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4

The fugacity of a gas in a mixture is equal to the product of its mole fraction and its fugacity in the pure state at the total pressure of the mixture. This is

A. The statement as per Gibbs-Helmholtz

B. Called Lewis-Randall rule

C. Henry's law

D. None of these

Correct Answer :

B. Called Lewis-Randall rule


Related Questions

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The chemical potential of any constituent of an ideal solution depends on the __________ of the solution.

A. Temperature

B. Pressure

C. Composition

D. All (A), (B) and (C)

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4

The melting point of paraffin wax (which contracts on solidification) __________ with pressure rise.

A. Increases

B. Decreases

C. Remains unchanged

D. Decreases linearly

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4

For an isothermal process, the internal energy of a gas

A. Increases

B. Decreases

C. Remains unchanged

D. Data insufficient, can't be predicted

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4

Cv for an ideal gas

A. Does not depend upon temperature

B. Is independent of pressure only

C. Is independent of volume only

D. Is independent of both pressure and volume

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4

The chemical potential for a pure substance is __________ its partial molal free energy.

A. More than

B. Less than

C. Equal to

D. Not related to

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4

It is desired to bring about a certain change in the state of a system by performing work on the system under adiabatic conditions.

A. The amount of work needed is path dependent

B. Work alone cannot bring out such a change of state

C. The amount of work needed is independent of path

D. More information is needed to conclude anything about the path dependence or otherwise of the work needed

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4

If the pressure on 100 c.c. of air is halved, then its volume (at the same temperature) would be __________ c.c.

A. 100

B. 50

C. 205

D. 200

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4

Which one is true for a throttling process?

A. A gas may have more than one inversion temperatures

B. The inversion temperature is different for different gases

C. The inversion temperature is same for all gases

D. The inversion temperature is the temperature at which Joule-Thomson co-efficient is infinity

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4

The Maxwell relation derived from the differential expression for the Helmholtz free energy (dA) is

A. (∂T/∂V)S = - (∂P/∂S)V

B. (∂S/∂P)T = - (∂V/∂T)P

C. (∂V/∂S)P = (∂T/∂P)S

D. (∂S/∂V)T = (∂P/∂T)V

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4

For an irreversible process involving only pressure-volume work

A. (dF)T, p <0

B. (dF)T, p = 0

C. (dF)T, p > 0

D. (dA)T, v >0

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4

If the vapour pressure at two temperatures of a solid phase in equilibrium with its liquid phase are known, then the latent heat of fusion can be calculated by the

A. Maxwell's equation

B. Clausius-Clapeyron Equation

C. Van Laar equation

D. Nernst Heat Theorem

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Which of the following exemplifies an adiabatic process?

A. Melting of ice

B. Condensation of alcohol vapor

C. Sudden bursting of a cycle tube

D. Evaporation of water

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4

The entropy change in a reversible isothermal process, when an ideal gas expands to four times its initial volume is

A. R loge 4

B. R log10 4

C. Cv log10 4

D. Cv loge 4

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4

When a system in equilibrium is subjected to a change in temperature, pressure or concentration, the equilibrium is displaced in a direction which tends to undo the effect of the change. This is called the

A. Le-Chatelier principle

B. Kopp's rule

C. Law of corresponding state

D. Arrhenius hypothesis

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4

The principle applied in liquefaction of gases is

A. Adiabatic expansion

B. Joule-Thomson effect

C. Both (A) and (B)

D. Neither (A) nor (B)

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4

Cv is given by

A. (∂E/∂T)V

B. (∂E/∂V)T

C. (∂E/∂P)V

D. (∂V/∂T)P

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4

When a system is in equilibrium for all possible processes, the differential or finite change of entropy is

A. < 0

B. > 0

C. = 0

D. None of these

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4

Compressibility factor for almost all the gases are approximately same at the same

A. Pressure and temperature

B. Reduced pressure and reduced temperature

C. Critical pressure and critical temperature

D. None of these

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4

In the reaction; N2 + O2 2NO, increasing the pressure will result in

A. Shifting the equilibrium towards right

B. Shifting the equilibrium towards left

C. No change in equilibrium condition

D. None of these

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4

The difference between isothermal compressibility and adiabatic compressibility for an ideal gas is

A. 0

B. +ve

C. -ve

D.

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4

Which of the following identities can be most easily used to verify steam table data for superheated steam?

A. (∂T/∂V)S = (∂p/∂S)V

B. (∂T/∂P)S = (∂V/∂S)P

C. (∂P/∂T)V = (∂S/∂V)T

D. (∂V/∂T)P = -(∂S/∂P)T

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4

An ideal liquid refrigerant should

A. Not have a sub-atmospheric vapour pressure at the temperature in the refrigerator coils

B. Not have unduly high vapour pressure at the condenser temperature

C. Both (A) and (B)

D. Have low specific heat

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Van Laar equation deals with the activity coefficients in

A. Binary solutions

B. Ternary solutions

C. Azeotropic mixture only

D. None of these

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4

__________ functions are exemplified by heat and work.

A. Path

B. Point

C. State

D. None of these

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4

An irreversible process

A. Is the analog of linear frictionless motion in machines

B. Is an idealised visualisation of behaviour of a system

C. Yields the maximum amount of work

D. Yields an amount of work less than that of a reversible process

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4

Gibbs-Duhem equation

A. States that n11 + n22 + ....njj = 0, for a system of definite composition at constant temperature and pressure

B. Applies only to binary systems

C. Finds no application in gas-liquid equilibria involved in distillation

D. None of these

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4

Entropy, which is a measure of the disorder of a system, is:

A. Independent of pressure

B. Independent of temperature

C. Zero at absolute zero temperature for a perfect crystalline substance

D. All (A), (B) & (C)

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4

Consider the reaction, C + O2 CO2; ΔH = - 94 kcal. What will be the value of ΔH for the reaction CO2 → C + O2?

A. -94 kcal

B. +94 kcal

C. > 94 kcal

D. < -94 kcal

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4

A cylinder contains 640 gm of liquid oxygen. The volume occupied (in litres) by the oxygen, when it is released and brought to standard conditions (0°C, 760 mm Hg) will be __________ litres.

A. 448

B. 224

C. 22.4

D. Data insufficient; can't be computed

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4

The root mean square speed of molecules of a gas is equal to (where, m = mass of the molecule K = Boltzmanns constant, T = absolute temperature)

A. √(2KT/m)

B. √(3KT/m)

C. √(6KT/m)

D. 3KT/m