Relate Enthalpy to Reactions - Chemistry

  1. Choose the correct expression for the enthalpy change of neutralization for strong acid and strong base.
    Approximately −57 kJ mol−1-57\ \mathrm{kJ\,mol^{-1}} per mol H2O\mathrm{H_2O} formed. Standard neutralization enthalpy for strong acids and bases.
  2. What happens to ΔH\Delta H when all coefficients in a reaction are multiplied by a factor kk?
    ΔH\Delta H is multiplied by kk. Scaling coefficients scales the enthalpy proportionally.
  3. State the meaning of stoichiometric coefficients in thermochemical equations with respect to ΔH\Delta H.
    ΔH\Delta H applies to the reaction as written with those coefficients. Enthalpy corresponds to exact stoichiometric amounts shown.
  4. What is ΔH\Delta H for a reaction that releases 250 kJ250\ \mathrm{kJ} of heat at constant pressure?
    ΔH=−250 kJ\Delta H=-250\ \mathrm{kJ}. Heat released means negative enthalpy change.
  5. Calculate ΔHrxn∘\Delta H_{rxn}^\circ given ∑nΔHf∘(prod)=−120 kJ\sum n\Delta H_f^\circ(\text{prod})=-120\ \mathrm{kJ} and ∑nΔHf∘(react)=−300 kJ\sum n\Delta H_f^\circ(\text{react})=-300\ \mathrm{kJ}.
    ΔHrxn∘=+180 kJ\Delta H_{rxn}^\circ=+180\ \mathrm{kJ}. Products minus reactants: −120−(−300)=+180-120 - (-300) = +180.
  6. State the relationship between heat at constant pressure and enthalpy change for a process.
    qp=ΔHq_p=\Delta H. At constant pressure, heat equals enthalpy change.
  7. What is the sign of ΔHvap\Delta H_{vap} for boiling a liquid under typical conditions?
    ΔHvap>0\Delta H_{vap}>0. Vaporization requires energy input, so positive.
  8. Which is more exothermic: a reaction with ΔH=−50 kJ\Delta H=-50\ \mathrm{kJ} or ΔH=−10 kJ\Delta H=-10\ \mathrm{kJ}?
    ΔH=−50 kJ\Delta H=-50\ \mathrm{kJ}. Larger negative value means more heat released.
  9. Estimate ΔH\Delta H given bonds broken total 800 kJ800\ \mathrm{kJ} and bonds formed total 650 kJ650\ \mathrm{kJ}.
    ΔH≈+150 kJ\Delta H\approx+150\ \mathrm{kJ}. Using bond formula: 800−650=+150800 - 650 = +150.
  10. Identify the enthalpy change name for converting 11 mol of a solid to a liquid at its melting point.
    Enthalpy of fusion, ΔHfus\Delta H_{fus}. Energy required to convert solid to liquid.
  11. What does a thermochemical equation include that a regular balanced equation may omit?
    A stated ΔH\Delta H value for the balanced reaction. Includes the enthalpy change alongside the chemical equation.
  12. Identify the enthalpy change name for forming 11 mol of a compound from its elements in standard states.
    Standard enthalpy of formation, ΔHf∘\Delta H_f^\circ. Enthalpy to form one mole from constituent elements.
  13. State the formula relating heat, mass, and temperature change for a substance with specific heat cc.
    q=mcΔTq=mc\Delta T. Basic calorimetry equation relating heat to temperature change.
  14. Calculate qq if n=2.0 moln=2.0\ \mathrm{mol} and ΔHvap=+40 kJ mol−1\Delta H_{vap}=+40\ \mathrm{kJ\,mol^{-1}}.
    q=+80 kJq=+80\ \mathrm{kJ}. Using q=nΔHvap=2.0×40q = n\Delta H_{vap} = 2.0 \times 40.
  15. Calculate ΔH\Delta H for a target reaction made by adding two steps with ΔH1=−90 kJ\Delta H_1=-90\ \mathrm{kJ} and ΔH2=−10 kJ\Delta H_2=-10\ \mathrm{kJ}.
    ΔH=−100 kJ\Delta H=-100\ \mathrm{kJ}. Adding individual step enthalpies: −90+(−10)=−100-90 + (-10) = -100.
  16. What is the enthalpy change name for heating 11 mol of a substance by 1 K1\ \mathrm{K} at constant pressure?
    Molar heat capacity at constant pressure, Cp,mC_{p,m}. Heat capacity measures energy per degree temperature change.
  17. What is ΔH\Delta H for a reaction that absorbs 18 kJ18\ \mathrm{kJ} of heat at constant pressure?
    ΔH=+18 kJ\Delta H=+18\ \mathrm{kJ}. Heat absorbed means positive enthalpy change.
  18. Identify the enthalpy change name for converting 11 mol of a liquid to a gas at its boiling point.
    Enthalpy of vaporization, ΔHvap\Delta H_{vap}. Energy required to convert liquid to gas.
  19. Identify the enthalpy change name for dissolving 11 mol of a solute in a solvent to infinite dilution.
    Enthalpy of solution, ΔHsoln\Delta H_{soln}. Energy change when dissolving solute completely.
  20. Calculate molar ΔH\Delta H if qp=−45 kJq_p=-45\ \mathrm{kJ} for n=1.5 moln=1.5\ \mathrm{mol} of reaction as written.
    ΔH=−30 kJ mol−1\Delta H=-30\ \mathrm{kJ\,mol^{-1}}. Molar enthalpy equals total heat divided by moles.
  21. What is the unit most commonly used for molar enthalpy changes in chemistry, such as ΔH\Delta H?
    kJ mol−1\mathrm{kJ\,mol^{-1}}. Standard unit for enthalpy per mole in chemical reactions.
  22. What is the enthalpy change name for complete combustion of 11 mol of a substance in O2(g)\mathrm{O_2(g)}?
    Enthalpy of combustion, ΔHcomb\Delta H_{comb}. Energy released when substance burns completely.
  23. What is the enthalpy change name for breaking 11 mol of a specific bond in the gas phase?
    Bond enthalpy (bond dissociation enthalpy). Energy required to break one mole of bonds.
  24. Calculate ΔHrxn\Delta H_{rxn} if Hreactants=120 kJH_{reactants}=120\ \mathrm{kJ} and Hproducts=80 kJH_{products}=80\ \mathrm{kJ}.
    ΔHrxn=−40 kJ\Delta H_{rxn}=-40\ \mathrm{kJ}. Using ΔH=Hproducts−Hreactants=80−120\Delta H = H_{products} - H_{reactants} = 80 - 120.
  25. Which process is endothermic: breaking a chemical bond or forming a chemical bond?
    Breaking a bond is endothermic. Breaking bonds requires energy input.
  26. Which sign of ΔH\Delta H indicates an endothermic reaction process?
    ΔH>0\Delta H>0. Positive ΔH\Delta H means heat is absorbed from surroundings.
  27. Calculate ΔH\Delta H for a target reaction made by adding two steps with ΔH1=−20 kJ\Delta H_1=-20\ \mathrm{kJ} and ΔH2=+55 kJ\Delta H_2=+55\ \mathrm{kJ}.
    ΔH=+35 kJ\Delta H=+35\ \mathrm{kJ}. Adding individual step enthalpies: −20+55=+35-20 + 55 = +35.
  28. What is the sign of ΔHfus\Delta H_{fus} for melting a solid under typical conditions?
    ΔHfus>0\Delta H_{fus}>0. Melting requires energy input, so positive.
  29. Estimate ΔH\Delta H given bonds broken total 1200 kJ1200\ \mathrm{kJ} and bonds formed total 1500 kJ1500\ \mathrm{kJ}.
    ΔH≈−300 kJ\Delta H\approx-300\ \mathrm{kJ}. Using bond formula: 1200−1500=−3001200 - 1500 = -300.
  30. Identify the process change that makes ΔH\Delta H change sign: reversing, scaling, or balancing only.
    Reversing the reaction changes the sign of ΔH\Delta H. Only reversing changes the sign, not scaling or balancing.
  31. Find ΔH\Delta H for the reverse reaction if the forward reaction has ΔH=+125 kJ\Delta H=+125\ \mathrm{kJ}.
    ΔH=−125 kJ\Delta H=-125\ \mathrm{kJ}. Reversing a reaction changes the sign of ΔH\Delta H.
  32. What is the standard temperature commonly assumed for tabulated ΔHf∘\Delta H_f^\circ values?
    298 K298\ \mathrm{K}. Standard temperature for thermodynamic data tables.
  33. Identify the sign of ΔH\Delta H if products are at higher enthalpy than reactants on an energy diagram.
    ΔH>0\Delta H>0. Higher energy products indicate endothermic reaction.
  34. Identify the sign of ΔH\Delta H if products are at lower enthalpy than reactants on an energy diagram.
    ΔH<0\Delta H<0. Lower energy products indicate exothermic reaction.
  35. Which process is exothermic: breaking a chemical bond or forming a chemical bond?
    Forming a bond is exothermic. Forming bonds releases energy.
  36. What is the value of ΔHf∘\Delta H_f^\circ for any element in its standard state?
    ΔHf∘=0\Delta H_f^\circ=0. Elements in standard state have zero formation enthalpy.
  37. What is the relationship between ΔH\Delta H and heat flow if the system releases heat to the surroundings?
    Heat released means ΔH<0\Delta H<0. Releasing heat corresponds to negative enthalpy change.
  38. Calculate ΔHrxn\Delta H_{rxn} if Hreactants=55 kJH_{reactants}=55\ \mathrm{kJ} and Hproducts=90 kJH_{products}=90\ \mathrm{kJ}.
    ΔHrxn=+35 kJ\Delta H_{rxn}=+35\ \mathrm{kJ}. Using ΔH=Hproducts−Hreactants=90−55\Delta H = H_{products} - H_{reactants} = 90 - 55.
  39. What happens to ΔH\Delta H when a chemical equation is reversed?
    The sign of ΔH\Delta H changes. Reversing makes products become reactants.
  40. What is the enthalpy change name for dissolving 11 mol of an ionic solid into aqueous ions?
    Enthalpy of hydration/solution (context-dependent). Energy change when ionic solid dissolves in water.
  41. What is the typical sign of ΔHcomb\Delta H_{comb} for a fuel undergoing complete combustion?
    ΔHcomb<0\Delta H_{comb}<0. Combustion reactions typically release energy.
  42. Which sign of ΔH\Delta H indicates an exothermic reaction process?
    ΔH<0\Delta H<0. Negative ΔH\Delta H means heat is released to surroundings.
  43. Find the new ΔH\Delta H if a reaction with ΔH=−80 kJ\Delta H=-80\ \mathrm{kJ} is multiplied by 33.
    ΔH=−240 kJ\Delta H=-240\ \mathrm{kJ}. Multiplying coefficients multiplies the enthalpy change.
  44. Find the new ΔH\Delta H if a reaction with ΔH=+60 kJ\Delta H=+60\ \mathrm{kJ} is multiplied by 12\frac{1}{2}.
    ΔH=+30 kJ\Delta H=+30\ \mathrm{kJ}. Dividing coefficients divides the enthalpy change proportionally.
  45. What is the enthalpy change name for forming 11 mol of gaseous ions from 11 mol of an ionic solid?
    Lattice enthalpy of dissociation (lattice enthalpy). Energy to separate ionic solid into gaseous ions.
  46. State the bond enthalpy estimate formula for reaction enthalpy using bonds broken and formed.
    ΔH≈∑D(broken)−∑D(formed)\Delta H\approx\sum D(\text{broken})-\sum D(\text{formed}). Energy to break bonds minus energy released forming bonds.
  47. State the formula for ΔHrxn∘\Delta H_{rxn}^\circ using standard enthalpies of formation.
    ΔHrxn∘=∑nΔHf∘(prod)−∑nΔHf∘(react)\Delta H_{rxn}^\circ=\sum n\Delta H_f^\circ(\text{prod})-\sum n\Delta H_f^\circ(\text{react}). Products minus reactants, weighted by stoichiometric coefficients.
  48. Identify the correct interpretation of ΔH=−100 kJ\Delta H=-100\ \mathrm{kJ} written under a balanced equation.
    The reaction as written releases 100 kJ100\ \mathrm{kJ} per stoichiometric reaction. Enthalpy refers to the complete balanced equation as written.
  49. Using Hess's law, find ΔH\Delta H for A→CA\to C if A→BA\to B is +40 kJ+40\ \mathrm{kJ} and B→CB\to C is −15 kJ-15\ \mathrm{kJ}.
    ΔHA→C=+25 kJ\Delta H_{A\to C}=+25\ \mathrm{kJ}. Using Hess's law: 40+(−15)=+2540 + (-15) = +25.
  50. State Hess's law in one sentence for reaction enthalpy changes.
    ΔH\Delta H depends on initial and final states, not the path. Enthalpy is a state function, path-independent.
  51. Calculate qq if n=0.50 moln=0.50\ \mathrm{mol} and ΔHfus=+12 kJ mol−1\Delta H_{fus}=+12\ \mathrm{kJ\,mol^{-1}}.
    q=+6.0 kJq=+6.0\ \mathrm{kJ}. Using q=nΔHfus=0.50×12q = n\Delta H_{fus} = 0.50 \times 12.
  52. What is the relationship between ΔH\Delta H and heat flow if the system absorbs heat from the surroundings?
    Heat absorbed means ΔH>0\Delta H>0. Absorbing heat corresponds to positive enthalpy change.
  53. What does the symbol ∘\circ mean in ΔH∘\Delta H^\circ?
    Standard-state conditions (typically 1 bar1\ \mathrm{bar}). Standard state means reference conditions for measurements.
  54. Calculate ΔHrxn∘\Delta H_{rxn}^\circ given ∑nΔHf∘(prod)=−500 kJ\sum n\Delta H_f^\circ(\text{prod})=-500\ \mathrm{kJ} and ∑nΔHf∘(react)=−200 kJ\sum n\Delta H_f^\circ(\text{react})=-200\ \mathrm{kJ}.
    ΔHrxn∘=−300 kJ\Delta H_{rxn}^\circ=-300\ \mathrm{kJ}. Products minus reactants: −500−(−200)=−300-500 - (-200) = -300.
  55. What is the definition of the enthalpy change of reaction, ΔHrxn\Delta H_{rxn}, at constant pressure?
    ΔHrxn=Hproducts−Hreactants\Delta H_{rxn}=H_{products}-H_{reactants} at constant PP. Enthalpy change equals final enthalpy minus initial enthalpy.
  56. Using Hess's law, find ΔH\Delta H for A→CA\to C if A→BA\to B is −10 kJ-10\ \mathrm{kJ} and B→CB\to C is −35 kJ-35\ \mathrm{kJ}.
    ΔHA→C=−45 kJ\Delta H_{A\to C}=-45\ \mathrm{kJ}. Using Hess's law: (−10)+(−35)=−45(-10) + (-35) = -45.
  57. State the formula for heat absorbed or released during a phase change using molar enthalpy ΔHphase\Delta H_{phase}.
    q=nΔHphaseq=n\Delta H_{phase}. Heat equals moles times molar enthalpy of phase change.

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