The heat of formation of \(\mathrm{NH}_{3}(g)\) is \(-46 \mathrm{~kJ} \mathrm{~mol}^{-1}\). The \(\Delta H\) (in \(\mathrm{kJ} \mathrm{mol}^{-1}\) ) of the reaction, \(2 \mathrm{NH}_{3}(g) \longrightarrow \mathrm{N}_{2}(g)+3 \mathrm{H}_{2}(g)\) is : (a) 46 (b) \(-46\) (c) 92 (d) \(-92\)

Short Answer

Expert verified
The \(\Delta H\) for the reaction is 92 \mathrm{~kJ} \mathrm{~mol}^{-1}\.

Step by step solution

01

Understand the Heat of Formation

The heat of formation is the change in enthalpy when one mole of a compound is formed from its elements in their standard states. For \(\mathrm{NH}_{3}(g)\), the given heat of formation is \-46 \mathrm{~kJ} \mathrm{~mol}^{-1}\, which means that 46 kJ of energy is released when one mole of \(\mathrm{NH}_{3}(g)\) is formed from its elements.
02

Write the Formation Equation for \(\mathrm{NH}_{3}(g)\)

To find the heat of reaction for the given process, we need to understand the formation reaction for ammonia which is \(\frac{1}{2} \mathrm{N}_{2}(g) + \frac{3}{2} \mathrm{H}_{2}(g) \longrightarrow \mathrm{NH}_{3}(g)\) with the heat of formation \-46 \mathrm{~kJ} \mathrm{~mol}^{-1}\.
03

Calculate the Change in Enthalpy (\(\Delta H\)) for the Reaction

Since each mole of \(\mathrm{NH}_{3}(g)\) releases 46 kJ of energy upon formation, reversing the reaction would require absorbing the same amount of energy. Thus, for the reverse reaction (the formation of 1 mole of \(\mathrm{NH}_{3}(g)\)), \(\Delta H\) is +46 \mathrm{~kJ} \mathrm{~mol}^{-1}\. For the given reaction, which is the reverse of the formation of two moles of \(\mathrm{NH}_{3}(g)\), the \(\Delta H\) would be twice that of a single mole, so \(\Delta H\) for the reaction is +46 \mathrm{~kJ} \mathrm{~mol}^{-1}\ times 2, which equals +92 \mathrm{~kJ} \mathrm{~mol}^{-1}\.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Enthalpy Change
Enthalpy change is a term used to describe the heat energy exchanged in a chemical process at constant pressure. It is denoted as \(\Delta H\), representing energy either released or absorbed by the system during a reaction. If \(\Delta H\) is negative, the process is exothermic, indicating that energy is released, often as heat, to the surroundings. Conversely, a positive \(\Delta H\) signals an endothermic process, where the system absorbs energy from the surroundings.

Understanding enthalpy changes is crucial when studying chemical reactions, as it helps predict how energy will flow. This knowledge, paired with the heat of formation values for substances involved, allows chemists to calculate the energy changes occurring in chemical processes.
Chemical Reaction
A chemical reaction is the process where substances, known as reactants, transform into new substances, termed as products. These reactions involve the breaking of bonds in the reactants and the formation of new bonds in the products. This bond rearrangement is associated with energy changes; energy is required to break bonds and is released when new bonds form.

The stoichiometry of a reaction – the quantitative relationship between reactants and products in a chemical equation – is essential for determining the enthalpy change of the reaction. In our exercise, the stoichiometry of the decomposition reaction of \(\mathrm{NH}_{3}(g)\) into \(\mathrm{N}_{2}(g)\) and \(\mathrm{H}_{2}(g)\) helps calculate the overall \(\Delta H\) of the process.
Standard States
Standard states refer to the physical states of substances at defined conditions of 1 atmosphere of pressure and a specified temperature, typically 298K (25 degrees Celsius). For pure substances, the standard state is the most stable form of the substance under standard conditions. For example, for hydrogen and nitrogen, it is the diatomic gases \(\mathrm{H}_{2}(g)\) and \(\mathrm{N}_{2}(g)\) respectively.

Heat of formation values, which are a form of enthalpy change, are always given for substances in their standard states. In the context of the exercise, it is important to note that the \(\Delta H\) provided for the formation of \(\mathrm{NH}_{3}(g)\) would apply when its constituent elements are in their standard states.
Reversible Reactions
Reversible reactions are processes that can proceed in both forward and backward directions. In the context of enthalpy, when a reversible reaction proceeds in one direction, it has a specific \(\Delta H\), and when the reaction is reversed, the sign of \(\Delta H\) changes. This is because the energy absorbed in the forward reaction is released in the reverse reaction, and vice versa.

In our given exercise, the synthesis of \(\mathrm{NH}_{3}(g)\) from its elements is exothermic, with a \(\Delta H\) of -46 \(\mathrm{kJ mol^{-1}}\). The reverse reaction, which is the decomposition of \(\mathrm{NH}_{3}(g)\) into \(\mathrm{N}_{2}(g)\) and \(\mathrm{H}_{2}(g)\), has a \(\Delta H\) of +46 \(\mathrm{kJ mol^{-1}}\) per mole of \(\mathrm{NH}_{3}(g)\) decomposed. Thus, for two moles of \(\mathrm{NH}_{3}(g)\), the total enthalpy change would be double this value.

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Most popular questions from this chapter

The entropies of \(\mathrm{H}_{2}(\mathrm{~g})\) and \(\mathrm{H}(\mathrm{g})\) are \(130.6\) and \(114.6 \mathrm{~J} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}\) respectively at \(298 \mathrm{~K}\). Using the data given below calculate the bond energy of \(\mathrm{H}_{2}\) (in \(\mathrm{kJ} / \mathrm{mol}\) ): \(\mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{H}(g) ; \Delta G^{\circ}=406.6 \mathrm{~kJ}\) (a) \(377.2\) (b) \(436.0\) (c) \(425.5\) (d) \(430.5\)

Using the listed \(\left[\Delta G^{\circ}{ }_{f}\right.\) values \(]\) calculate \(\Delta G^{\circ}\) for the reaction : \(3 \mathrm{H}_{2} \mathrm{~S}(g)[-33.6]+2 \mathrm{HNO}_{3}(l)[-80.6] \stackrel 2 \mathrm{NO}(g)[+86.6]+4 \mathrm{H}_{2} \mathrm{O}(l)[-237.1]+3 S(s)[0.0]\) (a) \(-513.0\) (b) \(-1037.0\) (c) \(+433.4\) (d) \(+225.0\)

Which of the following value of \(\Delta H_{f}^{\circ}\) represent that the product is least stable? (a) \(-94.0 \mathrm{kcal} \mathrm{mol}^{-1}\) (b) \(-231.6 \mathrm{kcal} \mathrm{mol}^{-1}\) (c) \(+21.4 \mathrm{kcal} \mathrm{mol}^{-1}\) (d) \(+64.8 \mathrm{kcal} \mathrm{mol}^{-1}\)

The entropies of \(\mathrm{H}_{2}(\mathrm{~g})\) and \(\mathrm{H}(\mathrm{g})\) are \(130.6\) and \(114.6 \mathrm{~J} \mathrm{~mol}^{-1} \mathrm{~K}^{-1}\) respectively at \(298 \mathrm{~K}\). Using the data given below calculate the bond energy of \(\mathrm{H}_{2}\) (in \(\mathrm{kJ} / \mathrm{mol}\) ): \(\mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{H}(g) ; \Delta G^{\circ}=406.6 \mathrm{~kJ}\) (a) \(377.2\) (b) \(436.0\) (c) \(425.5\) (d) \(430.5\)

The enthalpies of neutralization of a weak base \(A O H\) and a strong base \(B O H\) by \(H C l\) are \(-12250 \mathrm{cal} / \mathrm{mol}\) and \(-13000 \mathrm{cal} / \mathrm{mol}\) respectively. When one mole of \(\mathrm{HCl}\) is added to a solution containing 1 mole of \(A \mathrm{OH}\) and 1 mole of \(B O H\), the enthalpy change was \(-12500 \mathrm{cal} /\) mol. In what ratio is the acid distribution between \(A O H\) and \(B O H ?\) (a) \(2: 1\) (b) \(2: 3\) (c) \(1: 2\) (d) None of these

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