InterviewSolution
This section includes InterviewSolutions, each offering curated multiple-choice questions to sharpen your knowledge and support exam preparation. Choose a topic below to get started.
| 2301. |
Anything which separates the system from its surroundings is called ……(a) Boundary(b) Partition (c) Universe (d) Outer layer |
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Answer» (a) Boundary |
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| 2302. |
For a liquid the vapour pressure is given by `"log"_(10) P = (-400)/(T) + 10`. Vapour pressure of the liquid is `10^(x) mm` Hg. The value of x will be----- |
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Answer» Correct Answer - 9 `log_(10) P = - (400)/(T) + 10 = - (400)/(400) + 10 = 9` `P = 10^(@) mm Hg x = 9` |
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| 2303. |
Statement-1: There is a natural asymmetry between work to heat and converting heat to work . Statement-2: No process is possible in which the sole result is the absorption of heat from a reservoir and its complaete conversion into work .A. Statement-1 is True, Statement -2 is True, Statement-2 is a correct explanation for Statement-1.B. Statement -1 is True ,Starement -2 is True ,Statement-2 is not a correct explanation for Statement-1C. Statement-1 is True ,Statement-2 is False.D. Statement-1 is False ,Statement-2 is True. |
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Answer» Correct Answer - a |
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| 2304. |
The absolute enthalpy of neutralization of the reaction, `MgO(s)+2HCl(aq.)+H_(2)O(l)` will beA. less that 57 kJ `" mol"^(-1)`B. `-57 " kJ mol"^(-1)`C. greater than 57 kJ `" mol"^(-1)`D. 57 kJ `" mol"^(-1)` |
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Answer» Correct Answer - C `|"Enthalpy of change"|gt57` `2H^(+)` participate in reaction. |
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| 2305. |
The enthalpy of neutraliztion of weak base A OH and a strong base BOH by HCl are -12250 cal/mol and -13000 cal/mol respectively . When one mole of HCl is added to a solution containting 1 mole of A OH and 1 mole of BOH , the enthalpy change was -12500 cal/mol . In what ratio is the acid distribution between A OH and BOH?A. `2:1`B. `2:3`C. `1:2`D. None of these |
| Answer» Correct Answer - A | |
| 2306. |
Statement-1: There is a natural asymmetry between work to heat and converting heat to work . Statement-2: No process is possible in which the sole result is the absorption of heat from a reservoir and its complaete conversion into work .A. Statement-1 is true, statement 2 is true, statement 2 is a correct explanation for statement.3B. statement-1 is true, statement 2 is true, statement 2 is not a correc explanation for statement 3C. statement 1 is ture, statement 2 is falseD. statement-1 is false, statement-2 is true |
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Answer» Correct Answer - A Seconds law of thermodynamics states that total heat can never be converted into equivalent amount of work. Hence, (A) is correct optionxz. |
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| 2307. |
The enthalpy of neutraliztion of weak base A OH and a strong base BOH by HCl are -12250 cal/mol and -13000 cal/mol respectively . When one mole of HCl is added to a solution containting 1 mole of A OH and 1 mole of BOH , the enthalpy change was -12500 cal/mol . In what ratio is the acid distribution between A OH and BOH?A. `2 : 1`B. `2 : 3`C. `1 : 2`D. None of these |
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Answer» Correct Answer - A `-12250x-13000(1-x)=-12500` `750 x = 500 implies x=2//3" and "y = 1//3` So, `" "(x)/(y)=(2)/(1)` |
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| 2308. |
Water is supercooled to `-4^(@)C` . The enthalpy ( H ) isA. same as ice at `- 4^(@)C`B. more than ice at `- 4^(@)C`C. same as ice at `0^(@)C`D. less than ice at `-4^(@)C` |
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Answer» Correct Answer - d When ice is supercooled to`-4^(@)C` , heat is released . So,enthalpy decreases. |
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| 2309. |
Assertion: The heat absorbed during the isothermal expansion of an ideal gas against vacuum is zero. Reason: The volume occupied by the molecules of an ideal gas is zero.A. Statement-1 is true, statement 2 is true, statement 2 is a correct explanation for statement.1B. statement-1 is true, statement 2 is true, statement 2 is not a correc explanation for statement 1C. statement 1 is ture, statement 2 is falseD. statement-1 is false, statement-2 is true |
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Answer» Correct Answer - B By first law of thermodynamics `d q = dE + dW`. Under isothermal condition for ideal gas is zero. Also `(dE)_(T) = 0` as for ideal gas there is no change in internal energy at constant T due to no force of attraction between the molecular. `:. Dq = 0 + 0 = 0` hence, (B) is correct option |
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| 2310. |
Match the transformations In column I with appropriate options in column II. |
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Answer» Correct Answer - A::B::C::D (A) `s rarr g`, Phase transition, `Delta H = +ve, Delta S = +ve` (B) 0 mol `rarr` 1 mol gas, `Delta H = +ve, Delta S = +ve` (C) 2 mol `rarr P_("Read")`, Phase transition, Allotropic change, `Delta S = -ve` |
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| 2311. |
At `25^(@)C`, when 1 mole of `MgSO_(4)` was dissolved in water, the heat evolved was found to be 91.2 kJ. One mole of `MgSO_(4) . 7H_(2)O` on dissolution gives a solution of the same composition accompanied by an absorption of 13.8 kJ. The enthalpy of hydration, i.e., `DeltaH_(h)` for the reaction `MgSO_(4)(s) + 7H_(2)O(l)rarrMgSO_(4) . 7H_(2)O(s)` :A. `-105 kJ//"mol"`B. `-77.4 kJ//"mol"`C. 105 kJ/molD. None of these |
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Answer» Correct Answer - A Given that `MgSO_(4)(s)+nH_(2)OrarrMgSO_(4)(nH_(2)O),` `Delta_(r )H_(1)=-91.2 " kJ"//"mol ....(i)"` `MgSO_(4).7H_(2)O(s)+(n-7)H_(2)OrarrMgSO_(4)(nH_(2)O)` `Delta_(r )H_(2)=13.8 " kJ"//"mol ....(ii)"` Equation (i) - (ii) or `DeltaH_("hyd")=Delta_(r )H_(1)-Delta_(r)H_(2)` `=-91.2 " kJ"//"mol"-13.8 " kJ"//"mol"` `=-105" kJ"//"mol"` |
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| 2312. |
Water is supercooled to `- 4^(@)C`. The enthalpy `(H)` isA. more than ice at `- 4^(@)C`B. less than ice at `- 4^(@)C`C. same as ice at `-4^(@)C`D. same as ice at `0^(@)C` |
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Answer» Correct Answer - A When water is supercooled to `- 4^(@)C`, energy heat is released. However, during theis process, no ice is formed. Thus, the amount of energy released in the water `rarr` ice transition is missing. Consequently, the enthalpy `(H)` is more than ice at `- 4^(@)C`, |
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| 2313. |
At 298 K, the heat of solution of `MgSO_(4) (s)` is `-91.21 kJ mol^(-1)` and that of `MgSO_(4). 7H_(2)O(s)` is 13.81 kJ `mol^(-1)`. Calclate heat of hydration of `MgSO_(4)(s)` i.e., `DeltaH` for the reaction `MgSO_(4)(s)+7H_(2)O(l) to MgSO_(4).7H_(2)O(s)`A. `-105.02 kJ mol^(-1)`B. `105.02 kJ mol^(-1)`C. `-77.40 kJ mol^(-1)`D. `77.40 kJ mol^(-1)` |
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Answer» Correct Answer - A `DeltaH=H_(P) - H_(R), DeltaH=H_(MgSO_(4))-H_(MgSO_(4).7 H_(2)O)` |
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| 2314. |
Two moles of an ideal gas expanded isothermally and reversibly from `1L` to `10L` at `300K`. What is the enthalpy change?A. `- 11.47 kJ`B. `11.47 kJ`C. `0 kJ`D. `4.98 kJ` |
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Answer» Correct Answer - C Accroding to thermodynamics, `H = U + PV` `:. Delta H = Delta U + Delta (PV)` For an ideal gas, `pV = nRT` `:. Delta H = Delta U + Delta (nRT)` `= Delta U + nRT` For an isothermal and reversible process, we have `Delta T = 0` `Delta U = 0` `:. Delta H = 0` |
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| 2315. |
The standard enthalpies of formation of`CO_(2)(g), H_(2)O(l) ` and glucose (s)at `25^(@)C` are`-400 kJ //mol, - 300 kJ//mol` and`-1300kJ//mol` respectively.The standard enthalpy of combustion per gram of glucose at`25^(@)C` isA. ` + 2900kJ`B. ` -2900kJ`C. ` - 16.11kJ `D. `+16.11 kJ` |
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Answer» Correct Answer - C `C_(6)H_(12)O_(6)(s)+ 6O_(2)(g)rarr6 CO_(2)(g) +6 H_(2)O(l) ` `Delta_(r)H^(@) =Delta_(c) H^(@) = [ 6 Delta_(f)(CO_(2)) + 6 Delta_(f)H^(@) ( H_(2)O)]- [ Delta_(f) H^(@) ( C_(6)H_(12)O_(6)) + 6 Delta_(f) H^(@) ( O_(2))]` `= 6 xx ( - 400) + 6 ( - 300) -( - 1300)` `= -2900 kJ` `= - ( 2900)/( 180 ) kJ //g =- 16.11 kJ //g` |
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| 2316. |
Expansion of a gas in vacuum is called free expansion. Calculate the workdone and the change in internal energy when 1 litre of ideal gas expands isothermally into vacuum until its total volume is 5 litre ? |
| Answer» `w= -P _("ext") DeltaV`. As `P_(ext) = 0` , therefore, `w=0` . ltbrlt As internal energy of an idealgas depends only on temperature, therefore,for isothermal expansion of an ideal gas , internalenergy remains constant, i.e., `DeltaU =0`. [ Also,remember that as`H= U +PV, DeltaH = Delta ( U+PV)= DeltaU +P DeltaV = DeltaU _nR ( DeltaT)`. For isothermal process, `DeltaT = 0`, and also `DeltaU =0` as stated above, therefore, `DeltaH =0 ]` | |
| 2317. |
A system gives out 20 J of heat and also does 40 J of work. What is the internal energy change? |
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Answer» `Delta U = q + w` = -20 J + (-40) J = - 60 J |
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| 2318. |
Calculate the standard enthalpy of reaction for the following reaction using the listed enthalpies of reaction : `3Co(s)+2O_(2)(g)rarrCo_(3)O_(4)(s)` `2 Co(s)+O_(2)(g)rarr2CoO(s)," "DeltaH_(1)^(@)=-475.8 kJ` `6CoO(s)+O_(2)(g)rarr2Co_(3)O_(4)(s),DeltaH_(2)^(@)=-355.0 kJ`A. `-891.2 kJ`B. `-120.8 kJ`C. `+891.2 kJ`D. `-830.8 kJ` |
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Answer» Correct Answer - A `DeltaH^(@)=(3)/(2)xxDeltaH_(1)^(@)+(DeltaH_(2)^(@))/(2)` `=-713.7 - 177.5` `=-891.2 " kJ"` |
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| 2319. |
The free energy change `DeltaG = 0`, whenA. the system is at equilibriumB. catalyst is addedC. reactants are initially mixed thoroughlyD. the reactants are completely consumed |
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Answer» Correct Answer - A At equilibrium `DeltaG = 0` |
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| 2320. |
Calculate the enthalpy of formation of carbon monoxide (CO) from the following data`:` `(i) C(s) + O(g) rarr CO_(2)(g), Delta_(r)H^(@) = - 393.5 kJ mol^(-1)` (ii) `CO(g) + (1)/(2) O_(2)(g) rarrCO_(2)(g) , Delta _(r) H^(@) = - 283. 0 kJ mol^(-1)` |
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Answer» We aim at` : C(s) +(1)/(2) O_(2)(g) rarr CO(g) , Delta_(f) H^(@) = ?` Subtracting eqn. (ii) fromeqn. (i), we get `C(s) +(1)/(2) O_(2)(g) - CO(g) rarr0, Delta_(r) H^(@) = - 393.5 - (- 283.0) = - 110.5 kJ mol^(-1)` or `C(s) +(1)/(2) O_(2)(g) rarr CO (g) , Delta _(r) H^(@) = - 110.5 kJ` `:. ` Heat of formation of CO is `: Delta _(f) H^(@) = - 110.5 kJ mol^(-1)` |
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| 2321. |
Find the value of `Delta_(f) H^(@)` for the reaction `N_(2) O_(4) (g) + 3 CO(g) rarr N_(2) O (g) + 3 CO_(2) (g)` Standard enthalpies of formation of `CO(g), CO_(2) (g), N_(2) O (g)`, and `N_(2) O_(4) (g)` are `- 110, - 393, 81`, and `9.7 kJ mol^(-1)`, respectively. Strategy : The standard enthalpy change of a reaction is equal to the sum of the standard molar enthalpie of formation of the products each multiplied by its stiochiometric coefficient in the balanced equation, minus the corresponding sum of the standard molar enthalpies of formation of the reactants |
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Answer» Correct Answer - `Delta_(r)H=-778 kJ` `Delta_(r)H=` for a reaction is defined as the difference between `Delta_(f)H` value of products and `Delta_(f)H` value of reacteants. `Delta_(r)H=sumDelta_(f)H("products")-sumDelta_(f)H("reactants")` For the given reaction, `N_(2)O_(4(g))+_3CO_((g))rarrN_(2)O_((g))+3CO_(2(g))` `Delta_(r)H=[{Delta_(f)H(N_(2)O)+3Delta_(f)H(CO_(2))}-{Delta_(f)H(N_(2)O_(4))+3Delta_(f)H(CO)}]` Substituting the values of `Delta_(f)H "for"N_(2)O_(2),CO_(2)m_(2)O_(4)and CO` from the question, we get : `Delta_(r)H=[{81 K "mol"^(-1)+3(-393)kJ"mol"^(-1)}-{9.7 kJ "mol"^(-1)+3(-110)kJ "mol"^(-1)}]` `Delta_(r)H=-777.7 kJ "mol"^(-1)` Hence, the value of `Delta_(r)H` for the reactio is `-777.7 kJ "mol"^(-1)` |
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| 2322. |
`C + O_(2) rarr CO_(2),` `CO + (1)/(2) O_(2) rarr CO_(2),` Then `Delta_(f) H` for`CO` will beA. `2 X + Y`B. `X - Y`C. `Y - 2X`D. `Y - X` |
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Answer» Correct Answer - D `Delta_(f) H` for `CO` is given as `C + (1)/(2) O_(2) rarr CO` To get this equation, we need to subtract the second equation from the first one: `{:(" "C+O_(2)rarrCO_(2)),(" "CO_(2)rarrCO+(1)/(2)O_(2)),(bar(" "C+(1)/(2)O_(2)rarrCO" ")):}` `:. Delta_(f) H (CO) = (-X) - (-Y)` `= - X + Y = Y - X` |
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| 2323. |
The difference between heats of reaction at constant pressure and constant volume for a given reaction isA. `(Delta n_(g)) RT`B. `(Delta n_(g)) R//T`C. `(Delta n_(g)) T//R`D. `Delta n_(g) RT^(2)` |
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Answer» Correct Answer - A Heat of reaction at constant pressure is `Delta H` while heat of the reaction at constant volume is `Delta U` `Delta H = Delta U + (Delta n_(g)) RT` Thus, `Delta H - Delta U = (Delta n_(g) RT)` |
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| 2324. |
A system goes from P to Q by two different paths in the `p-V` diagram as shown in figure. Heat given to the system in path 1 is 1000 J. The work done by the system along path 1 is more than path 2 by 100 J. What is the heat exchanged by the system in path 2 ? |
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Answer» For path 1, Heat given `Q_(1)` = + 1000J ltBrgt Work done = `W_(1)` (let) For path 2, `" "` Work done `(W_(2))=(W_(1)-100)J` Heat given `Q_(2)`= ? As change in internal energy between two states for different path is same. `therefore " "DeltaU=Q_(1)-W_(1)=Q_(2)-W_(2)` `" "1000-W_(1)=Q_(2)-(W_(1)-100)` `rArr" "Q_(2)=1000-100=900J` |
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| 2325. |
A system goes from P to Q by two different paths in the `P-V` diagram as shown in (figure). Heat given to the system in path 1 is `1000J`. The work done by the system along path 1 is more than path 2 by `100J`. What is the exchange by the system in path 2? |
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Answer» In (figure) `dQ_(1)= dU+dW_(1)` and `Q_(2)=dU+dW_(2)` `:. dQ_(1)-dQ_(2)= dW_(1)-dW_(2)` `1000-dQ_(2)= 100` `dQ_(2)= 1000-100= 900J` |
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| 2326. |
A scientist has developed a system which goes from P to Q by two different paths. Heat given to the system in path 1 is 1000 J. The work done by the system along path 1 is more than path 2 by 100 J. What is the heat exchanged by the system in path 2? |
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Answer» For path 1: Heat given Q1 = + 1000 J Work done = W1(let) For path 2: Work done (W2) = (W1 − 100) J Heat given Q2 = ? As change in internal energy between two states for different paths is same. ∴ ∆U = Q1 − W1 = Q2 − W2 1000 – W1 = Q2 − (W1 − 100) or Q2 = (1000 – 100) J = 900 J |
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| 2327. |
A metallic sphere is heated. Out of its radius, surface area, volume and mass which will undergo the maximum percentage increase? |
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Answer» Mass remains same in this case. Radius of the sphere will increase. Surface area of sphere ∝ (radius)2 and Volume ∝ (Raidus)3 so the volume will undergo maximum percentage increase |
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| 2328. |
What is coefficient of performance of a refrigerator? |
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Answer» It is defined as the ratio of the amount of heat removed in a cycle from the refrigerator to the work done by some external agency to help the removal of this heat, i.e., β = \(\frac{Q_2}{W}\) = \(\frac{Q_2}{Q_1-Q_2}\) Also β = \(\frac{T_2}{T_1-T_2}\) For higher efficiency of refrigerator, β should be higher. |
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| 2329. |
On applying brakes to a car it is moving down a hill, at a constant speed. In this process of motion with constant speed, brakes become hot. Why? |
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Answer» If brakes were not applied, the car would have come down with acceleration. Hence, application of brakes is preventing this acceleration, i.e., brakes are putting frictional forces on the wheels. The work being done by these frictional forces shows up as heat. |
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| 2330. |
How can the internal energy of an ideal gas change? |
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Answer» Adiabatic process can bring a change in the internal energy of gas. The gas is compressed, that is work is done on it, its internal energy increases, when the gas is expanded, work id done by the gas, it’s internal energy decreases. |
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| 2331. |
Calculate `Delta H ^(298)` for the reaction `: 2Li (s) + 2H_(2)O(l) rarr 2Li^(+) ( aq) + 2OH^(-) (aq) + H_(2)(g)` Given that the standard enthalpies of formation of `Li^(+)(aq), OH^(-)(aq) ` and `H_(2)O(l)` are - 278.5, - 228.9 and - 285.8 kJ `mol^(-)` respectively ( all at 298 K ) |
| Answer» Correct Answer - `-443.2kJ` | |
| 2332. |
How do you distinguish between a gas and vapour? |
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Answer» A gas is a vapour above its critical temperature, while vapour is a gas below its critical temperature. Further, a gas cannot be liquefied by applying pressure alone; whereas a vapour can be liquefied by applying pressure only. |
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| 2333. |
Give an expression for the efficiency of Carnot’s engine? |
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Answer» Efficiency η = 1 –\(\frac{T_2}{T_1}\) Where T2 is the temperature of the sink and T1 is the temperature of the source. Also η = 1 –\(\frac{Q_2}{Q_1}\) Where Q2 is the amount of heat rejected to sink and Q2 is the amount of heat rejected to sink and Q1 is the amount of heat supplied by the source. |
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| 2334. |
Why is it impossible for a ship to use the internal energy of sea water to operate its engine? |
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Answer» For using the internal energy of sea water to operate the engine of a ship, the internal energy of the sea water has to be converted into mechanical energy. Since whole of the interned energy cannot be converted into mechanical energy, a part has to be rejected to a colder body (sink). Since, no such body is available, so the interned energy of the sea water cannot be used to operate the engine of the ship. |
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| 2335. |
State second law of thermodynamics. |
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Answer» Kelvin’s statement : No process is possible whose sole result is the absorption of heat from a reservoir and complete conversion of the heat into work. Clausius statement : It is not possible to transfer heat from a body at lower temperature to another at higher temperature without the help of some external energy. |
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| 2336. |
What is the origin of internal potential energy? |
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Answer» The attraction between molecules is the source of internal P.E. It results in change of distance between the molecules. Increase in internal P.E. increases the distance between the molecules. |
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| 2337. |
Generally what is the range of values of the specific heat of a gas? |
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Answer» Normally the specific heat of a gas varies from zero to infinity are shown here. We have ∆Q = mC∆T, hence specific heat, C = \(\frac{∆Q}{m∆T}\) (i) When a gas is compressed, its temperature rises without any heat supplied. This mean ∆Q = 0, ∆T ≠ 0 hence, C = 0. (ii) When a gas is expanded and heated simultaneously, its temperature rise can be zero. Hence ∆Q ≠ 0, ∆T = 0. Hence, C = ∞. |
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| 2338. |
What is the origin of internal K.E.? how does it affect a substance? |
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Answer» The random motion of molecules is the source of internal K.E. It affects temperature of the substance. Increase in internal K.E. increases temperature of the substance. |
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| 2339. |
What is the pressure of a gas in terms of kinetic parameters? |
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Answer» If a container has n molecules each of mass m, the pressure inside is P = \(\frac{1}{3}\frac{M}{V}C^2,\) where V is the volume of the container and c is the root mean square speed of the molecules. It is also written as P = \(\frac{1}{3}\frac{M}{V}c^2\) = \(\frac{1}{2}ρc^2\) |
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| 2340. |
Why does specific eat of gases increase with their atomicity? |
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Answer» In monoatomic gases molecules have only translational K.E., while in diatomic and triatomic gases, molecules have translational, rotational as well as vibrational kinetic energies. Due to presence of other type of motions, more heat is required to produce the transitional K.E. of the molecules and hence their temperature increases by certain amount. The specific heat increases accordingly. |
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| 2341. |
Same mass of a rarefied gas has more internal energy than the compressed gas when kept at same temperature. Why? |
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Answer» Equal masses of gases have equal amount of internal K.E. at same temperature. In rarefied gas, molecules are at more distance from each other than in compressed gas. These molecules possess more interned P.E. It makes total internal energy of the rarefied gas more than that of the compressed gas. |
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| 2342. |
Why heat changes reported are usually enthalpy changes and not internal energy changes ? |
| Answer» This is because most of the processes are carried out in open vessels,i.e., at constant pressure. | |
| 2343. |
Bond dissociation enthaply of the first H-S bond in hydrogen sulphide is `376 "Kj"//"mole".` The enthalpies of formatin of `H_(2)S(g)and S(g) are-20.0and277.0 "kj"//"mole"` respectively. The enthalpy of formation of gaseous hydrogen atomis `218 "Kj"//"mole".` Using above information, answer following questions : The bond disscociation enthalpy of the free radical HS is :A. `138kJ//"mole"`B. `276kJ//"mole"`C. `357kJ//"mole"`D. `376kJ//"mole"` |
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Answer» Correct Answer - c |
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| 2344. |
The species which by definition has ZERO standard molar enthalpy of formation at 298 K isA. `Br_(2)(g)`B. `Cl_(2)(g)`C. `H_(2)O(g)`D. `CH_(4)(g)` |
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Answer» Correct Answer - b `Delta_(f)H^(@) = 0` for elementary substances in standard state . `Br_(2)`is liquid in standard state. |
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| 2345. |
Bond dissociation enthaply of the first H-S bond in hydrogen sulphide is `376 "Kj"//"mole".` The enthalpies of formatin of `H_(2)S(g)and S(g) are-20.0and277.0 "kj"//"mole"` respectively. The enthalpy of formation of gaseous hydrogen atomis `218 "Kj"//"mole".` Using above information, answer following questions : The enthalpy of formation of free radical HS is :A. `138kJ//"mole"`B. `276kJ//"mole"`C. `-10kJ//"mole"`D. `357kJ//"mole"` |
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Answer» Correct Answer - a |
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| 2346. |
If a gas, at constant temperature and pressure expands, then itsA. Enthropy increases and then decreaseB. Internal energy increasesC. Internal energy remains the sameD. Internal energy decreases |
| Answer» Correct Answer - D | |
| 2347. |
Statement -1 in the following reaction : `C(s)+O_(2)(g)to CO_(2) (g), DeltaH=DeltaU-RT` Statement -2: `DeltaH` Is related to `DeltaU ` by the equation , `DeltaH=Delta+Deltan_(g)RT`A. Statement-1 is True, Statement -2 is True, Statement-2 is a correct explanation for Statement-1.B. Statement -1 is True ,Starement -2 is True ,Statement-2 is not a correct explanation for Statement-1C. Statement-1 is True ,Statement-2 is False.D. Statement-1 is False ,Statement-2 is True. |
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Answer» Correct Answer - d |
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| 2348. |
What is the value of `DeltaH` in the following reaction at 300 K ? `CH_(4)(g) 2O_(2)(g) rarr CO_(2)(g)+2H_(2)O(l), DeltaU = 885389J //mol.` |
| Answer» `DeltaH = DeltaU + Deltan_(g)RT = 885389+ ( -2) xx 8.314 xx 300 = - 880400 J mol^(-1)` | |
| 2349. |
Assertion. The enthalpy of formation of gaseous oxygen molecules at 298 K and under a pressure of one atmosphere is zero. Reason. The entropy of formation of geseous oxygen molecule under the same conditions is zero.A. If both A and R are true,andR is the true explanation of A.B. If both A and R are true,but R is not the true explanation of A.C. If A is true, but R is falseD. If both A and R are false. |
| Answer» Correct Answer - C | |
| 2350. |
Standard entropy of `X_(2)` , `Y_(2)` and `XY_(3)` are `60, 40 ` and `50JK^(-1)mol^(-1)` , respectively. For the reaction, `(1)/(2)X_(2)+(3)/(2)Y_(2)rarrXY_(3),DeltaH=-30KJ` , to be at equilibrium, the temperature will be:A. `1250 K`B. `500 K`C. `750 K`D. `1000 K` |
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Answer» Correct Answer - c `1/2X_(2)+3/2Y_(2)toXY_(3)` `DeltaS_("reaction")=50-(3/2xx40+1/2xx60)` `=-40 J mol^(-1), DeltaG=DeltaH-TDeltaS` at equilibrium , `DeltaG=0` `DeltaH=TDeltaS` `30xx10^(3)=Txx40, :. T=750 K` |
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