Enthalpy change negative

ANstreams = enthalpy change between feed and product streams AI/react = reaction enthalpy (negative in the case of exothermic reactions)... 

Negative ions also have two unique thennodynainic quantities associated with them the electron affinity, EA, defined as the negative of the enthalpy change for addition of an electron to a molecule at 0 K [117. 121. 122]... 

The chemistry of Lewis acid-base adducts (electron-pair donor-acceptor complexes) has stimulated the development of measures of the Lewis basicity of solvents. Jensen and Persson have reviewed these. Gutmann defined the donor number (DN) as the negative of the enthalpy change (in kcal moL ) for the interaction of an electron-pair donor with SbCls in a dilute solution in dichloroethane. DN has been widely used to correlate complexing data, but side reactions can lead to inaccurate DN values for some solvents. Maria and Gal measured the enthalpy change of this reaction... 

Air Enthalpy change T he heat of reaction, or difference in strength between the bonds broken in a reaction and tire bonds formed. When All is negative, the reaction releases heat and is exothermic. When A IT is positive, the reaction absorbs heat and is endothermic. 

Exothermic (Section 5.7) A reaction that releases heat and therefore has a negative enthalpy change. 

For many reactions, AH is a large negative number the reaction gives off a lot of heat In other cases, AH is positive heat must be absorbed for the reaction to occur. You may well wonder why the enthalpy change should vary so widely from one reaction to another. Is there some basic property of the molecules involved in the reaction that determines the sign and magnitude of AH ... 

The enthalpy change for a reverse reaction is the negative of the enthalpy change... 

We saw in Section 6.11 that the first law of thermodynamics implies that, because enthalpy is a state function, the enthalpy change for the reverse of a process is the negative of the enthalpy change of the forward process. The same relation applies to forward and reverse chemical reactions. For the reverse of reaction A, for instance, we can write... 

The lattice enthalpy of a solid cannot be measured directly. However, we can obtain it indirectly by combining other measurements in an application of Hess s law. This approach takes advantage of the first law of thermodynamics and, in particular, the fact that enthalpy is a state function. The procedure uses a Born-Haber cycle, a closed path of steps, one of which is the formation of a solid lattice from the gaseous ions. The enthalpy change for this step is the negative of the lattice enthalpy. Table 6.6 lists some lattice enthalpies found in this way. 

STRATEGY Decide which bonds are broken and which bonds are formed. Use the mean bond enthalpies in Table 6.8 to estimate the change in enthalpy when the reactant bonds break and the change in enthalpy when the new product bonds form. For diatomic molecules, use the information in Table 6.7 for the specific molecule. Finally, add the enthalpy change required to break the reactant bonds (a positive value) to the enthalpy change that occurs when the product bonds form (a negative value). 

In the second hypothetical step, we imagine the gaseous ions plunging into water and forming the final solution. The molar enthalpy of this step is called the enthalpy of hydration, AHhvd, of the compound (Table 8.7). Enthalpies of hydration are negative and comparable in value to the lattice enthalpies of the compounds. For sodium chloride, for instance, the enthalpy of hydration, the molar enthalpy change for the process... 

Measuring enthalpy changes for the dissolution of hydrocarbons, such as alkanes, in water shows that heat is evolved, i.e., A/f is negative and energetically water and alkanes attract each other. However, such attraction does not make alkanes soluble in water to any appreciable extent. This is because the free energy change AGsomtion opposes the process and is positive. 

Solid ammonium nitrate is an orderly, crystalline substance, a state considerably less random than a solution of ions in water. In this case, the positive entropy change outweighs the enthalpy change. That is TAS > AH. The Gibbs free energy change is negative, so the process will proceed spontaneously. 

Two types of situation may generally arise in respect of this equation. In the first, the enthalpy of the products exceeds that of the reactants (AH is positive), while in the second the converse happens (AH is negative). A reaction that conforms to the former situation is called an exothermic reaction and a reaction that corresponds to the latter situation is called an endothermic reaction. An exothermic reaction is accompanied by evolution of heat. An endothermic reaction, in contrast, occurs with absorption of heat. Enthalpy changes are... 

The reaction is exothermic and the enthalpy change AH° is therefore negative. The heat of reaction —AH° is positive. The superscript ° denotes a value at standard conditions and the subscript r implies that a chemical reaction is involved. 

Note A negative sign is necessary in equation 3.24 as Qr is positive when heat is evolved by the reaction, whereas the standard enthalpy change will be negative for exothermic reactions. Qp will be negative when cooling is required (see Section 3.4). 

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