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Kinetic Theory
KEY NOTES
Å Kinetic theory explains the behaviour of gases based on the It has been observed that, the value of K is same for all
idea that the gas consists of rapidly moving atoms or gases and it is called Boltzmann constant and is denoted
molecules. by kB which is given by
pV
kB =
Molecular Nature of Matter NT
Å According to the molecular theory of matter, (iii) According to Avogadro’s hypothesis, the number of
molecules per unit volume is the same for all gases at
(i) The atoms are much free in gases and can travel long
fixed temperature and pressure.
distances without colliding. If they are not enclosed,
gases disperse away. The number of molecules in 22.4 L of any gas is
6.02 × 1023 . This is known as Avogadro number and is
(ii) In solids and liquids, the closeness makes the denoted by N A .
interatomic force important. The force has a long range
attraction and a short range repulsion. The atoms attract (iv) The mass of 22.4 L of any gas is equal to its molecular
when they are at a few angstroms but repel when they weight in grams at STP (Standard Temperature 273 K
come closer. and Pressure 1 atm). This amount of substance is called
a mole.
(iii) In dynamic equilibrium, molecules collide with each
(v) The perfect gas equation can be written as
other and change their speeds during the collision.
However, only the average properties remain constant. pV = µRT
where, µ is the number of moles, R = N A kB which is a
Behaviour of Gases universal constant, T is absolute temperature in kelvin
Å Behaviour of gases can be stated as follows and R = 8. 314J mol −1 K−1 .
(i) Gases at low pressures and high temperatures much Another useful form of above perfect gas equation is
above that at which they liquefy (or solidify) ρRT
p=
approximately satisfy a simple relation between their M0
pressure, temperature and volume given by
where, ρ is the mass density of the gas.
pV = KT
(vi) If a gas that satisfies the relation, pV = µRT exactly at all
where, T is the temperature in kelvin or absolute scale pressures and temperatures, then it is defined to be an
and K is constant for a given sample but varies with the ideal gas.
volume of gas.
(vii) Keeping temperature constant, pressure of a given mass
(ii) With respect to atoms or molecules, K is proportional to of gas varies inversely with volume, i.e. pV = constant or
the number of molecules (N) in a sample of gas. p ∝ 1 / V.
i.e. K = Nk This is called Boyle’s law.
(viii) For a fixed pressure, the volume of a gas is proportional
to its absolute temperature T.
Law of Equipartition of Energy
i.e. V ∝T
Å It states that for any system in thermal equilibrium, the
total energy is equally distributed in all possible energy
This is called Charles’ law. modes, with each mode having an average energy equal
(ix) The total pressure of a mixture of ideal gases is equal to 1
to kBT.
the sum of the partial pressures of the individual gases. 2
µ RT µ 2 RT The kinetic energy of a single molecule is
i.e. p = p1 + p 2 + .... = 1 + + .... Å
V V 1 1 1
This is called Dalton’s law of partial pressure. ε t = mv x2 + mv y2 + mv z2
2 2 2
For a gas in thermal equilibrium at temperature T, the
Kinetic Theory of an Ideal Gas
Å
3
average value of energy denoted by < ε t > is kBT.
Å It is based on the molecular picture of matter. It correlates 2
the macroscopic properties like pressure and temperature of Since there is no preferred direction, hence
gases to microscopic properties like speed and kinetic energy 1 1 1 1
of gas molecules. < mv x2 > = < mv y2 > = < mv z2 > = kBT.
2 2 2 2
Å At ordinary pressure and temperature, the average distance Å A molecule has one degree of freedom for motion in a
between molecules is a factor of 10 or more than the typical line, two for motion in a plane and three for motion in
size of a molecule (2Å). Thus, interaction between molecules space.
is negligible.
Å Motion of a body as a whole from one point to another
Å When the molecules come close to each other, they is called translation. Thus, a molecule free to move in
experience intermolecular forces and their velocities change. space has three translational degrees of freedom.
These interactions are called collisions.
Å Molecules of a monoatomic gas have only translational
Å All collisions between molecules among themselves or degrees of freedom.
between molecules and the walls of the container are elastic,
Å Molecules of diatomic gas are made up of two atoms
i.e. total kinetic energy and momentum remain conserved.
joined rigidly to one another through a bond. Thus,
1
Å Total pressure exerted by a gas is p = nmv 2 diatomic molecule has 5 degree of freedom, i.e. 3
3 translational and 2 rotational. Hence, total energy
where, v 2 denotes the mean of the squared speed. consists of translational energy ε t and rotational
2 energy ε r .
Also, pV = E
3 1 2 1 2 1 2 1 1
i.e. ε t + ε r = mvx + mv y + mv z + I1ω12 + I 2ω 22
Å The internal energy E of an ideal gas can be given as 2 2 2 2 2
1 Diatomic molecule like CO, even at moderate
E = N × mv 2 Å
2 temperature have a mode of vibration, i.e. its atom
where, N ( = nV) is the number of molecules in the sample. oscillate along the interatomic axis and contribute
Å The average kinetic energy of one mole of an ideal gas is vibrational energy terms ε v to the total energy,
2
3 E 1 2 3 1 dy 1
E= kB NT or = mv = kB T ε v = m + ky 2
2 N 2 2 2 dt 2
Å In equilibrium, the average kinetic energy of the molecules of ⇒ ε = εt + εr + εv
different gases will be equal. where, k is the force constant of the oscillator and y is
1 1 3 the vibrational coordinate.
i.e. m1v12 = m2v 22 = kBT ⇒ p = (n1 + n2 + ...) kBT
2 2 2 Å Each translational and rotational degrees of freedom of
(Dalton’s law of partial pressure) 1
a molecule contributes kBT to the energy, while each
3k T 2
Å The mean square speed of a molecule is v 2 = B . 1
m vibrational frequency contributes 2 × kBT = kBT , since a
The square root of v 2 is known as root mean square (rms) 2
speed and is denoted by v rms. vibrational mode has both kinetic and potential energy
modes.
Å When gases diffuse, their rate of diffusion is inversely
proportional to square root of the masses.
Specific Heat Capacity Total internal energy,
(i) For monoatomic gas 3 3
U = kBT + kBT + f kBT N A
2 2
Degree of freedom, f = 3 (only translational)
The total internal energy of a mole of such a gas is ⇒ CV = ( 3 + f ) R
3 3 and Cp = ( 4 + f ) R
U = kBT N A = RT
2 2 where, f = number of vibrational modes.
The molar specific heat at constant volume, (4 + f )
γ=
dU 3 (3 + f)
CV = = R
dT 2 Å Specific heat capacity of solid is
The molar specific heat at constant pressure, ∆Q ∆U
5 C= = = 3R
C p = CV + R = R [QC p − CV = R] ∆T ∆T
2 Hence, total energy, U = 3 kBTN A = 3 RT
Cp 5
∴ Ratio of specific heats, γ = = Å Specific heat capacity of water is
CV 3
∆Q ∆U
(ii) For diatomic gas (for rigid diatomic) C= = = 9R
∆T ∆T
f = 5 (3 translational + 2 rotational) Hence, total energy , U = 3 ( 3 kBTN A ) = 9RT
5 5
Similarly, U = kB T × N A = RT Mean Free Path
2 2
The molar specific heats are Å The average distance travelled by a molecule between
5 7 two successive collisions is known as the mean free path
CV = R , C p = R (l) of the molecule.
2 2
1
Cp 7 Mean free path, l =
⇒ γ= = 2 nπ d 2
CV 5
where, d = diameter of each molecule
If the diatomic molecule is not rigid but in addition has a
and n = number of molecules per unit volume.
vibrational mode, then
Å The rate of collision of gas molecule is nπd 2 < v > or the
5 7
U = kBT + kBT N A = RT time between two successive collisions is on the
2 2 average,
7 9 9 1
⇒ CV = R , C p = R and γ = τ=
2 2 7 nπ < v > d 2
(iii) For polyatomic gas Å The mean free path, in gases, is of the order of
Generally, degree of freedom = ( 6 + f ) thousands of angstroms.
(3 translational + 3 rotational + f vibrational)
CHAPTER 13 > Kinetic Theory
Mastering NCERT
MULTIPLE CHOICE QUESTIONS
28 A gas at 300K is enclosed in a container. Now, the 33 The average translational kinetic energy of the
container is placed on a fast moving train. While the molecule of a gas is
3 1 2
train is in motion, the temperature of the gas (a) kB T (b) kB T (c) kB T (d) kB T
(a) rises above 300 K (b) falls below 300K 2 2 3
(c) remains unchanged (d) becomes unsteady 34 Oxygen and hydrogen are at the same temperature T.
The ratio of the mean kinetic energy of oxygen
29 When molecules of an isotropic gas travelling in
molecules to that of the hydrogen molecules will be
cubical box along + x-direction collides with the wall
(a) 16 : 1 (b) 1 : 1 (c) 4 : 1 (d) 1 : 4
of box elastically, the pressure exerted on the walls
due to gas is (where, n = number of molecules per unit 35 At what temperature, the kinetic energy of gas
volume, m = mass and v 2 = mean of squared speed) molecule is half of the value at 27°C?
1 (a) 13.5°C (b) 150°C (c) 75 K (d) − 123° C
(a) 3nmv 2 (b) nmv 2
3 36 The ratio of molecular masses of two gases in a
(c) nmv 2 (d) None of these container at a temperature T is 3 : 2. The ratio of the
30 The internal energy of an ideal gas is in the form of
kinetic energies of the molecule of two gases is
(a) 3 : 2 (b) 9 : 4 (c) 1 : 1 (d) 4 : 9
(a) kinetic energy of molecules
A
(a) same as the pressure initially
C
(b) 2 times the pressure initially
G
F (c) 10 times the pressure initially
E (d) 20 times the pressure initially
H
(a) the pressure on EFGH would be zero 97 A vessel of volume V contains a mixture of 1 mol of
(b) the pressure on all the faces will the equal hydrogen and 1 mol oxygen (both considered as
(c) the pressure of EFGH would be double of the pressure ideal). Let f 1 ( v ) dv denote the fraction of molecules
on ABCD with speed between v and ( v + dv ) with f 2 ( v ) dv,
(d) the pressure on EFGH would be half of that on ABCD similarly for oxygen. Then,
(a) f1 ( v ) + f2 ( v ) = f ( v ) obeys the Maxwell’s distribution (b) only the translational part of energy because
law rotational energy is very small compared to the
(b) f1 ( v ) and f2 ( v ) will obey the Maxwell’s distribution translational energy
law separately (c) only the translational part of the energy because during
(c) Neither f1 ( v ) nor f2 ( v ) will obey the Maxwell’s collisions with the wall pressure relates to change in
distribution law linear momentum
(d) f2 ( v ) and f1 ( v ) will be the same (d) the translational part of the energy because rotational
98 An inflated rubber balloon contains one mole of an energies of molecules can be of either sign and its
ideal gas, has a pressure p, volume V and temperature average over all the molecules is zero
T. If the temperature rises to 1.1 T and the volume is 100 When an ideal gas is compressed adiabatically, its
increased to 1.05 V , the final pressure will be temperature rises and the molecules on the average
(a) 1.1 p (b) p have more kinetic energy than before. The kinetic
(c) less than p (d) between p and 1.1p energy increases,
(a) because of collisions with moving parts of the wall only
99 Diatomic molecules like hydrogen have energies due
(b) because of collisions with the entire wall
to both translational as well as rotational motion.
2 (c) because the molecules gets accelerated in their motion
From the equation in kinetic theory pV = E , E is inside the volume
3
(d) because of redistribution of energy amongst the
(a) the total energy per unit volume molecules
Answers
>Mastering NCERT with MCQs
1 (c) 2 (d) 3 (b) 4 (b) 5 (b) 6 (a) 7 (a) 8 (b) 9 (b) 10 (d)
11 (c) 12 (b) 13 (b) 14 (c) 15 (d) 16 (a) 17 (b) 18 (c) 19 (c) 20 (a)
21 (a) 22 (a) 23 (a) 24 (c) 25 (c) 26 (a) 27 (c) 28 (c) 29 (b) 30 (a)
31 (a) 32 (*) 33 (a) 34 (b) 35 (d) 36 (c) 37 (d) 38 (c) 39 (d) 40 (a)
41 (b) 42 (a) 43 (b) 44 (c) 45 (a) 46 (c) 47 (c) 48 (a) 49 (c) 50 (c)
51 (b) 52 (b) 53 (c) 54 (d) 55 (a) 56 (a) 57 (a) 58 (c) 59 (b) 60 (b)
61 (a) 62 (d) 63 (c) 64 (c)
CV 7
7 −1
−1 V 5
On substituting Eq. (ii) in Eq. (i), we get ( 300 )V15 = T2 1
γ CV − CV = R 5
⇒ CV ( γ − 1) = R 300 × V12 / 5 300
⇒ T2 = 2
= −2
= 300 × 52 / 5
2/ 5
∴ CV =
R 1
V15 × 55
γ −1 5
3 = 300 × 1.903 = 570.9 −~ 571 K
48 (a) Energy of a gas, E = NkB T
2 Mean kinetic energy of a rotating molecules
Q N = µN A . × 10−23 × 571
= kB T = 138
3 = 787.98 × 10−23 J
∴ E = ⋅ µ ⋅ N A ⋅ kB .T
2
where, N A = Avogadro’s number and kB = Boltzmann 54 (d) Total internal energy of system = Internal energy of
constant. oxygen (diatomic) molecules + Internal energy of argon
m 1 (monoatomic) molecules
For helium molecule, µ = =
M 4 5 3
⇒ E = 2 × RT + 4 × RT = 11RT
∴ Heat energy required to raise temperature from T1 to 2 2
T2 is 55 (a) For hydrogen or diatomic gas, the internal energy is
3 3
∆E = N A kB ∆T = N A kB (T2 – T1 ) given by
8 8 5 5
U= kB T × N A = RT
49 (c) Given, number of moles of helium = 5 2 2
Number of atoms (He is monoatomic) dU 5
CV = = R
= Number of moles × Avogadro’s number dT 2
5 7 Cp 2
⇒ Cp = R + R = R [from C p = CV + R] γ= = 1+
2 2 CV f
Cp 7 We have,
∴ γ= =
CV 5 For gas A,
where, C p = molar heat capacity at constant pressure 2 29
1+ = ≈ 13
. ⇒ f = 6.67 ≈ 7
and CV = molar heat capacity at constant volume. f 22
For helium (or monoatomic) gas, the internal energy is So, gas A has vibrational mode of degree of freedom.
given by For gas B,
3 3
U = kB TN A = RT 1+ =
2 30
≈ 14
. ⇒ f =5
2 2 f 21
dU 3
⇒ CV = = R Hence, gas B does not have any vibrational mode of
dT 2 degree of freedom.
3 5
Cp = R + R = R 58 (c) A polyatomic molecule has 3 translational, 3
2 2
rotational degrees of freedom and a certain number f
Cp 5
∴ γ= = degree of freedom of vibrational modes. Therefore, total
CV 3 energy is
For ideal diatomic gas X (non-rigid, having an 3 3
U = kB T + kB T + f kB T N A
additional vibrational mode) the internal energy is 2 2
given by
7 7 = ( 3kB T + f kB T )N A
U = kB TN A = RT
2 2 59 (b) Internal energy of a gas with f degree of freedom is
dU 7 n f RT
⇒ CV = = R U= , where n is the number of moles.
dT 2 2
7 9 Internal energy due to O 2 gas which is a diatomic gas is
Cp = R + R = R
2 2 n f RT 5
U1 = 1 1 = 3 × RT
Cp 9 2 2
∴ γ= =
CV 7 (Q n1 = 3 moles, degree of freedom for a diatomic gas
f1 = 5)
56 (a) Molecule of CO at moderate temperature possess Internal energy due to Ar gas which is a monoatomic gas
vibrational modes, i.e. it oscillates like is
one-dimensional oscillator. n f RT 3
2 U2 = 2 2 = 5 × RT
1 dy 1 2 2
∴ Vibrational energy = m + ky2
2 dt 2 (Q n2 = 5 moles, degree of freedom
As, each vibrational mode contributes two square for a monoatomic gas f2 = 3)
1 ∴ Total internal energy = U1 + U 2
terms, so this mode will contribute 2 kB T energy.
2 ⇒ U = 15 RT
CO molecule has 3 translational and 2 rotational modes 61 (a) The prediction of specific heats, based on law of
1 equipartition of energy, are independent of temperature.
and each of them contributes kB T to the energy.
2 But as we go to low temperatures, there is a marked
∴ Total energy, departure from this prediction. Specific heat of all
1 1 1 substances approach zero as T → 0 K.
E = 3 kB T + 2 kB T + 2 kB T
2 2 2 This is related to the fact that degrees of freedom get
14243 14243 14243
Translational mode Rotational mode Vibrational mode
frozen and ineffective at low temperatures.
7 62 (d) As, mean free path,
= kB T 1
2 l=
57 (a) Now, in given case,
2 n πd 2
For gas A, C p = 29, CV = 22 1
⇒ l∝ 2 (Q n1 = n2 )
For gas B, C p = 30, CV = 21 d
2
By using l1 d 22 1 1
⇒ = = =
l2 d12 4 16
63 (c) For air at STP, n = 2.7 × 1025 m−3 68 (d) The translational motion of the gas chamber
and d = 2 × 10−10 m increases the total kinetic energy of the chamber but it
does not contribute to the internal energy of the system.
1
Mean free path, l= So, the temperature of gas in the chamber remains same.
2 nπd 2 Therefore, Assertion is incorrect but Reason is correct.
On putting values, we get 1
1 69 (c) Pressure of an ideal gas = nm v 2
l= 3
. × ( 2 × 10−10 )2
2 × 2.7 × 1025 × 314 µRT
Also, pressure of an ideal gas, p =
= 2.05 × 10−7 m V
1
64 (c) We know that, average time of collision between If µ and T are constants, p ∝
V
1
molecules, τ= So, pressure of an ideal gas increases with the decrease of
nπ 2 v rms d 2 volume.
where, n = number of molecules per unit volume Therefore, Assertion is correct but Reason is incorrect.
and v rms = rms velocity of molecules. 70 (c) In an ideal gas, there is no inter-particle interaction,
1 so vibrational kinetic energy remains constant,
⇒ τ∝
nv rms irrespective of temperature.
1 If the gas is monoatomic, no vibrational energy is there,
As, n ∝ and v rms ∝ T
V so the degree of freedom is always three.
Thus, we can write n = k1V −1 and v rms = k2 T 1 / 2 Therefore, Assertion is correct but Reason is incorrect.
where, k1 and k2 are constants. 71 (c) Statements II and III are correct but I is incorrect and
V it can be corrected as,
⇒ τ∝
T The kinetic theory relates the molecular properties like
viscosity, conduction and diffusion with bulk properties
For adiabatic process, TV γ − 1 = constant
of a gas.
or T ∝ V 1− γ
74 (a) In liquids, the atoms are not as rigidly fixed as in
Thus, we can write τ ∝ VT −1 / 2 ∝ V (V 1 − γ )−1 / 2
solid and can move around. This enables a liquid to flow.
γ +1
In liquids the separation between atoms is about 2Å.
⇒ τ ∝V 2
In case of gases, the atoms are not rigidly fixed but are
As, given that average time of collision between free to move.
molecules increases asV q , so on comparing, we get
Thus, the statement given in option (a) is correct, rest are
γ +1
q= incorrect.
2
75 (c) An ideal gas is that which satisfy the equation,
65 (a) The interatomic forces are negligible in gases. pV = µRT
Therefore in gases, the molecules are free and move
where, p = pressure,V = volume,
long distances without colliding, with faster speed.
µ = number of moles, R = gas constant
Therefore, Assertion and Reason are correct and
Reason is the correct explanation of Assertion. and T = temperature.
Here, µ and R are constant for a gas, so
66 (b) A real gas at low pressure and high temperature
T
behaves like ideal gas p∝
V
and satisfies pV = µRT .
Hence, pressure of an ideal gas depends on both the
Therefore, Assertion and Reason are correct but temperature and volume of the gas. Thus, both the
Reason is not the correct explanation of Assertion. statements given in options (a) and (b) are correct.
67 (b) Total translational kinetic energy of all molecules 76 (b) Due to the presence of external positive charge on the
(n moles) of a given mass of an ideal gas face ABCD, the usual expression for pressure p on the
3 3 basis of kinetic theory will not be valid.
= µRT = pV = 15 . pV
2 2 This is because ions present inside cube would also
[Q pV = µRT ] experience electrostatic forces other than the forces due
Due to collision of molecules of gas with each other, to collisions with the walls of the container. Also due to
their velocities continuously change. presence of positive charge, the isotropy is lost.
Therefore, Assertion and Reason are correct but Thus, the statement given in option (b) is correct, rest are
Reason is not the correct explanation of Assertion. incorrect.
78 (d) Pressure of a gas, D → As the x-component of velocities of all the
1 molecules are not same. So, we take average of vx2 .
p = nmv 2
3 ∴ Total pressure, p = nmvx2
where, n = number of molecules per unit volume, Hence, A → 2, B → 3, C → 4 and D → 1.
m = mass of gas and v 2 = mean of squared speed.
84 (b) Given, diameter of O2 molecule = 3Å
Thus we can conclude that, while finding out pressure,
∴ Radius of O2 = 1.5 Å = 1.5 × 10−8 cm
the shape of the vessel does not matter, as A and ∆t do
4
not appear in the above formula. Volume of each molecule, V = πr3
3
By Pascal’s law, the pressure of the gas in equilibrium
Number of molecules in one mole of gas = N A
is the same everywhere.
= Avogadro’s number = 6.023 × 1023 molecules/mol
Also, while deriving the expression of pressure, we
4
neglect the collisions between the molecules as it does ∴ Volume of total molecules at STP, V = πr3 N A
not make much difference. This is because the collisions 3
are too frequent and time spent is negligible. 4 −8 3
V = × 314 . × 10 ) × 6.023 × 1023
. (15
Thus, all the statements given in options (a), (b) and (c) 3
are correct. = 8.51 cm3
We know that, the volume of one mole of gas at STP
81 (b) All statements are correct except the statement given
in option (b) and it can be corrected as, = 22.4 L = 22.4 × 103 cm3
The average translational KE per molecule is same for = 22400 cm3
molecules of all gases like here O 2 and for each Fraction of molecular volume to the actual volume
3 8.51
molecule it is k B T. = = 3.8 × 10−4
2 22400
≈ 4.0 × 10−4
83 (b) A→ As only x-component of velocity changes, so
change in momentum of molecule 85 (a) Given, pressure, p = 1 atm
= − mvx − ( mvx ) = − 2mvx = 1.013 × 105 Nm−2
As collision is elastic, the total momentum of molecule Gas constant, R = 8.314 J mol −1 K −1
and wall is conserved. So, change in momentum of wall Number of mole, µ = 1
(momentum imparted to wall) = 2mvx . Temperature, T = 273.15 K
B → In time ∆t, the number of molecules with velocity Using ideal gas equation, pV = µRT
vx that could reach the wall is nAvx ∆t within volume of µRT 1 × 8.314 × 273.15
cylinder of length vx ∆t as shown below, where n → ⇒ V = =
number density. p 1.013 × 105
= 0.0224 m3
= 22.4 × 10−3 m3
= 22.4 L
A 86 (b) Given, volume of the room,V = 25.0 m3
vx∆t Temperature, T = 27° C = (273 + 27 ) K = 300 K
Pressure, p = 1 atm = 1.013 × 105 Pa
. × 10−23
Boltzmann constant, kB = 138
Using the relation, pV = µkB T
pV 1.013 × 105 × 25
But on an average half of these molecules will hit the ⇒ µ= =
1 kB T 1.38 × 10−23 × 300
wall in time, ∆t = n Avx ∆t
2 = 6.11 × 1026 molecules
The total momentum transferred to the wall in time ∆t
1 87 (c) Root mean square speed of argon atom,
= ( 2mvx ) n Avx ∆t = ( nmvx2 ) A ∆t
2 (v rms )Ar =
3kB TAr
…(i)
F Momentum M Ar
C → Pressure = =
A Area × Time Root mean square speed of helium atom,
( nmvx2 ) A ∆t 3kB THe
= = nmvx2 ( v rms )He = …(ii)
A ∆t M He
Dividing Eq. (i) by Eq. (ii), we get Hence, moles removed = µ 1 − µ 2
( v rms )Ar 3kB TAr M He = 19.48 − 1512
. = 4.36
= ×
( v rms )He M Ar 3kB THe Mass removed = 4.36 × 32 g
= 139.52g = 01396
. kg
Given, ( v rms )Ar = ( v rms )He
and THe = 27315 . − 20 = 25315
. K 90 (b) Given, T = 27°C = ( 27315
. + 27 ) K = 30015
. K
3
T M As average thermal energy, E = kB T
⇒ 1 = Ar ⋅ He 2
THe M Ar where, kB = Boltzmann’s constant
M He THe = 1.38 × 10−23 JK −1 .
⇒ = 3
M Ar TAr ∴ E = × 138. × 10−23 × 30015 .
2
M 39.9
∴ TAr = THe Ar = 253.15 = 6.21 × 10−21 J
He
M 4
91 (b) As the motion of the vessel as a whole does not
= 2525.171 K = 2.52 × 103 K
effect the relative motion of the gas molecules with
88 (d) respect to the walls of the vessel, hence pressure of the
I. The dotted line in the diagram shows that there is no gas inside the vessel, as observed by us, on the ground
pV remains the same.
deviation in the value of for different
T 92 (d) In an ideal gas, when a molecule collides elastically
temperatures T1 and T2 for increasing pressure, so with a wall, the momentum transferred to each molecule
this gas behaves ideally. Hence, dotted line will be twice the magnitude of its normal momentum.
corresponds to ideal gas behaviour. However, as the face EFGH absorbs the gas molecule
II. At high temperature, the deviation of the gas is less incident on it, thus the momentum transferred will be
and at low temperature the deviation of gas is more. only half.
In the graph, deviation for T2 is greater than for T1 , Therefore, the pressure on EFGH would be half of that
Thus, T1 > T2 . on ABCD.
III. Since, the two curves intersect at dotted line, so the 93 (b) Boyle’s law is applicable when temperature is
pV constant,
value of at that point on the Y -axis is same for
T i.e. pV = µRT = constant
all gases. ⇒ pV = constant (at constant temperature)
So, all statements are correct. 1
⇒ p ∝ (where , p = pressure and V =
89 (a) Absolute pressure, p1 = (15 + 1) atm V
( Q absolute pressure = gauge pressure + 1 atm) volume)
= 16 × 1.013 × 105 Pa As, this process is called as isothermal process, so
Boyle’s law is applicable for isothermal process.
V1 = 30 L = 30 × 10−3 m3
94 (c) Consider the diagram, where an ideal gas is
T1 = 27 + 273.15 = 300.15 K contained in a cylinder, having a piston of mass M
Using ideal gas equation, pV = µRT (friction is absent here).
pV
⇒ µ= M
RT pa
Initially number of moles,
p V 16 × 1.013 × 105 × 30 × 10−3 pa Mg/A
µ1 = 1 1 =
RT1 8.314 × 300.15
p
= 19.48
A
Finally, p2 = (11 + 1) = 12 atm p
= 12 × 1.013 × 105 Pa
V2 = 30 L = 30 × 10−3m 3 The pressure inside the gas will be
T2 = 17 + 27315
. = 29015 . K p = pa + Mg / A
Number of moles, where, pa = atmospheric pressure,
pV 12 × 1 . 013 × 105 × 30 × 10−3 A = area of cross-section of the piston
µ2 = 2 2 =
RT2 8. 314 × 29015
. and Mg = weight of piston.
= 1512
. As the mass remains constant, so the pressure p of the
gas remains the same.
As pV = µRT ⇒ V ∝ T , ( 2µ 1 ) ( 3000 )
= = 20
So, when temperature T increases, volumeV increases µ 1 ( 300 )
at constant pressure. ⇒ p2 = 20 p1
Hence,V will change but not p.
Hence, final pressure of the gas would be 20 times the
95 (a) We know for an ideal gas, pressure initially.
pV = µRT
97 (b) As the vessel contains 1 mole of hydrogen and
µR 1 mol of oxygen, therefore as per Maxwell’s law of
⇒ V = T
p speed distribution, speed of any molecule depend on its
where, p = pressure,V = volume, mass. The mass of hydrogen and oxygen are different,
so their speed will also be different. Hence, f1 ( v ) and
µ = number of moles of gas,
f2 ( v ) will obey the law separately.
R = gas constant and T = temperature.
Slope of the V-T graph, 98 (d) We know for an ideal gas, pV = µRT