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Question 481Question

A 500 cm3500\text{ cm}^3 sample of air collected near an industrial plant containing nitrogen (N2\text{N}_2), oxygen (O2\text{O}_2), carbon dioxide (CO2\text{CO}_2), and sulfur dioxide (SO2\text{SO}_2) pollutant was passed through concentrated potassium hydroxide (KOH\text{KOH}) solution, reducing the gas volume to 485 cm3485\text{ cm}^3. The residual gas mixture was subsequently passed through excess alkaline solution of pyrogallol, resulting in a final volume of 383 cm3383\text{ cm}^3. What is the percentage by volume of oxygen in the original air sample?

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Answer: 20.4

Answer

20.4%
Concentrated potassium hydroxide (KOH) absorbs the acidic gas pollutants (carbon dioxide and sulfur dioxide), causing an initial volume contraction of 15 cm315\text{ cm}^3. Alkaline pyrogallol then absorbs elemental oxygen gas (O2\text{O}_2), causing a further contraction from 485 cm3485\text{ cm}^3 to 383 cm3383\text{ cm}^3, which corresponds to 102 cm3102\text{ cm}^3 of O2\text{O}_2. Dividing this volume of oxygen by the original total sample volume of 500 cm3500\text{ cm}^3 and multiplying by 100%100\% yields 20.4%20.4\%.

Step-by-Step Solution

1
Identify the volume reduction caused by potassium hydroxide (KOH)
KOH absorbs acidic gases CO₂ and SO₂: 500 cm3485 cm3=15 cm3500\text{ cm}^3 - 485\text{ cm}^3 = 15\text{ cm}^3.
Potassium hydroxide is an alkaline reagent that selectively absorbs acidic oxides present in polluted air.
2
Determine the volume of oxygen gas absorbed by alkaline pyrogallol
Alkaline pyrogallol absorbs O₂: 485 cm3383 cm3=102 cm3485\text{ cm}^3 - 383\text{ cm}^3 = 102\text{ cm}^3.
Alkaline pyrogallol is a specific quantitative reagent used to absorb unreacted oxygen gas.
3
Calculate the percentage volume of oxygen in the initial sample
(102 cm3500 cm3)×100%=20.4%\left(\frac{102\text{ cm}^3}{500\text{ cm}^3}\right) \times 100\% = 20.4\%.
The volume percentage of a component in air is the ratio of its volume to the total initial unreacted air sample volume multiplied by 100.

Key Concept

Quantitative volumetric determination of atmospheric components and gaseous pollutants using selective absorbents
Estimated Time:2m 0s
Question 482Question

A uniform horizontal plank ABAB of length 5.0 m5.0\text{ m} and mass 40 kg40\text{ kg} rests on two smooth supports, CC and DD, located 1.0 m1.0\text{ m} from end AA and 1.0 m1.0\text{ m} from end BB respectively. What is the maximum mass, in kilograms, of an object that can be placed at end AA without causing the plank to tilt?

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Answer: 60

Answer

The maximum mass that can be placed at end A without tilting the plank is 60 kg.
Just before tilting, the plank rotates around support C, causing the normal reaction at support D to drop to zero. Equating the anticlockwise moment of the added mass at end A about support C ((mg)×1.0 m(m \cdot g) \times 1.0\text{ m}) to the clockwise moment of the plank's weight about support C ((40g)×1.5 m(40 \cdot g) \times 1.5\text{ m}) yields m=60 kgm = 60\text{ kg}.

Step-by-Step Solution

1
Identify the tipping condition and pivot point
Support C acts as the pivot; the reaction at support D becomes zero (RD=0R_D = 0).
When extra weight is added at end A, the plank rotates about C and lifts off support D.
2
Calculate perpendicular distances from the pivot C
Distance to added mass mm = 1.0 m1.0\text{ m}; Distance to plank's center of mass = 2.5 m1.0 m=1.5 m2.5\text{ m} - 1.0\text{ m} = 1.5\text{ m}.
The weight of a uniform beam acts at its midpoint (2.5 m from either end).
3
Equate clockwise and counterclockwise moments about C
m×g×1.0 m=40 kg×g×1.5 mm \times g \times 1.0\text{ m} = 40\text{ kg} \times g \times 1.5\text{ m}, giving m=60 kgm = 60\text{ kg}.
For the plank to remain balanced just before tipping, total anticlockwise moment must equal total clockwise moment.

Key Concept

Rotational Equilibrium and Tilting of Rigid Bodies
Estimated Time:1m 30s
Question 483Question

What volume of hydrogen gas, measured at STP, is produced when 4.8 g4.8\text{ g} of magnesium ribbon reacts completely with excess dilute tetraoxosulfate(VI) acid according to the chemical equation below?

Mg(s)+H2SO4(aq)MgSO4(aq)+H2(g)Mg(s) + H_2SO_4(aq) \rightarrow MgSO_4(aq) + H_2(g)

[Mg=24,Molar volume of gas at STP=22.4 dm3mol1][Mg = 24, \text{Molar volume of gas at STP} = 22.4\text{ dm}^3\text{mol}^{-1}]

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Answer: 4.48

Answer

The volume of hydrogen gas produced at STP is 4.48 dm34.48\text{ dm}^3.
From the stoichiometric relationship in the balanced reaction Mg(s)+H2SO4(aq)MgSO4(aq)+H2(g)Mg(s) + H_2SO_4(aq) \rightarrow MgSO_4(aq) + H_2(g), 1 mol1\text{ mol} of MgMg (24 g24\text{ g}) produces 1 mol1\text{ mol} of H2H_2 gas (22.4 dm322.4\text{ dm}^3 at STP). For 4.8 g4.8\text{ g} of MgMg, the number of moles is 4.824=0.20 mol\frac{4.8}{24} = 0.20\text{ mol}. Multiplying by the molar gas volume gives 0.20×22.4=4.48 dm30.20 \times 22.4 = 4.48\text{ dm}^3 of H2H_2 gas.

Step-by-Step Solution

1
Calculate the amount in moles of magnesium (MgMg) reacted.
n(Mg)=4.8 g24 g mol1=0.20 moln(Mg) = \frac{4.8\text{ g}}{24\text{ g mol}^{-1}} = 0.20\text{ mol}
Dividing given mass by relative atomic mass yields the number of moles.
2
Determine the amount in moles of hydrogen gas (H2H_2) produced.
n(H2)=0.20 moln(H_2) = 0.20\text{ mol}
The balanced chemical equation shows a 1:11:1 stoichiometric molar ratio between MgMg and H2H_2.
3
Calculate the volume of H2H_2 gas at STP.
V(H2)=0.20 mol×22.4 dm3mol1=4.48 dm3V(H_2) = 0.20\text{ mol} \times 22.4\text{ dm}^3\text{mol}^{-1} = 4.48\text{ dm}^3
At standard temperature and pressure (STP), one mole of any gas occupies 22.4 dm322.4\text{ dm}^3.

Key Concept

Mass-Volume stoichiometric calculation at STP
Question 484Question

In a Young's double-slit experiment, the separation between two narrow slits is 0.40 mm0.40\text{ mm} and the interference pattern is observed on a screen placed 1.20 m1.20\text{ m} away from the slits. If the distance between consecutive bright fringes on the screen is 1.80 mm1.80\text{ mm}, what is the wavelength of the light used in nanometers (nm\text{nm})?

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Answer: 600

Answer

The wavelength of the light used is 600 nm600\text{ nm}.
Using the Young's double-slit fringe spacing relation β=λDd\beta = \frac{\lambda D}{d}, rearranging yields λ=βdD\lambda = \frac{\beta d}{D}. Substituting β=1.80×103 m\beta = 1.80 \times 10^{-3}\text{ m}, d=4.0×104 md = 4.0 \times 10^{-4}\text{ m}, and D=1.20 mD = 1.20\text{ m} gives λ=6.00×107 m\lambda = 6.00 \times 10^{-7}\text{ m}, which corresponds to 600 nm600\text{ nm}.

Step-by-Step Solution

1
Convert given physical quantities into standard SI units (meters).
Slit separation d=0.40 mm=4.0×104 md = 0.40\text{ mm} = 4.0 \times 10^{-4}\text{ m}, distance to screen D=1.20 mD = 1.20\text{ m}, and fringe spacing β=1.80 mm=1.80×103 m\beta = 1.80\text{ mm} = 1.80 \times 10^{-3}\text{ m}.
Standard SI units ensure accuracy when applying wave speed and distance equations.
2
Write the Young's double-slit formula relating fringe width to wavelength.
\(\beta = \frac{\lambda D}{d}\)
This relationship defines the spatial period of interference fringes on a screen.
3
Rearrange the equation to isolate the wavelength λ\lambda.
\(\lambda = \frac{\beta d}{D}\)
The unknown parameter to solve for is the wavelength of the monochromatic source.
4
Substitute the numerical values and convert the final result to nanometers.
\(\lambda = \frac{1.80 \times 10^{-3}\text{ m} \times 4.0 \times 10^{-4}\text{ m}}{1.20\text{ m}} = 6.00 \times 10^{-7}\text{ m} = 600\text{ nm}\)
Multiply meters by 10910^9 to express the wavelength in nanometers.

Key Concept

Young's Double-Slit Interference Fringe Spacing
Question 485Question

In a metre bridge experiment, a standard resistor of 4.0 Ω4.0\text{ }\Omega is connected in the left gap and an unknown resistor RR is connected in the right gap. When balanced, the balance point is found at a distance of 40.0 cm40.0\text{ cm} from the left end of the 100.0 cm100.0\text{ cm} bridge wire. What is the value of the unknown resistance RR in ohms?

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Answer: 6

Answer

The value of the unknown resistance RR is 6.0 Ω6.0\text{ }\Omega.
The metre bridge operates on the Wheatstone bridge principle. At balance, the ratio of the resistance in the left gap to the length of the left segment equals the ratio of the resistance in the right gap to the length of the right segment. Substituting 4.0 Ω4.0\text{ }\Omega for the left gap and 40.0 cm40.0\text{ cm} and 60.0 cm60.0\text{ cm} for the two wire lengths yields R=6.0 ΩR = 6.0\text{ }\Omega.

Step-by-Step Solution

1
Determine the length of the wire segment corresponding to the right gap.
l2=100.0 cm40.0 cm=60.0 cml_2 = 100.0\text{ cm} - 40.0\text{ cm} = 60.0\text{ cm}.
The total length of a standard metre bridge wire is 100.0 cm100.0\text{ cm}.
2
Apply the Wheatstone bridge principle for the metre bridge balance condition.
Rleftl1=Rl2    R=Rleft×l2l1\frac{R_{\text{left}}}{l_1} = \frac{R}{l_2} \implies R = R_{\text{left}} \times \frac{l_2}{l_1}.
At balance, the potential drop per unit length across the two wire segments is proportional to their respective lengths.
3
Calculate the magnitude of the unknown resistor RR.
R=4.0×60.040.0=6.0 ΩR = 4.0 \times \frac{60.0}{40.0} = 6.0\text{ }\Omega.
Multiplying and simplifying yields the exact resistance value.

Key Concept

Metre Bridge Principle (Wheatstone Bridge)
Question 486Question

Monochromatic light of wavelength 600 nm600\text{ nm} is incident normally on a diffraction grating having 500 lines per mm500\text{ lines per mm}. What is the angle of diffraction, in degrees, for the first-order principal maximum?

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Answer: 17.5

Answer

The angle of diffraction for the first-order principal maximum is 17.517.5^\circ.
Using the grating equation dsinθ=nλd \sin \theta = n \lambda, the slit separation is d=103 m500=2.00×106 md = \frac{10^{-3}\text{ m}}{500} = 2.00 \times 10^{-6}\text{ m}. For n=1n = 1 and λ=6.00×107 m\lambda = 6.00 \times 10^{-7}\text{ m}, we get sinθ=6.00×1072.00×106=0.30\sin \theta = \frac{6.00 \times 10^{-7}}{2.00 \times 10^{-6}} = 0.30. Taking arcsin(0.30)\arcsin(0.30) gives approximately 17.517.5^\circ.

Step-by-Step Solution

1
Calculate the grating element (slit spacing) dd
d=2.00×106 md = 2.00 \times 10^{-6}\text{ m}
Grating spacing dd is the reciprocal of the line density N=500 lines/mm=500,000 lines/mN = 500\text{ lines/mm} = 500,000\text{ lines/m}.
2
Apply the diffraction grating equation dsinθ=nλd \sin \theta = n \lambda
sinθ=0.30\sin \theta = 0.30
For the first-order maximum (n=1n = 1), sinθ=1×600×109 m2.00×106 m=0.30\sin \theta = \frac{1 \times 600 \times 10^{-9}\text{ m}}{2.00 \times 10^{-6}\text{ m}} = 0.30.
3
Find the angle θ\theta by taking the inverse sine
θ=17.5\theta = 17.5^\circ
arcsin(0.30)17.46\arcsin(0.30) \approx 17.46^\circ, which rounds to 17.517.5^\circ.

Key Concept

Diffraction Grating Equation for Principal Maxima
Estimated Time:1m 30s
Question 487Question

A DC supply with an electromotive force (e.m.f.) of 24.0 V24.0\text{ V} and an internal resistance of 2.0 Ω2.0\text{ }\Omega is connected across three identical 12.0 Ω12.0\text{ }\Omega resistors connected in parallel. What is the terminal potential difference across the battery in volts?

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Answer: 16

Answer

The terminal potential difference across the battery is 16.0 V16.0\text{ V}.
The three identical 12.0 Ω12.0\text{ }\Omega resistors in parallel combine to yield an equivalent external resistance of 4.0 Ω4.0\text{ }\Omega. Adding the battery's internal resistance of 2.0 Ω2.0\text{ }\Omega gives a total circuit resistance of 6.0 Ω6.0\text{ }\Omega. The total current drawn from the battery is I=24.0 V6.0 Ω=4.0 AI = \frac{24.0\text{ V}}{6.0\text{ }\Omega} = 4.0\text{ A}. The terminal potential difference is the voltage drop across the external circuit, V=4.0 A×4.0 Ω=16.0 VV = 4.0\text{ A} \times 4.0\text{ }\Omega = 16.0\text{ V}.

Step-by-Step Solution

1
Find the equivalent external resistance of the three parallel resistors.
Rp=4.0 ΩR_p = 4.0\text{ }\Omega
Three identical resistors R=12.0 ΩR = 12.0\text{ }\Omega connected in parallel have an equivalent resistance of Rp=12.03=4.0 ΩR_p = \frac{12.0}{3} = 4.0\text{ }\Omega.
2
Find the total circuit resistance by adding internal resistance to the parallel combination.
Rtotal=6.0 ΩR_{total} = 6.0\text{ }\Omega
Internal resistance r=2.0 Ωr = 2.0\text{ }\Omega acts in series with the external parallel combination: Rtotal=Rp+r=4.0+2.0=6.0 ΩR_{total} = R_p + r = 4.0 + 2.0 = 6.0\text{ }\Omega.
3
Calculate the total current supplied by the cell.
I=4.0 AI = 4.0\text{ A}
Using the circuit formula I=ERtotalI = \frac{E}{R_{total}}, we divide the e.m.f. of 24.0 V24.0\text{ V} by the total resistance of 6.0 Ω6.0\text{ }\Omega.
4
Compute the terminal potential difference across the cell.
V=16.0 VV = 16.0\text{ V}
The potential drop across the external parallel network is V=IRp=4.0 A×4.0 Ω=16.0 VV = I R_p = 4.0\text{ A} \times 4.0\text{ }\Omega = 16.0\text{ V}, which equals EIr=24.0 V(4.0 A×2.0 Ω)=16.0 VE - Ir = 24.0\text{ V} - (4.0\text{ A} \times 2.0\text{ }\Omega) = 16.0\text{ V}.

Key Concept

Terminal Potential Difference and Internal Resistance
Estimated Time:1m 30s
Question 488Question

The solubility of copper(II) tetraoxosulfate(VI), CuSO4\text{CuSO}_4, at 60C60^\circ\text{C} and 20C20^\circ\text{C} is 40.0 g40.0\text{ g} and 21.0 g21.0\text{ g} per 100 g100\text{ g} of water respectively. Calculate the mass of CuSO4\text{CuSO}_4 in grams that will crystallize out of solution when a saturated solution containing 250 g250\text{ g} of water is cooled from 60C60^\circ\text{C} to 20C20^\circ\text{C}.

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Answer: 47.5

Answer

The mass of CuSO4\text{CuSO}_4 that crystallizes out of solution is 47.5 g47.5\text{ g}.
Subtracting the solubility at 20C20^\circ\text{C} (21.0 g21.0\text{ g}) from the solubility at 60C60^\circ\text{C} (40.0 g40.0\text{ g}) yields 19.0 g19.0\text{ g} of CuSO4\text{CuSO}_4 deposited per 100 g100\text{ g} of water. Multiplying by the ratio of actual solvent mass to reference solvent mass (250 g/100 g=2.5250\text{ g} / 100\text{ g} = 2.5) gives 47.5 g47.5\text{ g}.

Step-by-Step Solution

1
Determine the mass of CuSO4\text{CuSO}_4 deposited per 100 g100\text{ g} of water on cooling.
40.0 g21.0 g=19.0 g40.0\text{ g} - 21.0\text{ g} = 19.0\text{ g} per 100 g100\text{ g} of water.
The mass of solute precipitated per 100 g100\text{ g} of solvent is equal to the difference in solubility between the higher and lower temperatures.
2
Calculate the mass of solute deposited for 250 g250\text{ g} of water.
19.0 g×250 g100 g=47.5 g19.0\text{ g} \times \frac{250\text{ g}}{100\text{ g}} = 47.5\text{ g}.
The amount of solute crystallized out is directly proportional to the total mass of solvent present.

Key Concept

Crystallization and Mass of Solute Deposited on Cooling
Question 489Question

An electric iron rated at 1200W1200\,\text{W} is operated for 5hours5\,\text{hours} each day for a period of 30days30\,\text{days}. If electrical energy costs 20.00\text{₦}20.00 per kilowatt-hour (kWh\text{kWh}), what is the total cost of electricity consumed by the iron over this period in Naira (\text{₦})?

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Answer: 3600

Answer

The total cost of electricity consumed by the iron over the 30-day period is 3600 Naira.
To find the cost of electrical energy in commercial units, express power in kilowatts (1.2kW1.2\,\text{kW}) and time in total hours (150h150\,\text{h}). The energy consumed is 1.2×150=180kWh1.2 \times 150 = 180\,\text{kWh}. At a tariff of 20.00\text{₦}20.00 per kWh\text{kWh}, the total cost is 180×20=3600Naira180 \times 20 = 3600\,\text{Naira}.

Step-by-Step Solution

1
Convert the power rating of the appliance from watts to kilowatts
P=1200W1000=1.2kWP = \frac{1200\,\text{W}}{1000} = 1.2\,\text{kW}
Commercial energy consumption is calculated in kilowatt-hours (kWh), requiring power in kilowatts.
2
Calculate the total operating time in hours
t=5hours/day×30days=150hourst = 5\,\text{hours/day} \times 30\,\text{days} = 150\,\text{hours}
The usage duration across the month must be expressed in total hours.
3
Determine electrical energy consumed in kWh
E=P×t=1.2kW×150h=180kWhE = P \times t = 1.2\,\text{kW} \times 150\,\text{h} = 180\,\text{kWh}
Energy is the product of power in kilowatts and time in hours.
4
Calculate total cost of energy consumed
Total Cost=180kWh×20.00/kWh=3600\text{Total Cost} = 180\,\text{kWh} \times \text{₦}20.00/\text{kWh} = \text{₦}3600
Total cost is found by multiplying energy in kWh by the unit tariff rate.

Key Concept

Commercial electrical energy unit (kWh) and billing calculation
Question 490Question

A rigid metallic cylinder contains a fixed mass of gas at an initial pressure of 1.2 atm1.2\text{ atm} and a temperature of 27C27^\circ\text{C}. If the gas is heated until its temperature reaches 177C177^\circ\text{C} while the volume remains constant, what is the final pressure of the gas in atmospheres?

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Answer: 1.8

Answer

The final pressure of the gas is 1.8 atm1.8\text{ atm}.
Converting the temperatures to Kelvin (T1=300 KT_1 = 300\text{ K} and T2=450 KT_2 = 450\text{ K}) and applying Gay-Lussac's Pressure Law P1T1=P2T2\frac{P_1}{T_1} = \frac{P_2}{T_2} gives P2=1.2×450300=1.8 atmP_2 = 1.2 \times \frac{450}{300} = 1.8\text{ atm}.

Step-by-Step Solution

1
Convert given temperatures to the Kelvin scale
T1=300 KT_1 = 300\text{ K} and T2=450 KT_2 = 450\text{ K}
Gas laws require absolute temperature values measured in Kelvin (TK=tC+273T_K = t_C + 273).
2
Set up Gay-Lussac's Pressure Law proportion P1T1=P2T2\frac{P_1}{T_1} = \frac{P_2}{T_2}
P2=P1×T2T1=1.2×450300P_2 = P_1 \times \frac{T_2}{T_1} = 1.2 \times \frac{450}{300}
At constant volume, the pressure of a fixed mass of gas is directly proportional to its absolute temperature.
3
Perform the multiplication to determine the final pressure
P2=1.8 atmP_2 = 1.8\text{ atm}
Multiplying 1.21.2 by the ratio 1.51.5 yields 1.8 atm1.8\text{ atm}.

Key Concept

Pressure Law (Gay-Lussac's Law) states that for a given mass of gas at constant volume, the pressure is directly proportional to its absolute temperature in Kelvin (PTP \propto T).
Question 491Question

Chief Kalu insured his commercial supermarket building, valued at N50,000,000\text{N}50,000,000, against fire for a sum of N35,000,000\text{N}35,000,000. The policy contains an average clause. If a fire outbreak damages the building causing a loss of N10,000,000\text{N}10,000,000, what amount in Naira will the insurance company pay as indemnity?

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Answer: 7000000

Answer

7,000,000 Naira
Under the average clause in fire insurance policies, if a property is under-insured (insured for less than its true value), the insured is deemed to be their own insurer for the uninsured portion. Here, the building was insured for 70% of its full value (N35,000,000 / N50,000,000 = 0.70). Therefore, the insurance company pays only 70% of the actual loss incurred (70% of N10,000,000 = 7,000,000 Naira).

Step-by-Step Solution

1
Identify the property values given in the problem statement.
Actual Value = N50,000,000; Sum Insured = N35,000,000; Actual Loss = N10,000,000.
These figures are required to calculate indemnity under under-insurance.
2
Apply the average clause compensation formula.
Compensation = (Sum Insured / Actual Value) * Actual Loss
When property is insured for less than its full value and has an average clause, the insurer pays only a proportionate share of any loss.
3
Calculate the compensation payable.
Compensation = (35,000,000 / 50,000,000) * 10,000,000 = 7,000,000 Naira.
Since the owner insured 70% of the building's value, the insurer pays 70% of the actual loss suffered.

Key Concept

Average Clause in Insurance
Question 492Question

At a magnetic observation station, the horizontal component of the Earth's magnetic field is 40 μT40\text{ }\mu\text{T} and the vertical component is 30 μT30\text{ }\mu\text{T}. What is the total magnetic field intensity of the Earth at this station in μT\mu\text{T}?

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Answer: 50

Answer

The total magnetic field intensity of the Earth at this station is 50 μT50\text{ }\mu\text{T}.
The horizontal component (BhB_h) and vertical component (BvB_v) of the Earth's magnetic field act at right angles to each other. Therefore, the resultant total magnetic field intensity (BB) is calculated using vector addition: B=Bh2+Bv2=402+302=50 μTB = \sqrt{B_h^2 + B_v^2} = \sqrt{40^2 + 30^2} = 50\text{ }\mu\text{T}.

Step-by-Step Solution

1
Identify the vector relationship between the horizontal and vertical components of the Earth's magnetic field.
B=Bh2+Bv2B = \sqrt{B_h^2 + B_v^2}, where Bh=40 μTB_h = 40\text{ }\mu\text{T} and Bv=30 μTB_v = 30\text{ }\mu\text{T}.
The horizontal and vertical components of the Earth's magnetic field are mutually perpendicular vector components.
2
Substitute the values into the formula and solve for total magnetic field intensity BB.
B=(40)2+(30)2=1600+900=2500=50 μTB = \sqrt{(40)^2 + (30)^2} = \sqrt{1600 + 900} = \sqrt{2500} = 50\text{ }\mu\text{T}.
Applying the Pythagorean theorem yields the magnitude of the resultant magnetic field vector.

Key Concept

Resolution of Earth's magnetic field into horizontal (BhB_h) and vertical (BvB_v) components.
Estimated Time:1m 0s
Question 493Question

A rigid container holds a gas mixture containing 4.0 g4.0\text{ g} of methane (CH4\text{CH}_4) and 14.0 g14.0\text{ g} of nitrogen (N2\text{N}_2). If the partial pressure exerted by methane in the mixture is 125 kPa125\text{ kPa}, what is the total pressure of the gas mixture in kPa\text{kPa}? [Relative atomic masses: H=1\text{H} = 1, C=12\text{C} = 12, N=14\text{N} = 14]

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Answer: 375

Answer

The total pressure of the gas mixture is 375 kPa375\text{ kPa}.
The total pressure of 375 kPa375\text{ kPa} is determined by calculating the moles of methane (0.25 mol0.25\text{ mol}) and nitrogen (0.50 mol0.50\text{ mol}), giving a total of 0.75 mol0.75\text{ mol}. Methane constitutes one-third (1/31/3) of the total moles, so its partial pressure is one-third of the total pressure. Dividing the partial pressure of methane (125 kPa125\text{ kPa}) by its mole fraction (1/31/3) yields a total pressure of 375 kPa375\text{ kPa}.

Step-by-Step Solution

1
Calculate the amount of moles of each gas present in the mixture.
nCH4=4.0 g16 g/mol=0.25 moln_{\text{CH}_4} = \frac{4.0\text{ g}}{16\text{ g/mol}} = 0.25\text{ mol} and nN2=14.0 g28 g/mol=0.50 moln_{\text{N}_2} = \frac{14.0\text{ g}}{28\text{ g/mol}} = 0.50\text{ mol}.
Molar masses are determined from relative atomic masses: CH4=12+4(1)=16 g/mol\text{CH}_4 = 12 + 4(1) = 16\text{ g/mol} and N2=2(14)=28 g/mol\text{N}_2 = 2(14) = 28\text{ g/mol}.
2
Calculate total moles and the mole fraction of methane.
ntotal=0.25+0.50=0.75 moln_{\text{total}} = 0.25 + 0.50 = 0.75\text{ mol}; XCH4=0.25 mol0.75 mol=13X_{\text{CH}_4} = \frac{0.25\text{ mol}}{0.75\text{ mol}} = \frac{1}{3}.
Mole fraction is the ratio of the number of moles of a specific gas component to the total number of moles in the gas mixture.
3
Apply Dalton's Law of Partial Pressures to find total pressure.
Ptotal=PCH4XCH4=125 kPa1/3=375 kPaP_{\text{total}} = \frac{P_{\text{CH}_4}}{X_{\text{CH}_4}} = \frac{125\text{ kPa}}{1/3} = 375\text{ kPa}.
According to Dalton's Law, the partial pressure of a gas is equal to its mole fraction multiplied by the total pressure (Pi=Xi×PtotalP_i = X_i \times P_{\text{total}}).

Key Concept

Dalton's Law of Partial Pressures and Mole Fraction
Estimated Time:1m 30s
Question 494Question

The solubility of potassium trioxonitrate(V), KNO3\text{KNO}_3, in water at 40C40^\circ\text{C} is 6.0 mol dm36.0\text{ mol dm}^{-3}. What mass of KNO3\text{KNO}_3, in grams, is required to prepare a saturated solution in 250 cm3250\text{ cm}^3 of water at this temperature? (Molar mass of KNO3=101 g mol1\text{KNO}_3 = 101\text{ g mol}^{-1})

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Answer: 151.5

Answer

The mass of KNO3\text{KNO}_3 required to prepare a saturated solution in 250 cm3250\text{ cm}^3 of water at 40C40^\circ\text{C} is 151.5 g151.5\text{ g}.
To find the mass of solute required for saturation, convert the given volume of water to cubic decimeters (250 cm3=0.25 dm3250\text{ cm}^3 = 0.25\text{ dm}^3). Multiply the volume by the molar solubility (6.0 mol dm3×0.25 dm3=1.5 mol6.0\text{ mol dm}^{-3} \times 0.25\text{ dm}^3 = 1.5\text{ mol}) to obtain the number of moles, then multiply by the molar mass (1.5 mol×101 g mol1=151.5 g1.5\text{ mol} \times 101\text{ g mol}^{-1} = 151.5\text{ g}).

Step-by-Step Solution

1
Convert volume from cm3\text{cm}^3 to dm3\text{dm}^3
0.25 dm30.25\text{ dm}^3
Molar solubility is expressed per dm3\text{dm}^3, so the volume of solvent must be in dm3\text{dm}^3.
2
Determine moles of KNO3\text{KNO}_3 needed for saturation
1.5 mol1.5\text{ mol}
Multiply molar solubility by the volume in dm3\text{dm}^3.
3
Convert moles to mass in grams
151.5 g151.5\text{ g}
Multiply moles by the molar mass of KNO3\text{KNO}_3 (101 g mol1101\text{ g mol}^{-1}).

Key Concept

Calculating solute mass for saturation using molar solubility and volume
Question 495Question

A naturally occurring sample of neon gas consists of 90%90\% 20Ne^{20}\text{Ne} and 10%10\% 22Ne^{22}\text{Ne}. What is the relative atomic mass of neon in this sample?

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Answer: 20.2

Answer

The relative atomic mass of neon in the sample is 20.2.
The relative atomic mass of an element is calculated by summing the products of the mass number of each isotope and its fractional abundance: RAM=(20×0.90)+(22×0.10)=18.0+2.2=20.2\text{RAM} = (20 \times 0.90) + (22 \times 0.10) = 18.0 + 2.2 = 20.2.

Step-by-Step Solution

1
Calculate the weighted contribution of 20Ne^{20}\text{Ne}
20×0.90=18.020 \times 0.90 = 18.0
The isotope 20Ne^{20}\text{Ne} accounts for 90%90\% of the sample.
2
Calculate the weighted contribution of 22Ne^{22}\text{Ne}
22×0.10=2.222 \times 0.10 = 2.2
The isotope 22Ne^{22}\text{Ne} accounts for 10%10\% of the sample.
3
Sum the weighted contributions to find the relative atomic mass
18.0+2.2=20.218.0 + 2.2 = 20.2
The relative atomic mass is the weighted average of the atomic masses of naturally occurring isotopes.

Key Concept

Calculation of Relative Atomic Mass from Isotopic Abundance
Question 496Question

A solution of a monoprotic acid HXHX contains 3.65 g dm33.65\text{ g dm}^{-3} of the acid. If 25.0 cm325.0\text{ cm}^3 of this acid solution neutralizes 20.0 cm320.0\text{ cm}^3 of a 0.125 mol dm30.125\text{ mol dm}^{-3} sodium hydroxide (NaOH\text{NaOH}) solution, what is the molar mass of the acid HXHX in g mol3\text{g mol}^{-3}?

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Answer: 36.5

Answer

The molar mass of the acid HXHX is 36.5 g mol336.5\text{ g mol}^{-3}.
The reaction of monoprotic acid HXHX with NaOH\text{NaOH} follows a 1:1 stoichiometric ratio. Applying the titration formula CaVaCbVb=1\frac{C_a V_a}{C_b V_b} = 1 yields an acid concentration of 0.100 mol dm30.100\text{ mol dm}^{-3}. Dividing the mass concentration of 3.65 g dm33.65\text{ g dm}^{-3} by this molarity gives a molar mass of 36.5 g mol336.5\text{ g mol}^{-3}.

Step-by-Step Solution

1
Determine the stoichiometric mole ratio between acid and base.
The mole ratio na:nbn_a : n_b for HXHX reacting with NaOH\text{NaOH} is 1:11 : 1.
A monoprotic acid donates one proton per molecule to react with one mole of sodium hydroxide.
2
Calculate the molar concentration of the acid (CaC_a).
Ca=0.125 mol dm3×20.0 cm325.0 cm3=0.100 mol dm3C_a = \frac{0.125\text{ mol dm}^{-3} \times 20.0\text{ cm}^3}{25.0\text{ cm}^3} = 0.100\text{ mol dm}^{-3}.
Using the titration relation CaVaCbVb=nanb\frac{C_a V_a}{C_b V_b} = \frac{n_a}{n_b} allows determination of the acid molarity.
3
Calculate the molar mass of the acid.
Molar mass=Mass concentrationMolarity=3.65 g dm30.100 mol dm3=36.5 g mol3\text{Molar mass} = \frac{\text{Mass concentration}}{\text{Molarity}} = \frac{3.65\text{ g dm}^{-3}}{0.100\text{ mol dm}^{-3}} = 36.5\text{ g mol}^{-3}.
Molar mass is defined as mass of substance per mole.

Key Concept

Determination of molar mass using volumetric titration stoichiometry
Estimated Time:1m 30s
Question 497Question
Consider the redox reaction between dichromate ions (Cr2O72\text{Cr}_2\text{O}_7^{2-}) and iron(II) ions (Fe2+\text{Fe}^{2+}) in an acidic medium:
Cr2O72+xFe2++yH+2Cr3++xFe3++zH2O\text{Cr}_2\text{O}_7^{2-} + x\text{Fe}^{2+} + y\text{H}^+ \rightarrow 2\text{Cr}^{3+} + x\text{Fe}^{3+} + z\text{H}_2\text{O}
What is the stoichiometric coefficient xx of Fe2+\text{Fe}^{2+} when the ionic equation is completely balanced?
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Answer: 6

Answer

The stoichiometric coefficient x of Fe²⁺ in the balanced redox reaction is 6.
In the reduction half-reaction, dichromate (Cr2O72\text{Cr}_2\text{O}_7^{2-}) contains two Cr atoms in the +6 oxidation state converting to two Cr3+\text{Cr}^{3+} ions in the +3 state, which consumes 6 electrons. In the oxidation half-reaction, each Fe2+\text{Fe}^{2+} ion loses 1 electron to form Fe3+\text{Fe}^{3+}. To balance charge transfer, 6 Fe2+\text{Fe}^{2+} ions are needed for every 1 Cr2O72\text{Cr}_2\text{O}_7^{2-} ion, making the stoichiometric coefficient xx equal to 6.

Step-by-Step Solution

1
Determine the oxidation state changes for Chromium and Iron.
Chromium changes from +6 in Cr2O72\text{Cr}_2\text{O}_7^{2-} to +3 in Cr3+\text{Cr}^{3+}, requiring 3 electrons per Chromium atom (6e6e^- total for two Cr atoms). Iron changes from +2 in Fe2+\text{Fe}^{2+} to +3 in Fe3+\text{Fe}^{3+}, releasing 1e1e^- per Iron atom.
Identifying the number of electrons transferred in each half-reaction is required to balance the overall redox equation.
2
Balance the electron gain and loss.
The oxidation half-reaction (Fe2+Fe3++e\text{Fe}^{2+} \rightarrow \text{Fe}^{3+} + e^-) must be multiplied by 6 to balance the 6 electrons required by the dichromate ion.
The total number of electrons lost by the reducing agent must equal the total number of electrons gained by the oxidizing agent.
3
Combine the half-reactions and read the coefficient xx.
The balanced chemical equation is Cr2O72+6Fe2++14H+2Cr3++6Fe3++7H2O\text{Cr}_2\text{O}_7^{2-} + 6\text{Fe}^{2+} + 14\text{H}^+ \rightarrow 2\text{Cr}^{3+} + 6\text{Fe}^{3+} + 7\text{H}_2\text{O}, giving x=6x = 6.
The coefficient xx corresponds directly to the stoichiometric multiplier applied to Fe2+\text{Fe}^{2+}.

Key Concept

Balancing Redox Equations via Half-Reactions in Acidic Medium
Question 498Question

A galvanic cell is constructed under standard conditions using the following two reduction half-reactions:

Fe(aq)3++eFe(aq)2+,E=+0.77 V\text{Fe}^{3+}_{\text{(aq)}} + \text{e}^- \rightarrow \text{Fe}^{2+}_{\text{(aq)}}, \quad E^\circ = +0.77\text{ V}
Sn(aq)4++2eSn(aq)2+,E=+0.15 V\text{Sn}^{4+}_{\text{(aq)}} + 2\text{e}^- \rightarrow \text{Sn}^{2+}_{\text{(aq)}}, \quad E^\circ = +0.15\text{ V}

What is the standard cell potential (EcellE^\circ_{\text{cell}}) in volts for the spontaneous overall reaction?

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Answer: 0.62

Answer

The standard cell potential for the spontaneous reaction is +0.62 V.
In a spontaneous galvanic cell, reduction takes place at the cathode, which is the electrode with the higher standard reduction potential (+0.77 V for Fe3+/Fe2+\text{Fe}^{3+}/\text{Fe}^{2+}). Oxidation occurs at the anode (+0.15 V for Sn4+/Sn2+\text{Sn}^{4+}/\text{Sn}^{2+}). Substituting these values into Ecell=EcathodeEanodeE^\circ_{\text{cell}} = E^\circ_{\text{cathode}} - E^\circ_{\text{anode}} yields +0.77 V(+0.15 V)=+0.62 V+0.77\text{ V} - (+0.15\text{ V}) = +0.62\text{ V}.

Step-by-Step Solution

1
Identify the cathode and anode based on standard reduction potentials.
Cathode: Fe3+/Fe2+ half-cell (E° = +0.77 V); Anode: Sn4+/Sn2+ half-cell (E° = +0.15 V).
In a spontaneous galvanic cell, reduction occurs at the electrode with the more positive standard reduction potential.
2
Apply the standard electromotive force equation.
E°cell = E°cathode - E°anode = +0.77 V - (+0.15 V) = +0.62 V
The cell potential measures the overall potential difference between the reduction half-cell and oxidation half-cell.

Key Concept

Standard Cell Potential Calculation
Estimated Time:1m 30s
Question 499Question

A 1.5 mol1.5\text{ mol} sample of carbon dioxide gas (CO2\text{CO}_2) is held in a container of volume 0.60 dm30.60\text{ dm}^3 at a temperature of 300 K300\text{ K} under a pressure of 50 atm50\text{ atm}. What is the compressibility factor (ZZ) for the gas under these conditions? (Take R=0.082 atm dm3 mol1 K1R = 0.082\text{ atm dm}^3\text{ mol}^{-1}\text{ K}^{-1} and express your answer to two decimal places.)

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Answer: 0.81

Answer

The compressibility factor (Z) for carbon dioxide under these conditions is 0.81.
The compressibility factor ZZ is defined as Z=PVnRTZ = \frac{PV}{nRT}. Substituting the given values yields PV=50×0.60=30.0PV = 50 \times 0.60 = 30.0 and nRT=1.5×0.082×300=36.9nRT = 1.5 \times 0.082 \times 300 = 36.9. Dividing 30.030.0 by 36.936.9 yields approximately 0.810.81, which indicates negative deviation from ideality due to intermolecular attractive forces.

Step-by-Step Solution

1
Identify the given variables and the formula for the compressibility factor.
P=50 atmP = 50\text{ atm}, V=0.60 dm3V = 0.60\text{ dm}^3, n=1.5 moln = 1.5\text{ mol}, T=300 KT = 300\text{ K}, R=0.082 atm dm3 mol1 K1R = 0.082\text{ atm dm}^3\text{ mol}^{-1}\text{ K}^{-1}. Formula: Z=PVnRTZ = \frac{PV}{nRT}.
The compressibility factor ZZ measures the deviation of a real gas from ideal gas behavior (Z=1Z = 1 for an ideal gas).
2
Calculate the actual pressure-volume product (PVPV).
PV=50 atm×0.60 dm3=30.0 atm dm3PV = 50\text{ atm} \times 0.60\text{ dm}^3 = 30.0\text{ atm dm}^3.
This represents the numerator in the compressibility ratio.
3
Calculate the theoretical ideal pressure-volume product (nRTnRT).
nRT=1.5 mol×0.082 atm dm3 mol1 K1×300 K=36.9 atm dm3nRT = 1.5\text{ mol} \times 0.082\text{ atm dm}^3\text{ mol}^{-1}\text{ K}^{-1} \times 300\text{ K} = 36.9\text{ atm dm}^3.
This represents the expected PVPV value if the gas behaved ideally.
4
Compute the value of ZZ and round to two decimal places.
Z=30.036.90.81300.81Z = \frac{30.0}{36.9} \approx 0.8130 \rightarrow 0.81.
Dividing the observed PVPV by nRTnRT gives Z<1Z < 1, indicating that intermolecular attractive forces dominate under these conditions.

Key Concept

Compressibility factor Z of real gases
Question 500Question

Meridian Logistics Plc was registered with an authorized share capital of 5,000,0005,000,000 ordinary shares of 1.50\text{₦}1.50 each. The directors issued 3,000,0003,000,000 shares to the public and called up 1.00\text{₦}1.00 per share. If all called-up funds were received except a call of 0.20\text{₦}0.20 per share on 150,000150,000 shares, calculate the total paid-up share capital of the company in Naira.

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Answer: 2970000

Answer

The paid-up capital of Meridian Logistics Plc is ₦2,970,000.
Paid-up capital represents the actual cash received from shareholders for called-up shares. The called-up capital is 3,000,000 shares×1.00=3,000,0003,000,000 \text{ shares} \times \text{₦}1.00 = \text{₦}3,000,000. Calls in arrears are 150,000 shares×0.20=30,000150,000 \text{ shares} \times \text{₦}0.20 = \text{₦}30,000. Deducting calls in arrears from called-up capital gives 3,000,00030,000=2,970,000\text{₦}3,000,000 - \text{₦}30,000 = \text{₦}2,970,000.

Step-by-Step Solution

1
Calculate Total Called-up Capital
₦3,000,000
Multiply issued shares by called-up value per share (3,000,000 shares × ₦1.00).
2
Calculate Calls in Arrears
₦30,000
Multiply defaulting shares by unpaid call per share (150,000 shares × ₦0.20).
3
Compute Paid-up Capital
₦2,970,000
Subtract Calls in Arrears from Total Called-up Capital (₦3,000,000 - ₦30,000).

Key Concept

Classification of Share Capital - Paid-up Capital Calculation
Estimated Time:1m 30s
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