The enthalpy change of a reaction does not depend on

The enthalpy change of a reaction does not depend on
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The enthalpy change of a reaction does not depend on A. State of reactants and products B. ... D. Initial and final ethalpy change of reaction
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What is the standard enthalpy change at 298 K for the following reaction? `CO_(2) (g)+ C("diamond") rarr 2CO(g)` Given : `DeltaH_(f)^(@)(CO,g) = - 110

Description : What is the standard enthalpy change at 298 K for the following reaction? `CO_(2) (g)+ C("diamond") rarr 2CO(g)` Given : `DeltaH_(f)^(@)(CO,g) = - 110

Last Answer : What is the standard enthalpy change at 298 K for the following reaction? `CO_(2) (g)+ C("diamond") rarr 2CO(g ... `+172.5 kJ//mol` D. `170.5 kJ//mol`

The enthalpy change for the reaction `2C("graphite")+3H_(2)(g)rarrC_(2)H_(6)(g)` is called

Description : The enthalpy change for the reaction `2C("graphite")+3H_(2)(g)rarrC_(2)H_(6)(g)` is called

Last Answer : The enthalpy change for the reaction `2C("graphite")+3H_(2)(g)rarrC_(2)H_(6)(g ... combustion C. Enthalpy of hydrogenation D. Enthalpy of vaporisation

The enthalpy of formation of ammonia is `-46.0 KJ mol^(-1)` . The enthalpy change for the reaction `2NH_(3)(g)rarr N_(2)(g)+3H_(2)(g)` is :

Description : The enthalpy of formation of ammonia is `-46.0 KJ mol^(-1)` . The enthalpy change for the reaction `2NH_(3)(g)rarr N_(2)(g)+3H_(2)(g)` is :

Last Answer : The enthalpy of formation of ammonia is `-46.0 KJ mol^(-1)` . The enthalpy change for the reaction `2NH_(3)(g) ... mol^(-1)` D. `-92.0 KJ mol^(-1)`

The enthalpy change for a given reaction at `298 K` is `-x cal mol^(-1)`. If the reaction occurs spontaneously at `298 K`, the entropy change at that

Description : The enthalpy change for a given reaction at `298 K` is `-x cal mol^(-1)`. If the reaction occurs spontaneously at `298 K`, the entropy change at that

Last Answer : The enthalpy change for a given reaction at `298 K` is `-x cal mol^(-1)`. If the reaction occurs ... (-1)` C. Cannot be negative D. Cannot be positive

The value of enthalpy change `(DeltaH)` for the reaction `C_(2)H_(5)OH (l)+3O_(2) (g) rarr 2CO_(2) (g) +3H_(2)O (l)` at `27^(@)C` is `-1366.5 kJ mol^(

Description : The value of enthalpy change `(DeltaH)` for the reaction `C_(2)H_(5)OH (l)+3O_(2) (g) rarr 2CO_(2) (g) +3H_(2)O (l)` at `27^(@)C` is `-1366.5 kJ mol^(

Last Answer : The value of enthalpy change `(DeltaH)` for the reaction `C_(2)H_(5)OH (l)+3O_(2) (g) rarr 2CO_(2) (g) + ... 1369. kJ` C. `-1364.0 kJ` D. `-1361.5 kJ`

Consider the reaction: `N_(2) + 3H_(2) hArr 2NH_(3)` carried out at constant pressure and temperature. If `DeltaH` and `DeltaU` are change in enthalpy

Description : Consider the reaction: `N_(2) + 3H_(2) hArr 2NH_(3)` carried out at constant pressure and temperature. If `DeltaH` and `DeltaU` are change in enthalpy

Last Answer : Consider the reaction: `N_(2) + 3H_(2) hArr 2NH_(3)` carried out at constant pressure and temperature. If ` ... Delta H = 0` D. `Delta H = Delta U`

The enthalpy change `(Delta H)` for the reaction `N_(2) (g)+3H_(2)(g) rarr 2NH_(3)(g)` is `-92.38 kJ` at `298 K`. What is `Delta U` at `298 K`?

Description : The enthalpy change `(Delta H)` for the reaction `N_(2) (g)+3H_(2)(g) rarr 2NH_(3)(g)` is `-92.38 kJ` at `298 K`. What is `Delta U` at `298 K`?

Last Answer : The enthalpy change `(Delta H)` for the reaction `N_(2) (g)+3H_(2)(g) rarr 2NH_(3)(g)` is `-92.38 kJ` at ` ... -87.42 kJ` C. `-97.34 kJ` D. `-89.9 kJ`

The enthalpy and entropy change for the reaction, `Br_(2)(l)+Cl_(2)(g)rarr2BrCl(g)` are `30KJmol^(-1)` and `105JK^(-1)mol^(-1)` respectively. The temp

Description : The enthalpy and entropy change for the reaction, `Br_(2)(l)+Cl_(2)(g)rarr2BrCl(g)` are `30KJmol^(-1)` and `105JK^(-1)mol^(-1)` respectively. The temp

Last Answer : The enthalpy and entropy change for the reaction, `Br_(2)(l)+Cl_(2)(g)rarr2BrCl(g)` are `30KJmol^(-1)` and ` ... 285.7 K B. 273 K C. 450 K D. 300 K

What is meant by entropy driven reaction? How can the reaction with positive change of enthalpy and entropy be made entropy driven?

Description : What is meant by entropy driven reaction? How can the reaction with positive change of enthalpy and entropy be made entropy driven?

Last Answer : Ans.The free energy change of a reaction is given by ΔG = ΔH - TΔS For a reaction to be spontaneous, ΔG should be -ve. If both ΔH and ΔS are positive ΔG can be -ve if TΔS>ΔH in magnitude. Thus, entropy ... is low, TΔS should be greater than ΔH (ii) If ΔS is small, T should be so large that TΔS>ΔH.

Entropy change of the reaction, H2O (liquid) → H2O (gas), is termed as the enthalpy of (A) Solution (B) Vaporisation (C) Formation (D) Sublimation

Description : Entropy change of the reaction, H2O (liquid) → H2O (gas), is termed as the enthalpy of (A) Solution (B) Vaporisation (C) Formation (D) Sublimation

Last Answer : (B) Vaporisation

The total change in the enthalpy of a system is independent of the (A) Number of intermediate chemical reactions involved (B) Pressure and temperature (C) State of combination and aggregation in the beginning and at the end of the reaction (D) None of these

Description : The total change in the enthalpy of a system is independent of the (A) Number of intermediate chemical reactions involved (B) Pressure and temperature (C) State of combination and aggregation in the beginning and at the end of the reaction (D) None of these

Last Answer : (A) Number of intermediate chemical reactions involved

"If different processes are used to bring about the same chemical reaction, the enthalpy change is same for all of them". This is __________ law. (A) Hess's (B) Kirchoff's (C) Lavoisier and Laplace (D) None of these

Description : "If different processes are used to bring about the same chemical reaction, the enthalpy change is same for all of them". This is __________ law. (A) Hess's (B) Kirchoff's (C) Lavoisier and Laplace (D) None of these

Last Answer : (A) Hess's

For an exothermic reaction (A) Only enthalpy change (ΔH) is negative (B) Only internal energy change (ΔE) is negative (C) Both ΔH and ΔE are negative (D) Enthalpy change is zero

Description : For an exothermic reaction (A) Only enthalpy change (ΔH) is negative (B) Only internal energy change (ΔE) is negative (C) Both ΔH and ΔE are negative (D) Enthalpy change is zero

Last Answer : (C) Both ΔH and ΔE are negative

“The enthalpy change for any chemical reaction is independent of the intermediate stages, provided the initial and final conditions are the same for each route.” This statement is known as:

Description : “The enthalpy change for any chemical reaction is independent of the intermediate stages, provided the initial and final conditions are the same for each route.” This statement is known as:  A. Dulong’s Law  B. Dalton’s Law  C. Hess’s Law  D. Petit Law

Last Answer : Hess’s Law

Assertion :- Entropy of system increases for a spontaneous reactions. Reason :- Enthalpy of reaction always decreases for spontaneous reaction.

Description : Assertion :- Entropy of system increases for a spontaneous reactions. Reason :- Enthalpy of reaction always decreases for spontaneous reaction.

Last Answer : Assertion :- Entropy of system increases for a spontaneous reactions. Reason :- Enthalpy of reaction ... D. If both Assertion & Reason are false.

The enthalpy of a reaction at 273 K. is -3.57 KJ. What will be the enthalpy of reaction at 373 K if `DeltaC_(p)` = zero :-

Description : The enthalpy of a reaction at 273 K. is -3.57 KJ. What will be the enthalpy of reaction at 373 K if `DeltaC_(p)` = zero :-

Last Answer : The enthalpy of a reaction at 273 K. is -3.57 KJ. What will be the enthalpy of reaction at 373 K if `DeltaC_ ... C. `-3.57xx(373)/(273)` D. `-375`

The enthalpy of formation of `CO(g), CO_(2)(g),N_(2)O(g)` and `N_(2)O_(4)(g)` is `-110,-393,+81` and 10 kJ / mol respectively. For the reaction `N_(2)

Description : The enthalpy of formation of `CO(g), CO_(2)(g),N_(2)O(g)` and `N_(2)O_(4)(g)` is `-110,-393,+81` and 10 kJ / mol respectively. For the reaction `N_(2)

Last Answer : The enthalpy of formation of `CO(g), CO_(2)(g),N_(2)O(g)` and `N_(2)O_(4)(g)` is `-110,-393,+81` and 10 ... is A. `-212` B. `+212` C. `+778` D. `-778`

The absolute enthalpy of neutralization of the reaction, `MgO(s)+2HCl(aq.)+H_(2)O(l)` will be

Description : The absolute enthalpy of neutralization of the reaction, `MgO(s)+2HCl(aq.)+H_(2)O(l)` will be

Last Answer : The absolute enthalpy of neutralization of the reaction, `MgO(s)+2HCl(aq.)+H_(2)O(l)` will be A. `57.33" kj ... )` D. Less than `=57.33" kj mol"^(-1)`

If you need to reverse the following reaction and multiply it by 2 in order for it to be an intermediate reaction in a Hess's law problem what would be the final value for the enthalpy of reaction yo?

Description : If you need to reverse the following reaction and multiply it by 2 in order for it to be an intermediate reaction in a Hess's law problem what would be the final value for the enthalpy of reaction yo?

Last Answer : 2820 kJ

If you need to reverse the following reaction in order for it to be an intermediate reaction in a Hess's law problem what would be the final value for the enthalpy of rea?

Description : If you need to reverse the following reaction in order for it to be an intermediate reaction in a Hess's law problem what would be the final value for the enthalpy of rea?

Last Answer : 286 kJ

Which reaction shows that the enthalpy of formation of H2S is Hf -20.6 kJmol?

Description : Which reaction shows that the enthalpy of formation of H2S is Hf -20.6 kJmol?

Last Answer : H2(g) + S(s) —> H2S + 20.6 kJ

If a reaction has an enthalpy of -54.32 kJ/mol and an entropy of -354.2 J/(K*mol), what is the Gibbs free Energy at 54.3(degrees c)?

Description : If a reaction has an enthalpy of -54.32 kJ/mol and an entropy of -354.2 J/(K*mol), what is the Gibbs free Energy at 54.3(degrees c)?

Last Answer : DeltaG = DeltaH - TDeltaS dG = -54.32 kJ/mol - (54'32+273)K(-354.2J/molK) NB Thevtemperature is quoted in Kelvin(K) and the Entropy must be converted to kJ by dividing by '1000'/ Hence dG = ... 115.94 kJ/mol dG = (+)61.61 kJ/mol Since dG is positive, the reaction is NOT thermodynamically feasible.

In the reaction, C + O2 → CO2; ΔH = - 94 kcal. What is the heat content (enthalpy) of O2? (A) -94 kcal (B) > -94 kcal (C) < - 94 kcal (D) Zero

Description : In the reaction, C + O2 → CO2; ΔH = - 94 kcal. What is the heat content (enthalpy) of O2? (A) -94 kcal (B) > -94 kcal (C) < - 94 kcal (D) Zero

Last Answer : (D) Zero

The isentropic enthalpy drop in moving blade is two-third of the isentropic enthalpy drop in fixed blades of a turbine. The degree of reaction will be (A) 0.4 (B) 0.56 (C) 0.67 (D) 1.67

Description : The isentropic enthalpy drop in moving blade is two-third of the isentropic enthalpy drop in fixed blades of a turbine. The degree of reaction will be (A) 0.4 (B) 0.56 (C) 0.67 (D) 1.67

Last Answer : (A) 0.4

The first law of thermodynamics is based on which of the following principles?  a. conservation of mass  b. the enthalpy-entropy relationship  c. action – reaction  d. conservation of energy

Description : The first law of thermodynamics is based on which of the following principles?  a. conservation of mass  b. the enthalpy-entropy relationship  c. action – reaction  d. conservation of energy

Last Answer : conservation of energy

What is the energy absorbed during chemical reaction under constant volume conditions?  A. Entropy  B. Ion exchange  C. Enthalpy  D. Enthalpy of reaction

Description : What is the energy absorbed during chemical reaction under constant volume conditions?  A. Entropy  B. Ion exchange  C. Enthalpy  D. Enthalpy of reaction

Last Answer : Enthalpy

In any chemical reaction, a quantity that decrease to a minimum is: w) free energy x) entropy y) temperature z) enthalpy

Description : In any chemical reaction, a quantity that decrease to a minimum is: w) free energy x) entropy y) temperature z) enthalpy

Last Answer : ANSWER: W -- FREE ENERGY

What does the reaction rate depend on ?

Last Answer : : The reaction rate depends on the time and density

Rate constant for a first order reaction does not depend upon reaction time, extent of reaction and the initial concentration of reactants; but it is afunction of reaction temperature. In a chemical reaction, the time requiredto reduce the concentration of reactant from 100 gm moles/litre to 50 gmmoles/litre is same as that required to reduce it from 2 gm moles/litre to 1gm mole/litre in the same volume. Then the order of this reaction is:(A) 0(B) 1(C) 2(D) 3

Description : Rate constant for a first order reaction does not depend upon reaction time, extent of reaction and the initial concentration of reactants; but it is afunction of reaction temperature. In a chemical reaction, the time required to ... Then the order of this reaction is: (A) 0 (B) 1 (C) 2 (D) 3

Last Answer : (B) 1

The units of frequency factor in Arrhenius equation (A) Are the same as those of the rate constant (B) Depend on the order of the reaction (C) Depend on temperature, pressure etc. of the reaction (D) Are cycles per unit time

Description : The units of frequency factor in Arrhenius equation (A) Are the same as those of the rate constant (B) Depend on the order of the reaction (C) Depend on temperature, pressure etc. of the reaction (D) Are cycles per unit time

Last Answer : (A) Are the same as those of the rate constant

Photochemical reaction rate does not depend significantly on temperature, because (A) It is a reversible reaction (B) It is an exothermic reaction (C) The energy of reacting molecules exceeds the activation energy by absorption of light (D) None of these

Description : Photochemical reaction rate does not depend significantly on temperature, because (A) It is a reversible reaction (B) It is an exothermic reaction (C) The energy of reacting molecules exceeds the activation energy by absorption of light (D) None of these

Last Answer : (C) The energy of reacting molecules exceeds the activation energy by absorption of light

An irreversible first order reaction is being carried out in a CSTR and PFR of same volume. The liquid flow rates are same. The relative conversion will (A) Be more in CSTR than in PFR (B) Be more in PFR than in CSTR (C) Be same in both cases (D) Depend on the temperature

Description : An irreversible first order reaction is being carried out in a CSTR and PFR of same volume. The liquid flow rates are same. The relative conversion will (A) Be more in CSTR than in PFR (B) Be more in PFR than in CSTR (C) Be same in both cases (D) Depend on the temperature

Last Answer : (B) Be more in PFR than in CSTR

For the gaseous phase chemical reaction, C2H4(g) + H2O(g) ↔ C2H5OH(g), the equilibrium conversion does not depend on the (A) Steam to ethylene ratio (B) Temperature (C) Pressure (D) None of these

Description : For the gaseous phase chemical reaction, C2H4(g) + H2O(g) ↔ C2H5OH(g), the equilibrium conversion does not depend on the (A) Steam to ethylene ratio (B) Temperature (C) Pressure (D) None of these

Last Answer : (D) None of these

Does anyone know of a link for help on solving the change in enthalpy?

Description : Does anyone know of a link for help on solving the change in enthalpy?

Last Answer : Wikipedia explains it well. http://en.wikipedia.org/wiki/Enthalpy

What is Enthalpy Change ?

Description : What is Enthalpy Change ?

Last Answer : : The matte energy that is obtained by combining the product of pressure and volume with the internal energy of a system is called enthalpy. Enthalpy is expressed by H. Therefore - enthalpy = ... of a system can be accurately determined. Change of enthalpy = [product enthalpy - reactive enthalpy]

The change in the enthalpy of `NaOH+HCl rarr NaCl+H_(2)O` is called :

Description : The change in the enthalpy of `NaOH+HCl rarr NaCl+H_(2)O` is called :

Last Answer : The change in the enthalpy of `NaOH+HCl rarr NaCl+H_(2)O` is called : A. Heat of ... of reaction C. Heat of hydration D. Heat of solution

`Delta_(f)^(@)` for `CO_(2(g)), CO_((g))` and `H_(2)O_((g))` are `-393.5,-110.5` and `-241.8kJ mol^(-1)` respectively. The standard enthalpy change `(

Description : `Delta_(f)^(@)` for `CO_(2(g)), CO_((g))` and `H_(2)O_((g))` are `-393.5,-110.5` and `-241.8kJ mol^(-1)` respectively. The standard enthalpy change `(

Last Answer : `Delta_(f)^(@)` for `CO_(2(g)), CO_((g))` and `H_(2)O_((g))` are `-393.5,-110.5` and `-241.8kJ mol^(-1 ... A. `524.1` B. `41.2` C. `-262.5` D. `-41.2`

Standard enthalpy of formation of ethane is -84.7kjper mol calculate the enthalpy change for the formation of 0.1kg ethane

Description : Standard enthalpy of formation of ethane is -84.7kjper mol calculate the enthalpy change for the formation of 0.1kg ethane

Last Answer : Standard enthalpy of formation of ethane is -84.7kjper mol calculate the enthalpy change for the formation of 0.1kg ethane

The change in enthalpy per unit weight of adsorbed gas when adsorbed on gas free or "outgassed" adsorbent to from a definite concentration of adsorbate is called its (A) Integral heat of adsorption (B) Heat of wetting (C) Differential heat of adsorption (D) Heat of normal condensation

Description : The change in enthalpy per unit weight of adsorbed gas when adsorbed on gas free or "outgassed" adsorbent to from a definite concentration of adsorbate is called its (A) Integral heat of adsorption (B) Heat of wetting (C) Differential heat of adsorption (D) Heat of normal condensation

Last Answer : (A) Integral heat of adsorption

The change in enthalpy, when a unit quantity of gas is absorbed by relatively large quantity of adsorbent (on which a definite concentration of the adsorbed gas already exists) is termed as the (A) Differential heat of adsorption (B) Heat of wetting (C) Integral heat of adsorption (D) None of these

Description : The change in enthalpy, when a unit quantity of gas is absorbed by relatively large quantity of adsorbent (on which a definite concentration of the adsorbed gas already exists) is termed as the (A) ... (B) Heat of wetting (C) Integral heat of adsorption (D) None of these

Last Answer : (A) Differential heat of adsorption

Pick out the wrong statement. (A) Minimum number of degree of freedom of a system is zero (B) Degree of freedom of a system containing a gaseous mixture of helium, carbon dioxide and hydrogen is 4 (C) For a two phase system in equilibrium made up of fourchemical species, the number of degrees of freedom is 4 (D) Enthalpy and internal energy change is zero during phase change processes like melting, vaporisation and sublimation

Description : Pick out the wrong statement. (A) Minimum number of degree of freedom of a system is zero (B) Degree of freedom of a system containing a gaseous mixture of helium, carbon ... ) Enthalpy and internal energy change is zero during phase change processes like melting, vaporisation and sublimation

Last Answer : (D) Enthalpy and internal energy change is zero during phase change processes like melting, vaporisation and sublimation

For a constant pressure reversible process, the enthalpy change (ΔH) of the system is (A) Cv.dT (B) Cp.dT (C) ∫ Cp.dT (D) ∫ Cv.dT

Description : For a constant pressure reversible process, the enthalpy change (ΔH) of the system is (A) Cv.dT (B) Cp.dT (C) ∫ Cp.dT (D) ∫ Cv.dT

Last Answer : (C) ∫ Cp.dT

(∂E/∂T)V is the mathematical expression for (A) CV (B) Enthalpy change (C) Free energy change (D) None of these

Description : (∂E/∂T)V is the mathematical expression for (A) CV (B) Enthalpy change (C) Free energy change (D) None of these

Last Answer : (D) None of these

Specific __________ does not change during phase change at constant temperature and pressure. (A) Entropy (B) Gibbs energy (C) Internal energy (D) Enthalpy

Description : Specific __________ does not change during phase change at constant temperature and pressure. (A) Entropy (B) Gibbs energy (C) Internal energy (D) Enthalpy

Last Answer : (B) Gibbs energy

The enthalpy change when ammonia gas is dissolved in water is called the heat of (A) Solution (B) Formation (C) Dilution (D) Combustion

Description : The enthalpy change when ammonia gas is dissolved in water is called the heat of (A) Solution (B) Formation (C) Dilution (D) Combustion

Last Answer : (A) Solution

High pressure steam is expanded adiabatically and reversibly through a well insulated turbine, which produces some shaft work. If the enthalpy change and entropy change across the turbine are represented by ΔH and ΔS respectively for this process: (A) Δ H = 0 and ΔS = 0 (B) Δ H ≠ 0 and ΔS = 0 (C) Δ H ≠ 0 and ΔS ≠ 0 (D) Δ H = 0 and ΔS ≠ 0

Description : High pressure steam is expanded adiabatically and reversibly through a well insulated turbine, which produces some shaft work. If the enthalpy change and entropy change across the turbine are represented by ΔH and ΔS respectively for this process: ... (C) Δ H ≠ 0 and ΔS ≠ 0 (D) Δ H = 0 and ΔS ≠ 0

Last Answer : (B) Δ H ≠ 0 and ΔS = 0

Specific __________ does not change during a phase change (e.g. sublimation, melting, vaporisation etc.). (A) Entropy (B) Internal energy (C) Enthalpy (D) Gibbs free energy

Description : Specific __________ does not change during a phase change (e.g. sublimation, melting, vaporisation etc.). (A) Entropy (B) Internal energy (C) Enthalpy (D) Gibbs free energy

Last Answer : (D) Gibbs free energy

If two pure liquid constituents are mixed in any proportion to give an ideal solution, there is no change in (A) Volume (B) Enthalpy (C) Both (A) & (B) (D) Neither (A) nor (B)

Description : If two pure liquid constituents are mixed in any proportion to give an ideal solution, there is no change in (A) Volume (B) Enthalpy (C) Both (A) & (B) (D) Neither (A) nor (B)

Last Answer : (C) Both (A) & (B)

Pressure-enthalpy chart is useful in refrigeration. The change in internal energy of an ideal fluid used in ideal refrigeration cycle is (A) Positive (B) Negative (C) Zero (D) Infinity

Description : Pressure-enthalpy chart is useful in refrigeration. The change in internal energy of an ideal fluid used in ideal refrigeration cycle is (A) Positive (B) Negative (C) Zero (D) Infinity

Last Answer : C) Zero

The change in __________ is equal to the reversible work for compression in steady state flow process under isothermal condition. (A) Internal energy (B) Enthalpy (C) Gibbs free energy (D) Helmholtz free energy

Description : The change in __________ is equal to the reversible work for compression in steady state flow process under isothermal condition. (A) Internal energy (B) Enthalpy (C) Gibbs free energy (D) Helmholtz free energy

Last Answer : (C) Gibbs free energy