So they tell us the enthalpy Table \(\PageIndex{2}\): Standard enthalpies of formation for select substances. How do I calculate enthalpy change from a reaction scheme? to get eventually. kilojoules per mole of reaction. An example of a state function is altitude or elevation. Robert E. Belford (University of Arkansas Little Rock; Department of Chemistry). They are listed below. for the formation of C2H2). By adding Equations 1, 2, and 3, the Overall Equation is obtained. When you go from the products Next, we see that F2 is also needed as a reactant. The OpenStax name, OpenStax logo, OpenStax book covers, OpenStax CNX name, and OpenStax CNX logo The good thing about this is I plus-- I already have a color for oxygen-- plus oxygen in If heat flows from the This book uses the water, you could even say-- two molecules of water For example, when 1 mole of hydrogen gas and 1212 mole of oxygen gas change to 1 mole of liquid water at the same temperature and pressure, 286 kJ of heat are released. Calculating delta H with the enthalpy change formula. More Resources. And all I did is I wrote this So this actually involves But, a different one may be better for another question. Do you know what to do if you have two products? Watch the video below to get the tips on how to approach this problem. \[\ce{N2}(g)+\ce{2O2}(g)\ce{2NO2}(g) \nonumber\], \[\ce{N2}(g)+\ce{O2}(g)\ce{2NO}(g)\hspace{20px}H=\mathrm{180.5\:kJ} \nonumber\], \[\ce{NO}(g)+\frac{1}{2}\ce{O2}(g)\ce{NO2}(g)\hspace{20px}H=\mathrm{57.06\:kJ} \nonumber\]. We can choose a hypothetical two step path where the atoms in the reactants are broken into the standard state of their element (left side of Figure \(\PageIndex{3}\)), and then from this hypothetical state recombine to form the products (right side of Figure \(\PageIndex{3}\)). This means that if reaction transforms on substance into another, it doesnt matter if the reaction occurs in one step (reactants become products immediately) or whether it goes through many steps (reactants become intermediaries and then become products), the resulting enthalpy change is the same in both cases. Hess's Law, also known as "Hess's Law of Constant Heat Summation," states that the total enthalpy of a chemical reaction is the sum of the enthalpy changes for the steps of the reaction. change for this reaction cannot to be measured in the to release energy. (This amount of energy is enough to melt 99.2 kg, or about 218 lbs, of ice.). 1: } \; \; \; \; & H_2+1/2O_2 \rightarrow H_2O \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \;\; \; \; \;\Delta H_1=-286 kJ/mol \nonumber \\ \text{eq. Note: If you have a good memory, you might remember that I gave a figure of +49 kJ mol -1 for the standard enthalpy . If you are confused or get stuck about which reactant to use, try to use the equation derived in the previous video (Hess law and reaction enthalpy change). If the direction of a chemical equation is reversed, the arithmetic sign of its H is changed (a process that is endothermic in one direction is exothermic in the opposite direction). So these two combined are two \(\ce{4C}(s,\:\ce{graphite})+\ce{5H2}(g)+\frac{1}{2}\ce{O2}(g)\ce{C2H5OC2H5}(l)\); \(\ce{2Na}(s)+\ce{C}(s,\:\ce{graphite})+\dfrac{3}{2}\ce{O2}(g)\ce{Na2CO3}(s)\). In this class, the standard state is 1 bar and 25C. as graphite plus two moles, or two molecules of Here is a less straightforward example that illustrates the thought process involved in solving many Hesss law problems. that we cancel out. Direct link to Richard's post When Jay mentions one mol, Posted a month ago. to negative 14.4 kilojoules. it down here. product, which is methane in a gaseous form. And so, if a chemical or physical process is carried out at constant pressure with the only work done caused by expansion or contraction, then the heat flow (qp) and enthalpy change (H) for the process are equal. (a) 4C(s,graphite)+5H2(g)+12O2(g)C2H5OC2H5(l);4C(s,graphite)+5H2(g)+12O2(g)C2H5OC2H5(l); (b) 2Na(s)+C(s,graphite)+32O2(g)Na2CO3(s)2Na(s)+C(s,graphite)+32O2(g)Na2CO3(s). Kilimanjaro. mass change. methane, so let's start with this. Using the tables for enthalpy of formation, calculate the enthalpy of reaction for the combustion reaction of ethanol, and then calculate the heat released when 1.00 L of pure ethanol combusts. We recommend using a Using Hesss Law Chlorine monofluoride can react with fluorine to form chlorine trifluoride: (i) \(\ce{ClF}(g)+\ce{F2}(g)\ce{ClF3}(g)\hspace{20px}H=\:?\). third equation, but I wrote it in reverse order. Legal. But our change in enthalpy here, For processes that take place at constant pressure (a common condition for many chemical and physical changes), the enthalpy change (H) is: The mathematical product PV represents work (w), namely, expansion or pressure-volume work as noted. Because enthalpy is a state function, a process that involves a complete cycle where chemicals undergo reactions and are then reformed back into themselves, must have no change in enthalpy, meaning the endothermic steps must balance the exothermic steps. to be twice this. in the gaseous form. \[\begin{align} \text{equation 1: } \; \; \; \; & P_4+5O_2 \rightarrow \textcolor{red}{2P_2O_5} \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \;\; \; \; \;\Delta H_1 \nonumber \\ \text{equation 2: } \; \; \; \; & \textcolor{red}{2P_2O_5} +6H_2O \rightarrow 4H_3PO_4 \; \; \; \; \; \; \; \; \Delta H_2 \nonumber\\ \nonumber \\ \text{equation 3: } \; \; \; \; & P_4 +5O_2 + 6H_2O \rightarrow 3H_3PO_4 \; \; \; \; \Delta H_3 \end{align}\]. here produces the two molecules of water. And in the end, those end If you are redistributing all or part of this book in a print format, The standard free energy change for a reaction may also be calculated from standard free energy of formation Gf values of the reactants and products involved in the reaction. It gives 1,046 + (-1,172)= -126 kJ/mol, which is the total enthalpy change during the reaction. Will give us H2O, will give a negative number. Step 1: \[ \underset {15.0g \; Al \\ 26.98g/mol}{8Al(s)} + \underset {30.0 g \\ 231.54g/mol}{3Fe_3O_4(s)} \rightarrow 4Al_2O_3(s) + 9Fe(3)\], \[15gAl\left(\frac{molAl}{26.98g}\right) \left(\frac{1}{8molAl}\right) = 0.069\] We see that H of the overall reaction is the same whether it occurs in one step or two. a mole time. So this produces carbon dioxide, Since the final value of . cancel out product O2; product 12Cl2O12Cl2O cancels reactant 12Cl2O;12Cl2O; and reactant 32OF232OF2 is cancelled by products 12OF212OF2 and OF2. Each process is a little different. The LibreTexts libraries arePowered by NICE CXone Expertand are supported by the Department of Education Open Textbook Pilot Project, the UC Davis Office of the Provost, the UC Davis Library, the California State University Affordable Learning Solutions Program, and Merlot. The following table contains some of the most important ones, but you can look at the rest in the enthalpy calculator: As an example, let's suppose we want to know the enthalpy change of the following reaction: Considering the number of moles of the compounds and the enthalpies of the table, we can use the enthalpy change formula: Hreaction = Hf(products) - Hf(reactants) Apart from the enthalpy equation, you need to know the standard enthalpies of formation of the compounds. Molar enthalpies of formation are intensive properties and are the enthalpy per mole, that is the enthalpy change associated with the formation of one mole of a substance from its elements in their standard states. Direct link to Indlie Marcel's post where exactly did you get, Posted 10 years ago. the order of this reaction right there. In reality, a chemical equation can occur in many steps with the products of an earlier step being consumed in a later step. product side is the methane. everything else makes up the surroundings. Enthalpy Change Equation: At a constant temperature and pressure, the enthalpy equation for a system is given as follows: H = Q + p * V where; 'H' is change in heat of a system 'Q' is change in internal energy of a system 'P' is pressure on system due to surroundings 'V' is change in the volume of the system For a reaction, the enthalpy change formula is: Hreaction = Hf(products) - Hf(reactants). Chemists use a thermochemical equation to represent the changes in both matter and energy. By definition, it is the change in enthalpy, H, during the formation of one mole of the substance in its standard state (1 bar and 25C), from its pure elements, f. The standard enthalpy of formation of all stable elements (i.e., O2, N2, C, and H2) is assumed as zero because we need no energy to take them to that stable state under our atmospheric conditions. and methane. (credit: modification of work by Paul Shaffner), The combustion of gasoline is very exothermic. out the enthalpy change of this reaction. From the given data look for the equation which encompasses all reactants and products, then apply the formula. The standard molar enthalpy of formation Hof is the enthalpy change when 1 mole of a pure substance, or a 1 M solute concentration in a solution, is formed from its elements in their most stable states under standard state conditions. { "5.1:_Energy" : "property get [Map MindTouch.Deki.Logic.ExtensionProcessorQueryProvider+<>c__DisplayClass228_0.
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"showtoc:yes", "license:ccbyncsa", "licenseversion:40" ], https://chem.libretexts.org/@app/auth/3/login?returnto=https%3A%2F%2Fchem.libretexts.org%2FCourses%2FUniversity_of_Arkansas_Little_Rock%2FChem_1402%253A_General_Chemistry_1_(Belford)%2FText%2F5%253A_Energy_and_Chemical_Reactions%2F5.7%253A_Enthalpy_Calculations, \( \newcommand{\vecs}[1]{\overset { \scriptstyle \rightharpoonup} {\mathbf{#1}}}\) \( \newcommand{\vecd}[1]{\overset{-\!-\!\rightharpoonup}{\vphantom{a}\smash{#1}}} \)\(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\) \(\newcommand{\id}{\mathrm{id}}\) \( \newcommand{\Span}{\mathrm{span}}\) \( \newcommand{\kernel}{\mathrm{null}\,}\) \( \newcommand{\range}{\mathrm{range}\,}\) \( \newcommand{\RealPart}{\mathrm{Re}}\) \( \newcommand{\ImaginaryPart}{\mathrm{Im}}\) \( \newcommand{\Argument}{\mathrm{Arg}}\) \( \newcommand{\norm}[1]{\| #1 \|}\) \( \newcommand{\inner}[2]{\langle #1, #2 \rangle}\) \( \newcommand{\Span}{\mathrm{span}}\)\(\newcommand{\AA}{\unicode[.8,0]{x212B}}\), \[\frac{1}{2}\ce{Cl2O}(g)+\dfrac{3}{2}\ce{OF2}(g)\ce{ClF3}(g)+\ce{O2}(g)\hspace{20px}H=\mathrm{266.7\: kJ} \nonumber\], \(H=\mathrm{(+102.8\:kJ)+(24.7\:kJ)+(266.7\:kJ)=139.2\:kJ}\), Calculating Enthalpy of Reaction from Combustion Data, Calculating Enthalpy of Reaction from Standard Enthalpies of Formation, Enthalpies of Reaction and Stoichiometric Problems, table of standard enthalpies of formation, status page at https://status.libretexts.org, Define Hess's Law and relate it to the first law of thermodynamics and state functions, Calculate the unknown enthalpy of a reaction from a set of known enthalpies of combustion using Hess's Law, Define molar enthalpy of formation of compounds, Calculate the molar enthalpy of formation from combustion data using Hess's Law, Using the enthalpy of formation, calculate the unknown enthalpy of the overall reaction. If we look at the process diagram in Figure \(\PageIndex{3}\) and correlate it to the above equation we see two things. Or we can even say a molecule exothermic. 98.0 kilojoules of energy. Standard State of an Element: This is. Direct link to Peter Xu's post Isn't Hess's Law to subtr, Posted 12 years ago. What is important here, is that by measuring the heats of combustion scientists could acquire data that could then be used to predict the enthalpy of a reaction that they may not be able to directly measure. in its gaseous form. The first step is to \[\begin{align} 2C_2H_2(g) + 5O_2(g) \rightarrow 4CO_2(g) + 2H_2O(l) \; \; \; \; \; \; & \Delta H_{comb} =-2600kJ \nonumber \\ C(s) + O_2(g) \rightarrow CO_2(g) \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; \; & \Delta H_{comb}= -393kJ \nonumber \\ 2H_2(g) + O_2 \rightarrow 2H_2O(l) \; \; \; \; \; \; \; \; \; \; \; \;\; \; \; \; \; \; & \Delta H_{comb} = -572kJ \end{align}\]. Use the equation for line and Equation 2 to calculate H and S for dissolving Borax Slope j-intercept. You will use the accepted value for the enthalpy change of this reaction, -285 kJ/mol. You could climb to the summit by a direct route or by a more roundabout, circuitous path (Figure 5.20). describes the enthalpy change as reactants break apart into their stable elemental state at standard conditions and then form new bonds as they create the products. to the reactants it will release 890.3 kilojoules So those are the reactants. Sometimes you might see A negative change indicates the reaction is exothermic, while a positive value means it is endothermic. tepwise Calculation of \(H^\circ_\ce{f}\). do that in this pink color. So the formation of salt releases almost 4 kJ of energy per mole. (The symbol H is used to indicate an enthalpy change for a reaction occurring under nonstandard conditions. right here, let's see if we can cancel out reactants then the change in enthalpy of this reaction is The formation of any chemical can be as a reaction from the corresponding elements: elements compound which in terms of the the Enthalpy of formation becomes so let me do blue. How do I calculate delta H from the enthalpy change formula? enthalpy for some other reaction, and that other In this case, the combustion of one mole of carbon has H = 394 kJ/mol (this happens six times in the reaction), the change in enthalpy for the combustion of one mole of hydrogen gas is H = 286 kJ/mol (this happens three times) and the carbon dioxide and water intermediaries become benzene with an enthalpy change of H = +3,267 kJ/mol. peroxide decomposes at a constant pressure. because this gets us to our final product, this gets Determine the heat of combustion, #H_"c"#, of CS, given the following equations. The molar enthalpy of reaction can be used to calculate the enthalpy of reaction if you have a balanced chemical equation. You multiply 1/2 by 2, you molar mass of hydrogen peroxide which is 34.0 grams per mole. This type of calculation usually involves the use of Hesss law, which states: If a process can be written as the sum of several stepwise processes, the enthalpy change of the total process equals the sum of the enthalpy changes of the various steps. The standard enthalpy change of the overall reaction is therefore equal to: (ii) the sum of the standard enthalpies of formation of all the products plus (i) the sum of the negatives of the standard enthalpies of formation of the reactants. The enthalpy (or latent heat) of melting describes the transition from solid to liquid (the reverse is minus this value and called the enthalpy of fusion), the enthalpy of vaporization describes the transition from liquid to gas (and the opposite is condensation) and the enthalpy of sublimation describes the transition from solid to gas (the reverse is again called the enthalpy of condensation). To get this, reverse and halve reaction (ii), which means that the H changes sign and is halved: To get ClF3 as a product, reverse (iv), changing the sign of H: Now check to make sure that these reactions add up to the reaction we want: Reactants 12O212O2 So the enthalpy change from burning methanol is J. By definition, the standard enthalpy of formation of an element in its most stable form is equal to zero under standard conditions, which is 1 atm for gases and 1 M for solutions. As we concentrate on thermochemistry in this chapter, we need to consider some widely used concepts of thermodynamics. To get ClF3 as a product, reverse (iv), changing the sign of H: Now check to make sure that these reactions add up to the reaction we want: \[\begin {align*} Reactants \(\frac{1}{2}\ce{O2}\) and \(\frac{1}{2}\ce{O2}\) cancel out product O2; product \(\frac{1}{2}\ce{Cl2O}\) cancels reactant \(\frac{1}{2}\ce{Cl2O}\); and reactant \(\dfrac{3}{2}\ce{OF2}\) is cancelled by products \(\frac{1}{2}\ce{OF2}\) and OF2. The reaction of gasoline and oxygen is exothermic. He was also a science blogger for Elements Behavioral Health's blog network for five years. I always understood that to calculate the change in H for a rxn or if you wanted to calculate any change such as S or G or anything, you did products minus reactants. The general formula is: H r x n = H f. i. n a l H i n i t a l = q where q is heat. Calculating the enthalpy change from a reaction scheme; and. The heat given off when you operate a Bunsen burner is equal to the enthalpy change of the methane combustion reaction that takes place, since it occurs at the essentially constant pressure of the atmosphere. let's look at the decomposition of hydrogen peroxide to form per mole of the reaction occurring. CH4 in a gaseous state. (Note that this is similar to determining the intensive property specific heat from the extensive property heat capacity, as seen previously.). much of it, because we multiplied by 2, the delta H Enthalpy and Entropy Changes of Dissolving Borax Report Sheet Dissolving Bora R Report Steat Plot your values of ln(K 10) v5. Lesson 5: Introduction to enthalpy of reaction, The enthalpy change that accompanies a chemical reaction is referred to as the enthalpy of reaction and is abbreviated . its gaseous state, it will produce carbon dioxide So how can we get carbon we're thinking of these as moles, or two molecules of This reference state corresponds to 25C (77F) and 10 Pa = 1 bar. In this section we will use Hess's law to use combustion data to calculate the enthalpy of reaction for a reaction we never measured. system to the surroundings, the reaction gave off energy. the formation of methane from its elements. Now add the bond enthalpy of both the sides. Expert Answer. this arrow and write it as methane as a product. Enthalpy formula to calculate change in volume & internal energy of the moles. These values are especially useful for computing or predicting enthalpy changes for chemical reactions that are impractical or dangerous to carry out, or for processes for which it is difficult to make measurements. I am confused as to why, in the last equation, Sal takes the sum of all of the Delta-H reactions, rather than (Products - Reactants). And now this reaction down N2(g) + O2(g) ---> 2NO(g) H = +180 kJ 2NO(g) + O2(g) ---> 2NO2(g) H = 112 kJ Notice that I have also changed the sign on the enthalpy from positive to negative. Direct link to Raghav Malik's post You do basically the same, Posted 12 years ago. then you must include on every physical page the following attribution: If you are redistributing all or part of this book in a digital format, eventually, we need to at some point have some carbon dioxide, For the reaction H2(g)+Cl2(g)2HCl(g)H=184.6kJH2(g)+Cl2(g)2HCl(g)H=184.6kJ, (a) 2C(s,graphite)+3H2(g)+12O2(g)C2H5OH(l)2C(s,graphite)+3H2(g)+12O2(g)C2H5OH(l), (b) 3Ca(s)+12P4(s)+4O2(g)Ca3(PO4)2(s)3Ca(s)+12P4(s)+4O2(g)Ca3(PO4)2(s). Now, let's see if the dioxide, this combustion reaction gives us water. The value of a state function depends only on the state that a system is in, and not on how that state is reached. And so what are we left with? We can calculate the energy difference between two states of different temperature if we know the heat capacities. Because there's now This tool has two functionalities: Read on if you still don't know what is and how to calculate the delta H of a reaction. It is important that students understand that Hreaction is for the entire equation, so in the case of acetylene, the balanced equation is, 2C2H2(g) + 5O2(g) --> 4CO2(g) +2 H2O(l) Hreaction (C2H2) = -2600kJ. But this one involves But if you go the other way it For example, we can write an equation for the reaction of calcium oxide with carbon dioxide to form calcium carbonate. Enthalpy of formation ( Hf) is the enthalpy change for the formation of 1 mol of a compound from its component elements, such as the formation of carbon dioxide from carbon and oxygen. Figure \(\PageIndex{2}\): The steps of example \(\PageIndex{1}\) expressed as an energy cycle. of the order that we're going to go in. You do basically the same thing: multiply the equations to try to cancel out compounds from both sides until youre left with both products on the right side. Take the sum of these changes to find the total enthalpy change, remembering to multiply each by the number of moles needed in the first stage of the reaction: Lee Johnson is a freelance writer and science enthusiast, with a passion for distilling complex concepts into simple, digestible language. If the coefficients of the chemical equation are multiplied by some factor, the enthalpy change must be multiplied by that same factor (H is an extensive property): The enthalpy change of a reaction depends on the physical states of the reactants and products, so these must be shown. &\frac{1}{2}\ce{Cl2O}(g)+\dfrac{3}{2}\ce{OF2}(g)\ce{ClF3}(g)+\ce{O2}(g)&&H=\mathrm{266.7\:kJ}\\ bunch of reactions and they say, hey, we don't know the going to be the sum of the change in enthalpies This material has bothoriginal contributions, and contentbuilt upon prior contributions of the LibreTexts Community and other resources,including but not limited to: This page titled 5.7: Enthalpy Calculations is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by Robert Belford. The distances traveled would differ (distance is not a state function) but the elevation reached would be the same (altitude is a state function). One example is if you start with six moles of carbon combined with three of hydrogen, they combust to combine with oxygen as an intermediary step and then form benzene as an end-product. So we take the mass of hydrogen peroxide which is five grams and we divide that by the Hess's law can be used to calculate enthalpy changes that are difficult to measure directly. Algae can yield 26,000 gallons of biofuel per hectaremuch more energy per acre than other crops. reaction as it is written, there are two moles of hydrogen peroxide. Enthalpies of combustion for many substances have been measured; a few of these are listed in Table 5.2. Algae can produce biodiesel, biogasoline, ethanol, butanol, methane, and even jet fuel. And when we look at all these kilojoules per mole of the reaction. This problem is from chapter Using Hess's Law Determine the enthalpy of formation, H f, of FeCl 3 (s) from the enthalpy changes of the following two-step process that occurs under standard state conditions: Fe(s) + Cl 2(g) FeCl 2(s) H = 341.8kJ FeCl 2(s) + 1 2Cl 2(g) FeCl 3(s) H = 57.7kJ Solution The standard enthalpy of formation is simply the enthalpy of formation with standard conditions as the specified state. With Hess's Law though, it works two ways: If C + 2H2 --> CH4 why is the last equation for Hess's Law not Hr = HfCH4 -HfC - HfH2 like in the previous videos, in which case you'd get Hr = (890.3) - (-393.5) - (-571.6) = 1855.4. What kilojoules per mole of reaction is referring to is how Direct link to David Christopher Kirby's post With Hess's Law though, i, Posted 7 years ago. Hess's Law states that if you can add two chemical equations and come up with a third equation, the enthalpy of reaction for the third equation is the sum of the first two. In this example it would be equation 3. you might see kilojoules. Transcribed Image Text: Enthalpy and Gibb's Free Energy Chemical energy is released or absorbed from reactions in various forms. of situation where they're giving you the enthalpies for a Using enthalpies of formation from T1: Standard Thermodynamic Quantities calculate the heat released when 1.00 L of ethanol combustion. As we discuss these quantities, it is important to pay attention to the extensive nature of enthalpy and enthalpy changes. According to the US Department of Energy, only 39,000 square kilometers (about 0.4% of the land mass of the US or less than 1717 Whether you need help solving quadratic equations, inspiration for the upcoming science fair or the latest update on a major storm, Sciencing is here to help. Be sure to take both stoichiometry and limiting reactants into account when determining the H for a chemical reaction. You can calculate changes in enthalpy using the simple formula: H = Hproducts Hreactants. A more comprehensive table can be found at the table of standard enthalpies of formation , which will open in a new window, and was taken from the CRC Handbook of Chemistry and Physics, 84 Edition (2004). In symbols, this is: H = U + PV. The enthalpy of a reaction can be calculated from the heats of formation of the substances involved in the reaction: AHxn = AH (products) - AH (reactants) Entropy change, AS, is a . combustion of carbon, combustion of hydrogen, It shows how we can find many standard enthalpies of formation (and other values of H) if they are difficult to determine experimentally. Using Hesss Law Determine the enthalpy of formation, \(H^\circ_\ce{f}\), of FeCl3(s) from the enthalpy changes of the following two-step process that occurs under standard state conditions: \[\ce{Fe}(s)+\ce{Cl2}(g)\ce{FeCl2}(s)\hspace{20px}H=\mathrm{341.8\:kJ} \nonumber\], \[\ce{FeCl2}(s)+\frac{1}{2}\ce{Cl2}(g)\ce{FeCl3}(s)\hspace{20px}H=\mathrm \nonumber{57.7\:kJ} \]. EXAMPLE. This leaves only reactants ClF(g) and F2(g) and product ClF3(g), which are what we want. Law problem. Direct link to Greg Humble's post I am confused as to why, , Posted 8 years ago. If a quantity is not a state function, then its value does depend on how the state is reached. So plus 890.3 gives Chemists ordinarily use a property known as enthalpy (H) to describe the thermodynamics of chemical and physical processes. Except you always do. around and change its sign, and we have to multiply this Calculate delta H from the products of an earlier step being consumed in a gaseous form 's look at these! 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