Point out the wrong statement in relation to enthalpy
It is a state function
It is an intensive property
It is independent of the path followed for the change
Its value depends upon the amount of substance in the system
Which of the following is zero for an isochoric process
dP
dV
dT
dE
Mark the correct statement
For a chemical reaction to be feasible, ΔG should be zero
Entropy is a measure of order in a system
For a chemical reaction to be feasible, ΔG should be positive
The total energy of an isolated system is constant
Internal energy is an example of [Pb. PMT 2000]
Path function
State function
Both (1) and (2)
None of these
The intensive property among these quantities is
Enthalpy
Mass/volume
Mass
Volume
Which of the following is not a state function?
ΔS
ΔG
ΔH
ΔQ
Which of the following is true for an adiabatic process [DCE 2002; MP PET 1995, 98, 2004; CPMT 1990; MP PMT 1998, 2002]
ΔH = 0
ΔW = 0
ΔQ = 0
ΔV = 0
Which of the following is not a state function
Internal energy
Work
Entropy
Among them, intensive property is [AFMC 2004]
Surface tension
First law of thermodynamics is the law of conservation of=
Linear momentum
Energy
Angular momentum
A mixture of two moles of carbon monoxide and one mole of oxygen, in a closed vessel is ignited to convert the carbon monoxide to carbon dioxide. If ΔH is the enthalpy change and ΔE is the change in internal energy, then
ΔH > ΔE
ΔH < ΔE
ΔH = ΔE
The relationship depends on the capacity of the vessel
The relation between ΔE and ΔH is [MP PET 1992; MP PMT 1996; MP PET/PMT 1998]
ΔH=ΔE−P ΔV
ΔH=ΔE+P ΔV
ΔE=ΔV+ΔH
ΔE=ΔH+P ΔV
At constant T and P, which one of the following statements is correct for the reaction, CO(g)+12O2(g)→CO2(g)
ΔH is independent of the physical state of the reactants of that compound
For the reaction of one mole of zinc dust with one mole of sulphuric acid in a bomb calorimeter, ΔU and w correspond to
ΔU<0, w=0
ΔU=0, w<0
ΔU>0, w=0
ΔU<0, w>0
If ΔH is the change in enthalpy and ΔE the change in internal energy accompanying a gaseous reaction
ΔH is always greater than ΔE
ΔH < ΔE only if the number of moles of the products is greater than the number of the reactants
ΔH is always less than ΔE
ΔH < ΔE only if the number of moles of the products is less than the number of moles of the reactants
Enthalpy for the reaction C + O2 → CO2 is-
Positive
Negative
Zero
None
The work done in ergs for the reversible expansion of one mole of an ideal gas from a volume of 10 liters to 20 liters at 25°C is -
-2.303×298×0.082 log 2
-298×107×8.31×2.303 log 2
2.303×298×0.082 log 0.5
-8.31×107×298−2.303 log 0.5
In a reversible isothermal process, the change in internal energy is-
None of the above
The enthalpy of neutralization of which of the following acids and bases is nearly –13.6 Kcal [Roorkee 1999]
HCN and NaOH
HCl and KOH
HCl and HCN
HCl and NH4OH
Work done during isothermal expansion of one mole of an ideal gas from 10 atm to 1 atm at 300 K is (Gas constant = 2)
938.8 cal.
1138.8 cal.
1381.8 cal.
1581.8 cal.
Joule-Thomson expansion is [JIPMER 2000]
Isobaric
Isoenthalpic
Isothermal
In an adiabatic expansion of an ideal gas-
W = ΔE
ΔE = 0
W = 0
For the reaction
CH3COOH(l)+2O2(g)⇌2CO2(g)+2H2O(l)
at 25°C and 1 atm. pressure, ΔH = –874 kJ. The change in internal energy (ΔE) is -
– 874 kJ
– 971.53 kJ
+ 971.53 kJ
+ 874 kJ
One mole of an ideal gas is allowed to expand freely and adiabatically into a vacuum until its volume has doubled. A statement that is not true concerning this expression is [Pb. PMT 1998]
ΔS = 0
At 27°C, one mole of an ideal gas is compressed isothermally and reversibly from a pressure of 2 atm to 10 atm. The values of ΔE and q are (R = 2)
0, – 965.84 cal
– 965.84 cal, + 965.84 cal
+ 865.58 cal, – 865.58 cal
– 865.58 cal, – 865.58 cal
ΔE° of combustion of isobutylene is –X kJ mol–1. The value of ΔH° is [DCE 2004]
= ΔE°
> ΔE°
= 0
< ΔE°
An ideal gas expands in volume from 1 × 10–3 m3 to 1 × 10–2 m3 at 300 K against a constant pressure of 1 × 105 Nm–2. The work done is [AIEEE 2004]
270 kJ
–900 kJ
–900 J
900 kJ
The spontaneous flow of heat is always
From low to high pressure
From high to high pressure
Unidirectional from lower temperature to higher temperature
Unidirectional from the higher to lower temperature
The mixing of non-reacting gases is generally accompanied by
Decrease in entropy
Increase in entropy
Change in enthalpy
Change in free energy
An irreversible process occuring isothermally in an isolated system leads to
Zero entropy
An increase in the total entropy of the system
A decrease in the total entropy of the system
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