A. Saturated

B. None of these

C. Non-solidifiable

A. None of these

B. Decreases, for an exothermic reaction

D. Increases, for an endothermic reaction

B. 0

C. < 0

D. ?

A. 0.2528

B. 0.5

D. 0.25

A. Isochoric

C. Adiabatic

D. Isobaric

A. 1

B. 3

C. 0

A. ?

B. #NAME?

C. #NAME?

A. Temperature

B. Composition

D. Pressure

A. Volume

C. Pressure

D. All A, B. & C

B. 3.389

C. 1.9398

D. 4.238

A. Pressure

B. Volume

D. Neither A. nor B.

A. Molar free energy change

C. Molal concentration difference

D. Molar free energy

A. Decreases

B. Remains constant

D. Decreases logarithmically

A. Unity

B. Activity

D. Neither A. nor B

A. 1

C. 3

D. 4

A. Steady

C. Equilibrium

D. Adiabatic

A. 10-Oct

C. 13-Oct

D. 3-Oct

B. High temperature and high pressure

C. Low pressure and low temperature

D. Low pressure and high temperature

A. Simultaneous pressure & temperature change

B. Heating

C. Cooling

B. 2

C. 1

D. 3

B. Less than

C. Data insufficient, cant be predicted

D. More than

A. Compressibility

B. Co-efficient of thermal expansion

C. None of these

B. The physical state (e.g., solid, liquid or gaseous) of reactants and products

C. Whether the reaction is carried out at constant temperature or constant pressure

D. None of these

A. Joule-Thomson co-efficient

B. Specific heat at constant volume (CV)

D. Specific heat at constant pressure (Cp)

B. Normally, the gases which are easily liquefied are more soluble in common solvents

C. The gases which are capable of forming ions in aqueous solution are much more soluble in

D. er than in other solvents

E. At constant pressure, solubility of a gas in a liquid increases with rise in temperature

A. Pressure

B. Temperature

D. Neither A. nor B

B. dW dE = Tds

C. Tds dW + dE >0

D. dE dW = Tds

A. dQ = CpdT + Vdp

B. Tds = dE PdV

C. dQ = CvdT + PdV

A. rogen is 4

C. For a two phase system in equilibrium made up of four non-reacting chemical species, the

D. orisation and sublimation</strong>

E. ber of degrees of freedom is 4

F. Minimum number of degree of freedom of a system is zero

A. Entropy

B. Pressure

D. None of these

A. Molecules possess appreciable volume

B. Energy is lost during molecular collisions

C. None of these

B. None of these

C. Adiabatic

D. Reversible

A. Pressure

B. Specific heat

D. Volume

A. State function

B. Extensive property

D. Macroscopic property

A. Activity

B. Mole fraction

C. Activity co-efficient

A. 760 mm wc

B. 100 N/m2

C. 13.6 cms of Hg

A. Decrease

B. Remain same

C. Increase in summer and will decrease in winter

B. The amount of work needed is independent of path

C. work needed

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

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

B. 12 P1V1

C. 6 P1 V1

D. P1 V1

A. Critical

B. Inversion

D. Reduced

A. Tds dT + dW < 0

B. Tds = dE dW = 0

D. dE dW Tds = 0

A. Volume in the liquid state is negligible compared with that in the vapour state

B. Vapour pressure is relatively low and the temperature does not vary over wide limits

D. Vapour obeys the ideal gas law and the latent heat of vaporisation is constant

A. Isobaric

B. Adiabatic

C. Isenthalpic

A. its internal energy (U) decreases and its entropy (S) increases

C. U decreases but S is constant

D. U is constant but S decreases

B. Same as

C. More than

D. Half

A. First

B. Zeroth

D. Third

A. Cp.dT

B. ? Cv.dT

D. Cv.dT

A. High temperature

B. Low pressure

C. Low temperature only

B. Adiabatic compression of a perfect gas

C. Ideal compression of air

D. Adiabatic expansion of steam in a turbine

B. API scale

C. None of these

D. Baume scale