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ization forward In this chapter, we will look more closely at some of the ways that my father motivated people If there was one thing that my father understood above all else, it was how to motivate and inspire people My father felt that success depended on a leader s ability to get others to act He was an expert in dealing with people, the best motivator in his business and in my own experience better than most in other businesses, too In this chapter, I draw out the key lessons on how to motivate both teams and individuals, and I discuss ways to apply these lessons to the workplace Leaders motivate and inspire by creating a climate for success They motivate by kindling passion, painting a picture of success (through mission, vision, and values), fanning the flame of team spirit, and inspiring confidence They motivate by demanding accountability, and obtaining results These themes recur throughout this book, but they have special significance when seen through the lens of motivation

Hence, for any species at a concentration low enough for Henry's law to hold,

10 10 10 23 10

and The advantage of this standard state is that it provides a very simple relation between fugacity and concentration for cases in which Henry's law is at least approximately valid Its range does not commonly extend to a concentration of 1 molal In the rare case where it does, the standard state is a real state of the solute This standard state is useful only where AGO data are available

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SETTING THE MOTIVATIONAL TABLE Today, perhaps more than ever before, people are examining what they re doing and why they re doing it This is not a cosmetic change or a small shifting of priorities Rather, it s a real sea change in the way people look at their lives One reason this has happened is that employers have broken almost all the rules that used to govern the employer employee relationship We ve all seen the list of offenses a thousand times: downsizing, reorganizing, re-engineering, inept or insensitive intrusions of technology, excessive executive compensation, managers interested only in short-term results, and managers who micromanage rather than lead

7 ~ o l a l i t is a measure of solute concentration, expressed as moles of solute per kilogram of solvent y

for the standard state of a 1-molal solution, for otherwise the equilibrium constant cannot be evaluated by Eq (1311)

If the initial molarity and Ka of the weak acid are known, the [H+ ] (or [A ]) can be + calculated easily And if the initial molarity and [H ] are known, Ka can be calculated

Suppose a single reaction occurs in a homogeneous system, and suppose the equilibrium constant is known In this event, the calculation of the phase composition at equilibrium is straightforward if the phase is assumed an ideal gas [Eq (1328)] or an ideal solution [Eq (1327) or (1333)] When an assumption of ideality is not reasonable, the problem is still tractable for gas-phase reactions through application of an equation of state and solution by computer For heterogeneous systems, where more than one phase is present, the problem is more complicated and requires the superposition of the criterion for phase equilibrium developed in Sec 116 At equilibrium, there can be no tendency for change to occur, either by mass transfer between phases or by chemical reaction We present in what follows, mainly by example, the procedures in use for equilibrium calculations, first, for single-phase reactions, and second, for heterogeneous reactions

W H AT I T TA K E S T O B E # 1

When liquid and gas phases are both present in an equilibrium mixture of reacting species, Eq (1 144), a criterion of vaporlliquid equilibrium, must be satisfied along with the equation of chemical-reaction equilibrium Consider, for example, the reaction of gas A with liquid water B to form an aqueous solution C Several choices in the method of treatment exist The reaction may be assumed to occur entirely in the gas phase with simultaneous transfer of material between phases to maintain phase equilibrium In this case, the equilibrium constant is evaluated from AGO data based on standard states for the species as gases, ie, the ideal-gas states at 1 bar and the reaction temperature On the other hand, the reaction may be assumed to occur in the liquid phase, in which case AGO is based on standard states for the species as liquids Alternatively, the reaction may be written:

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