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.
| 1451. |
Give examples of endothermic and exothermic reactions. |
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Answer» Reaction in which heat is given out along with the products is called exothermic reaction: |
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| 1452. |
Heat of neutralisation of strong acid and strong base is constant. Why? |
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Answer» The enthalpy of neutralization of all strong acids and strong bases is always constant, i.e., -57.1 kJ. The explanation to this generalization can be provided on the basis of Arrhenius theory of ionization. The strong acids and strong bases are almost completely ionized in dilute aqueous solutions. The neutralization of strong acid and strong bases simply involve the combination of H+ ions (from acid) and OH– ions (from base) to form water molecules. It has been found experimentally that when 1 mole of water is formed by the neutralization of 1 mole of H+ ions and 1 mol of OH– in aqueous solutions, 57.1 kJ of energy is released. |
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| 1453. |
Which of the following reactions have maximum heat of neutralisation?(a) NH4 OH and CH3 COOH(b) NH4 OH and HCl(c) NaOH and CH3 COOH(d) NaOH and HCl |
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Answer» (d) NaOH and HCl |
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| 1454. |
A Carnot engine converts one-fifth of heat given into work. If temperature of sink is reduced by `80^(@)`, efficiency gets doubled. If temperature of sourceand sink is `T_(1)`and `T_(2)` respectively then calculate value of `(T_(1)-T_(2))/(10)` |
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Answer» Correct Answer - 8 |
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| 1455. |
Define internal energy change. |
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Answer» Internal energy change:- If E1 is the internal energy of the system in the initial state (that is, before the change) and E2 is the internal energy of the system in the final state (after change), then the internal energy change (ΔE) is given by ΔE = E2 - E1 = Efinal - Einitial |
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| 1456. |
With the help of thermochemical equation, calculate ΔfH° at 298 K for the following reactions: C(graphite) + O2(g) → CO2(g) ; ΔfH° = -393.5kJ/mol H2(g) + 1/2O2(g) → H2O(l) ; ΔfH° = -285.8kJ/mol CO2(g) + 2H2O(l) → CH4(g) + 2O2(g) ; ΔfH° = +890.3kJ/mol |
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Answer» C(graphite) + O2(g) → CO2(g) ; ΔfH° = -393.5 kJ/mol …(1) H2(g) + 1/2O2(g) → H2O(l) ; ΔfH° = -285.8 kJ/mol …(2) CO2(g) + 2H2O(l) → CH4(g) + 2O2(g) ΔfH° = +890.3 kJ/mol …(3) Here we want one mole of C(graphite) as reactant, so we write down equation (1) as such, we want two moles of H2(g) as reactant, so we multiply equation (2) by 2, we want C(graphite) + O2 (g) → CO2(g) ; ΔfH° = -393.5 kJ / mol …(1) 2H2(g) + O2(g) → 2H2O(l) ; ΔfH° = 2(-285.8 kJ/mol) …(2) CO2(g) + 2H2O(l) → CH4(g) + 2O2(g) ; ΔfH° = +890.3 kJ/mol . … (3) Adding we obtain: C(graphite) + 2H2(g) → CH4(g); ΔfH° = -74.8 kJ/mol |
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| 1457. |
For a reaction :`2A(g) to B(g), DeltaH =-40 Kcal`. If rate constant for disapperance of A is `10^(-2) M^(-1) sec^(-1)` then identify the opations which will be correct [Assume gases to behave ideally and reaction to be occuring at 300 K] [Take : R=2 cal/mole K]A. The reaction must be elementary reaction.B. Change in internal energy of the reaction will be `-19.7 kcal//"mole"` ofA consumed.C. The rate at which heat will be liberated initially when 2 moles of A is taken in 3 litre rigid vessel will be approx `0.26 kcal//sec`.D. Time requried for concentration of A |
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Answer» Correct Answer - b,d |
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| 1458. |
If the heats of formation of `C_(2)H_(2)` and `C_(6)H_(6)` are `230 kJ mol^(-1)` and `85 kJ mol^(-1)` respectively, the `DeltaH` value for the trimerisation of `C_(2)H_(2)` isA. `-605 kJ`B. `-205 kJ`C. `205 kJ`D. `605 kJ` |
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Answer» Correct Answer - A `3C_(2)H_(2) rarr C_(6)H_(6) , DeltaH=H_(P)-H_(R)` |
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| 1459. |
The expansion of a gas into an evacuated space takes place non-spontaneously. A process in which all steps cannot be retraced by themselves is called a spontaneous process.A. If both the statements are TRUE and STATEMENT-2 is the correct explanation of STATEMENT-18B. If both the statements are TRUE but STATEMENT-2 is NOT the correct explanation of STATEMENT-18C. If STATEMENT-1 is TRUE and STATEMENT-2 is FALSED. If STATEMENT-1 is FALSE and STATEMENT-2 is TRUE |
| Answer» Correct Answer - D | |
| 1460. |
A gobar gas plant produces methane and supplies to the families. If a family requires 15,000 kJ of energy per day, how many days will the quote of 10 kg will last ? `(Delta_(c)H "of" CH_(4) = - "1665 kJ "mol^(-1))` |
| Answer» Correct Answer - 69.37 days | |
| 1461. |
An athlete is given 180 g of glucose `(C_(6)H_(12)O_(6))`. He utilises 50% of the energy due to internal combustion in the body. In order to avoid storage of energy in the body, calculate the masss of water he would need to perspire. Given enthalpy of combustion of glucose is -2800 kJ `mol^(-1)` and enthalpy of evaporation of water is 44 kJ `mol^(-1)` |
| Answer» Correct Answer - 572.73 g | |
| 1462. |
90 g of water spilled out from a vessel in the room on the floor. Assuming that water vapour behaving as an ideal gas, calculate the internal energy change when the spilled water undergoes complete evaporation at `100^(@)C`. (Given the molar enthalpy of vaporisation of water at 1 bar and 373 K = 41 kJ `mol^(-1)`). |
| Answer» Correct Answer - 25.49 kJ `mol^(-1)` | |
| 1463. |
What is Extensive property? Give example. |
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Answer» It is a property of which depends on the amount of the substance present in the system. Example: Mass, Volume, Energy |
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| 1464. |
Write any two differences between Isothermal and Adiabatic process. |
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| 1465. |
A sample of an ideal monoatomic gas is taken round the cycle ABCA as shown in the figure the work done during the cycle is A. ZeroB. 2 PVC. 6 PVD. 9 PV |
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Answer» Correct Answer - B |
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| 1466. |
Assume ideal gas behavior for all the gases considered and vibratonal degree of freedom to be active. Separated equimolar sample of `Ne,O_(2), So_(2) and CH_(4)` were subjedted to a two step process as mentioned . Initiallyt all are at same state of temperture and pressure. Step -I: All undergo reversible abiabatic expansion to attain same final volume thereby causing the decreasae in their temperature. Step -II : After step I, all are given appropriate amount of heat isochorically to restore the original temperature . Mark the correct optoin(s).A. Due to step I only , the decrease in temperature will be maximum for Ne.B. During step II , heat given will be minimum for `CH_(4)`C. There will be no net change in internal energy for any of the gas after both the steps of process are completed.D. The `(@) P-V` graph of `CH_(4)` and `SO_(2)` wll be same for overall process. |
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Answer» Correct Answer - a,c |
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| 1467. |
A bomb calorimeter has a heat capacity of `783J xx^(@)c^(-1)` and contains 254 g of water which has a specific heat of `4.184Jxxg^(-1)xx^(@)C_(-1)` .How much heat is enolved or absorbed by a reaction when the temperature goes from `23.73^(@) "to" 26.01^(@)` C ?A. 1.78 KJ absorbedB. 2.42KJ absorbedC. 1.78 KJ evolvedD. 4.21KJ evolved |
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Answer» Correct Answer - d |
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| 1468. |
For which reaction from the following, `DeltaS` will be maximum?A. `Ca(s)+1//2O_(2)(g)rarr CaO(s)`B. `CaCO_(3)(s)rarr CaO(s)+CO_(2)(g)`C. `C(s)+O_(2)(g)rarr CO_(2)(g)`D. `N_(2)(g)+O_(2)(g)rarr 2NO(g)` |
| Answer» Correct Answer - B | |
| 1469. |
An adiabatic process is one in which :-A. Temperature of the system does not changeB. The system is not closed to heat transferC. There is no entropy changeD. None of these |
| Answer» Correct Answer - C | |
| 1470. |
Entropy meansA. DisordernessB. RanomnessC. OrdernessD. both 1 & 2 |
| Answer» Correct Answer - D | |
| 1471. |
`Delta S` for the reaction , `MgCO_(3)(s)rarr MgO(s)+CO_(2)(g)` will be : |
| Answer» Correct Answer - C | |
| 1472. |
Change in entropy is negative forA. Bromine `(l) rarr` Bromine (g)B. `C(s)+H_(2)O(g)rarrCO(g)+H_(2)(g)`C. `N_(2)(g,10 atm)rarr N_(2)(g, 1 atm)`D. `Fe(at 400 K)rarr Fe(at 300 K)` |
| Answer» Correct Answer - D | |
| 1473. |
When two gases are mixed the entropy :-A. Remains constantB. DecreasesC. IncreasesD. Becomes zero |
| Answer» Correct Answer - C | |
| 1474. |
In which reaction `Delta S` is positive :-A. `H_(2)O(l)rarr H_(2)O(s)`B. `3O_(2)(g)rarr 2O_(3)(g)`C. `H_(2)O(l)rarr H_(2)O(g)`D. `N_(2)(g)+3H_(2)(g)rarr 2NH_(3)(g)` |
| Answer» Correct Answer - C | |
| 1475. |
When the egg is hard boiled, there isA. Increase in disorderB. Decrease in disorderC. No change in disorderD. `Delta G` is negative |
| Answer» Correct Answer - A | |
| 1476. |
The heat of combustion of `H_(2)(g)` at constant pressure and `300k` is `-280kJ mol^(-1)`. What will be the heat of combustion at constant volume and at `300K`? |
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Answer» `H_(2)(g) = (1)/(2)O_(2)(g) rarr H_(2)O(l) DeltaH =- 280 kJ mol^(-1)` `DeltaH = DeltaU +DeltanRT, Deltan = 0 - (3)/(2) =- (3)/(2)`, `DeltaH = DeltaU -(3)/(2) xx 8.314 xx 300` `- 280 kJ = DeltaU - (74826)/(20) xx (1)/(1000) kJ` `rArr DeltaU =- 276.2587 kJ` |
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| 1477. |
The standard absolute entropy of a substance, `(S^(Theta))` is the entropy of the substance in its standard state at `1` atm, temperature beingA. `0K`B. `298K`C. `398K`D. `273 K` |
| Answer» Correct Answer - `298 K` | |
| 1478. |
Heat of reaction for `C_(6)H_(12)O_(6(s))+6O_(2(g)) rarr 6CO_(2(g))+6H_(2)O_(v)` at constant pressure is `-651 kcal` at `17^(@)C`. Calculate the heat of reaction at constant volume at `17^(@)C`. |
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Answer» `DeltaH = DeltaU +DeltanRT….(i)` Given `DeltaH =- 651 xx10^(3) cal, R = 2 cal` Substituting all value in equation (i), we get `T = 290 K`, `Deltan = 6+6 -6 = 6` `:. =- 651 xx 10^(3) = DeltaU +6 xx 2xx 290` and `DeltaU =- 654480 cla or -654.48 kcal ` Note: For `C_(6)H_(12)O_(6)(g) +6O_(2)(g) rarr 6CO_(2)(g) +6H_(2)O(v) Deltan =` Number of products molecules -Number of reactants molecules (only in gaseous phase) `=6 +6 -6 = 6` Here, `H_(2)O(v)` is also in gaseous state. |
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| 1479. |
The enthalpy change of a reaction does not depand onA. State of reactants and productsB. Nature of reactants and productsC. Different intermediate reactionsD. Initial and final enthalpy change of reaction |
| Answer» Correct Answer - C | |
| 1480. |
What is Equation of state and examples ? |
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Answer» The mathematical relation between the pressure, volume and temperature of a thermodynamic system is called its equation of state. For example, the equation of state of n moles of an ideal gas can be written as PV = n RT |
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| 1481. |
What is meant by Thermodynamic equilibrium ? |
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Answer» A system is said to be in the state of thermodynamic equilibrium, if the microscopic variables of the describing the thermodynamic state of the system do not change with time. A system in a state of thermodynamic equilibrium possess mechanical, thermal and chemical equilibria simultaneously. |
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| 1482. |
Difference between heat and work. |
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Answer» (i) Heat is a mode of energy transfer due to temperature difference between the system and the surroundings. Work is the mode of energy transfer brought about by means that do not involve temperature difference such as moving the piston of a cylinder containing the gas, by raising or lowering the weight connected to it. (ii) When heat is supplied to a gas, its molecules move faster in all directions at random. So heat is a mode of energy transfer that produces random motion, when a piston compresses a gas to do work on it, it forces the molecules to move in the direction of piston’s motion. So work may be regarded as the mode of energy transfer that produces organised motion. |
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| 1483. |
What is Zeroth Law of Thermodynamics ? |
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Answer» If systems A and B are each in thermal equilibrium with a third system separately C, then A and B are in thermal equilibrium with each other. The zeroth law leads to the concept of temperature. |
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| 1484. |
Define Thermodynamic variables. Give the state of Thermodynamic variables. |
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Answer» Pressure, volume, temperature, internal energy and the number of moles are called thermodynamic variables. For µ moles of an ideal gas, equation of state is PV = µRT. Thermodynamic State Variables : (i) Intensive variables (ii) Extensive variables. |
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| 1485. |
Enthalpy of neutralization is defined as the enthalpy change when `1` mole of acid/base is completely neutralized by base/acid in dilute solution. For strong acid and strong base neutralization net chemical change is `" "H^(+)(aq) + OH^(-)(aq) rarr H_(2)O(l), " " Delta_(r)H^(@) = -55.84 KJ//mol` `DeltaH_("ionization")^(@)` of aqueous solution of strong acid and strong base is zero. When a dilute solution of a weak acid or base is neutalized, teh enthalpy of neutralization is some what less because of the absorption of heat in the ionization of the weak acid or base, for weak acid/base `DeltaH_("neutrilization")^(2) = DeltaH_("ionization")^(@) + Delta_(r)H^(@) " " (H^(+) + OH^(-) rarr H_(2)O)` Under the same condition how many mL of `0.1` M NaOH and `0.05` M `H_(2)`A (strong diprotic acid) solution should be mixed for a total volume of `100` mL produce the highest rise in temperature:A. `25:75`B. `50:50`C. `75:25`D. `66.66:33.33` |
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Answer» Correct Answer - B For max. rise in temp. max. neutralization of `H^(+)` and `OH^(-)` required . If we take equal volume , all `H^(+) (5 m-"mole")` will react with all `OH^(-)(5 m-"mole").` |
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| 1486. |
Heat of dissociation of acetic acidis 0.30 kcal`mol^(-1)` . Hence,enthalpy change when 1 mol of`Ca(OH)_(2)` is completely neutralized by acetic acid would beA. `-13.4 kcal`B. `-27.1 kcal`C. `-26.8 kcal`D. `-27.4 kcal` |
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Answer» Correct Answer - c `Ca(OH)_(2) rarr Ca^(2+) + 2OH^(-) , i.e., 1` mole of`Ca(OH)_(2)` gives two moles of `OH^(-)` ions. Hence, when `Ca(OH)_(2)` is completely neutralized,heat produced `= 2 xx 13.7 kcal = 27.4 kcal` 2 moles of `OH^(-)` ions require 2 moles of `H^(+)` ions for complete neutralization. Heat of dissociation of acetic acidto produce 2 moles of`H^(+)` ions `= 2 xx 0.30 kcal = 0.6 kcal`. Hence, net heat produced `=27.4 - 0.6 =26.8 kcal, i.e., DeltaH = - 26.8 kcal` |
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| 1487. |
The enthalpy change when 1 L of 1 M `H _(2)SO_(4)` is completely neutralized by 1L of1 M `Ca(OH)_(2)` will beA. `-13.7 kcal`B. `-27.4 kcal`C. `-1.37 kcal`D. `- 2.74 kcal` |
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Answer» Correct Answer - b 1 L of 1 M `H_(2)SO_(4)` gives 2 moles of`H^(+)` ions 1L of`M Ca9OH)_(2)` gives 2 moles of `OH^(-) ` ions Hence, for complete neutralization of 2 molesof `H^(+)` ions by 2 molesof `OH^(-)` ions. `DeltaH = 2 ( - 13.7) kcal =- 27.4 kcal` |
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| 1488. |
The enthalpies of elements in their standard states are takeen as zero. The enthalpy of formation of a compoundA. is always negativeB. is always positiveC. may be positive or negativeD. is never negative |
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Answer» Correct Answer - c Combination of elements to form a compound can be exothermic or endothermic`( e.g., C + O_(2) rarrCO_(2)` is exothermic whereas `C + 2S rarrCS_(2)` is endothermic ). Hence, enthalpy of formation can be `+ve` or `-ve`. |
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| 1489. |
ΔU of combustion of methane is -x kJ mol-1. The value of ΔH° is(a) = ΔU°(b) > ΔU°(c) < ΔU°(d) = 0 |
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Answer» Answer is (b) > ΔU° |
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| 1490. |
The enthalpies of all elements in their standard states are:(a) unity(b) zero(c) < 0(d) different for each element |
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Answer» Answer is (b) zero |
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| 1491. |
For the process to occur under adiabatic conditions, the correct condition is(a) ΔT = 0(b) Δp = 0(c) q = 0(d) W = 0 |
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Answer» Answer is (c) q = 0 |
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| 1492. |
A thermodynamic state function is a quantity:(a) used to determine heat changes(b) whose value is independent of path(c) used to determine pressure volume work(d) whose value depends on temperature only |
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Answer» Answer is (b) whose value is independent of path |
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| 1493. |
If we mix `H_(2)` and `O_(2)`, they do not combine to form `H_(2)O`, is the reaction spontaneous or non-spontaneous ? Give reason. |
| Answer» Reaction is spontaneous because it takes place when intiated by an electric spark. | |
| 1494. |
Calculate `Delta H ^(@)` for the reaction `CH_(2)= CH_(2) + 3O_(2) rarr 2CO_(2)+ 2H_(2)O` Given that the average bond energies of the different bonds are `:` `{:("Bond",C-H,O=O,C=O,O-H,C=C),("Bond energy " ( kJ mol^(-1)),414,499,724,460,619):}` |
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Answer» Correct Answer - `-964 Kj mol^(-1)` `Deta_(r)H [B.E. (C=C) + 4B.E. (C-H) + 3 B.E.(O-O) ] - [ 2 xx 2 xx B.E. ( C=O) + 2 xx 2 xx B.E.(O-H) ]` ` [619+ 4 ( 414)]+ 3 ( 499) ] - [ 4 ( 724)+ 4 ( 460 ) ] kJ = - 964 kJ` |
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| 1495. |
If an additional pressure `Delta p` of a saturated vapour over a convex spherical surface of a liquid is considerably less than the vapour pressure over a plane surface, then `Delta p = (rho_v//rho_l) 2 alpha//r`, where `rho_v` and `rho_l)` are the densities of the vapour and the liquid, `alpha` is the surface tension, and `r` is the radius of curvature of the surface. Using this formula, find the diameter of water droplets at which the saturated vapour pressure exceeds the vapour pressure over the plane surface by `eta = 1.0 %` at a temperature `t = 27 ^@C`. The vapour is assumed to be an ideal gas. |
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Answer» Given `Delta P = (rho_v)/(rho_l) (2 alpha)/(r) = (rho_v)/(rho_l) xx (4 alpha)/(d) = eta p_(vap) = eta ((m)/(M) RT)/(V_(vap)) = (eta RT)/(M) rho_v` or `d = (4 alpha M)/(rho_1 RT eta)` For water `alpha = 73 "dynes"//cm, M = 18 gm, rho_l = gm//c c, T = 300 K`, and with `eta ~~ 0.01`, we get `d ~~ 0.2 mu m`. |
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| 1496. |
Hydrazine , `N_(2)H_(4) ,` contains aN-N single bond and 4N -H bonds . Use bond energies to calculate `DeltaH`in KJ for the reaction : `N_(2)+2H_(2)toN_(2)H_(4)` `{:(Bond ,"Energies" (KJ.mol^(-1))),(H-H,436),(H-N,386),(N-N,193),(N=N,418),(N-=N,941):}`A. `-425KJ`B. `-76KJ`C. `76KJ`D. `245KJ` |
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Answer» Correct Answer - c |
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| 1497. |
Bomb calorimeters are the devices that are used to experimentally determine `DeltaH` and `DeltaU` of any reaction by measuring the temperature change in the water bath Hence , the experimatal data can be used for cross-checking theortical data, From the following theoretical data answer the question that follow: Thermodynamic data: `DeltaH_(f)^(@)Ch_(4)(g)=- 15 kcal //"mole", DeltaH_(f)^(@) CO_(2)(g)=-90 kcal//"mole",` `DeltaH_(f)^(@)H_(2)O(l)=-60 Kcal//"mole"` `S_(m)^(@) CH_(4)(g)= 40 cal//"mole Kelivn"` `S_(m)^(@) O(g)= 45 cal//"mole Kelivn"` `S_(m)^(@) H_(2)O(g)= 15 cal//"mole Kelivn"` `S_(m)^(@) CO_(2)(g)= 50 cal//"mole Kelivn"` Calorimeter data: (1) Water equivlent of calorimaeter = 36 gm (2) Sepcific heat capacity of water = `1 cal//gm .^(@)C` (2) mass of water inthe water bath =164 gm All data at 300 K, `R=2 cal//"mol "K` . If calorimeter is modified so as to convert chemical energy into electrical by ensuring that the reaction is occurring at constant pressure then how much electron work can be obtained by combustion of 0.1 mole of `CH_(4) (g)`?A. `19.5 kcal`B. `18 kcal`C. `19.62 kcal`D. `18.12 kcal` |
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Answer» Correct Answer - b |
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| 1498. |
Find the mass of all molecules leaving one square centimetre of water surface per second into a saturated water vapour above it at a temperature `t = 100 ^@C`. It is assumed that `eta = 3.6 %` of all water vapour molecules falling on the water surface are retained in the liquid phase. |
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Answer» In equilibrium the number of "liquid" molecules evaporoting must equals the number of "vapour" molecules condensing. By kinetic theory, this number is `eta xx (1)/(4) n lt v gt = eta xx (1)/(4) n xx sqrt((8)/(pi)(kT)/(m))` Its mass is `mu = m xx eta xx n xx sqrt((kT)/(2 pi m)) = eta n k T sqrt((m)/(2 pi kt))` `=eta p_0 sqrt((M)/(2 pi RT)) = 0.35 g//cm^2.s.` where `p_0` is atmospheric pressure and `T = 373 K` and `M` = molecular weight of water. |
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| 1499. |
Bomb calorimeters are the devices that are used to experimentally determine `DeltaH` and `DeltaU` of any reaction by measuring the temperature change in the water bath Hence , the experimatal data can be used for cross-checking theortical data, From the following theoretical data answer the question that follow: Thermodynamic data: `DeltaH_(f)^(@)Ch_(4)(g)=- 15 kcal //"mole", DeltaH_(f)^(@) CO_(2)(g)=-90 kcal//"mole",` `DeltaH_(f)^(@)H_(2)O(l)=-60 Kcal//"mole"` `S_(m)^(@) CH_(4)(g)= 40 cal//"mole Kelivn"` `S_(m)^(@) O(g)= 45 cal//"mole Kelivn"` `S_(m)^(@) H_(2)O(g)= 15 cal//"mole Kelivn"` `S_(m)^(@) CO_(2)(g)= 50 cal//"mole Kelivn"` Calorimeter data: (1) Water equivlent of calorimaeter = 36 gm (2) Sepcific heat capacity of water = `1 cal//gm .^(@)C` (2) mass of water inthe water bath =164 gm All data at 300 K, `R=2 cal//"mol "K` . 1. Calculate `DeltaU_("combustion")` of `CH_(4)(g)` at 300 K.A. `-195 kcal//"mole"`B. `-196.2 kcal//"mole"`C. `-193.8 kcal//"mole"`D. `-235 kcal//"mole"` |
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Answer» Correct Answer - c |
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| 1500. |
Bomb calorimeters are the devices that are used to experimentally determine `DeltaH` and `DeltaU` of any reaction by measuring the temperature change in the water bath Hence , the experimatal data can be used for cross-checking theortical data, From the following theoretical data answer the question that follow: Thermodynamic data: `DeltaH_(f)^(@)Ch_(4)(g)=- 15 kcal //"mole", DeltaH_(f)^(@) CO_(2)(g)=-90 kcal//"mole",` `DeltaH_(f)^(@)H_(2)O(l)=-60 Kcal//"mole"` `S_(m)^(@) CH_(4)(g)= 40 cal//"mole Kelivn"` `S_(m)^(@) O(g)= 45 cal//"mole Kelivn"` `S_(m)^(@) H_(2)O(g)= 15 cal//"mole Kelivn"` `S_(m)^(@) CO_(2)(g)= 50 cal//"mole Kelivn"` Calorimeter data: (1) Water equivlent of calorimaeter = 36 gm (2) Sepcific heat capacity of water = `1 cal//gm .^(@)C` (2) mass of water inthe water bath =164 gm All data at 300 K, `R=2 cal//"mol "K` . Calculate rise in temperature of calorimeter if 0.01 moles of `CH_(4)(g)` undergoes combustion in the above bonb calorimeter at 300 K .A. `9.18 K`B. `9.696 K`C. `12 K`D. `8.8 K` |
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Answer» Correct Answer - b |
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