11th class (FSc) chemistry Unit 7 MCQs

a. Bond energy
b. Enthalpy change
c. Internal energy change
d. Heat of sublimation

b. Enthalpy change

a. In an adiabatic process, work done is independent of its path
b. Energy can neither created nor destroy
c. Continuous productions of mechanical work without supplying an equivalent amount of heat is possible
d. One form of energy can be transformed into an equivalent amount of other kind of energy

c. Continuous productions of mechanical work without supplying an equivalent amount of heat is possible

a. pq>pv
b. pq=pv
c. pq=pv/2
d. pq<pv

a. pq>pv

a. Heat of neutralization
b. Heat of reaction
c. Heat of combustion
d. Heat of formation

a. Heat of neutralization

a. Joule’s law
b. Henry’s law
c. Law of conservation or energy
d. Hess’s law

d. Hess’s law

a. Acids always gives H+ ions and bases OH ions
b. Neutralization to formation of salt and water
c. The net chemical change involves the combination of H+ and OH to form water
d. Stong acids and bases are ionic substance

c. The net chemical change involves the combination of H+ and OH to form water

a. Dissolution
b. Combustion
c. Formation
d. Dissociation

b. Combustion

a. Increases then decreases
b. Remain unchanged
c. Decrease
d. Increase

b. Remain unchanged

a. Dissociation reactions
b. Exothermic reactions
c. Endothermic reactions
d. Decomposition reactants

b. Exothermic reactions

a. Dissolution
b. Combustion
c. Formation
d. Dissociation

b. Combustion

a. -294KJ/mole
b. -394 KJ/mole
c. -390KJ/mole
d. +394 KJ/mole

b. -394 KJ/mole

a. Photochemical reactions
b. Exothermic reactions
c. Non-spontaneous reactions
d. Endothermic reactions

b. Exothermic reactions

a. H = -393.7 KJmol-1
b. C+O2→ CO2
c. H =?
d. C+1/2O2 → CO

b. C+O2→ CO2

a. -202.5 KJ/mol
b. 205.5 KJ/mol
c. 1 KJ/mol
d. Zero KJ/mol

b. 205.5 KJ/mol

a. 110 KJ mol-1
b. -676 KJ molc
c. 676 KJ mol-1
d. -110 KM mol-1

b. -676 KJ molc

a. 1/2 H2(g) → H(g) +218 KJmol-1
b. 1/2 H2O(i) → H2(g) + 1/2 O(g)
c. 1/2 H2(g) → H(g) +-218 KJmol-1
d. 1/2 H2O(i) → H2(g) – 1/2 O(g)

b. 1/2 H2O(i) → H2(g) + 1/2 O(g)

a. Enrthalpy of formation
b. Enthalpy of atomization
c. Enthalpy of dissociation
d. Enthalpy of decomposition

b. Enthalpy of atomization

a. 1/2 H2(g) → H(g) +218 KJmol-1
b. 1/2 H2O(i) → H2(g) + 1/2 O(g)
c. 1/2 H2(g) → H(g) +-218 KJmol-1
d. 1/2 H2O(i) → H2(g) – 1/2 O(g)

b. 1/2 H2O(i) → H2(g) + 1/2 O(g)

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