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Question 8141Question

The electromagnetic spectrum consists of waves with varying frequencies, wavelengths, and photon energies, each associated with distinct physical detection mechanisms and applications. Consider the following types of electromagnetic radiation:

I. Radiation emitted by warm bodies, primarily detected using a thermopile.
II. Radiation utilized in radar systems and satellite communications.
III. Radiation emitted during nuclear decay processes, detected using a Geiger-Müller counter.
IV. Radiation responsible for sun tanning and detected by its ability to induce fluorescence on zinc sulfide screens.

Arrange these four types of electromagnetic radiation in order of increasing photon energy (from lowest photon energy to highest photon energy).

Drag items to arrange them in the correct order

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Answer

The correct sequence in order of increasing photon energy is: Radiation utilized in radar systems (Microwaves) < Radiation emitted by warm bodies (Infrared) < Radiation causing sun tanning (Ultraviolet) < Radiation emitted during nuclear decay (Gamma rays).
Microwaves possess the lowest frequency among the four types, followed by infrared radiation, then ultraviolet radiation, and finally gamma rays which possess the highest frequency and photon energy.

Step-by-Step Solution

1
Identify the region of the electromagnetic spectrum corresponding to each property and detector described.
Item I corresponds to Infrared radiation; Item II corresponds to Microwaves; Item III corresponds to Gamma rays; Item IV corresponds to Ultraviolet radiation.
Thermopiles detect thermal radiation (IR); radar uses microwaves; Geiger-Müller counters detect nuclear ionizing radiation (Gamma rays); fluorescence on ZnS is caused by UV light.
2
Relate photon energy EE to frequency ff and wavelength λ\lambda using Planck's relation E=hf=hcλE = hf = \frac{hc}{\lambda}.
Photon energy is directly proportional to frequency (EfE \propto f) and inversely proportional to wavelength (E1λE \propto \frac{1}{\lambda}).
Higher frequency radiation consists of more energetic individual photons.
3
Sequence the identified electromagnetic waves from lowest frequency to highest frequency.
Microwaves (f1091011 Hzf \approx 10^9 - 10^{11}\text{ Hz}) < Infrared (f10114×1014 Hzf \approx 10^{11} - 4 \times 10^{14}\text{ Hz}) < Ultraviolet (f7.5×10143×1016 Hzf \approx 7.5 \times 10^{14} - 3 \times 10^{16}\text{ Hz}) < Gamma rays (f>1019 Hzf > 10^{19}\text{ Hz}).
This sequence reflects the fundamental order of increasing photon energy across the spectrum.

Key Concept

Electromagnetic Spectrum Spectral Regions, Detection Devices, and Photon Energy Ordering
Question 8142Question

A quality control analyst evaluated a synthesized sample of benzoic acid using thin-layer chromatography. The solvent front advanced 10.0 cm10.0\text{ cm} from the origin line, while the compound produced a single distinct spot that moved 7.5 cm7.5\text{ cm}. What is the retardation factor (RfR_f) of the compound, and what does the result reveal about the purity of the sample?

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Answer: Rf=0.75R_f = 0.75, indicating that the sample is pure.

Answer

The retardation factor is Rf=0.75R_f = 0.75, and the single chromatogram spot confirms that the sample is pure.
Calculating the retardation factor gives Rf=7.5 cm10.0 cm=0.75R_f = \frac{7.5\text{ cm}}{10.0\text{ cm}} = 0.75. In paper or thin-layer chromatography, pure substances yield a single spot under specified solvent conditions, confirming chemical purity.

Step-by-Step Solution

1
Calculate the retardation factor (RfR_f) using the chromatography ratio formula.
Rf=Distance moved by soluteDistance moved by solvent front=7.5 cm10.0 cm=0.75R_f = \frac{\text{Distance moved by solute}}{\text{Distance moved by solvent front}} = \frac{7.5\text{ cm}}{10.0\text{ cm}} = 0.75
The RfR_f value is the ratio of solute migration distance to solvent migration distance.
2
Interpret the number of spots on the chromatogram to assess purity.
A single distinct spot indicates only one component is present.
Impure samples produce multiple spots corresponding to different components in the mixture.

Key Concept

Criteria of Purity and Retardation Factor (RfR_f) Calculation
Estimated Time:1m 0s
Question 8143Question

Complete the following statement regarding manganese redox species by filling in the correct numerical oxidation states.

Fill in the blanks below

In potassium manganate(VI), K2MnO4K_2MnO_4, the oxidation state of the central manganese atom is , whereas in potassium tetraoxomanganate(VII), KMnO4KMnO_4, the oxidation state of manganese is .
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Answer

The oxidation state of manganese in K2MnO4K_2MnO_4 is +6, and in KMnO4KMnO_4 it is +7.
In potassium manganate(VI), K2MnO4K_2MnO_4, two potassium ions yield a +2+2 total charge and four oxide ions yield 8-8, requiring manganese to be +6+6 to balance to zero. In potassium tetraoxomanganate(VII), KMnO4KMnO_4, one potassium ion (+1+1) and four oxide ions (8-8) leave manganese at +7+7.

Step-by-Step Solution

1
Calculate the oxidation state of manganese in K2MnO4K_2MnO_4.
Assign standard oxidation numbers: K=+1K = +1 and O=2O = -2. For the neutral molecule K2MnO4K_2MnO_4, 2(+1)+Mn+4(2)=0    +2+Mn8=0    Mn=+62(+1) + \text{Mn} + 4(-2) = 0 \implies +2 + \text{Mn} - 8 = 0 \implies \text{Mn} = +6.
The sum of oxidation states in a neutral chemical compound must equal zero.
2
Calculate the oxidation state of manganese in KMnO4KMnO_4.
Assign standard oxidation numbers: K=+1K = +1 and O=2O = -2. For the neutral molecule KMnO4KMnO_4, 1(+1)+Mn+4(2)=0    +1+Mn8=0    Mn=+71(+1) + \text{Mn} + 4(-2) = 0 \implies +1 + \text{Mn} - 8 = 0 \implies \text{Mn} = +7.
The sum of oxidation states in a neutral chemical compound must equal zero.

Key Concept

Determining oxidation states of central transition metal atoms in oxoanions and neutral salts.
Question 8144Question

In the preparation of potassium ferrate, K2FeO4K_2FeO_4, elemental iron (FeFe) is oxidized in an alkaline medium. What is the change in the oxidation number of iron per atom during this reaction, and what is the systematic IUPAC name of K2FeO4K_2FeO_4?

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Answer: Increase of 6; potassium tetraoxoferrate(VI)

Answer

The oxidation number of iron increases by 6, and the systematic IUPAC name of K2FeO4K_2FeO_4 is potassium tetraoxoferrate(VI).
Free uncombined iron (FeFe) has an oxidation number of 00. In K2FeO4K_2FeO_4, potassium is +1+1 and oxygen is 2-2. Solving 2(+1)+Fe+4(2)=02(+1) + Fe + 4(-2) = 0 yields Fe=+6Fe = +6. The change in oxidation number is +60=+6+6 - 0 = +6. The polyatomic anion FeO42FeO_4^{2-} contains four oxo ligands attached to iron in the +6+6 oxidation state, making its systematic IUPAC name potassium tetraoxoferrate(VI).

Step-by-Step Solution

1
Determine the oxidation state of uncombined elemental iron (FeFe).
Oxidation state of Fe=0Fe = 0.
By IUPAC rules, elements in their free uncombined elemental state always have an oxidation number of zero.
2
Calculate the oxidation state of iron in K2FeO4K_2FeO_4.
Oxidation state of Fe=+6Fe = +6.
Potassium has an oxidation state of +1+1 and oxygen has 2-2. Setting up the charge balance equation: 2(+1)+Fe+4(2)=0    +2+Fe8=0    Fe=+62(+1) + Fe + 4(-2) = 0 \implies +2 + Fe - 8 = 0 \implies Fe = +6.
3
Calculate the change in oxidation number.
Change =+60=+6= +6 - 0 = +6 (an increase of 6).
The change in oxidation state is the final state minus the initial state.
4
Formulate the systematic IUPAC name for K2FeO4K_2FeO_4.
Potassium tetraoxoferrate(VI).
The salt consists of potassium cations and the polyatomic anion FeO42FeO_4^{2-}. With four oxygen atoms surrounding iron in oxidation state +6+6, the IUPAC name is potassium tetraoxoferrate(VI).

Key Concept

Determination of oxidation state changes from elemental forms and IUPAC Stock nomenclature of oxoanions
Question 8145Question

A student investigates two unlabelled water samples, XX and YY. Boiling sample XX eliminates its soap-consuming property, allowing it to lather readily, whereas sample YY continues to form scum with soap after boiling. Which solute present in sample YY accounts for its persistent hardness?

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Answer: Calcium tetraoxosulfate(VI)

Answer

Calcium tetraoxosulfate(VI) accounts for the persistent (permanent) water hardness in sample Y.
Permanent water hardness is caused by dissolved calcium tetraoxosulfate(VI) or magnesium chloride. These salts do not decompose upon heating, so boiling does not precipitate the metal ions responsible for consuming soap.

Step-by-Step Solution

1
Classify the type of hardness based on response to boiling.
Sample X exhibits temporary hardness because boiling removes its soap-consuming capability. Sample Y exhibits permanent hardness because boiling fails to remove its scum-forming property.
Temporary hardness is caused by hydrogen trioxocarbonates which decompose on boiling, whereas permanent hardness is caused by soluble sulfate or chloride salts of calcium or magnesium.
2
Identify the specific chemical species responsible for permanent hardness in sample Y.
Calcium tetraoxosulfate(VI) (CaSO4\text{CaSO}_4) remains dissolved after boiling.
Tetraoxosulfate(VI) ions do not undergo thermal decomposition at boiling temperatures to form insoluble precipitates.

Key Concept

Temporary vs. Permanent Water Hardness
Estimated Time:1m 0s
Question 8146Question

A liquid sample collected from a reaction vessel is tested in a laboratory and observed to boil continuously over a temperature range of 102C102^\circ\text{C} to 106C106^\circ\text{C} at standard atmospheric pressure. Which classification of matter best describes this sample?

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Answer: A mixture

Answer

The correct answer is a mixture, because impure substances and mixtures boil over a range of temperatures rather than at a distinct, sharp boiling point.
A liquid that boils over a temperature range rather than at a single, fixed temperature is impure and constitutes a mixture. Pure substances (both elements and compounds) have definite compositions and sharp boiling points.

Step-by-Step Solution

1
Analyze the physical behavior described in the question.
The liquid boils across a temperature range of 102C102^\circ\text{C} to 106C106^\circ\text{C}.
Determining whether a substance has a sharp or broad boiling point is a key test of chemical purity.
2
Apply the criteria of purity for elements, compounds, and mixtures.
Pure elements and compounds have fixed compositions and fixed, sharp boiling points. Mixtures contain varying amounts of components and therefore boil over a temperature range.
The presence of multiple substances in variable proportions alters the vapor pressure continuously during boiling.

Key Concept

Distinction between pure substances (elements and compounds) which have sharp boiling points, and mixtures which boil over a range of temperatures.
Question 8147Question

A sample of a radioactive nuclide has a half-life of 4 hours4\text{ hours}. What is the ratio of the number of nuclei that have decayed to the number of undecayed nuclei remaining after a total elapsed time of 16 hours16\text{ hours}?

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Answer: 15:115 : 1

Answer

The ratio of decayed nuclei to remaining undecayed nuclei is 15:115 : 1.
In an elapsed time of 16 hours16\text{ hours} (which is 44 half-lives), the remaining undecayed portion of the sample is (1/2)4=1/16(1/2)^4 = 1/16 of the original amount. Consequently, 11/16=15/161 - 1/16 = 15/16 of the nuclei have decayed. The ratio of decayed nuclei to remaining nuclei is (15/16):(1/16)=15:1(15/16) : (1/16) = 15 : 1.

Step-by-Step Solution

1
Determine the number of half-lives (nn) that have elapsed.
n=tT1/2=16 hours4 hours=4 half-livesn = \frac{t}{T_{1/2}} = \frac{16\text{ hours}}{4\text{ hours}} = 4\text{ half-lives}.
The number of half-lives is the total time divided by the half-life duration.
2
Calculate the fraction of original nuclei remaining undecayed (N/N0N/N_0).
NN0=(12)n=(12)4=116\frac{N}{N_0} = \left(\frac{1}{2}\right)^n = \left(\frac{1}{2}\right)^4 = \frac{1}{16}.
After nn half-lives, the remaining fraction is (1/2)n(1/2)^n.
3
Find the fraction of original nuclei that have decayed (Ndecayed/N0N_{\text{decayed}}/N_0).
\frac{N_{\text{decayed}}}{N_0} = 1 - \frac{N}{N_0} = 1 - \frac{1}{16} = \frac{15}{16}.
Decayed fraction equals total initial fraction (1) minus the undecayed fraction.
4
Compute the ratio of decayed nuclei to remaining undecayed nuclei.
\text{Ratio} = \frac{N_{\text{decayed}}}{N} = \frac{15/16}{1/16} = 15 : 1.
The question asks for the ratio of decayed nuclei to remaining undecayed nuclei.

Key Concept

Radioactive Decay Law and Half-life calculations involving ratios of decayed versus remaining quantities.
Question 8148Question

An alternating voltage source of root-mean-square (RMS) voltage 200 V200\ \text{V} is connected across a series combination of a resistor with resistance 60 Ω60\ \Omega and a capacitor with capacitive reactance 80 Ω80\ \Omega. Calculate the root-mean-square current in the circuit.

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Answer: 2

Answer

The root-mean-square current flowing through the circuit is 2 A.
The total impedance of the series RC circuit is obtained via quadrature sum Z=R2+XC2=602+802=100 ΩZ = \sqrt{R^2 + X_C^2} = \sqrt{60^2 + 80^2} = 100\ \Omega. Dividing the RMS supply voltage (200 V200\ \text{V}) by this impedance gives an RMS current of 2 A2\ \text{A}.

Step-by-Step Solution

1
Calculate the total impedance of the series RC circuit.
Z = \sqrt{R^2 + X_C^2} = \sqrt{60^2 + 80^2} = \sqrt{3600 + 6400} = 100\ \Omega
In an AC circuit with resistance and capacitive reactance in series, the total Opposition (impedance) is found by phasor addition.
2
Apply Ohm's law for alternating current circuits to find RMS current.
I_{\text{rms}} = \frac{V_{\text{rms}}}{Z} = \frac{200\ \text{V}}{100\ \Omega} = 2\ \text{A}
The RMS current is equal to the RMS voltage divided by the total circuit impedance.

Key Concept

Impedance and RMS Current in AC Series Circuits
Question 8149Question

Complete the following statement regarding industrial chemical manufacturing processes by identifying the correct categories of chemicals.

Fill in the blanks below

Chemicals manufactured on a large scale in continuous processes with relatively lower purity for widespread utility are classified as chemicals, whereas specialized compounds like pharmaceuticals and analytical reagents produced in small batches with extremely high purity are known as chemicals.
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Answer

The first blank is heavy and the second blank is fine.
Heavy chemicals are manufactured in massive bulk quantities through continuous processes for general industrial applications, while fine chemicals are produced in small batch quantities with high purity standards for specialized uses such as medicine and research.

Step-by-Step Solution

1
Analyze the production scale, process type, and purity level of the first class of chemicals.
Chemicals produced in high tonnage, continuously, and with lower purity (e.g., H2SO4H_2SO_4, NaOHNaOH) are heavy chemicals.
Large-scale utility and industrial demand define heavy (bulk) chemicals.
2
Analyze the production scale, process type, and purity level of the second class of chemicals.
Chemicals produced in smaller quantities, via batch processes, with high degree of purity (e.g., drugs, dyes) are fine chemicals.
High purity and specific end-use application define fine chemicals.

Key Concept

Classification and properties of heavy vs fine chemicals
Question 8150Question

When 10.0 g10.0\text{ g} of pure calcium carbonate (CaCO3\text{CaCO}_3) is strongly heated, it completely decomposes into solid calcium oxide (CaO\text{CaO}) and carbon(IV) oxide gas (CO2\text{CO}_2). According to the Law of Conservation of Mass, if 5.6 g5.6\text{ g} of calcium oxide remains in the container, what is the mass of carbon(IV) oxide gas released in grams?

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Answer: 4.4

Answer

The mass of carbon(IV) oxide gas released is 4.4 g4.4\text{ g}.
According to the Law of Conservation of Mass, the total mass of reactants must equal the total mass of products in a chemical change. For the reaction CaCO3(s)CaO(s)+CO2(g)\text{CaCO}_3(s) \rightarrow \text{CaO}(s) + \text{CO}_2(g), the initial mass of 10.0 g10.0\text{ g} of CaCO3\text{CaCO}_3 must equal the combined mass of CaO\text{CaO} (5.6 g5.6\text{ g}) and CO2\text{CO}_2. Subtracting 5.6 g5.6\text{ g} from 10.0 g10.0\text{ g} yields 4.4 g4.4\text{ g} for the gas produced.

Step-by-Step Solution

1
Apply the Law of Conservation of Mass
Total mass of reactants (10.0 g10.0\text{ g}) = Total mass of products (solid residue + gas)
Mass cannot be created or destroyed in a chemical reaction.
2
Calculate the missing mass of carbon(IV) oxide gas
Mass of CO2=10.0 g5.6 g=4.4 g\text{Mass of CO}_2 = 10.0\text{ g} - 5.6\text{ g} = 4.4\text{ g}
Subtracting the mass of the solid product from the initial mass of reactant gives the mass of the gaseous product evolved.

Key Concept

Law of Conservation of Mass
Estimated Time:45s
Question 8151Question

A light rigid lever of length 2.5 m2.5\text{ m} is pivoted horizontally at one end OO. A downward vertical weight of 60 N60\text{ N} is hung from the lever at a distance of 1.5 m1.5\text{ m} from OO. An upward force FF inclined at an angle of 3030^\circ to the lever is applied at the free end. What is the magnitude of the force FF required to maintain horizontal equilibrium?

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Answer: 72 N72\text{ N}

Answer

The magnitude of the force FF required to maintain equilibrium is 72 N72\text{ N}.
According to the Principle of Moments, for a body in rotational equilibrium, the total clockwise moment about a pivot equals the total counterclockwise moment. The load creates a clockwise moment of 60 N×1.5 m=90 Nm60\text{ N} \times 1.5\text{ m} = 90\text{ N}\cdot\text{m}. The force FF applied at 3030^\circ has a perpendicular component of Fsin30=0.5FF \sin 30^\circ = 0.5F. The counterclockwise moment is 0.5F×2.5 m=1.25F0.5F \times 2.5\text{ m} = 1.25F. Setting 1.25F=90 Nm1.25F = 90\text{ N}\cdot\text{m} gives F=72 NF = 72\text{ N}.

Step-by-Step Solution

1
Calculate the clockwise moment about the pivot OO caused by the hanging load.
Clockwise Moment=60 N×1.5 m=90 Nm\text{Clockwise Moment} = 60\text{ N} \times 1.5\text{ m} = 90\text{ N}\cdot\text{m}
The force of 60 N60\text{ N} acts perpendicularly at a distance of 1.5 m1.5\text{ m} from the pivot.
2
Express the counterclockwise moment about the pivot OO exerted by the force FF.
Counterclockwise Moment=Fsin(30)×2.5 m=1.25F Nm\text{Counterclockwise Moment} = F \sin(30^\circ) \times 2.5\text{ m} = 1.25 F\text{ N}\cdot\text{m}
Only the perpendicular component of the force, Fsin(30)F \sin(30^\circ), contributes to the moment about pivot OO.
3
Equate the clockwise and counterclockwise moments according to the Principle of Moments.
1.25F=90    F=901.25=72 N1.25 F = 90 \implies F = \frac{90}{1.25} = 72\text{ N}
For rotational equilibrium, the sum of clockwise moments must equal the sum of counterclockwise moments.

Key Concept

Principle of Moments and Perpendicular Force Components
Question 8152Question

Planet PP has a mean uniform density that is twice that of Planet QQ, and a radius that is half that of Planet QQ. What is the ratio of the escape velocity at the surface of Planet PP to the escape velocity at the surface of Planet QQ?

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Answer: 12\frac{1}{\sqrt{2}}

Answer

12\frac{1}{\sqrt{2}}
The correct answer is derived by substituting the planet's mass in terms of radius and density (M=43πR3ρM = \frac{4}{3}\pi R^3 \rho) into the escape velocity equation ve=2GMRv_e = \sqrt{\frac{2GM}{R}}. Simplifying gives ve=R83πGρv_e = R\sqrt{\frac{8}{3}\pi G \rho}, which means escape velocity is proportional to RρR\sqrt{\rho}. Halving the radius and doubling the density yields a factor of 12×2=22=12\frac{1}{2} \times \sqrt{2} = \frac{\sqrt{2}}{2} = \frac{1}{\sqrt{2}}.

Step-by-Step Solution

1
Express the mass of a uniform spherical planet in terms of its radius RR and density ρ\rho.
M=43πR3ρM = \frac{4}{3}\pi R^3 \rho
Mass equals volume multiplied by mean density.
2
Substitute mass into the escape velocity formula ve=2GMRv_e = \sqrt{\frac{2GM}{R}}.
ve=2G(43πR3ρ)R=R83πGρv_e = \sqrt{\frac{2G \left(\frac{4}{3}\pi R^3 \rho\right)}{R}} = R\sqrt{\frac{8}{3}\pi G \rho}
This establishes the proportionality veRρv_e \propto R\sqrt{\rho}.
3
Set up the ratio of escape velocity for Planet PP to Planet QQ using RP=12RQR_P = \frac{1}{2}R_Q and ρP=2ρQ\rho_P = 2\rho_Q.
\frac{v_{e,P}}{v_{e,Q}} = \frac{R_P\sqrt{\rho_P}}{R_Q\sqrt{\rho_Q}} = \frac{\left(\frac{1}{2}R_Q\right)\sqrt{2\rho_Q}}{R_Q\sqrt{\rho_Q}} = \frac{1}{2}\sqrt{2} = \frac{1}{\sqrt{2}}
Evaluating the ratio of proportional quantities yields the final scale factor.

Key Concept

Dependence of Escape Velocity on Planet Density and Radius
Estimated Time:2m 0s
Question 8153Question

What is the oxidation state of chlorine in uncombined chlorine gas, Cl2Cl_2?

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Answer: 00

Answer

The oxidation state of chlorine in uncombined chlorine gas (Cl2Cl_2) is 00.
According to standard rules for assigning oxidation states, any element in its free or uncombined elemental state has an oxidation number of zero. Because Cl2Cl_2 consists of identical chlorine atoms sharing bonding electrons equally, its oxidation state is 00.

Step-by-Step Solution

1
Identify the chemical state of the given species.
Chlorine is present as free, uncombined diatomic chlorine gas (Cl2Cl_2).
Redox rules distinguish uncombined elemental states from elements bound in chemical compounds.
2
Apply the fundamental oxidation number rule for uncombined elements.
The oxidation number assigned to any atom in an uncombined element is 00.
In a homonuclear diatomic molecule like Cl2Cl_2, electrons are shared equally between identical atoms, resulting in zero net charge allocation.

Key Concept

Oxidation state of uncombined elements
Question 8154Question
Ammonia gas (NH3\text{NH}_3) reacts with oxygen gas (O2\text{O}_2) over a platinum-rhodium catalyst to form nitrogen(II) oxide (NO\text{NO}) and water vapor (H2O\text{H}_2\text{O}) according to the equation:
4NH3(g)+5O2(g)4NO(g)+6H2O(g)4\text{NH}_{3(g)} + 5\text{O}_{2(g)} \rightarrow 4\text{NO}_{(g)} + 6\text{H}_2\text{O}_{(g)}

Which of the following statements correctly interprets the oxidation process occurring in this reaction from both classical and modern redox perspectives?

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Answer: Ammonia is oxidized because nitrogen loses hydrogen classically, which corresponds to an increase in the oxidation state of nitrogen from 3-3 to +2+2.

Answer

Ammonia is oxidized because nitrogen loses hydrogen classically, which corresponds to an increase in the oxidation state of nitrogen from 3-3 to +2+2.
In classical terminology, oxidation involves the removal of hydrogen or addition of oxygen. Ammonia (NH3\text{NH}_3) loses hydrogen to form nitrogen(II) oxide (NO\text{NO}), fulfilling classical oxidation. In modern electronic terms, the oxidation number of nitrogen increases from 3-3 in NH3\text{NH}_3 to +2+2 in NO\text{NO}, representing a loss of 5 electrons per nitrogen atom, which directly aligns with the modern definition of oxidation.

Step-by-Step Solution

1
Analyze classical redox definitions for ammonia
In NH3\text{NH}_3, nitrogen is combined with hydrogen. In forming NO\text{NO}, hydrogen is removed and oxygen is added. Classically, loss of hydrogen and gain of oxygen both define oxidation.
Classical redox concepts define oxidation as the gain of oxygen or loss of hydrogen.
2
Determine oxidation states for nitrogen in reactants and products
In NH3\text{NH}_3, hydrogen is +1+1, so N+3(+1)=0N=3N + 3(+1) = 0 \Rightarrow N = -3. In NO\text{NO}, oxygen is 2-2, so N+(2)=0N=+2N + (-2) = 0 \Rightarrow N = +2.
Sum of oxidation numbers in a neutral molecule equals zero.
3
Correlate modern redox definition with classical observation
The change in oxidation state of nitrogen from 3-3 to +2+2 is an increase of 55, which corresponds to loss of electrons (oxidation).
Modern redox concepts define oxidation as an increase in oxidation state due to loss of electrons.

Key Concept

Integration of Classical (Hydrogen/Oxygen Transfer) and Modern (Oxidation Number/Electron Transfer) Redox Concepts
Estimated Time:2m 0s
Question 8155Question

A sample of neon gas occupies a volume of 300 cm3300\text{ cm}^3 at a pressure of 100 kPa100\text{ kPa} under isothermal conditions. If the pressure on the gas is increased to 150 kPa150\text{ kPa}, what is the final volume of the gas?

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Answer: 200 cm3200\text{ cm}^3

Answer

The final volume of the gas is 200 cm3200\text{ cm}^3.
According to Boyle's law, pressure and volume are inversely proportional at constant temperature (P1V1=P2V2P_1 V_1 = P_2 V_2). Multiplying the initial pressure (100 kPa100\text{ kPa}) by the initial volume (300 cm3300\text{ cm}^3) gives 30000 kPacm330000\text{ kPa}\cdot\text{cm}^3. Dividing this product by the final pressure (150 kPa150\text{ kPa}) yields the correct volume of 200 cm3200\text{ cm}^3.

Step-by-Step Solution

1
Identify the given parameters and constant conditions
P1=100 kPaP_1 = 100\text{ kPa}, V1=300 cm3V_1 = 300\text{ cm}^3, P2=150 kPaP_2 = 150\text{ kPa}, temperature is constant.
Boyle's law applies when mass and temperature are kept constant.
2
State Boyle's Law formula
P1V1=P2V2P_1 V_1 = P_2 V_2
Pressure and volume are inversely proportional for a fixed mass of gas at constant temperature.
3
Substitute the values into the formula and solve for the unknown volume (V2V_2)
V2=P1V1P2=100×300150=200 cm3V_2 = \frac{P_1 V_1}{P_2} = \frac{100 \times 300}{150} = 200\text{ cm}^3
Rearranging the equation yields the new volume following compression.

Key Concept

Boyle's Law states that for a fixed mass of gas at constant temperature, the volume of the gas is inversely proportional to its pressure (P1V1=P2V2P_1 V_1 = P_2 V_2).
Question 8156Question
A Plutonium-239 nucleus (94239Pu{^{239}_{94}\text{Pu}}) captures a thermal neutron (01n{^{1}_{0}\text{n}}) and undergoes nuclear fission according to the reaction equation:
94239Pu+01n56144Ba+3893Sr+x01n+Q{^{239}_{94}\text{Pu}} + {^{1}_{0}\text{n}} \rightarrow {^{144}_{56}\text{Ba}} + {^{93}_{38}\text{Sr}} + x\,{^{1}_{0}\text{n}} + Q

Given the rest masses:
- Mass of 94239Pu=239.0522 u{^{239}_{94}\text{Pu}} = 239.0522\text{ u}
- Mass of 01n=1.0087 u{^{1}_{0}\text{n}} = 1.0087\text{ u}
- Mass of 56144Ba=143.9229 u{^{144}_{56}\text{Ba}} = 143.9229\text{ u}
- Mass of 3893Sr=92.9154 u{^{93}_{38}\text{Sr}} = 92.9154\text{ u}
- 1 u=931.5 MeV1\text{ u} = 931.5\text{ MeV}

What is the number of emitted neutrons xx and the total energy QQ released in this fission process?

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Answer: x=3x = 3 neutrons and Q=183.04 MeVQ = 183.04\text{ MeV}

Answer

The reaction releases x=3x = 3 neutrons and an energy Q=183.04 MeVQ = 183.04\text{ MeV}.
The conservation of nucleon number requires 239+1=144+93+x239 + 1 = 144 + 93 + x, giving x=3x = 3 neutrons. The mass defect is calculated by subtracting the mass of products (143.9229+92.9154+3×1.0087=239.8644 u143.9229 + 92.9154 + 3 \times 1.0087 = 239.8644\text{ u}) from the mass of reactants (239.0522+1.0087=240.0609 u239.0522 + 1.0087 = 240.0609\text{ u}), yielding Δm=0.1965 u\Delta m = 0.1965\text{ u}. Converting this to energy gives Q=0.1965×931.5 MeV=183.04 MeVQ = 0.1965 \times 931.5\text{ MeV} = 183.04\text{ MeV}.

Step-by-Step Solution

1
Balance mass number (AA) to find the number of neutrons xx
239+1=144+93+x    240=237+x    x=3239 + 1 = 144 + 93 + x \implies 240 = 237 + x \implies x = 3
Total mass number must be conserved in a nuclear reaction.
2
Calculate the total mass of the reactants (mreactantsm_{\text{reactants}})
mreactants=239.0522 u+1.0087 u=240.0609 um_{\text{reactants}} = 239.0522\text{ u} + 1.0087\text{ u} = 240.0609\text{ u}
The reactants consist of one Plutonium-239 nucleus and one thermal neutron.
3
Calculate the total mass of the products (mproductsm_{\text{products}})
mproducts=143.9229 u+92.9154 u+3(1.0087 u)=239.8644 um_{\text{products}} = 143.9229\text{ u} + 92.9154\text{ u} + 3(1.0087\text{ u}) = 239.8644\text{ u}
The products consist of one Barium-144 nucleus, one Strontium-93 nucleus, and three neutrons.
4
Calculate the mass defect (Δm\Delta m)
Δm=240.0609 u239.8644 u=0.1965 u\Delta m = 240.0609\text{ u} - 239.8644\text{ u} = 0.1965\text{ u}
Mass defect is the difference between total mass of reactants and total mass of products.
5
Calculate the liberated energy (QQ)
Q=0.1965 u×931.5 MeV/u=183.03975 MeV183.04 MeVQ = 0.1965\text{ u} \times 931.5\text{ MeV/u} = 183.03975\text{ MeV} \approx 183.04\text{ MeV}
Using Einstein's mass-energy equivalence conversion factor 1 u=931.5 MeV1\text{ u} = 931.5\text{ MeV}.

Key Concept

Nuclear fission conservation laws (mass/atomic number conservation) and mass defect energy equivalence (Q=Δm931.5 MeV/uQ = \Delta m \cdot 931.5\text{ MeV/u}).
Estimated Time:2m 0s
Question 8157Question

In a saturated acyclic alkane such as propane (C3H8\text{C}_3\text{H}_8), each carbon atom exhibits tetrahedral geometry through sp3sp^3 hybridization. What is the percentage of ss-orbital character present in each of these hybrid orbitals?

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Answer: 25%25\%

Answer

The percentage of ss-orbital character in each sp3sp^3 hybrid orbital of a tetrahedral carbon atom is 25%25\%.
In tetrahedral carbon compounds, sp3sp^3 hybridization involves mixing one ss orbital and three pp orbitals to produce four degenerate orbitals. Therefore, the proportion of ss-character in each hybrid orbital is 14\frac{1}{4}, which equals 25%25\%.

Step-by-Step Solution

1
Determine the composition of orbitals in sp3sp^3 hybridization.
An sp3sp^3 hybrid orbital is produced by combining one ss atomic orbital and three pp atomic orbitals, yielding a total of 4 equivalent hybrid orbitals.
Hybridization mixes pure atomic orbitals to form equivalent hybrid orbitals around a central tetrahedral carbon atom.
2
Calculate the fractional contribution of the ss orbital.
The fraction of ss-character is 11+3=14=0.25\frac{1}{1 + 3} = \frac{1}{4} = 0.25.
One out of the four constituent atomic orbitals is an ss orbital.
3
Convert the fraction into a percentage.
0.25×100%=25%0.25 \times 100\% = 25\%.
Multiplying the fractional contribution by 100 gives the percentage of ss-character.

Key Concept

Orbital Hybridization and s/p Character in Tetrahedral Carbon
Question 8158Question

A satellite revolves around a planet in a circular orbit of radius 1.0×104 km1.0 \times 10^4 \text{ km} with an orbital period of 12 hours12 \text{ hours}. Calculate the orbital period, in hours, of a second satellite orbiting the same planet in a circular path of radius 4.0×104 km4.0 \times 10^4 \text{ km}.

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Answer: 96

Answer

96 hours
According to Kepler's Third Law (T2r3T^2 \propto r^3), the orbital period TT scales with radius rr as Tr3/2T \propto r^{3/2}. Increasing the orbital radius by a factor of 4 increases the period by a factor of 43/2=84^{3/2} = 8. Multiplying the original period of 12 hours by 8 yields 96 hours.

Step-by-Step Solution

1
Set up Kepler's Third Law equation relating orbital period and orbital radius.
T22T12=r23r13\frac{T_2^2}{T_1^2} = \frac{r_2^3}{r_1^3}
Kepler's Third Law states that the square of the orbital period of a body in circular orbit is directly proportional to the cube of the radius of its orbit.
2
Substitute the given orbital radii and evaluate the scaling factor.
\frac{r_2}{r_1} = \frac{4.0 \times 10^4 \text{ km}}{1.0 \times 10^4 \text{ km}} = 4
Simplifying the ratio of the two orbital radii gives a factor of 4 increase in radius.
3
Calculate the period multiplier by taking the ratio to the power of 3/2.
4^{3/2} = (\sqrt{4})^3 = 2^3 = 8
Taking T2=T1×(r2r1)3/2T_2 = T_1 \times \left(\frac{r_2}{r_1}\right)^{3/2} shows the period scales by a factor of 8.
4
Multiply the initial orbital period by the scaling factor to find the final answer.
T_2 = 12 \text{ hours} \times 8 = 96 \text{ hours}
Multiplying the baseline period of 12 hours by 8 yields the new orbital period.

Key Concept

Kepler's Third Law of Planetary Motion
Estimated Time:1m 30s
Question 8159Question

A concentrated solution of ethanoic acid (CH3COOHCH_3COOH) exhibits higher electrical conductivity than a dilute solution of hydrochloric acid (HClHCl) because the higher concentration provides a greater total number of free mobile ions.

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Answer: False

Answer

The statement is False. Dilute hydrochloric acid conducts electricity more effectively than concentrated ethanoic acid because hydrochloric acid is a strong acid that ionizes completely to yield a higher concentration of free mobile ions.
The statement is false because the electrical conductivity of an electrolyte solution depends strictly on the concentration of free mobile ions available to carry electric current. Hydrochloric acid (HClHCl) is a strong acid that ionizes completely in water, yielding a high density of H+H^+ and ClCl^- ions. Ethanoic acid (CH3COOHCH_3COOH) is a weak acid that ionizes only slightly in water, leaving most molecules unionized. Consequently, even a dilute solution of HClHCl has a much higher concentration of mobile ions and a higher electrical conductivity than a concentrated solution of ethanoic acid.

Step-by-Step Solution

1
Analyze the acid strength and degree of ionization of both compounds.
Hydrochloric acid (HClHCl) is a strong acid that undergoes complete ionization (HCl(aq)H+(aq)+Cl(aq)HCl(aq) \rightarrow H^+(aq) + Cl^-(aq)), whereas ethanoic acid (CH3COOHCH_3COOH) is a weak acid that undergoes partial ionization (CH3COOH(aq)H+(aq)+CH3COO(aq)CH_3COOH(aq) \rightleftharpoons H^+(aq) + CH_3COO^-(aq)).
Electrical conductivity in aqueous solutions depends directly on the concentration of free, mobile charge-carrying ions.
2
Compare the concentration of mobile ions in concentrated weak acid vs. dilute strong acid.
Despite having a high molecular concentration, concentrated ethanoic acid contains mostly neutral, unionized molecules and very few free ions. Dilute HClHCl, even at lower molarity, yields a significantly higher concentration of free ions due to complete dissociation.
Only ionized species conduct electricity in solution; neutral molecules do not carry current.
3
Determine the relative electrical conductivity and evaluate the statement.
Dilute HClHCl is a far better conductor of electricity than concentrated CH3COOHCH_3COOH. Thus, the claim in the statement is false.
High acid concentration does not guarantee high conductivity if the acid is weak.

Key Concept

Electrical Conductivity and Ionization of Strong vs. Weak Acids
Question 8160Question

Match each structural feature or carbon center of 2-methylbut-1-en-3-yne (HCCC(CH3)=CH2HC\equiv C-C(CH_3)=CH_2) on the left with its corresponding hybridization state, geometric descriptor, or orbital overlap description on the right.

Click a left item, then click its matching right item

Items

The C2C3C_2-C_3 single bond connecting the alkyne and alkene carbon centers
The methyl carbon center (CH3-CH_3)
The alkene double bond between C3C_3 and C4C_4
The terminal acetylenic carbon center (C1C_1)

Matches

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Answer

The correct pairings are: (1) The C2C3C_2-C_3 single bond matches with the σ\sigma-bond formed by head-on spsp2sp-sp^2 hybrid orbital overlap. (2) The methyl carbon center matches with sp3sp^3 hybridization, tetrahedral geometry, and 109.5\approx 109.5^\circ bond angles. (3) The alkene double bond matches with one σ\sigma-bond (sp2sp2sp^2-sp^2) and one π\pi-bond (2p2p2p-2p). (4) The terminal acetylenic carbon matches with spsp hybridization, linear geometry, and 180180^\circ bond angle.
Each carbon atom in 2-methylbut-1-en-3-yne adopts a hybridization state determined by its steric number (number of attached atoms and lone pairs). C1C_1 and C2C_2 are spsp-hybridized (linear, 180180^\circ), C3C_3 and C4C_4 are sp2sp^2-hybridized (trigonal planar, 120120^\circ), and the methyl group carbon is sp3sp^3-hybridized (tetrahedral, 109.5109.5^\circ). Consequently, single bonds between differently hybridized carbons utilize hybrid orbitals corresponding to each carbon (spsp2sp-sp^2 for C2C3C_2-C_3), and double bonds consist of one σ\sigma bond (sp2sp2sp^2-sp^2) plus one π\pi bond (2p2p2p-2p).

Step-by-Step Solution

1
Analyze the expanded structural formula of 2-methylbut-1-en-3-yne
HC(1)C(2)C(3)(CH3)=C(4)H2H-C(1)\equiv C(2)-C(3)(CH_3)=C(4)H_2
Determining the bonding domains around each carbon atom establishes its hybridization state and structural role.
2
Determine hybridization state for each carbon center
C1C_1 (spsp), C2C_2 (spsp), C3C_3 (sp2sp^2), C4C_4 (sp2sp^2), and methyl carbon (sp3sp^3)
Carbons with 2 electron domains are spsp (linear), 3 domains are sp2sp^2 (trigonal planar), and 4 domains are sp3sp^3 (tetrahedral).
3
Map orbital overlap types to specific bonds
C2C3C_2-C_3 is an spsp2sp-sp^2 σ\sigma-bond; double bond C3=C4C_3=C_4 comprises an sp2sp2sp^2-sp^2 σ\sigma-bond and a 2p2p2p-2p π\pi-bond.
Single bonds are formed by head-on overlap of hybrid orbitals, while double bonds consist of one coaxial σ\sigma bond and one collateral π\pi bond.
4
Match left items with their corresponding right item descriptions based on hybridization and geometry principles
All 4 items are accurately matched to their structural characteristics.
Ensures complete alignment between structural features and underlying orbital hybridization properties.

Key Concept

Orbital Hybridization and Overlap Types in Hydrocarbon Frameworks
Estimated Time:2m 0s
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