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Page 1 1. (b) K p = K c (RT) ?n since ?n = 0, K p = K c . 2. (c) pH = pK a + log 5 = 4 + log [ Q pK a = – log K a ] Given, K a = 1 × 10 – 4 ? pK a = – log (1× 10 – 4 ) = 4 Now from Handerson equation pH = pK a + Putting the values 5 =4 + = 5 – 4 = 1 Taking antilog [Salt]/[Acid] = 10 = 10 : 1 3. (a) The reaction given is an exothermic reaction thus according to Le chatalier’s principle lowering of temperature, addition of F 2 and Cl 2 favour the forward direction and hence the production of ClF 3 . 4. (c) Ag 2 CrO 4 K sp = [Ag + ] 2 = 1.1 × 10 –12 AgCl K sp = [Ag + ] [Cl – ] = 1.8 × 10 –10 Page 2 1. (b) K p = K c (RT) ?n since ?n = 0, K p = K c . 2. (c) pH = pK a + log 5 = 4 + log [ Q pK a = – log K a ] Given, K a = 1 × 10 – 4 ? pK a = – log (1× 10 – 4 ) = 4 Now from Handerson equation pH = pK a + Putting the values 5 =4 + = 5 – 4 = 1 Taking antilog [Salt]/[Acid] = 10 = 10 : 1 3. (a) The reaction given is an exothermic reaction thus according to Le chatalier’s principle lowering of temperature, addition of F 2 and Cl 2 favour the forward direction and hence the production of ClF 3 . 4. (c) Ag 2 CrO 4 K sp = [Ag + ] 2 = 1.1 × 10 –12 AgCl K sp = [Ag + ] [Cl – ] = 1.8 × 10 –10 [Ag + ] = AgBr K sp = [Ag + ] [Br – ] = 5.0 × 10 –13 AgI K sp = [Ag + ] [I – ] = 8.3 × 10 –17 If we take than maximum [Ag + ] will be required in case of Ag 2 CrO 4 . 5. (b) MY M + + Y – K SP = s 2 ? = 6.2 × 10 –13 ? s = s = 7.87 × 10 –7 mol L –1 NY 3 N 3+ + 3Y – K SP = s × (3s) 3 = 27s 4 = 6.2 × 10 –13 s = s = 3.89 × 10 –4 mol L –1 ? molar solubility of NY 3 is more than MY in water. 6. (b) ?G° NO(g) = 86.6k J/mol = 86600 J/mol = x J/mol T = 298, K P = 1.6 × 10 12 ?G° = – RT ln K P Given equation, 2NO(g) + O 2 (g) 2NO 2 (g) ? 2?G° NO2 – 2?G° NO = – R (298) ln (1.6 × 10 12 ) Page 3 1. (b) K p = K c (RT) ?n since ?n = 0, K p = K c . 2. (c) pH = pK a + log 5 = 4 + log [ Q pK a = – log K a ] Given, K a = 1 × 10 – 4 ? pK a = – log (1× 10 – 4 ) = 4 Now from Handerson equation pH = pK a + Putting the values 5 =4 + = 5 – 4 = 1 Taking antilog [Salt]/[Acid] = 10 = 10 : 1 3. (a) The reaction given is an exothermic reaction thus according to Le chatalier’s principle lowering of temperature, addition of F 2 and Cl 2 favour the forward direction and hence the production of ClF 3 . 4. (c) Ag 2 CrO 4 K sp = [Ag + ] 2 = 1.1 × 10 –12 AgCl K sp = [Ag + ] [Cl – ] = 1.8 × 10 –10 [Ag + ] = AgBr K sp = [Ag + ] [Br – ] = 5.0 × 10 –13 AgI K sp = [Ag + ] [I – ] = 8.3 × 10 –17 If we take than maximum [Ag + ] will be required in case of Ag 2 CrO 4 . 5. (b) MY M + + Y – K SP = s 2 ? = 6.2 × 10 –13 ? s = s = 7.87 × 10 –7 mol L –1 NY 3 N 3+ + 3Y – K SP = s × (3s) 3 = 27s 4 = 6.2 × 10 –13 s = s = 3.89 × 10 –4 mol L –1 ? molar solubility of NY 3 is more than MY in water. 6. (b) ?G° NO(g) = 86.6k J/mol = 86600 J/mol = x J/mol T = 298, K P = 1.6 × 10 12 ?G° = – RT ln K P Given equation, 2NO(g) + O 2 (g) 2NO 2 (g) ? 2?G° NO2 – 2?G° NO = – R (298) ln (1.6 × 10 12 ) 2?G° NO2 – 2 × 86600 = – R (298) ln (1.6 × 10 12 ) 2?G° NO2 = 2 × 86600 – R (298) ln (1.6 × 10 12 ) ?G° NO2 = [2 × 86600 – R(298) ln (1.6 × 10 12 ] = 0.5 [2 × 86600 – R (298) ln (1.6 × 10 12 )] 7. (a) (i) (ii) (iii) Applying (II + 3 × III – I) we will get = ? K = K 2 × / K 1 8. (b) Initially on increasing temperature rate of reaction will increase, so % yield will also increase with time. But at equilibrium % yield at high temperature (T 2 ) would be less than at T 1 as reaction is exothermic so the graph is 9. (c) Page 4 1. (b) K p = K c (RT) ?n since ?n = 0, K p = K c . 2. (c) pH = pK a + log 5 = 4 + log [ Q pK a = – log K a ] Given, K a = 1 × 10 – 4 ? pK a = – log (1× 10 – 4 ) = 4 Now from Handerson equation pH = pK a + Putting the values 5 =4 + = 5 – 4 = 1 Taking antilog [Salt]/[Acid] = 10 = 10 : 1 3. (a) The reaction given is an exothermic reaction thus according to Le chatalier’s principle lowering of temperature, addition of F 2 and Cl 2 favour the forward direction and hence the production of ClF 3 . 4. (c) Ag 2 CrO 4 K sp = [Ag + ] 2 = 1.1 × 10 –12 AgCl K sp = [Ag + ] [Cl – ] = 1.8 × 10 –10 [Ag + ] = AgBr K sp = [Ag + ] [Br – ] = 5.0 × 10 –13 AgI K sp = [Ag + ] [I – ] = 8.3 × 10 –17 If we take than maximum [Ag + ] will be required in case of Ag 2 CrO 4 . 5. (b) MY M + + Y – K SP = s 2 ? = 6.2 × 10 –13 ? s = s = 7.87 × 10 –7 mol L –1 NY 3 N 3+ + 3Y – K SP = s × (3s) 3 = 27s 4 = 6.2 × 10 –13 s = s = 3.89 × 10 –4 mol L –1 ? molar solubility of NY 3 is more than MY in water. 6. (b) ?G° NO(g) = 86.6k J/mol = 86600 J/mol = x J/mol T = 298, K P = 1.6 × 10 12 ?G° = – RT ln K P Given equation, 2NO(g) + O 2 (g) 2NO 2 (g) ? 2?G° NO2 – 2?G° NO = – R (298) ln (1.6 × 10 12 ) 2?G° NO2 – 2 × 86600 = – R (298) ln (1.6 × 10 12 ) 2?G° NO2 = 2 × 86600 – R (298) ln (1.6 × 10 12 ) ?G° NO2 = [2 × 86600 – R(298) ln (1.6 × 10 12 ] = 0.5 [2 × 86600 – R (298) ln (1.6 × 10 12 )] 7. (a) (i) (ii) (iii) Applying (II + 3 × III – I) we will get = ? K = K 2 × / K 1 8. (b) Initially on increasing temperature rate of reaction will increase, so % yield will also increase with time. But at equilibrium % yield at high temperature (T 2 ) would be less than at T 1 as reaction is exothermic so the graph is 9. (c) K SP = [Ag + ] 2 [C 2 O 4 ? 2– ] [Ag + ] = 2.2 × 10 –4 M Given that: ? Concentration of C 2 O 4 ? 2– ions, ? K SP = (2.2 × 10 –4 ) 2 (1.1 × 10 –4 ) = 5.324 × 10 –12 10. (b) + 1 – = = or, = = when = 1 11. (d) Max. pressure of CO 2 = Pressure of CO 2 at equilibrium For reaction, SrCO 3 (s) SrO(s) + CO 2 K p = P CO2 = 1.6 atm = maximum pressure of CO 2 volume of container at this stage. V = …(i) Since container is sealed and reaction was not earlier at equilibrium. ? n = constant. n = …(ii) Put equation (ii) in equation (i) V = Page 5 1. (b) K p = K c (RT) ?n since ?n = 0, K p = K c . 2. (c) pH = pK a + log 5 = 4 + log [ Q pK a = – log K a ] Given, K a = 1 × 10 – 4 ? pK a = – log (1× 10 – 4 ) = 4 Now from Handerson equation pH = pK a + Putting the values 5 =4 + = 5 – 4 = 1 Taking antilog [Salt]/[Acid] = 10 = 10 : 1 3. (a) The reaction given is an exothermic reaction thus according to Le chatalier’s principle lowering of temperature, addition of F 2 and Cl 2 favour the forward direction and hence the production of ClF 3 . 4. (c) Ag 2 CrO 4 K sp = [Ag + ] 2 = 1.1 × 10 –12 AgCl K sp = [Ag + ] [Cl – ] = 1.8 × 10 –10 [Ag + ] = AgBr K sp = [Ag + ] [Br – ] = 5.0 × 10 –13 AgI K sp = [Ag + ] [I – ] = 8.3 × 10 –17 If we take than maximum [Ag + ] will be required in case of Ag 2 CrO 4 . 5. (b) MY M + + Y – K SP = s 2 ? = 6.2 × 10 –13 ? s = s = 7.87 × 10 –7 mol L –1 NY 3 N 3+ + 3Y – K SP = s × (3s) 3 = 27s 4 = 6.2 × 10 –13 s = s = 3.89 × 10 –4 mol L –1 ? molar solubility of NY 3 is more than MY in water. 6. (b) ?G° NO(g) = 86.6k J/mol = 86600 J/mol = x J/mol T = 298, K P = 1.6 × 10 12 ?G° = – RT ln K P Given equation, 2NO(g) + O 2 (g) 2NO 2 (g) ? 2?G° NO2 – 2?G° NO = – R (298) ln (1.6 × 10 12 ) 2?G° NO2 – 2 × 86600 = – R (298) ln (1.6 × 10 12 ) 2?G° NO2 = 2 × 86600 – R (298) ln (1.6 × 10 12 ) ?G° NO2 = [2 × 86600 – R(298) ln (1.6 × 10 12 ] = 0.5 [2 × 86600 – R (298) ln (1.6 × 10 12 )] 7. (a) (i) (ii) (iii) Applying (II + 3 × III – I) we will get = ? K = K 2 × / K 1 8. (b) Initially on increasing temperature rate of reaction will increase, so % yield will also increase with time. But at equilibrium % yield at high temperature (T 2 ) would be less than at T 1 as reaction is exothermic so the graph is 9. (c) K SP = [Ag + ] 2 [C 2 O 4 ? 2– ] [Ag + ] = 2.2 × 10 –4 M Given that: ? Concentration of C 2 O 4 ? 2– ions, ? K SP = (2.2 × 10 –4 ) 2 (1.1 × 10 –4 ) = 5.324 × 10 –12 10. (b) + 1 – = = or, = = when = 1 11. (d) Max. pressure of CO 2 = Pressure of CO 2 at equilibrium For reaction, SrCO 3 (s) SrO(s) + CO 2 K p = P CO2 = 1.6 atm = maximum pressure of CO 2 volume of container at this stage. V = …(i) Since container is sealed and reaction was not earlier at equilibrium. ? n = constant. n = …(ii) Put equation (ii) in equation (i) V = 12. (d) K 1 = 1.0 × 10 –5 = (Given) (Given) = (1.0 × 10 –5 ) × (5 × 10 –10 ) = 5 × 10 –15 13. (c) Let s = solubility K sp = [Ag + ] [IO 3 ? – ] = s × s = s 2 Given K sp = 1 × 10 –8 = = 1.0 × 10 –4 mol/lit = 1.0 × 10 –4 × 283 g/lit = = 2.83 × 10 –3 gm/ 100 ml 14. (a) (HSO 4 ) – can accept and donate a proton (HSO 4 ) – + H + H 2 SO 4 (acting as base) (HSO 4 ) – – H + SO 4 ? 2– . (acting as acid) 15. (d) [Cu(H 2 O) 4 ] 2+ + 4NH 3 [Cu(NH 3 ) 4 ] 2+ + 4H 2 O involves lose and gain of electrons. H 2 O is coordinated to Cu by donating electrons (LHS). It is then removed by withdrawing electrons. 16. (b) pH of an acidic solution should be less than 7. The reason is that from H 2 O. [H + ] = 10 –7 M which cannot be neglected in comparison to 10 –8 M. The pH can be calculated as. from acid, [H + ] = 10 –8 M. from H 2 O, [H + ] = 10 –7 M ? Total [H + ] = 10 –8 + 10 –7Read More
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1. What is the concept of equilibrium in chemistry? |
2. How is equilibrium achieved in a chemical reaction? |
3. What is Le Chatelier's principle and how does it relate to equilibrium? |
4. How does temperature affect the equilibrium in a chemical reaction? |
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