Q.Assertion (A): D(+)-Glucose is dextrorotatory in nature.
Reason (R): 'D' represents its dextrorotatory nature.
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🔒 Start your 14-day free trial to unlock the full solution →Concept understanding — De Broglie Wavelength
De Broglie Wavelength: When Particles Start Acting Like Waves
Imagine you're holding a cricket ball. You know exactly where it is, and if you throw it, you can predict its path. That's a particle — localised, definite, following Newton's laws. Now think of light. You can't "hold" a beam of light; it spreads out, bends around corners, creates interference patterns. That's a wave — spread out, not localised.
For centuries, physics kept these two worlds separate. Particles were particles. Waves were waves. Never the twain shall meet.
Then came a young French physicist, Louis de Broglie, in 1924. He asked a question that seemed almost absurd: If light — which we thought was a wave — can behave like a particle (the photoelectric effect), then why can't a particle — say, an electron — behave like a wave?
That question turned physics upside down.
The Core Idea
De Broglie proposed that every moving particle has a wave associated with it. The wavelength of that wave depends on the particle's momentum. The faster or heavier the particle, the shorter the wavelength.
λ=ph=mvh
Where:
- λ = de Broglie wavelength (in metres)
- h = Planck's constant (6.626×10−34 J⋅s)
- p = momentum of the particle (mv for non-relativistic speeds)
This is not a mathematical trick. It's a physical reality. An electron moving through a crystal actually behaves like a wave of this wavelength — it can diffract, interfere, and form patterns just like light does.
Why You Don't See It in Daily Life
Here's the crucial point: the de Broglie wavelength is incredibly tiny for everyday objects.
Take a cricket ball of mass 0.16 kg moving at 30 m/s. Its de Broglie wavelength is:
λ=0.16×306.626×10−34≈1.38×10−34 m
That's about a hundred trillion trillion times smaller than the nucleus of an atom. No experiment can detect such a wave — it's effectively zero for all practical purposes.
Now take an electron (mass 9.1×10−31 kg) accelerated through 100 volts. Its speed is about 5.9×106 m/s. Its de Broglie wavelength:
λ=9.1×10−31×5.9×1066.626×10−34≈1.23×10−10 m
That's about 0.12 nanometres — comparable to the spacing between atoms in a crystal. This is measurable. And indeed, in 1927, Davisson and Germer fired electrons at a nickel crystal and observed diffraction — the unmistakable signature of a wave.
The de Broglie wavelength is only observable when it is comparable to the size of objects the particle interacts with. For macroscopic objects, it's far too small to matter. For subatomic particles, it's the key to understanding their behaviour.
What This Means Physically
The wave is not a physical wave in space like a water wave. It's a probability wave — its amplitude at any point tells you the probability of finding the particle there. Where the wave amplitude is large, you're likely to find the particle; where it's zero, you won't.
This wave-particle duality is not a compromise. It's the actual nature of reality. An electron is neither a pure particle nor a pure wave — it's something that shows particle-like behaviour in some experiments (like hitting a screen at a point) and wave-like behaviour in others (like passing through two slits and interfering with itself). …
Why this formula?
De Broglie Wavelength: Why the Formula Holds
Let's build this from the ground up — understanding why matter has a wavelength, not just memorizing λ=ph.
The Core Insight: Nature's Symmetry
Before de Broglie, physics had two separate worlds:
- Light — showed wave behaviour (diffraction, interference) but also particle behaviour (photoelectric effect)
- Matter — showed particle behaviour (momentum, collisions) but no wave behaviour yet
De Broglie asked a daring question in his 1924 PhD thesis:
If light (a wave) can behave like a particle, why can't a particle (like an electron) behave like a wave?
Nature should be symmetric — what applies to one should apply to the other.
Step 1: Start with Light (What We Already Knew)
For a photon, Einstein had given us two key relations:
- Energy: E=hf (Planck's relation)
- Momentum: p=λh (from E=pc for light, combined with c=fλ)
So for light:
λ=ph
This was experimentally verified for photons.
Step 2: De Broglie's Bold Hypothesis
De Broglie said: This relation is not special to light. It is universal.
For any particle with momentum p:
λ=ph
Where:
- λ = de Broglie wavelength
- h = Planck's constant (6.626×10−34 J⋅s)
- p = momentum of the particle
Step 3: Why Momentum and Not Velocity?
This is crucial. The formula uses momentum (p=mv), not just velocity.
For a non-relativistic particle (slow compared to light):
λ=mvh
For a relativistic particle (like an electron at high speed):
p=γmvwhereγ=1−v2/c21
λ=γmvh
Why momentum? Because momentum is the more fundamental quantity — it's conserved, it's frame-independent in a deeper sense, and it connects directly to the wave's phase.
Step 4: The Deeper Reasoning — Wave-Particle Duality
De Broglie didn't just guess. He reasoned:
- Every moving particle has an associated wave — called the "matter wave" or "pilot wave"
- The frequency of this wave comes from energy: f=hE
- The wavelength comes from momentum: λ=ph
These two relations are linked by the phase velocity of the wave:
vphase=fλ=hE⋅ph=pE
For a free particle with kinetic energy E=2mp2:
vphase=2mp=2v
This is half the particle's speed — a strange but mathematically consistent result.
Step 5: Experimental Confirmation (Why We Believe It)
De Broglie's idea was confirmed when electrons showed wave behaviour: …
The key idea here is that the D in D(+)-Glucose refers to the configuration at the chiral carbon farthest from the aldehyde group (based on Fischer projection), not to the direction of optical rotation. Dextrorotatory (+) means it rotates plane-polarized light to the right, which is a separate experimental observation.
- Assertion (A) is true: D(+)-Glucose is indeed dextrorotatory (rotates light right). …
The assertion is true (D(+)-glucose is dextrorotatory), but the reason is false — the 'D' in D-glucose refers to the configuration at the chiral carbon farthest from the aldehyde group, not to its optical rotation. The correct option is (C).
Understanding the Concept: Dextrorotatory vs. D-Configuration
This question tests a classic confusion in carbohydrate chemistry. You need to separate two ideas that sound similar but are completely independent:
- Optical rotation — whether a compound rotates plane-polarised light to the right (dextrorotatory, +) or left (laevorotatory, −). This is a physical property measured experimentally.
- D/L configuration — a naming convention based on the orientation of the −OH group on the chiral carbon farthest from the carbonyl group (the penultimate carbon). This is a structural assignment, not a measurement of rotation.
The 'D' in D-glucose has nothing to do with dextrorotation. It comes from the Fischer projection: if the −OH on the bottom-most chiral centre points to the right, the sugar is D; if it points left, it is L. The actual optical rotation is indicated separately by a (+) or (−) sign.
Many students assume 'D' stands for dextrorotatory. This is the single most common mistake in carbohydrate nomenclature. D-glucose happens to be dextrorotatory, but D-fructose is laevorotatory — proving the D/L label and rotation are unrelated.
Step-by-Step Analysis
1. Check the Assertion (A): D(+)-Glucose is dextrorotatory in nature.
D(+)-Glucose is the naturally occurring form of glucose. The (+) sign explicitly tells us it rotates plane-polarised light to the right. This is a well-established experimental fact. So Assertion (A) is true.
2. Check the Reason (R): 'D' represents its dextrorotatory nature. …
Method: Conceptual Analysis of D/L and (+)/(−) Nomenclature in Carbohydrates
Relevant Concept
In carbohydrate chemistry, D and L refer to the absolute configuration at the chiral carbon farthest from the carbonyl group (the penultimate carbon), based on Fischer projection orientation of the −OH group.
The symbols (+) and (−) denote optical rotation — the direction in which the compound rotates plane-polarized light (dextrorotatory = clockwise, levorotatory = anticlockwise).
These two systems are independent — a D-sugar can be either dextrorotatory or levorotatory.
Steps to Solve
-
Check Assertion (A):
- D(+)-Glucose is indeed dextrorotatory (rotates light clockwise).
- This is a fact — glucose has a specific rotation of +52.7°.
- Therefore, A is true.
-
Check Reason (R):
- The statement says: 'D' represents its dextrorotatory nature. …
Here are the common mistakes students make with this Assertion-Reason question, along with how to avoid each.
Mistake 1: Confusing ‘D’ with Dextrorotatory
The Mistake:
Students assume that the ‘D’ in D(+)-Glucose stands for dextrorotatory (i.e., it rotates plane-polarized light to the right). They then think the Reason (R) is correct, leading them to choose option (A) or (B).
Why it’s wrong:
- The ‘D’ in carbohydrate nomenclature refers to the configuration at the chiral carbon farthest from the aldehyde group (C-5 in glucose). It indicates that the -OH group on that carbon is on the right in the Fischer projection.
- The ‘(+)’ sign (or ‘+’) is what actually denotes dextrorotatory (clockwise rotation of light).
- So, ‘D’ does not mean dextrorotatory — it is a configurational label.
How to Avoid:
- Memorise the distinction:
- D/L = configuration (relative to glyceraldehyde).
- (+)/(-) = observed optical rotation (experimental).
- Always check the symbols in the question: D(+)-Glucose has both a configurational label (D) and a rotation sign (+). They are independent.
Mistake 2: Thinking the Reason Explains the Assertion
The Mistake:
Even if a student knows that D(+)-Glucose is dextrorotatory (Assertion is true), they might still think the Reason correctly explains why it is dextrorotatory — because they confuse ‘D’ with rotation.
Why it’s wrong:
- The Assertion (A) is true: D(+)-Glucose is indeed dextrorotatory (it rotates light to the right).
- The Reason (R) is false because ‘D’ does not represent dextrorotatory nature.
- Since R is false, it cannot be the correct explanation of A.
How to Avoid:
- In Assertion-Reason questions, first independently check the truth of each statement.
- A: True (D(+)-Glucose is dextrorotatory).
- R: False (D does not mean dextrorotatory).
- Then check if R explains A — if R is false, it cannot explain anything.
- The correct answer here is (C) A is true but R is false.
Mistake 3: Forgetting that ‘D’ and ‘L’ are Configurational, Not Rotational
The Mistake: …
Showing the 12 most recent of 53 on this concept.
- TG EAPCET 2026Set eng-2026-05-09-FN1 markMCQQ.Law of conservation of mass was regarded as another basic conservation law of nature until the advent of (A) Bose-Einstein statistics (B) Theory of relativity (C) Chandrasekhar limit (D) Uncertainty principle
›Reveal solutionSolution
The law of conservation of mass was overturned as a fundamental principle by Einstein’s theory of relativity, which showed mass and energy are interchangeable. The correct option is (B).
The key idea here is that before the 20th century, scientists believed mass could neither be created nor destroyed — it was a bedrock of chemistry and physics. But the theory of relativity changed that by revealing that mass is a form of energy, so mass can be “lost” when converted into energy (as in nuclear reactions). The other options deal with quantum statistics, stellar limits, or quantum uncertainty — none directly challenge mass conservation.
Let’s walk through each option:
-
Bose-Einstein statistics — This describes how identical particles (bosons) behave at low temperatures, leading to phenomena like Bose-Einstein condensates. It doesn’t alter the conservation of mass; it’s about quantum statistical behavior, not mass-energy equivalence.
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Theory of relativity — Einstein’s special relativity (1905) introduced E=mc2, showing that mass and energy are two sides of the same coin. In nuclear reactions, a tiny amount of mass disappears and reappears as a huge amount of energy. This directly breaks the classical law of conservation of mass, replacing it with the more general conservation of mass-energy.
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Chandrasekhar limit — This is the maximum mass (about 1.4 solar masses) a white dwarf star can have before collapsing into a neutron star. It’s a consequence of quantum mechanics and gravity, not a challenge to mass conservation itself. …
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- TG EAPCET 2026Set eng-2026-05-09-FN1 markMCQQ.The ratio of wavenumber of first line of Balmer series and wavenumber of second line of Lyman series of hydrogen atom is (A) 5:32 (B) 32:5 (C) 22:7 (D) 7:22
›Reveal solutionSolution
The wavenumber ratio is found by applying the Rydberg formula to the first Balmer line (transition from n=3 to n=2) and the second Lyman line (transition from n=4 to n=1). The ratio simplifies to 5:32, so the correct option is (A).
The key concept here is the Rydberg formula for wavenumber of spectral lines in hydrogen. The wavenumber ν~ (inverse wavelength) for a transition from a higher energy level n2 to a lower level n1 is given by:
ν~=RH(n121−n221)
where RH is the Rydberg constant. The Balmer series corresponds to transitions ending at n1=2, and the Lyman series to transitions ending at n1=1. The "first line" of a series means the transition with the smallest energy difference (longest wavelength), and the "second line" means the next smallest.
Let’s work through the calculation step by step.
- Identify the transitions.
- First line of Balmer series: This is the transition from n2=3 to n1=2.
- Second line of Lyman series: This is the transition from n2=4 to n1=1. (The first Lyman line is from n=2 to n=1; the second is from n=3 to n=1; wait — careful: the second line of Lyman is actually from n=3 to n=1? Let’s double-check: Lyman series: n1=1. The first line: n2=2. The second line: n2=3. The third line: n2=4. So the second line of Lyman is from n=3 to n=1, not n=4. This is a common pitfall — see the warning below.)
Watch outA classic mistake is to think the "second line" means the second possible upper level, which is n=3 for Lyman, not n=4. The first line uses n=2, the second uses n=3, the third uses n=4, etc. So for the second Lyman line, n2=3.
- Write the wavenumber for each line.
- For the first Balmer line (n1=2,n2=3): ν~B=RH(221−321)=RH(41−91)=RH(369−4)=RH⋅365…
- Identify the transitions.
- TG EAPCET 2026Set eng-2026-05-10-AN1 markMCQQ.If the activities of a radioactive substance at times t=0 and t=3T are A and B respectively, then the activity of the substance at a time t=9T is (A) B2A3 (B) BA2 (C) AB2 (D) A2B3
›Reveal solutionSolution
Radioactive decay follows an exponential law: activity R(t)=R0e−λt. Using the given values at t=0 and t=3T, we find e−λT=(B/A)1/3. Then activity at t=9T becomes A⋅(B/A)3=B3/A2, which matches option (D).
The key idea is that radioactive decay is exponential: the activity decreases by a constant factor over equal time intervals. So if we know the factor over 3T, we can raise it to the appropriate power to get the factor over 9T.
-
Write the decay law
Activity at time t is R(t)=R0e−λt, where R0 is the initial activity and λ the decay constant.
At t=0: R(0)=R0=A.
At t=3T: R(3T)=Ae−λ⋅3T=B.
-
Find the decay factor over 3T
From Ae−3λT=B, we get
e−3λT=AB.
Taking the cube root:
e−λT=(AB)1/3.
This is the factor by which activity drops every T seconds.
- Activity at t=9T 9T is three intervals of 3T, or nine intervals of T. Using the factor per T: R(9T)=A⋅(e−λT)9=A⋅[(AB)1/3]9. …
-
- TG EAPCET 2026Set eng-2026-05-10-AN1 markMCQQ.The velocity of the photoelectron (in ms−1) emitted when a smooth surface of a metal is made to strike with a photon of wavelength 4×10−7 m is (W0 of metal = 2.13 eV; 1 eV = 1.6×10−19 J ; h=6.6×10−34 Js ; me=9.1×10−31 kg) (A) 51×106 (B) 31×105 (C) 31×106 (D) 71×105
›Reveal solutionSolution
The photoelectron’s velocity is found from Einstein’s photoelectric equation: kinetic energy = photon energy minus work function. After converting units and solving, the speed is 31×106 m/s, which matches option (C).
The core idea is Einstein’s photoelectric effect: a photon gives all its energy to an electron. Some of that energy is used to overcome the work function W0 (the minimum energy to free the electron), and the rest becomes the electron’s kinetic energy. Since the electron is non‑relativistic here, we use K=21mv2. The question gives wavelength, so we first find photon energy from E=hc/λ.
- Find the photon energy in joules. Photon wavelength λ=4×10−7 m.
Ephoton=λhc
Using h=6.6×10−34 J·s and c=3×108 m/s:
Ephoton=4×10−7(6.6×10−34)(3×108)=4×10−719.8×10−26=4.95×10−19 J
- Convert the work function to joules. Given W0=2.13 eV and 1 eV = 1.6×10−19 J:
W0=2.13×1.6×10−19=3.408×10−19 J
- Apply Einstein’s photoelectric equation. Kinetic energy of the emitted electron:
K=Ephoton−W0=(4.95−3.408)×10−19=1.542×10−19 J
- Relate kinetic energy to velocity.
21mev2=K⇒v=me2K
With me=9.1×10−31 kg:
v=9.1×10−312×1.542×10−19=9.1×10−313.084×10−19=0.3389×1012
v=3.389×1011≈3.389×105.5
More neatly: 3.389×1011=2.951012, but let’s compute exactly. …
- TG EAPCET 2026Set eng-2026-05-10-FN1 markMCQQ.The kinetic energy of photo electron emitted from the surface of a metal is 7.2×10−20 J, when the metal is made to strike with light having wavelength x nm. What is the value of x? (Work function of metal = 4.5 eV; h=6.6×10−34 Js; c=3×108 ms−1; 1 eV =1.6×10−19 J) (A) 125 (B) 250 (C) 175 (D) 150
›Reveal solutionSolution
We use Einstein's photoelectric equation, KE=E−ϕ, to find the incident photon energy, ensuring all terms are in Joules. Then, we use E=hc/λ to calculate the wavelength. The value of x is 250 nm.
The photoelectric effect is a fundamental phenomenon in quantum physics where electrons are emitted from a material when light shines on it. This effect demonstrates the particle nature of light, where light energy is carried in discrete packets called photons.
When a photon strikes the surface of a metal, it transfers its energy to an electron. For an electron to be ejected, the photon's energy (E) must be greater than or equal to the work function (ϕ) of the metal. The work function is the minimum energy required to remove an electron from the surface of the metal. Any energy supplied by the photon beyond this work function is converted into the kinetic energy (KE) of the emitted electron.
This energy conservation principle is described by Einstein's photoelectric equation:
KE=E−ϕ
Where:
- KE is the maximum kinetic energy of the emitted photoelectron.
- E is the energy of the incident photon.
- ϕ is the work function of the metal.
The energy of an incident photon is also related to its wavelength (λ) by the formula:
E=λhc
Where:
- h is Planck's constant.
- c is the speed of light in vacuum.
The crucial step in solving such problems is to ensure all energy terms are expressed in consistent units, typically Joules (J), before performing calculations. The work function is often given in electron volts (eV), which must be converted to Joules.
Step-by-Step Solution:
-
Identify given values and the target:
We are provided with the following information:
- Kinetic energy of the photoelectrons, KE=7.2×10−20 J.
- Work function of the metal, ϕ=4.5 eV.
- Planck's constant, h=6.6×10−34 Js.
- Speed of light, c=3×108 ms−1.
- Conversion factor, 1 eV =1.6×10−19 J. We need to find the wavelength of the incident light, x nm. This means we will calculate the wavelength λ in meters and then convert it to nanometers.
-
Convert the work function to Joules:
Since the kinetic energy is given in Joules, we must convert the work function from electron volts to Joules to maintain unit consistency in the photoelectric equation.
ϕ=4.5 eV×(1.6×10−19 J/eV)
ϕ=7.2×10−19 J
-
Calculate the energy of the incident photon (E):
Using Einstein's photoelectric equation, KE=E−ϕ, we can rearrange it to solve for the incident photon energy E:
E=KE+ϕ
Substitute the given kinetic energy and the converted work function:
E=(7.2×10−20 J)+(7.2×10−19 J) …
- TG EAPCET 2026Set eng-2026-05-11-AN1 markMCQQ.The work function of three metals A, B and C is respectively 2.25, 2.42 and 3.6 eV. All the three metals were irradiated with light of wavelength 330 nm. The kinetic energy of photoelectrons emitted from A, B and C is respectively EA,EB and EC. The correct relationship of EA,EB and EC is (h=6.6×10−34 Js; c=3×108 ms−1) (A) EA>EB>EC (B) EA=EB=EC (C) EA<EB<EC (D) EC>EA>EB
›Reveal solutionSolution
The photoelectric effect tells us that kinetic energy equals photon energy minus work function.
For a fixed wavelength (330 nm), the photon energy is constant, so the metal with the smallest work function gives the largest kinetic energy.
Since work functions are A = 2.25 eV, B = 2.42 eV, C = 3.6 eV, we get EA>EB>EC.
The correct option is (A).
Concept & Intuition
The photoelectric effect is beautifully simple: a photon gives all its energy to an electron. The electron uses some of that energy to escape the metal (the work function ϕ), and the rest becomes kinetic energy.
So for each metal:
Kmax=hf−ϕ
Here, the light’s wavelength is fixed (330 nm), so every photon carries the same energy. That means the metal with the smallest work function will give the electron the most leftover kinetic energy. It’s like three toll booths with different tolls — if you have the same amount of cash, the one with the smallest toll leaves you with the most change.
Step‑by‑step reasoning
- Find the photon energy The energy of a single photon is
Ephoton=λhc
Given h=6.6×10−34 Js, c=3×108 m/s, and λ=330 nm=330×10−9 m:
Ephoton=330×10−9(6.6×10−34)(3×108)=3.3×10−71.98×10−25=6.0×10−19 J
Convert to electronvolts (1 eV = 1.6×10−19 J):
Ephoton=1.6×10−196.0×10−19=3.75 eV
- Apply the photoelectric equation for each metal
EA=3.75−2.25=1.50 eV
- TG EAPCET 2026Set ap-2026-05-04-AN1 markMCQQ.The scientific principle useful for the working of a fusion test reactor is (A) Trapping and cooling of atoms by laser beams and magnetic fields (B) Controlled nuclear fission (C) Magnetic confinement of plasma (D) Wave nature of electrons
›Reveal solutionSolution
Fusion test reactors aim to harness nuclear fusion, which requires extremely high temperatures to create plasma; this plasma is then confined and controlled using powerful magnetic fields. The correct option is (C).
Concept and Intuition
Nuclear fusion is the process by which two light atomic nuclei combine to form a heavier nucleus, releasing a tremendous amount of energy. This is the same process that powers the Sun and other stars. On Earth, achieving controlled nuclear fusion is incredibly challenging because atomic nuclei are positively charged and repel each other strongly (due to electrostatic repulsion). To overcome this repulsion and allow them to fuse, the nuclei must be brought very close together with immense kinetic energy.
This requires extremely high temperatures, typically tens to hundreds of millions of degrees Celsius. At such extreme temperatures, atoms ionize, meaning their electrons are stripped away, forming a superheated, electrically charged gas called plasma. This plasma is the "fuel" for fusion.
The core challenge for a fusion reactor is twofold:
- Heating: Reaching and maintaining these extreme temperatures.
- Confinement: Containing this superheated plasma for long enough and at sufficient density for fusion reactions to occur efficiently. No physical material can withstand temperatures of millions of degrees, so traditional containers are impossible. This is where the scientific principle of confinement becomes critical.
Step-by-Step Analysis
Let's examine each option in the context of a fusion test reactor:
-
Trapping and cooling of atoms by laser beams and magnetic fields
- This technique is primarily used in fields like quantum physics to study ultra-cold atoms, create Bose-Einstein condensates, or develop highly precise atomic clocks. It involves slowing down and cooling atoms to temperatures very close to absolute zero.
- Why it's incorrect for fusion: Fusion requires heating matter to millions of degrees Celsius, not cooling it. The goal is to give nuclei enough energy to overcome their electrostatic repulsion, which is the opposite of cooling.
-
Controlled nuclear fission
- Nuclear fission is the process where a heavy atomic nucleus (like uranium or plutonium) is split into two or more smaller nuclei, releasing energy. This is the principle behind current commercial nuclear power plants and atomic bombs.
- Why it's incorrect for fusion: While both fission and fusion are nuclear reactions that release energy, they are fundamentally different processes. Fusion involves combining light nuclei, whereas fission involves splitting heavy nuclei. A fusion reactor aims to achieve fusion, not fission.
-
Magnetic confinement of plasma
- As discussed, fusion requires plasma at extremely high temperatures. This plasma is too hot to be contained by any material walls, as it would instantly melt or vaporize them and cool down rapidly, stopping the fusion reactions. …
- TG EAPCET 2026Set ap-2026-05-05-FN1 markMCQQ.The concept that provided a convincing evidence of the atomic picture of matter is (A) Photo electric effect (B) Brownian motion theory (C) Superconductivity (D) Wave nature of electrons
›Reveal solutionSolution
The concept that gave the most direct and convincing evidence for the atomic (discrete) picture of matter was the Brownian motion theory, which explained the jittery motion of visible particles as the result of invisible molecular collisions.
The question asks for the concept that provided convincing evidence of the atomic picture of matter — that is, proof that matter is made of discrete, indivisible particles (atoms or molecules), not a continuous substance.
Let’s look at each option carefully.
-
Photo electric effect — This showed that light behaves as discrete packets of energy (photons), and that electrons are emitted from a metal surface only when light of a certain minimum frequency strikes it. While this was revolutionary for quantum theory and the particle nature of light, it did not directly prove that matter itself is made of atoms. It proved something about light, not about the structure of matter.
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Brownian motion theory — In 1827, Robert Brown observed that pollen grains suspended in water moved in a constant, random, zigzag path. Einstein (1905) and later Perrin (1908) showed theoretically and experimentally that this motion is caused by the continuous, random bombardment of the pollen grains by invisible water molecules. The quantitative agreement between theory and experiment — especially Perrin’s measurement of Avogadro’s number — was the first direct, convincing proof that molecules (and hence atoms) really exist. This is the correct answer.
-
Superconductivity — This is a macroscopic quantum phenomenon where certain materials conduct electricity with zero resistance below a critical temperature. It reveals important quantum properties of matter but does not serve as evidence for the atomic (discrete) nature of matter itself. It assumes atoms exist; it doesn’t prove they do. …
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- TG EAPCET 2025Set eng-2025-05-02-FN1 markMCQQ.The RMS velocity of dihydrogen is 7 times more than that of dinitrogen. If TH2 and TN2 are the temperatures of dihydrogen and dinitrogen, then the correct relationship between them is (A) TH2=TN2 (B) TH2>TN2 (C) TH2=7TN2 (D) TH2=2TN2
›Reveal solutionSolution
The RMS velocity formula vrms=M3RT shows that for a given gas, velocity depends on temperature and molar mass. Given vH2=7vN2, we find TH2=21TN2, so the correct option is (D).
The key concept here is the root-mean-square (RMS) velocity of gas molecules, given by
vrms=M3RT
where R is the gas constant, T is the absolute temperature, and M is the molar mass.
The problem tells us that the RMS velocity of dihydrogen (H2) is 7 times that of dinitrogen (N2). That means
vH2=7vN2
We need to relate their temperatures. The trick: the molar masses are different — MH2=2 g/mol and MN2=28 g/mol. So the ratio of velocities depends on both T and M. Let’s work it out step by step.
- Write the RMS velocity expressions for each gas.
vH2=MH23RTH2,vN2=MN23RTN2
- Use the given relation vH2=7vN2. Substitute the formulas:
MH23RTH2=7⋅MN23RTN2
- Square both sides to remove square roots.
MH23RTH2=7⋅MN23RTN2
Cancel 3R from both sides:
MH2TH2=7⋅MN2TN2
- Plug in the molar masses. MH2=2, MN2=28:
2TH2=7⋅28TN2
- Simplify the right-hand side. 2TH2=287TN2=41TN2 …
- TG EAPCET 2025Set eng-2025-05-03-AN1 markMCQQ.The potential energy of an electron in an orbit of hydrogen atom is −6.8 eV. The de Broglie wavelength of the electron in this orbit is (r0 is Bohr radius) (A) 2πr0 (B) 4πr0 (C) πr0 (D) 3πr0
›Reveal solutionSolution
The key idea is that the de Broglie wavelength of an electron in a Bohr orbit equals the circumference of that orbit divided by the principal quantum number n. Given the potential energy −6.8 eV, we find n=2, so the wavelength is 4πr0, which corresponds to option (B).
Concept and Intuition
In the Bohr model of the hydrogen atom, an electron moves in circular orbits around the nucleus. A central condition is that the angular momentum is quantized:
mvr=n2πh
where n=1,2,3,… is the principal quantum number.
The de Broglie wavelength of the electron is λ=h/(mv). Combining these, we get:
λ=mvh=n2πr
So the wavelength is simply the circumference of the orbit divided by n. This means that if we know the orbit's radius (in terms of the Bohr radius r0) and the quantum number n, we can find λ.
The problem gives the potential energy U=−6.8 eV. In the Bohr model, the total energy of an electron in the n-th orbit is:
En=−n213.6 eV
and the potential energy is twice the total energy (by the virial theorem for a Coulomb force):
U=2En=−n227.2 eV
Thus, from U=−6.8 eV, we can solve for n, then find the radius rn=n2r0, and finally the de Broglie wavelength.
Step-by-Step Solution
- Find the principal quantum number n from the potential energy. The potential energy in the n-th Bohr orbit is:
U=−n227.2 eV
Set this equal to −6.8 eV:
−n227.2=−6.8
Cancel the negatives and solve:
n227.2=6.8⇒n2=6.827.2=4
So n=2.
- Determine the radius of the orbit. The radius of the n-th Bohr orbit is:
rn=n2r0
For n=2:
- TG EAPCET 2025Set eng-2025-05-03-AN1 markMCQQ.In the atomic spectrum of hydrogen, the wavelengths of the spectral lines corresponding to electronic transitions(i) n=4 to n=2 and(ii) n=3 to n=1 are λ1 and λ2 A˚ respectively. The value of (λ1−λ2) (in cm) is (RH = Rydberg constant) (A) RH1[10124] (B) RH[10124] (C) RH1[24101] (D) RH[24101]
›Reveal solutionSolution
The key idea is to use the Rydberg formula for hydrogen to express each wavelength in terms of RH, then subtract them and simplify. The result is λ1−λ2=RH1⋅24101, so the correct option is (C).
The problem asks for the difference in wavelengths (in cm) between two spectral lines of hydrogen, given in terms of the Rydberg constant RH. The Rydberg formula directly gives the wavenumber (inverse wavelength) for any transition, so we can compute each wavelength, subtract, and simplify. The trick is to handle the units carefully — the answer choices are expressed as fractions involving RH, so we keep everything symbolic.
Why this approach works:
The Rydberg formula is the fundamental relation for hydrogen spectral lines. It expresses the wavenumber ν~=1/λ as RH(nf21−ni21). By writing each λ as the reciprocal of this, we can directly compute λ1−λ2 algebraically. The answer choices are all in the form of either RH times a fraction or 1/RH times a fraction, so our result will match one of these.
- Write the Rydberg formula for each transition. For hydrogen, the wavenumber is:
λ1=RH(nf21−ni21)
where RH is the Rydberg constant (in cm−1 if λ is in cm).
- Transition (i): ni=4, nf=2
λ11=RH(221−421)=RH(41−161)=RH(164−161)=RH⋅163
So:λ1=RH1⋅316
- Transition (ii): ni=3, nf=1
λ21=RH(121−321)=RH(1−91)=RH⋅98
So:λ2=RH1⋅89
- Compute the difference λ1−λ2. Both are expressed as multiples of 1/RH, so:
λ1−λ2=RH1(316−89)
Find a common denominator (24):
- TG EAPCET 2025Set eng-2025-05-03-FN1 markMCQQ.The potential energy of an electron in an orbit of hydrogen atom is −6.8 eV. The de Broglie wavelength of the electron in this orbit is (r0 is Bohr radius) (A) 3πr0 (B) πr0 (C) 2πr0 (D) 4πr0
›Reveal solutionSolution
The de Broglie wavelength of an electron in a Bohr orbit equals n2πrn. The given potential energy −6.8 eV identifies n=2, and the radius r2=4r0, giving λ=4πr0 — option (D).
Concept and Intuition
The de Broglie wavelength of a particle is λ=h/p, where p is its momentum. In the Bohr model of hydrogen, a stable orbit must support a standing wave around its circumference — the circumference must be an integer number of wavelengths: 2πrn=nλ, so λ=n2πrn.
Given the potential energy, we first find which orbit (n) the electron occupies, then find that orbit's radius rn=n2r0, and finally compute λ.
Step-by-step solution
- Relate potential energy to the orbit number The total energy of the nth Bohr orbit is En=−n213.6 eV. By the virial theorem, the potential energy is twice the total energy:
U=2En=−n227.2 eV.
Given U=−6.8 eV,
−n227.2=−6.8⇒n2=6.827.2=4⇒n=2.
- Find the radius of the n=2 orbit The Bohr radius r0 is the radius of the n=1 orbit, and rn=n2r0. So
r2=4r0.
- Apply the standing-wave (Bohr quantization) condition …
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