Explore topic-wise InterviewSolutions in Current Affairs.

This section includes 7 InterviewSolutions, each offering curated multiple-choice questions to sharpen your Current Affairs knowledge and support exam preparation. Choose a topic below to get started.

1.

Enzyme trypsin converts:

Answer»

AMINO ACIDS into proteins
Glucose into GLYCOGENS
STARCH into sugar
Proteins into amino acids

Answer :D
2.

Enzyme inhibitors may attack on

Answer»

ACTIVE site of enzyme
ALLOSTERIC site of enzyme
Tongue
Stomach walls

SOLUTION :They may attack on active SITES or allosteric sites.
3.

Enzyme inhibitors may attack on a) Active site of enzyme b) Allosteric site of enzyme c) Tongue d) Stomach walls Correct answers are

Answer»

a only
B only
a and b
a, b, C and d

Answer :C
4.

Enzyme catalysis are more effective and efficient than ordinary catalysis. Prove this statement.

Answer»

Solution : (i) Effective and EFFICIENT CONVERSION is the special charcteristic of ENZYME catalysed reactions. An enzyme MAY transform a million molecules of reactant to PRODUCT in a minute.
For e.g. `2H_2O_2 to 2H_2O + O_2`
(ii) For this reaction colloidal platinum as a catalyst the activation energy is 11.7k.cal/mole. But with the enzyme catalyst the activation energy of this reaction is less than 2k.cal/mole.
5.

Enzyme catalyst are:

Answer»

HIGHLY SPECIFIC in nature
Non-specific
Solids
Always liquid

Answer :A
6.

Enzyme catalysed reaction has maximum rate at optimum temperature. Prove it.

Answer»

SOLUTION :(i) At first rate of REACTION increases with the increase of temperature, but above a PARTICULAR temperature, the activity of enzyme is destroyed. The rate may even drop to ZERO. The temperature at which enzymic activity in HIGH or maximum is called optimum temperature.
(ii) For e.g., enzymes involved in human body have an optimum temperature `37^(@)C//98^(@)F`.
7.

Enzyme catalysis is highly specific in nature. Justify this statement.

Answer»

Solution :(i) Urea can be hydrolysed to urea by the enzyme urease.
`UNDERSET("Urea")(NH_2-underset(O)underset(||)C-NH_2) + H_2O OVERSET("Urease")to 2NH_3 + H_2O`
The catalyst MEASE (enzyme) CATALYSES urea but it does not hydrolyse methyl urea.
8.

Enzyme catalysed reaction are :

Answer»

HIGHLY specific
Usually HYDROLYTIC in nature
Usually OCCURS with EVOLUTION of gases
All

Answer :D
9.

Enzymes are:

Answer»

Moulds
Complex NITROGEN compounds
Micro-organisms
Inorganic sulphides

Answer :B
10.

Enzyme are:

Answer»

SUBSTANCES made by CHEMISTS to ACTIVATE washing powder
Very active VEGETABLE catalysts
Catalysts found in organisms
Synthetic catalysts

Answer :C
11.

Enumerate the reactions of D-glucose which cannot be explained by its open chain structure.

Answer»

SOLUTION :(1) D-glucose does not form `NaHSO_(3)` additional product, aldehyde ammonia adduct, 2, 4-DNP derivative and does not respond to SCHIFF's reagent test.
(2) When dissolved in aqueous solution, both `alpha`-D-glucose exhibit the phenomenon of mutarotation.
(3) Glucose reacts with `NH_(2)OH` to form an oxime but pentaacetyl derivative of glucose does not react with `NH_(2)OH`.
(4) D-glucose reacts with methanol in presence of dry HCl gas to form TWO isomeric methyl-D-glucosides.
12.

Enumerate the reaction and facts of D - glucosewhichcannot be explained by its open chain structure .

Answer»

Solution :REACTION of glucosethat cannot be explained byopen chain structure .
(i)Glucose gives the characteristic reactiono of alcohols and carbonyl GROP (aldehydes and ketones).
However it does not form ADDITION compoundwith ammonia and sodium bisulphiteand does not respond to 2,4-DNP TESTAND schiffs test .
(ii) The penta - acetate of glucosedoes not react within hydroxyl amine indicating the absence of FREE - CHO group.
13.

Entropy is a measure of :

Answer»

disorder
internal energy
efficiency
useful WORK DONE by the system

Answer :A
14.

Entropy will not change for the reaction

Answer»

Crystallization of sucrose from the solution
Corrosion of iron
Conversion of ice into WATER
VAPORISATION of Camphor

Solution :The change in entropy in going from one state to another is INDEPENDENT of the PATH.
15.

Entropy of vaporisation of water at 100^@C, if molar heat of vaporisation is 9710 cal mol^-1 will be:

Answer»

20 CAL `mol^-1 K^-1`
26.0 cal `mol^-1 K^-1`
24 cal `mol^-1 K^-1`
28.0 cal `mol^-1 K^-1`

ANSWER :B
16.

Entropy of ice is _____ than entropy of water vapour.

Answer»


ANSWER :LESS
17.

Entropy of the universe is

Answer»

constant
zero
continuously decreasing
continuously INCREASING

Solution :ENTROPY of the universe is increasing continuously.This is THIRD law of THERMODYNAMICS as `Delta S = + ve`
18.

Entropy of a system may depend upon

Answer»

VOLUME only
Temperature only
Pressure only
All of these

Answer :D
19.

Entropy is measure of degree of randomness. Entropy is directly proportional to temperature. Every system tries to acquire maximum state of randomness or disorder. Entropy is measure of unavailable energy. Unavailable energy = Entropy x Temperature. The ratio of entropy of vaporization and boiling point of substance remains almost constant. Which of the following process have DeltaS = -ve

Answer»

ADSORPTION
dissolution of `NH_(4)Cl` in water
`H_(2) to 2H`
`2NaHCO_(3)(s) to Na_(2)CO_(3) + CO_(2) + H_(2)O`

Answer :A
20.

Entropy is measure of degree of randomness. Entropy is directly proportional to temperature. Every system tries to acquire maximum state of randomness or disorder. Entropy is measure of unavailable energy. Unavailable energy = Entropy x Temperature. The ratio of entropy of vaporization and boiling point of substance remains almost constant. Observe the graph and identify the correct statement (s) The law of thermodynamics invented by Nernst, which helps to determine absolute entropy is

Answer»

Zero th LAW
1st law
2ND law
3RD law.

ANSWER :D
21.

Entropy is measure of degree of randomness. Entropy is directly proportional to temperature. Every system tries to acquire maximum state of randomness or disorder. Entropy is measure of unavailable energy. Unavailable energy = Entropy x Temperature. The ratio of entropy of vaporization and boiling point of substance remains almost constant. The sign of DeltaS in the reaction. N_(2)(g) + O_(2)(g) to 2NO (g)

Answer»

`+ve`
`-ve`
zero
none of these

ANSWER :A
22.

Entropy is measure of degree of randomness. Entropy is directly proportional to temperature. Every system tries to acquire maximum state of randomness or disorder. Entropy is measure of unavailable energy. Unavailable energy = Entropy x Temperature. The ratio of entropy of vaporization and boiling point of substance remains almost constant. Which of the following has DeltaS = +ve?

Answer»

`H_(2)(G) + Cl_(2)(g) to 2HCl(g)`
BOILING of egg
Crystallization of sugar
Formation of COMPLEX compound

Answer :B
23.

Entropy is a measure of disoder. For perfect crystalline substance at 0 K, entropy becomes:

Answer»

Minus
Zero
Constant
Very low

Answer :B
24.

Entropy is

Answer»

a thermodynamic CONCEPT
a state FUNCTION
independent of path
all of these

Solution :Entropy is thermodynamic concept. Entropy like any other thermodynamic property such as INTERNAL energy (U) and enthalpy (H) is a state function and `DeltaS` is independent of path.
25.

Entropy has great importance in thermodynamics. It is a state function and it is a measure of the degree of disorder or randomness of the system. More is the disorder of the system, greater will be the entropy and vice versa. It is normally expressed in terms of change of entropy. (i) For a reaction entropy change is given by DeltaS=sumS("product")-sumS("reactant") (ii) DeltaS=(Q_(rev))/(T)=(W_(rev))/(T)=(nRT ln (V_(2)//V_(1)))/(T) =nRT ln (V_(2))/(V_(1))=nR ln (P_(1))/(P_(2)) (iii) DeltaS=DeltaH-TDeltaS (iv) Entropy change in reversible and irreversible process : Consider a Carnot cycle as shown in figure below in which ab and cd are isothermal. Irrespective of the path of the system in its reversible change, dq//T is same For entire Carnot cycle (dq_(1))/(T_(1))-(dq_(2))/(T_(2))=0 :. DeltaS_("universe")=DeltsS_("system")+DeltaS_("surrounding") DeltaS_("Surrounding")=(q_(1))/(T_(1))+(q_(2))/(T_(2)) (q term includes their own sign) bc and da are adiabatics. Let dq_(1) be the heat supplied to the working system at T_(1) K and dq_(2) be heat rejected by it to the sink at T_(2) K. All these steps are reversible. In a Carnot cycle. (dq_(1)-dq_(2))/(dq_(1))=(T_(1)-T_(2))/(T_(1)) or (dq_(1))/(T_(1))=(dq_(2))/(T_(2)) Let us now confine our attention only to the change of the system from point 'a' to point 'c' and attempt to find out the ratio of heat change to the temperature at which thermal changes occur by proceeding from a to c either along abc or adc. Along the path abc, ("Heat change")/("Temp.")=(dq_(1))/(T_(1)) Along the path adc, ("Heat change")/("Temp")=(dq_(2))/(T_(2)) In case of spontaneous and irreversible expansion to volume V_(1)+V_(2), W=0 and so will be DeltaU In the reversible expansion of the gas at T K from volume V_(1) to V_(1)+V_(2), heat absorbed DeltaU+RT ln (V_(1)+V_(2))/(V_(1)) (v) Suppose n moles of an ideal gas are enclosed in a vessel A of volume V_(1) which is connected through a stop cock to a completely evacuated vessel B of volume V_(2). The system is insulated and has temperature T K. If the stop cock is opened, the gas will attain the volume V_(1)+V_(2). In a reversible isothermal expansion of the gas at T K as shown in figure II, the DeltaS_("system"), DeltaS_("surroundings") and DeltaS_("universe") will be respectively ?

Answer»

`R LN (V_(1)+V_(2))/(V_(1))`, `0`, `+ve`
`0`, `R ln (V_(1)+V_(2))/(V_(1))`, `+ve`
`R ln (V_(1)+V_(2))/(V_(2))`, `0`, `+ve`
`R ln (V_(2)+V_(1))/(V_(2))`, `0`, `-ve`

Answer :A
26.

Entropy has great importance in thermodynamics. It is a state function and it is a measure of the degree of disorder or randomness of the system. More is the disorder of the system, greater will be the entropy and vice versa. It is normally expressed in terms of change of entropy. (i) For a reaction entropy change is given by DeltaS=sumS("product")-sumS("reactant") (ii) DeltaS=(Q_(rev))/(T)=(W_(rev))/(T)=(nRT ln (V_(2)//V_(1)))/(T) =nRT ln (V_(2))/(V_(1))=nR ln (P_(1))/(P_(2)) (iii) DeltaS=DeltaH-TDeltaS (iv) Entropy change in reversible and irreversible process : Consider a Carnot cycle as shown in figure below in which ab and cd are isothermal. Irrespective of the path of the system in its reversible change, dq//T is same For entire Carnot cycle (dq_(1))/(T_(1))-(dq_(2))/(T_(2))=0 :. DeltaS_("universe")=DeltsS_("system")+DeltaS_("surrounding") DeltaS_("Surrounding")=(q_(1))/(T_(1))+(q_(2))/(T_(2)) (q term includes their own sign) bc and da are adiabatics. Let dq_(1) be the heat supplied to the working system at T_(1) K and dq_(2) be heat rejected by it to the sink at T_(2) K. All these steps are reversible. In a Carnot cycle. (dq_(1)-dq_(2))/(dq_(1))=(T_(1)-T_(2))/(T_(1)) or (dq_(1))/(T_(1))=(dq_(2))/(T_(2)) Let us now confine our attention only to the change of the system from point 'a' to point 'c' and attempt to find out the ratio of heat change to the temperature at which thermal changes occur by proceeding from a to c either along abc or adc. Along the path abc, ("Heat change")/("Temp.")=(dq_(1))/(T_(1)) Along the path adc, ("Heat change")/("Temp")=(dq_(2))/(T_(2)) In case of spontaneous and irreversible expansion to volume V_(1)+V_(2), W=0 and so will be DeltaU In the reversible expansion of the gas at T K from volume V_(1) to V_(1)+V_(2), heat absorbed DeltaU+RT ln (V_(1)+V_(2))/(V_(1)) (v) Suppose n moles of an ideal gas are enclosed in a vessel A of volume V_(1) which is connected through a stop cock to a completely evacuated vessel B of volume V_(2). The system is insulated and has temperature T K. If the stop cock is opened, the gas will attain the volume V_(1)+V_(2). In figure I, which is a reversible cyclic process, what will be the value of DeltaU, DeltaH, oint(dq)/(T) respectively ?

Answer»

`0`, `0`, `0`
`0`, `0`, `(dq_(1))/(T_(1))`
`0`, `0`, `(dq_(2))/(T_(2))`
NONE of these

Answer :A
27.

Entropy has great importance in thermodynamics. It is a state function and it is a measure of the degree of disorder or randomness of the system. More is the disorder of the system, greater will be the entropy and vice versa. It is normally expressed in terms of change of entropy. (i) For a reaction entropy change is given by DeltaS=sumS("product")-sumS("reactant") (ii) DeltaS=(Q_(rev))/(T)=(W_(rev))/(T)=(nRT ln (V_(2)//V_(1)))/(T) =nRT ln (V_(2))/(V_(1))=nR ln (P_(1))/(P_(2)) (iii) DeltaS=DeltaH-TDeltaS (iv) Entropy change in reversible and irreversible process : Consider a Carnot cycle as shown in figure below in which ab and cd are isothermal. Irrespective of the path of the system in its reversible change, dq//T is same For entire Carnot cycle (dq_(1))/(T_(1))-(dq_(2))/(T_(2))=0 :. DeltaS_("universe")=DeltsS_("system")+DeltaS_("surrounding") DeltaS_("Surrounding")=(q_(1))/(T_(1))+(q_(2))/(T_(2)) (q term includes their own sign) bc and da are adiabatics. Let dq_(1) be the heat supplied to the working system at T_(1) K and dq_(2) be heat rejected by it to the sink at T_(2) K. All these steps are reversible. In a Carnot cycle. (dq_(1)-dq_(2))/(dq_(1))=(T_(1)-T_(2))/(T_(1)) or (dq_(1))/(T_(1))=(dq_(2))/(T_(2)) Let us now confine our attention only to the change of the system from point 'a' to point 'c' and attempt to find out the ratio of heat change to the temperature at which thermal changes occur by proceeding from a to c either along abc or adc. Along the path abc, ("Heat change")/("Temp.")=(dq_(1))/(T_(1)) Along the path adc, ("Heat change")/("Temp")=(dq_(2))/(T_(2)) In case of spontaneous and irreversible expansion to volume V_(1)+V_(2), W=0 and so will be DeltaU In the reversible expansion of the gas at T K from volume V_(1) to V_(1)+V_(2), heat absorbed DeltaU+RT ln (V_(1)+V_(2))/(V_(1)) (v) Suppose n moles of an ideal gas are enclosed in a vessel A of volume V_(1) which is connected through a stop cock to a completely evacuated vessel B of volume V_(2). The system is insulated and has temperature T K. If the stop cock is opened, the gas will attain the volume V_(1)+V_(2). In irreversible cyclic process, which of the following is correct ?

Answer»

`DeltaS_("UNIVERSE") GT 0`, `DeltaS_("system")=0`, `DeltaS_("surroundings) gt 0`
`DeltaS_("universe") gt 0`, `DeltaS_("system")GT0`, `DeltaS_("surroundings) = 0`
`DeltaS_("universe") gt 0`, `DeltaS_("system")gt0`, `DeltaS_("surroundings) = 0`
`DeltaS_("universe") = 0`, `DeltaS_("system")=0`, `DeltaS_("surroundings) = 0`

ANSWER :A
28.

Entropy has great importance in thermodynamics. It is a state function and it is a measure of the degree of disorder or randomness of the system. More is the disorder of the system, greater will be the entropy and vice versa. It is normally expressed in terms of change of entropy. (i) For a reaction entropy change is given by DeltaS=sumS("product")-sumS("reactant") (ii) DeltaS=(Q_(rev))/(T)=(W_(rev))/(T)=(nRT ln (V_(2)//V_(1)))/(T) =nRT ln (V_(2))/(V_(1))=nR ln (P_(1))/(P_(2)) (iii) DeltaS=DeltaH-TDeltaS (iv) Entropy change in reversible and irreversible process : Consider a Carnot cycle as shown in figure below in which ab and cd are isothermal. Irrespective of the path of the system in its reversible change, dq//T is same For entire Carnot cycle (dq_(1))/(T_(1))-(dq_(2))/(T_(2))=0 :. DeltaS_("universe")=DeltsS_("system")+DeltaS_("surrounding") DeltaS_("Surrounding")=(q_(1))/(T_(1))+(q_(2))/(T_(2)) (q term includes their own sign) bc and da are adiabatics. Let dq_(1) be the heat supplied to the working system at T_(1) K and dq_(2) be heat rejected by it to the sink at T_(2) K. All these steps are reversible. In a Carnot cycle. (dq_(1)-dq_(2))/(dq_(1))=(T_(1)-T_(2))/(T_(1)) or (dq_(1))/(T_(1))=(dq_(2))/(T_(2)) Let us now confine our attention only to the change of the system from point 'a' to point 'c' and attempt to find out the ratio of heat change to the temperature at which thermal changes occur by proceeding from a to c either along abc or adc. Along the path abc, ("Heat change")/("Temp.")=(dq_(1))/(T_(1)) Along the path adc, ("Heat change")/("Temp")=(dq_(2))/(T_(2)) In case of spontaneous and irreversible expansion to volume V_(1)+V_(2), W=0 and so will be DeltaU In the reversible expansion of the gas at T K from volume V_(1) to V_(1)+V_(2), heat absorbed DeltaU+RT ln (V_(1)+V_(2))/(V_(1)) (v) Suppose n moles of an ideal gas are enclosed in a vessel A of volume V_(1) which is connected through a stop cock to a completely evacuated vessel B of volume V_(2). The system is insulated and has temperature T K. If the stop cock is opened, the gas will attain the volume V_(1)+V_(2). In the figure-I, what will be the value of (dq)/(T) along the line bc ?

Answer»

`0`
`dq_(1)//T`
`(dq_(2))/(T_(2))`
`(dq_(1))/(T_(1))-(dq_(2))/(T_(2))`

ANSWER :A
29.

Entropy has great importance in thermodynamics. It is a state function and it is a measure of the degree of disorder or randomness of the system. More is the disorder of the system, greater will be the entropy and vice versa. It is normally expressed in terms of change of entropy. (i) For a reaction entropy change is given by DeltaS=sumS("product")-sumS("reactant") (ii) DeltaS=(Q_(rev))/(T)=(W_(rev))/(T)=(nRT ln (V_(2)//V_(1)))/(T) =nRT ln (V_(2))/(V_(1))=nR ln (P_(1))/(P_(2)) (iii) DeltaS=DeltaH-TDeltaS (iv) Entropy change in reversible and irreversible process : Consider a Carnot cycle as shown in figure below in which ab and cd are isothermal. Irrespective of the path of the system in its reversible change, dq//T is same For entire Carnot cycle (dq_(1))/(T_(1))-(dq_(2))/(T_(2))=0 :. DeltaS_("universe")=DeltsS_("system")+DeltaS_("surrounding") DeltaS_("Surrounding")=(q_(1))/(T_(1))+(q_(2))/(T_(2)) (q term includes their own sign) bc and da are adiabatics. Let dq_(1) be the heat supplied to the working system at T_(1) K and dq_(2) be heat rejected by it to the sink at T_(2) K. All these steps are reversible. In a Carnot cycle. (dq_(1)-dq_(2))/(dq_(1))=(T_(1)-T_(2))/(T_(1)) or (dq_(1))/(T_(1))=(dq_(2))/(T_(2)) Let us now confine our attention only to the change of the system from point 'a' to point 'c' and attempt to find out the ratio of heat change to the temperature at which thermal changes occur by proceeding from a to c either along abc or adc. Along the path abc, ("Heat change")/("Temp.")=(dq_(1))/(T_(1)) Along the path adc, ("Heat change")/("Temp")=(dq_(2))/(T_(2)) In case of spontaneous and irreversible expansion to volume V_(1)+V_(2), W=0 and so will be DeltaU In the reversible expansion of the gas at T K from volume V_(1) to V_(1)+V_(2), heat absorbed DeltaU+RT ln (V_(1)+V_(2))/(V_(1)) (v) Suppose n moles of an ideal gas are enclosed in a vessel A of volume V_(1) which is connected through a stop cock to a completely evacuated vessel B of volume V_(2). The system is insulated and has temperature T K. If the stop cock is opened, the gas will attain the volume V_(1)+V_(2). Ethanol boils at 78.4^(@)C and standard enthalpy of vaporisation of ethanol is 42.4 kJ//mol. Calculate the enthropy of vaporisation of ethanol

Answer»

`0`
`90 J K^(-1)MOL^(-1)`
`50 J K^(-1)mol^(-1)`
`120.66J K^(-1)mol^(-1)`

Answer :D
30.

Entropy has great importance in thermodynamics. It is a state function and it is a measure of the degree of disorder or randomness of the system. More is the disorder of the system, greater will be the entropy and vice versa. It is normally expressed in terms of change of entropy. (i) For a reaction entropy change is given by DeltaS=sumS("product")-sumS("reactant") (ii) DeltaS=(Q_(rev))/(T)=(W_(rev))/(T)=(nRT ln (V_(2)//V_(1)))/(T) =nRT ln (V_(2))/(V_(1))=nR ln (P_(1))/(P_(2)) (iii) DeltaS=DeltaH-TDeltaS (iv) Entropy change in reversible and irreversible process : Consider a Carnot cycle as shown in figure below in which ab and cd are isothermal. Irrespective of the path of the system in its reversible change, dq//T is same For entire Carnot cycle (dq_(1))/(T_(1))-(dq_(2))/(T_(2))=0 :. DeltaS_("universe")=DeltsS_("system")+DeltaS_("surrounding") DeltaS_("Surrounding")=(q_(1))/(T_(1))+(q_(2))/(T_(2)) (q term includes their own sign) bc and da are adiabatics. Let dq_(1) be the heat supplied to the working system at T_(1) K and dq_(2) be heat rejected by it to the sink at T_(2) K. All these steps are reversible. In a Carnot cycle. (dq_(1)-dq_(2))/(dq_(1))=(T_(1)-T_(2))/(T_(1)) or (dq_(1))/(T_(1))=(dq_(2))/(T_(2)) Let us now confine our attention only to the change of the system from point 'a' to point 'c' and attempt to find out the ratio of heat change to the temperature at which thermal changes occur by proceeding from a to c either along abc or adc. Along the path abc, ("Heat change")/("Temp.")=(dq_(1))/(T_(1)) Along the path adc, ("Heat change")/("Temp")=(dq_(2))/(T_(2)) In case of spontaneous and irreversible expansion to volume V_(1)+V_(2), W=0 and so will be DeltaU In the reversible expansion of the gas at T K from volume V_(1) to V_(1)+V_(2), heat absorbed DeltaU+RT ln (V_(1)+V_(2))/(V_(1)) (v) Suppose n moles of an ideal gas are enclosed in a vessel A of volume V_(1) which is connected through a stop cock to a completely evacuated vessel B of volume V_(2). The system is insulated and has temperature T K. If the stop cock is opened, the gas will attain the volume V_(1)+V_(2). Which of the following statement is correct about entropy ?

Answer»

It is a FUNCTION of TEMPERATURE only
It is a function of PRESSURE only
It is a function of VOLUME only
It is a function of pressure, temperature and volume.

Answer :D
31.

Entropy decreases during:

Answer»

CRYSTALLISATION of SUCROSE from solution
Rusting of iron
Melting of ice
Vaporisation of camphor

Answer :A
32.

Entropy changes for the process, H_(2)O_((l))rarrH_(2)O_((s)) at normal pressure and 274 K are given below DeltaS_("system")=-22.13, DeltaS_("surr")=+22.05,the process is non-spontaneous because

Answer»

`DeltaS_("SYSTEM") " is " -ve`
`DeltaS_("surr")" is +ve"`
`DeltaS_(U)" is -ve"`
`DeltaS_("system")ne DeltaS_("surr")`

Solution :`DeltaS_(u)=DeltaS_("system")+DeltaS_("SURROUNDING")=-22.13+22.05 =-0.08`
For a spontaneous process, `DeltaS_(u)` MUST be positive i.e.,
`DeltaS_(u)=DeltaS_("system")+DeltaS_("surrounding")gt0`.
33.

Entropy changes for the process H_(2)O(l) rarr H_(2)O(g) at normal pressure and 274 K are given below Delta G_(system) = - 22.13, Delta S_("surroundings") = + 22.05 Then process is non spontaneous because

Answer»

`Delta G_("system")` is -ve
`Delta G_("SURROUNDING")` is +ve
`Delta S_("UNIVERSE")` is -ve
`Delta G_(system) ne Delta S_("surrounding")`

SOLUTION :For a process to be spontaneous `Delta S_("universe")` must be positive. Here,
`Delta S_("universe") = - 22.13 + 22.05 = - 0.08 KJ`
34.

Entropy change in a process where 1 litre of liquid He is poured into ice cold water is

Answer»

FINITE and positive
Finite and negative
Zero
Infinity

ANSWER :A
35.

Entropy change for an isothermal expansion of one mole of an ideal gas from volume V_(1) to V_(2) is :

Answer»

`R "ln" (V_(2))/(V_(1))`
`2.303 R "ln" (V_(2))/(V_(1))`
`R "ln" (V_(1))/(V_(2))`
`R "ln" (V_(2) - V_(1))`

ANSWER :A
36.

Entropy change for an adiabatic reversible process is

Answer»

POSITIVE
zero
negative
INFINITE

ANSWER :B
37.

Entropy change for an adiabatic reversible process is :

Answer»

ZERO
`+ve`
`-ve`
NEGATIVE or zero

Answer :A
38.

Entries of Column-I are to be matched with entries of Coloumn-II. Each entry of Column-I may have the matching with one or more than one entries of Column-II.

Answer»


ANSWER :A::B::C::D
39.

Entries of Column-I are to be matched with entries of Coloumn-II. Each entry of Column-I may have the matching with one or more than one entries of Column-II.

Answer»


ANSWER :A::B::C::D
40.

Entries of Column-I are to be matched with entries of Coloumn-II. Each entry of Column-I may have the matching with one or more than one entries of Column-II. Column-I contains four statements following reason and Column-II consists of four options P, Q, R, S Answer the following P-If both statement and reason are true and reason is correct explanation of statement. Q-If both statement and reason are true and reason is not correct explanation of statement. R-If statement is correct and reason is incorrect. S-If both statement and reason are incorrect.

Answer»


ANSWER :A::B::C::D
41.

Entries of Column-I are to be matched with entries of Coloumn-II. Each entry of Column-I may have the matching with one or more than one entries of Column-II.

Answer»


ANSWER :A::B::C::D
42.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
43.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
44.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
45.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
46.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
47.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
48.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
49.

Entries of Column-I are to be matched with entrices of Column-II. Each entry of Column-I may have the matching with one or more than entries of Column-II

Answer»


ANSWER :A::B::C::D
50.

Enthalpy of which of the following reactions does not represent the standard enthalpy of formation?

Answer»

`H_2(g)+FRAC{1}{2}O_2(g)rightarrow H_2O(L)`
`H_2(g)+Br_2(l)rightarrow 2HBr(g)`
S(rhombic, s) + `O_2(g)rightarrowSO_2(g)`
2C (graphite, s)+`3H_2(g)+frac{1}{2}O_2(g)rightarrow C_2H_5OH(l)`

Answer :B