Enthalpy of Combustion
Trending Questions
Q.
Why do bonds release energy?
Q. The heat of combustion of sucrose (C12H22O11) is −5.65×103 kJ. If complete combustion of 1.0 kg sucrose is done, heat evloved will be:
- 1.65×104 kJ
- 5.65×103 kJ
- 7.38×105 kJ
- 3.51×105 kJ
Q. In the combustion of 2 g of methane, 25 kcal heat is liberated. Find the molar heat of combustion of methane.
- 100 kcal
- 200 kcal
- 75 kcal
- 150 kcal
Q. When 1.0 g of oxalic acid (H2C2O4) is burned in a bomb calorimeter whose heat capacity is 8.75 kJ/K, the temperature increases by 0.312 K. The enthalpy of combustion of oxalic acid at 27oC is:
- −300.7 kJ/mol
- −280.452 kJ/mol
- −241.947 kJ/mol
- None of these
Q. The combustion of hydrogen-oxygen mixture is used to produce very high temperatures (≈2500oC) needed for certain types of welding operations.
H2(g)+12O2(g)→H2O(g); △H=−230.9 kJ
Quantity of heat, (in kJ) evolved when a 200 g mixture containing equal parts of H2 and O2 by mass is burned, is
H2(g)+12O2(g)→H2O(g); △H=−230.9 kJ
Quantity of heat, (in kJ) evolved when a 200 g mixture containing equal parts of H2 and O2 by mass is burned, is
- 2.72×103kJ
- 1.36×103kJ
- 1.44×103kJ
- 4.3524×104kJ
Q.
How will you provide the following information in a chemical equation?
Evolution of heat
Q. Efficiency of a fuel is based on it's :
- Specific heat
- Calorific value
- Cost
- Ignition temperature
Q.
The standard heat of combustion of Al is −837.8 kJ mol−1 25∘C which of the following releases 250 kcal of heat?
- The reaction of 0.624 mol of Al
- The formation of 0.624 mol of Al2O3
- The reaction of 0.312 mol of Al
- The formation of 0.150 mol of Al2O3
Q. The standard enthalpy of formation of octane (C8H18) is −250 kJ/mol. Calculate the enthalpy of combustion of C8H18.
Given : enthalpy of formation of CO2(g) and H2O(l) are −394 kJ/mol and −286 kJ/mol respectively:
Given : enthalpy of formation of CO2(g) and H2O(l) are −394 kJ/mol and −286 kJ/mol respectively:
- −5200 kJ/mol
- −5726 kJ/mol
- −5476 kJ/mol
- −5310 kJ/mol
Q. (i) Cis - 2 - butene → trans-2-butene, △H1
(ii) Cis - 2 - butene → 1 - butene, △H2
(iii) Trans-2-butene is more stable than cis - 2 - butene.
(iv) Enthalpy of combustion of 1 - butene, △H=−649.8 kcal/mol
(v) 9△H1+5△H2=0
(vi) Enthalpy of combustion of trans 2 - butene, △H=−647.0 kcal/mol.
The value of △H1 and △H2 in kcal/mol are
(ii) Cis - 2 - butene → 1 - butene, △H2
(iii) Trans-2-butene is more stable than cis - 2 - butene.
(iv) Enthalpy of combustion of 1 - butene, △H=−649.8 kcal/mol
(v) 9△H1+5△H2=0
(vi) Enthalpy of combustion of trans 2 - butene, △H=−647.0 kcal/mol.
The value of △H1 and △H2 in kcal/mol are
- - 1.0, 1.8
- 1.8, -1.0
- -5, 9
- -2, 3.6
Q. The standard enthalpy of combustion at 25o C of hydrogen, cyclohexene (C6H10) and cyclohexane (C6H12 ) are −241, −3800 and −3920kJ mol−1 respectively. Calculate the heat of hydrogenation of cyclohexene ( in kJ mol−1)
- − 121
- + 121
- + 221
- − 221
Q. The enthalpy of combustion of H2(g) at 298 K to give H2O(g) is −249 kJ mol−1 and bond enthalpies of H - H and O = O are 433 kJ mol−1 and 492 kJ mol−1, respectively. The bond enthalpy of O - H is
- 464 kJ mol−1
- 928 kJ mol−1
- 232 kJ mol−1
- −232 kJ mol−1
Q. When 1.0 g of oxalic acid (H2C2O4) is burned in a bomb calorimeter whose heat capacity is 8.75 kJ/K, the temperature increases by 0.312 K. The enthalpy of combustion of oxalic acid at 27oC is:
- −300.7 kJ/mol
- −280.452 kJ/mol
- −241.947 kJ/mol
- None of these
Q. The standard enthalpy of combustion at 25o C of hydrogen, cyclohexene (C6H10) and cyclohexane (C6H12 ) are −241, −3800 and −3920kJ mol−1 respectively. Calculate the heat of hydrogenation of cyclohexene ( in kJ mol−1)
- − 121
- + 121
- + 221
- − 221
Q. The heat of combustion of carbon to CO2 is -393.5 kJ/mol. The heat released upon formation of 35.2g of CO2 from carbon and oxygen gas is
- +315 kJ
- -630 kJ
- -3.15 kJ
- -315 kJ
Q. The heat of combustion of benzene in a bomb calorimeter (i.e., constant volume) was found to be 3263.9 kJmol−1 at 25oC. Calculate the heat of combustion of benzene at constant pressure.
- −4767.6 kJmol−1
- 3667.6 kJmol−1
- −3267.6 kJmol−1
- 2767.6 kJmol−1
Q. The combustion of benzene (l) gives CO2(g) and H2O(l). Given that the heat of combustion of benzene at constant volume is —3263.9 kJ mol−1 at 25∘C. The heat of combustion (in kJ mol−1) of benzene at constant pressure will be:
(R=8.314 JK−1mol−1)
(R=8.314 JK−1mol−1)
- -3267.6
- 4152.6
- -452.46
- 3260
Q.
The heats of combustion of carbon and carbon monoxide are −283.5 and −283.5 kJ mol−1 respectively. The heat of formation (in kJ) of carbon monoxide per mole is
676.5
– 676.5
– 110.5
110.5
Q. The enthalpy change for the reaction,
C2H4(g) + 3O2(g) ⟶2CO2(g) + 2H2O(g) is called:
C2H4(g) + 3O2(g) ⟶2CO2(g) + 2H2O(g) is called:
Enthalpy of formation
Enthalpy of combustion
Enthalpy of vaporization
Enthalpy of sublimation
Q. The standard enthalpy of formation of octane (C8H18) is −250 kJ/mol. Calculate the enthalpy of combustion of C8H18.
Given : enthalpy of formation of CO2(g) and H2O(l) are −394 kJ/mol and −286 kJ/mol respectively:
Given : enthalpy of formation of CO2(g) and H2O(l) are −394 kJ/mol and −286 kJ/mol respectively:
- −5200 kJ/mol
- −5726 kJ/mol
- −5476 kJ/mol
- −5310 kJ/mol
Q. When 5 litres of a gas mixture of methane and propane is perfectly combusted at 0∘C and 1 atmosphere, 16 litres of oxygen at the same temperature and pressure is consumed. The amount of heat released from this combustion in kJ(ΔHcomb.(CH4)=890 kJ mol−1, ΔHcomb.(C3H8)=2220 kJ mol−1) is
- 38
- 317
- 477
- 32
Q. The standard heat of combustion of solid boron is equal to
ΔH0f(B2O3)
12ΔH0f(B2O3)
2ΔH0f(B2O3)
−12ΔH0f(B2O3)
Q. When a certain amount of ethylene was combusted, 6226 kJ heat was evolved. If heat of combustion of 1 mole of ethylene is 1411 kJ, the volume of O2 (at NTP) that entered into the reaction is:
- 296.5 mL
- 296.5 litres
- 6226×22.4 litres
- 22.4 litres
Q. Which of the following is not an endothermic process
- Combustion of methane
- Decomposition of water
- Dehydrogenation of ethane to ethylene
- Conversion of graphite to diamond
Q. The value of log10K for a reaction A⇌B is: Given:△rH∘298 K=−54.07 kJ mol−1, △rS∘298 K=10 J K−1 mol−1 and R=8.314 J K−1 mol−1
- 10
- 100
- 5
- 95
Q. When 5 litres of a gas mixture of methane and propane is perfectly combusted at 0∘C and 1 atmosphere, 16 litres of oxygen at the same temperature and pressure is consumed. The amount of heat released from this combustion in kJ(ΔHcomb.(CH4)=890 kJ mol−1, ΔHcomb.(C3H8)=2220 kJ mol−1) is
- 38
- 317
- 477
- 32
Q. The combustion of hydrogen-oxygen mixture is used to produce very high temperatures (=2500∘ C) needed for certain types of welding operations.
H2(g)+12O2(g)→H2O(g); ΔH=−230.9 kJ
Quantity of heat, (in kJ) evolved when a 200 g mixture containing equal parts of H2 and O2 mass is burned, is
H2(g)+12O2(g)→H2O(g); ΔH=−230.9 kJ
Quantity of heat, (in kJ) evolved when a 200 g mixture containing equal parts of H2 and O2 mass is burned, is
- −2.72×103 kJ
- −1.36×103 kJ
- −1.44×103 kJ
- −4.3524×104 kJ
Q. The heat of combustion of benzene in a bomb calorimeter (i.e., constant volume) was found to be 3263.9 kJmol−1 at 25oC. Calculate the heat of combustion of benzene at constant pressure.
- −4767.6 kJmol−1
- 3667.6 kJmol−1
- −3267.6 kJmol−1
- 2767.6 kJmol−1
Q. The total entropy change (△Stotal) for the system and the surrounding of a spontaneous process is given by:
- △Stotal=△Ssystem+△Ssurr>0
- △Stotal=△Ssystem−△Ssurr>0
- △Ssystem=△Stotal+△Ssurr>0
- △Ssurr=△Stotal−△Ssystem<0
Q. The heat of formation of CO and CO2 are −26.4 kcal and −94 kcal respectively. The heat of combustion of carbon monoxide will be:
- +26.4 kcal
- −67.6 kcal
- −120.4 kcal
- +52.8 kcal