A. Adiabatic
B. Isentropic
D. None of these
A. Pressure
C. Both A. & B.
D. Neither A. nor B.
B. Pressure vs. enthalpy
C. Pressure vs. volume
D. Temperature vs. entropy
A. Work done under adiabatic condition
B. Co-efficient of thermal expansion
C. Compressibility
A. 6 P1 V1
C. 12 P1V1
D. P1 V1
A. Closed
C. Isolated
A. 2
B. 1
C. 3
A. Equal to
B. Either B. or C; depends on the type of alloy
C. More than
A. Third
B. Zeroth
D. First
B. Molten lead
C. Molten potassium
D. Mercury
B. F = E + A
C. F = A TS
D. F = A + TS
A. Vary as square of the absolute temperature
B. None of these
C. Vary as square of the absolute pressure
A. May be positive or negative
C. Positive
D. Negative
A. < 0
B. 0
D. ?
A. Increases linearly
B. Decreases
D. Remain constant
B. Vapor compression cycle using expansion valve
C. Air refrigeration cycle
D. Vapor compression cycle using expansion engine
A. Sublimation
C. Fusion
D. Vaporisation
A. Does not change in volume
B. Either (A), B. or (C)
C. Expands
A. Increase in summer and will decrease in winter
C. Decrease
D. Remain same
B. Chemical potentials of all components should be same in a particular phase
C. Sum of the chemical potentials of any given component in all the phases should be the same
A. Composition
B. Temperature
D. Pressure
A. 4.238
C. 1.9398
D. 3.389
A. Supersaturated
C. Both A. and B
D. Neither A. nor B
A. Violates second law of thermodynamics
B. 7058.3
C. 9000
D. 6738.9
A. Adiabatic expansion
B. Joule-Thomson effect
A. Ammonia
C. Methyl chloride
D. Liquid sulphur dioxide
A. None of these
C. Momentum
D. Mass
A. During heating of an ideal gas
B. During cooling of an ideal gas
C. Under reversible isothermal volume change
C. None of these
D. Isobaric
A. C = P F + 2
C. P = F C 2
D. F = C P 2
A. Zero
C. Minimum
B. Heating takes place
C. Temperature is constant
D. Pressure is constant
A. Does not depend upon temperature
B. Is independent of pressure only
C. Is independent of volume only
A. Temperature
B. Entropy
C. Volume
B. Equals 0.24 kcal/kmol K
C. Becomes zero
D. Equals 1 kcal/kmol K
A. Isolated
B. Closed
D. Non-thermodynamic
A. Low freezing point
C. High thermal conductivity
D. Large latent heat of vaporisation
B. Directly proportional to pressure
D. Inversely proportional to pressure
C. unpredictable
D. 50%
B. Dependent on climatic conditions
C. More
D. Same
A. Nernst Heat Theorem
C. Van Laar equation
D. Maxwells equation
A. Decreases linearly
B. Remain same
C. Decreases
B. Activity co-efficient
C. Activity
D. Mole fraction
B. Dilution
C. Formation
D. Combustion
B. Specific heat
C. Latent heat of vaporisation
D. Specific vapor volume
C. Viscosity
D. Molar heat capacity
A. (dF)T, p > 0
B. (dF)T, p = 0
C. (dA)T, v >0
A. dE dW Tds = 0
C. Tds dT + dW < 0
D. Tds = dE dW = 0
A. #NAME?
C. #NAME?
D. Dependent on the path
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