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Column Company.CompanyID is invalid in the select list because it is not contained in either an aggregate function or the GROUP BY clause.

Infrared reflectance spectroscopy provides information on the vibrational states in the interphase It can be interpreted in terms of molecular symmetry, force constants and chemical bond lengths The intensity of the spectral peaks of the adsorbed molecules is determined both by standard.

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If so, it is because you wrote an SQL statement that attempted to produce an impossible result set. We discuss what is and isn t possible with SELECT statements that use GROUP BY, HAVING, DISTINCT, and aggregate functions later on, in 9, but for now, we concentrate on writing a few more basic SELECT statements. Listing 5-3 seems simple enough, but what if you want only those columns for the one company with a CompanyID of 10 For that, you need to add a WHERE clause to the SQL statement, as shown in Listing 5-4.

Listing 5-4: Adding a WHERE clause to the SELECT statement returns only those rows that satisfy its criterion

<cfquery name= GetSupportCalls datasource= #Request.MainDSN# > SELECT SupportCallID, Status, Description FROM SupportCall ORDER BY Status ASC </cfquery> <h1>Support Calls</h1> <table cellspacing= 2 cellpadding= 2 border= 1 > <tr> <td><b>Call #</b></td> <td><b>Status</b></td> <td><b>Description</b></td> </tr> <cfoutput> <cfloop query= GetSupportCalls > <tr bgcolor= <cfif GetSupportCalls.Status EQ 0>Lime<cfelse>White</cfif> > <td align= Right >#SupportCallID#</td> <td> <cfswitch expression= #GetSupportCalls.Status# > <cfcase value= 0 > Opened

selection rules and also by specific surface selection rules, differentiating various directions of the polarization of radiation and molecular orientation with respect to the surface of the electrode. Infrared reflectance spectroscopy has been used, for example, to study the structure of water in the electrical double layer, adsorption of H2 and CO on a platinum electrode and the adsorption of intermediates in the oxidation of organic substances on Pt, Au, Rh and Pd electrodes. The spectra can be interpreted in terms of the symmetry changes in the molecules in the electrochemical interface, bonding to the electrode surface, aggregation, etc. An example of the SNIFTIRS study of a Pt electrode in contact with 0.5 M LiClO4 in propylene carbonate (PC) is demonstrated in Fig. 5.35. The reference potential, E was 2 V versus Li/Li + , the working potential, w was 3.2 V versus Li/Li + . Anodic oxidation of PC is clearly apparent at these conditions; it is accompanied by the relative intensity drop of the C = O stretching vibration at 1785 cm"1 (from the intact PC), and increase of the C=O stretching vibration at 1766 cm"1 (from the oxidized PC). The oxidation products are further characterized by several new negative going peaks in the 1000-1800 cm"1 region, whereas the content of CH3 groups remains unchanged by oxidation. The most characteristic oxidation product of PC is molecular CO2 identified at 2342 cm"1. The onset of PC oxidation (CO2 formation) was detected by SNIFTIRS already at 2.1 V versus Li/Li + , which indicates that propylene carbonate is much less stable against oxidative decomposition than it was formerly believed on the basis of electrochemical methods (anodic currents at the platinum electrode in the mentioned electrolyte are practically negligible in the interval 2-4 V versus

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