5.3 Bond enthalpies

What is the $\mathrm{H}-\mathrm{H}$ bond enthalpy, in $\mathrm{kJ} {\mathrm{mol}}^{-1}$, in the ${\mathrm{H}}_2$ molecule?

$2{\mathrm{H}}_2\left(\mathrm{g}\right)+{\mathrm{O}}_2\left(\mathrm{g}\right)\to 2{\mathrm{H}}_2\mathrm{O}\left(\mathrm{g}\right)$

$∆H_{\mathrm{f}}\left({\mathrm{H}}_2\mathrm{O}\right)=x \mathrm{kJ} {\mathrm{mol}}^{-1}$

A.  $x-y+4z$

B.  $\frac{1}{2}\left(x-y+4z\right)$

C.  $x-y+2z$

D.  $\frac{1}{2}\left(x-y+2z\right)$

What is the $\mathrm{H}-\mathrm{H}$ bond enthalpy, in $\mathrm{kJ} {\mathrm{mol}}^{-1}$, in the ${\mathrm{H}}_2$ molecule?

$2{\mathrm{H}}_2\left(\mathrm{g}\right)+{\mathrm{O}}_2\left(\mathrm{g}\right)\to 2{\mathrm{H}}_2\mathrm{O}\left(\mathrm{g}\right)$

$∆H_{\mathrm{f}}\left({\mathrm{H}}_2\mathrm{O}\right)=x \mathrm{kJ} {\mathrm{mol}}^{-1}$

A.  $x-y+4z$

B.  $\frac{1}{2}\left(x-y+4z\right)$

C.  $x-y+2z$

D.  $\frac{1}{2}\left(x-y+2z\right)$

Calculate the standard enthalpy change, $∆H^{⦵}$, for this reaction using section 12 of the data booklet.

Calculate the standard enthalpy change, $∆H^{⦵}$, for this reaction using section 12 of the data booklet.

Calculate the standard enthalpy change, $∆H^{⦵}$, for this reaction using section 12 of the data booklet.

Calculate the standard enthalpy change, $∆H^{⦵}$, for this reaction using section 12 of the data booklet.

Calculate the standard enthalpy change, $∆H^{⦵}$, for this reaction using section 12 of the data booklet.

Calculate the standard enthalpy change, $∆H^{⦵}$, for this reaction using section 12 of the data booklet.

Determine the standard enthalpy change, $∆H^{⦵}$, for this reaction, using section 11 of the data booklet.

Determine the standard enthalpy change, $∆H^{⦵}$, for this reaction, using section 11 of the data booklet.

Determine the standard enthalpy change, $∆H^{⦵}$, for this reaction, using section 11 of the data booklet.

State one reason why you would expect the value of ΔH calculated from the $∆H_f^{\mathrm{⦵}}$ values, given in section 12 of data booklet, to differ from your answer to (d)(i).

State one reason why you would expect the value of ΔH calculated from the $∆H_f^{\mathrm{⦵}}$ values, given in section 12 of data booklet, to differ from your answer to (d)(i).

State one reason why you would expect the value of ΔH calculated from the $∆H_f^{\mathrm{⦵}}$ values, given in section 12 of data booklet, to differ from your answer to (d)(i).

Determine the change in enthalpy, ΔH, for the combustion of but-2-ene, using section 11 of the data booklet. 

CH₃CH=CHCH₃(g) + 6O₂ (g) → 4CO₂(g) + 4H₂O (g)

Determine the change in enthalpy, ΔH, for the combustion of but-2-ene, using section 11 of the data booklet. 

CH₃CH=CHCH₃(g) + 6O₂ (g) → 4CO₂(g) + 4H₂O (g)

Determine the change in enthalpy, ΔH, for the combustion of but-2-ene, using section 11 of the data booklet. 

CH₃CH=CHCH₃(g) + 6O₂ (g) → 4CO₂(g) + 4H₂O (g)

Determine the change in enthalpy, ΔH, for the combustion of but-2-ene, using section 11 of the data booklet. 

CH₃CH=CHCH₃(g) + 6O₂ (g) → 4CO₂(g) + 4H₂O (g)

Determine the change in enthalpy, ΔH, for the combustion of but-2-ene, using section 11 of the data booklet. 

CH₃CH=CHCH₃(g) + 6O₂ (g) → 4CO₂(g) + 4H₂O (g)

Determine the change in enthalpy, ΔH, for the combustion of but-2-ene, using section 11 of the data booklet. 

CH₃CH=CHCH₃(g) + 6O₂ (g) → 4CO₂(g) + 4H₂O (g)

Under certain conditions, ethyne can be converted to benzene.

Determine the standard enthalpy change, ΔH^Θ, for the reaction stated, using section 11 of the data booklet.

3C₂H₂(g) → C₆H₆(g)

Under certain conditions, ethyne can be converted to benzene.

Determine the standard enthalpy change, ΔH^Θ, for the reaction stated, using section 11 of the data booklet.

3C₂H₂(g) → C₆H₆(g)

Under certain conditions, ethyne can be converted to benzene.

Determine the standard enthalpy change, ΔH^Θ, for the reaction stated, using section 11 of the data booklet.

3C₂H₂(g) → C₆H₆(g)

Explain, giving two reasons, the difference in the values for (c)(i) and (ii). If you did not obtain answers, use −475 kJ for (i) and −600 kJ for (ii).

Explain, giving two reasons, the difference in the values for (c)(i) and (ii). If you did not obtain answers, use −475 kJ for (i) and −600 kJ for (ii).

Explain, giving two reasons, the difference in the values for (c)(i) and (ii). If you did not obtain answers, use −475 kJ for (i) and −600 kJ for (ii).

Outline why the value of enthalpy of reaction calculated from bond enthalpies is less accurate.

Outline why the value of enthalpy of reaction calculated from bond enthalpies is less accurate.

Outline why the value of enthalpy of reaction calculated from bond enthalpies is less accurate.

Which combustion reaction releases the least energy per mole of C₃H₈?

Approximate bond enthalpy / kJ mol⁻¹
O=O    500
C=O    800
 C≡O   1000

A.  C₃H₈(g) + 5O₂(g) → 3CO₂(g) + 4H₂O (g)

B.  C₃H₈(g) + $\frac{9}{2}$O₂(g) → 2CO₂(g) + CO (g) + 4H₂O (g)

C.  C₃H₈(g) + 4O₂(g) → CO₂(g) + 2CO (g) + 4H₂O (g)

D.  C₃H₈(g) + $\frac{7}{2}$O₂(g) → 3CO (g) + 4H₂O (g)

Chemistry: Atoms First 2e, https://openstax.org/books/chemistry-atoms-first-2e/pages/9-4-strengths-of-ionic-andcovalent-bonds © 1999–2021, Rice University. Except where otherwise noted, textbooks on this site are licensed under a Creative Commons Attribution 4.0 International License.
(CC BY 4.0) https://creativecommons.org/licenses/ by/4.0/.

Which combustion reaction releases the least energy per mole of C₃H₈?

Approximate bond enthalpy / kJ mol⁻¹
O=O    500
C=O    800
 C≡O   1000

A.  C₃H₈(g) + 5O₂(g) → 3CO₂(g) + 4H₂O (g)

B.  C₃H₈(g) + $\frac{9}{2}$O₂(g) → 2CO₂(g) + CO (g) + 4H₂O (g)

C.  C₃H₈(g) + 4O₂(g) → CO₂(g) + 2CO (g) + 4H₂O (g)

D.  C₃H₈(g) + $\frac{7}{2}$O₂(g) → 3CO (g) + 4H₂O (g)

Chemistry: Atoms First 2e, https://openstax.org/books/chemistry-atoms-first-2e/pages/9-4-strengths-of-ionic-andcovalent-bonds © 1999–2021, Rice University. Except where otherwise noted, textbooks on this site are licensed under a Creative Commons Attribution 4.0 International License.
(CC BY 4.0) https://creativecommons.org/licenses/ by/4.0/.

Determine the enthalpy change, ΔH, for the Haber–Bosch process, in kJ. Use Section 11 of the data booklet.

Determine the enthalpy change, ΔH, for the Haber–Bosch process, in kJ. Use Section 11 of the data booklet.

Determine the enthalpy change, ΔH, for the Haber–Bosch process, in kJ. Use Section 11 of the data booklet.

Outline why the value obtained in (b)(i) might differ from a value calculated using ΔH_f data.

Outline why the value obtained in (b)(i) might differ from a value calculated using ΔH_f data.

Outline why the value obtained in (b)(i) might differ from a value calculated using ΔH_f data.

The enthalpy change for the reaction to produce B is −213 kJ. Predict, giving a reason, which product is the most stable.

The enthalpy change for the reaction to produce B is −213 kJ. Predict, giving a reason, which product is the most stable.

The enthalpy change for the reaction to produce B is −213 kJ. Predict, giving a reason, which product is the most stable.

Determine the enthalpy change for the reaction, in kJ, to produce A using section 11 of the data booklet.

Determine the enthalpy change for the reaction, in kJ, to produce A using section 11 of the data booklet.

Determine the enthalpy change for the reaction, in kJ, to produce A using section 11 of the data booklet.

Determine the enthalpy of combustion of this compound, in kJ mol⁻¹, using data from section 11 of the data booklet.

Determine the enthalpy of combustion of this compound, in kJ mol⁻¹, using data from section 11 of the data booklet.

Determine the enthalpy of combustion of this compound, in kJ mol⁻¹, using data from section 11 of the data booklet.

The diagram shows the Maxwell–Boltzmann distribution and potential energy profile for the reaction without a catalyst.

Annotate both charts to show the activation energy for the catalysed reaction, using the label E_{a (cat)}.

The diagram shows the Maxwell–Boltzmann distribution and potential energy profile for the reaction without a catalyst.

Annotate both charts to show the activation energy for the catalysed reaction, using the label E_{a (cat)}.

The diagram shows the Maxwell–Boltzmann distribution and potential energy profile for the reaction without a catalyst.

Annotate both charts to show the activation energy for the catalysed reaction, using the label E_{a (cat)}.

Determine the enthalpy of combustion of the organic product in (b), in kJ mol⁻¹, using data from section 11 of the data booklet.

Determine the enthalpy of combustion of the organic product in (b), in kJ mol⁻¹, using data from section 11 of the data booklet.

Determine the enthalpy of combustion of the organic product in (b), in kJ mol⁻¹, using data from section 11 of the data booklet.

The diagram shows the Maxwell–Boltzmann distribution and potential energy profile for the reaction without a catalyst.

Annotate both charts to show the activation energy for the catalysed reaction, using the label E_{a (cat)}.

The diagram shows the Maxwell–Boltzmann distribution and potential energy profile for the reaction without a catalyst.

Annotate both charts to show the activation energy for the catalysed reaction, using the label E_{a (cat)}.

The diagram shows the Maxwell–Boltzmann distribution and potential energy profile for the reaction without a catalyst.

Annotate both charts to show the activation energy for the catalysed reaction, using the label E_{a (cat)}.

What is the enthalpy change, in kJ, of the following reaction?

3H₂ (g) + N₂ (g) $\rightleftharpoons$ 2NH₃ (g)

A. (6 × 391) − [(3 × 436) + 945]

B. (3 × 391) − (436 + 945)

C. −[(3 × 436) + 945] + (3 × 391)

D. −(6 × 391) + [(3 × 436) + 945]

What is the enthalpy change, in kJ, of the following reaction?

3H₂ (g) + N₂ (g) $\rightleftharpoons$ 2NH₃ (g)

A. (6 × 391) − [(3 × 436) + 945]

B. (3 × 391) − (436 + 945)

C. −[(3 × 436) + 945] + (3 × 391)

D. −(6 × 391) + [(3 × 436) + 945]

Hydrogen gas can be formed industrially by the reaction of natural gas with steam.

                                          CH₄(g) + H₂O(g) → 3H₂(g) + CO(g)

Determine the enthalpy change, ΔH, for the reaction, in kJ, using section 11 of the data booklet.

Bond enthalpy for C≡O: 1077 kJ mol⁻¹

Hydrogen gas can be formed industrially by the reaction of natural gas with steam.

                                          CH₄(g) + H₂O(g) → 3H₂(g) + CO(g)

Determine the enthalpy change, ΔH, for the reaction, in kJ, using section 11 of the data booklet.

Bond enthalpy for C≡O: 1077 kJ mol⁻¹

Hydrogen gas can be formed industrially by the reaction of natural gas with steam.

                                          CH₄(g) + H₂O(g) → 3H₂(g) + CO(g)

Determine the enthalpy change, ΔH, for the reaction, in kJ, using section 11 of the data booklet.

Bond enthalpy for C≡O: 1077 kJ mol⁻¹

Under certain conditions, ethyne can be converted to benzene.

Determine the standard enthalpy change, ΔH^ϴ, for the reaction stated, using section 11 of the data booklet.

                                        3C₂H₂(g) → C₆H₆(g)

Under certain conditions, ethyne can be converted to benzene.

Determine the standard enthalpy change, ΔH^ϴ, for the reaction stated, using section 11 of the data booklet.

                                        3C₂H₂(g) → C₆H₆(g)

Under certain conditions, ethyne can be converted to benzene.

Determine the standard enthalpy change, ΔH^ϴ, for the reaction stated, using section 11 of the data booklet.

                                        3C₂H₂(g) → C₆H₆(g)

Explain, giving two reasons, the difference in the values for (b)(i) and (ii). If you did not obtain answers, use −475 kJ for (i) and −600 kJ for (ii).

Explain, giving two reasons, the difference in the values for (b)(i) and (ii). If you did not obtain answers, use −475 kJ for (i) and −600 kJ for (ii).

Explain, giving two reasons, the difference in the values for (b)(i) and (ii). If you did not obtain answers, use −475 kJ for (i) and −600 kJ for (ii).

Hydrogen gas can be formed industrially by the reaction of natural gas with steam.

                                          CH₄(g) + H₂O(g) → 3H₂(g) + CO(g)

Determine the enthalpy change, ΔH, for the reaction, in kJ, using section 11 of the data booklet.

Bond enthalpy for C≡O: 1077 kJ mol⁻¹

Hydrogen gas can be formed industrially by the reaction of natural gas with steam.

                                          CH₄(g) + H₂O(g) → 3H₂(g) + CO(g)

Determine the enthalpy change, ΔH, for the reaction, in kJ, using section 11 of the data booklet.

Bond enthalpy for C≡O: 1077 kJ mol⁻¹

Hydrogen gas can be formed industrially by the reaction of natural gas with steam.

                                          CH₄(g) + H₂O(g) → 3H₂(g) + CO(g)

Determine the enthalpy change, ΔH, for the reaction, in kJ, using section 11 of the data booklet.

Bond enthalpy for C≡O: 1077 kJ mol⁻¹

Consider the following reaction:

N₂ (g) + 3H₂ (g) $\rightleftharpoons$ 2NH₃ (g)

Which calculation gives ΔH^Θ, in kJ, for the forward reaction?

A.   2z − y − 3x

B.   y + 3x − 2z

C.   y + 3x − 6z

D.   6z − y − 3x

Consider the following reaction:

N₂ (g) + 3H₂ (g) $\rightleftharpoons$ 2NH₃ (g)

Which calculation gives ΔH^Θ, in kJ, for the forward reaction?

A.   2z − y − 3x

B.   y + 3x − 2z

C.   y + 3x − 6z

D.   6z − y − 3x

Outline why bond enthalpy values are not valid in calculations such as that in (g)(i).

Outline why bond enthalpy values are not valid in calculations such as that in (g)(i).

Outline why bond enthalpy values are not valid in calculations such as that in (g)(i).

An allotrope of molecular oxygen is ozone. Compare, giving a reason, the bond enthalpies of the O to O bonds in O₂ and O₃.

An allotrope of molecular oxygen is ozone. Compare, giving a reason, the bond enthalpies of the O to O bonds in O₂ and O₃.

An allotrope of molecular oxygen is ozone. Compare, giving a reason, the bond enthalpies of the O to O bonds in O₂ and O₃.

The IR spectrum and low resolution ¹H NMR spectrum of the actual product formed are shown.

Deduce whether the product is A or B, using evidence from these spectra together with sections 26 and 27 of the  data booklet.

Identity of product:

One piece of evidence from IR:

One piece of evidence from ¹H NMR:

The IR spectrum and low resolution ¹H NMR spectrum of the actual product formed are shown.

Deduce whether the product is A or B, using evidence from these spectra together with sections 26 and 27 of the  data booklet.

Identity of product:

One piece of evidence from IR:

One piece of evidence from ¹H NMR:

The IR spectrum and low resolution ¹H NMR spectrum of the actual product formed are shown.

Deduce whether the product is A or B, using evidence from these spectra together with sections 26 and 27 of the  data booklet.

Identity of product:

One piece of evidence from IR:

One piece of evidence from ¹H NMR:

Outline why ozone in the stratosphere is important.

Outline why ozone in the stratosphere is important.

Outline why ozone in the stratosphere is important.

Methane undergoes incomplete combustion.

2CH₄ (g) + 3O₂ (g) → 2CO (g) + 4H₂O (g)

What is the enthalpy change, in kJ, using the bond enthalpy data given below?

A. [2(1077) + 4(463)] − [2(414) + 3(498)]

B. [2(414) + 3(498)] − [2(1077) + 4(463)]

C. [8(414) + 3(498)] − [2(1077) + 8(463)]

D. [2(1077) + 8(463)] − [8(414) + 3(498)]

Methane undergoes incomplete combustion.

2CH₄ (g) + 3O₂ (g) → 2CO (g) + 4H₂O (g)

What is the enthalpy change, in kJ, using the bond enthalpy data given below?

A. [2(1077) + 4(463)] − [2(414) + 3(498)]

B. [2(414) + 3(498)] − [2(1077) + 4(463)]

C. [8(414) + 3(498)] − [2(1077) + 8(463)]

D. [2(1077) + 8(463)] − [8(414) + 3(498)]

Outline why bond enthalpy values are not valid in calculations such as that in (c)(i).

Outline why bond enthalpy values are not valid in calculations such as that in (c)(i).

Outline why bond enthalpy values are not valid in calculations such as that in (c)(i).

Outline why ozone in the stratosphere is important.

Outline why ozone in the stratosphere is important.

Outline why ozone in the stratosphere is important.

Which is correct for the reaction?

2Al (s) + 6HCl (aq) → 2AlCl₃ (aq) + 3H₂ (g)         ΔH = −1049 kJ

A. Reactants are less stable than products and the reaction is endothermic.

B. Reactants are more stable than products and the reaction is endothermic.

C. Reactants are more stable than products and the reaction is exothermic.

D. Reactants are less stable than products and the reaction is exothermic.

Which is correct for the reaction?

2Al (s) + 6HCl (aq) → 2AlCl₃ (aq) + 3H₂ (g)         ΔH = −1049 kJ

A. Reactants are less stable than products and the reaction is endothermic.

B. Reactants are more stable than products and the reaction is endothermic.

C. Reactants are more stable than products and the reaction is exothermic.

D. Reactants are less stable than products and the reaction is exothermic.

Methane undergoes incomplete combustion.

2CH₄ (g) + 3O₂ (g) → 2CO (g) + 4H₂O (g)

What is the enthalpy change, in kJ, using the bond enthalpy data given below?

A. [2(1077) + 4(463)] − [2(414) + 3(498)]

B. [2(414) + 3(498)] − [2(1077) + 4(463)]

C. [8(414) + 3(498)] − [2(1077) + 8(463)]

D. [2(1077) + 8(463)] − [8(414) + 3(498)]

Methane undergoes incomplete combustion.

2CH₄ (g) + 3O₂ (g) → 2CO (g) + 4H₂O (g)

What is the enthalpy change, in kJ, using the bond enthalpy data given below?

A. [2(1077) + 4(463)] − [2(414) + 3(498)]

B. [2(414) + 3(498)] − [2(1077) + 4(463)]

C. [8(414) + 3(498)] − [2(1077) + 8(463)]

D. [2(1077) + 8(463)] − [8(414) + 3(498)]

Which equation represents the N–H bond enthalpy in NH₃?

A.  NH₃ (g) → N (g) + 3H (g)

B.  $\frac{1}{3}$NH₃ (g) → $\frac{1}{3}$N (g) + H (g)

C.  NH₃ (g) → $\frac{1}{2}$N₂ (g) + $\frac{3}{2}$H₂ (g)

D.  NH₃ (g) → •NH₂ (g) + •H (g)

Which equation represents the N–H bond enthalpy in NH₃?

A.  NH₃ (g) → N (g) + 3H (g)

B.  $\frac{1}{3}$NH₃ (g) → $\frac{1}{3}$N (g) + H (g)

C.  NH₃ (g) → $\frac{1}{2}$N₂ (g) + $\frac{3}{2}$H₂ (g)

D.  NH₃ (g) → •NH₂ (g) + •H (g)

Which statement is correct?

A.  ${\mathrm{O}}_3$ bond dissociation occurs at a longer wavelength of light than ${\mathrm{O}}_2$ bond dissociation.

B.  ${\mathrm{O}}_3$ bond dissociation occurs at a higher energy than ${\mathrm{O}}_2$ bond dissociation.

C.  ${\mathrm{O}}_3$ bond lengths are shorter than ${\mathrm{O}}_2$ bond lengths.

D.  ${\mathrm{O}}_3$ bond dissociation occurs at a higher frequency of light than ${\mathrm{O}}_2$ bond dissociation.

Which statement is correct?

A.  ${\mathrm{O}}_3$ bond dissociation occurs at a longer wavelength of light than ${\mathrm{O}}_2$ bond dissociation.

B.  ${\mathrm{O}}_3$ bond dissociation occurs at a higher energy than ${\mathrm{O}}_2$ bond dissociation.

C.  ${\mathrm{O}}_3$ bond lengths are shorter than ${\mathrm{O}}_2$ bond lengths.

D.  ${\mathrm{O}}_3$ bond dissociation occurs at a higher frequency of light than ${\mathrm{O}}_2$ bond dissociation.

Which statements about bond strength and activation energy are correct for this reaction?

${\mathrm{CH}}_4 \left(\mathrm{g}\right)+2{\mathrm{O}}_2 \left(\mathrm{g}\right)\to {\mathrm{CO}}_2 \left(\mathrm{g}\right)+2{\mathrm{H}}_2\mathrm{O} \left(\mathrm{l}\right)$      $∆H^{⦵}=-891 \mathrm{kJ}$

Which statements about bond strength and activation energy are correct for this reaction?

${\mathrm{CH}}_4 \left(\mathrm{g}\right)+2{\mathrm{O}}_2 \left(\mathrm{g}\right)\to {\mathrm{CO}}_2 \left(\mathrm{g}\right)+2{\mathrm{H}}_2\mathrm{O} \left(\mathrm{l}\right)$      $∆H^{⦵}=-891 \mathrm{kJ}$

Determine the standard enthalpy change, $∆H^{⦵}$, for this reaction, using section 11 of the data booklet.

Determine the standard enthalpy change, $∆H^{⦵}$, for this reaction, using section 11 of the data booklet.

Determine the standard enthalpy change, $∆H^{⦵}$, for this reaction, using section 11 of the data booklet.

Determine the enthalpy change, ΔH, in kJ. Use section 11 of the data booklet.

Bond enthalpy of CO = 1077 kJ mol⁻¹.

Determine the enthalpy change, ΔH, in kJ. Use section 11 of the data booklet.

Bond enthalpy of CO = 1077 kJ mol⁻¹.

Determine the enthalpy change, ΔH, in kJ. Use section 11 of the data booklet.

Bond enthalpy of CO = 1077 kJ mol⁻¹.

Determine the enthalpy change, ΔH, in kJ. Use section 11 of the data booklet.

Bond enthalpy of CO = 1077 kJ mol⁻¹.

Determine the enthalpy change, ΔH, in kJ. Use section 11 of the data booklet.

Bond enthalpy of CO = 1077 kJ mol⁻¹.

Determine the enthalpy change, ΔH, in kJ. Use section 11 of the data booklet.

Bond enthalpy of CO = 1077 kJ mol⁻¹.

Explain, using equations, how the presence of ${\text{CCl}}_{\text{2}}{\text{F}}_{\text{2}}$ results in a chain reaction that decreases the concentration of ozone in the stratosphere.

Explain, using equations, how the presence of ${\text{CCl}}_{\text{2}}{\text{F}}_{\text{2}}$ results in a chain reaction that decreases the concentration of ozone in the stratosphere.

Explain, using equations, how the presence of ${\text{CCl}}_{\text{2}}{\text{F}}_{\text{2}}$ results in a chain reaction that decreases the concentration of ozone in the stratosphere.

Sketch an energy profile for the decomposition of calcium carbonate based on your answer to b(i), labelling the axes and activation energy, E_a.

Sketch an energy profile for the decomposition of calcium carbonate based on your answer to b(i), labelling the axes and activation energy, E_a.

Sketch an energy profile for the decomposition of calcium carbonate based on your answer to b(i), labelling the axes and activation energy, E_a.

Which equation represents the bond enthalpy for H–Br in hydrogen bromide?

A.  HBr (g) → H⁺ (g) + Br⁻ (g)

B.  HBr (g) → H (g) + Br (g)

C.  HBr (g) → $\frac{1}{2}$H₂ (g) + $\frac{1}{2}$Br₂ (l)

D.  HBr (g) → $\frac{1}{2}$H₂ (g) + $\frac{1}{2}$Br₂ (g)

Which equation represents the bond enthalpy for H–Br in hydrogen bromide?

A.  HBr (g) → H⁺ (g) + Br⁻ (g)

B.  HBr (g) → H (g) + Br (g)

C.  HBr (g) → $\frac{1}{2}$H₂ (g) + $\frac{1}{2}$Br₂ (l)

D.  HBr (g) → $\frac{1}{2}$H₂ (g) + $\frac{1}{2}$Br₂ (g)

Determine the enthalpy change, ΔH, for the Haber–Bosch process, in kJ. Use Section 11 of the data booklet.

Determine the enthalpy change, ΔH, for the Haber–Bosch process, in kJ. Use Section 11 of the data booklet.

Determine the enthalpy change, ΔH, for the Haber–Bosch process, in kJ. Use Section 11 of the data booklet.

Suggest why the values obtained in (d)(i) and (d)(ii) differ.

Suggest why the values obtained in (d)(i) and (d)(ii) differ.

Suggest why the values obtained in (d)(i) and (d)(ii) differ.

Calculate the enthalpy change of the reaction, ΔH, using section 11 of the data booklet.

Calculate the enthalpy change of the reaction, ΔH, using section 11 of the data booklet.

Calculate the enthalpy change of the reaction, ΔH, using section 11 of the data booklet.

Draw and label an enthalpy level diagram for this reaction.

Draw and label an enthalpy level diagram for this reaction.

Draw and label an enthalpy level diagram for this reaction.

Calculate the enthalpy change of the reaction, ΔH, using section 11 of the data booklet.

Calculate the enthalpy change of the reaction, ΔH, using section 11 of the data booklet.

Calculate the enthalpy change of the reaction, ΔH, using section 11 of the data booklet.