium chemically reacts with mercury to form a distinct crystalline ionic compound in routine practice
C Mercury metal directly oxidises the sodium as the two substances come into contact overall in most cases
D Sodium and mercury are actually largely immiscible and rarely form an alloy under typical conditions
Show answer & explanation
Answer: A. Na dissolves in mercury forming a liquid alloy (amalgam) that is safer and less reactive than pure Na
Why: Amalgams are alloys of mercury; Na dissolves in Hg, diluting its reactivity while retaining reducing power, making it safer to handle.
Q75.
Why does group 2 hydroxides become more basic and more soluble down the group?
A Increasing cation size reduces lattice energy and increases hydration enthalpy advantage; larger M<sup>2+</sup> also holds OH- less tightly
B The atomic mass of each successive Group 2 metal supposedly decreases steadily down the group according to standard textbooks
C The electronegativity of the metal supposedly increases steadily down the group toward fluorine-like values in general practice
D The first ionisation energy of the metal supposedly increases steadily down the group instead of falling as frequently described
Show answer & explanation
Answer: A. Increasing cation size reduces lattice energy and increases hydration enthalpy advantage; larger M<sup>2+</sup> also holds OH- less tightly
Why: From Mg(OH)<sub>2</sub> (sparingly soluble, weakly basic) to Ba(OH)<sub>2</sub> (soluble, strongly basic): larger, less polarising cations release OH- more freely and their hydroxides have lower lattice energies.