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The standard free energy change for the formation of H2(g)=12O2(g) from H2O(l) is G°=+237.13KJ The reactions are

cathode:2H2O+2e-H2(g)+20H-Anode:H2O12O2(g)+2H++2e-

Calculate the standard voltageE°needed to decompose water into its elements by electrolysis. What does the word standard mean in this question?

Short Answer

Expert verified
  • The standard voltage E = -1.229 V needed to decompose water into its elements by electrolysis.

Step by step solution

01

Definition of Standard free energy:

  • The standard free energy of a substance represents the free energy change associated with the formation of the substance from the elements in their most stable forms as they exist under standard conditions.
02

Step 2: Method of calculating Standard Voltage:

We can calculate standard voltage using this equation:

G=-n.F.E

So, the is,

E=-Gn.FE=-237.13.103j2.96485C/molE=--1.229V

03

Elucidating the word Standard:

  • The word standard mean that the reluctant and products are in standard states.

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Most popular questions from this chapter

The cyclic voltammogram of the antibiotic chloramphenicol (abbreviated) is shown here. The first cathodic scan goes from 0 to -1.0 V. The first cathodic wave, , is from the reaction RNO2+4e-+4H+RNHOH+H2O. Peak B in the reverse anodic scan could be assigned to RNHOHRNO+2H++2e-. In the second cathodic scan from +0.9 to -0.4 V, the new peak C appears. Write a reaction for peak C and explain why peak C was not seen in the initial scan.


Cyclic voltammogram of 3.7 ×10-4 chloramphenicol in 0.1 M acetate buffer, pH 4.62. The voltage of the carbon paste working electrode was scanned at a rate of 350 mV/s. [Data from P. T. Kissinger and W. R. Heineman, “Cyclic Voltammetry,” J. Chem. Ed. 1983, 60, 702.]

The drug Librium gives a polarographic wave withE1/2=-0.265V(versus S.C.E.) in 0.05MH2SO4. A 50.0 - Mlsample containing Librium gave a wave height of0.37μA. When 2.00mLof 3.00mMLibrium in0.05MH2SO4were added to the sample, the wave height increased to0.80μA. Find the molarity of Librium in the unknown.

From the two standard additions of 50 pm Fe(III) in the figure, find the concentration of Fe(III) in the seawater. Estimate where the baseline should be drawn for each trace and measure the peak height from the baseline. Consider the volume to be constant for all three solutions.

For a rotating disk electrode operating at sufficiently great potential, the redox reaction rate is governed by the rate at which analyte diffuses through the diffusion layer to the electrode (Figure 17-15b). The thickness of the diffusion layer is

δ=1.61D1/3V1/6ω-1/2

whereis the diffusion coefficient of reactant (m2/s),vis the kinematic viscosity of the liquid

(=viscosity/debsity=(m2/s),v and ωis the rotation rate (radians/s) of the electrode. There are 2π radians in a circle. The current densityis localid="1655441451764" (A/m2)is

localid="1655441445229" Currentdebsity=0.62nFD2/3v-1/6ω1/2C0

where nis the number of electrons in the half-reaction, Fis the Faraday constant, and localid="1655441459070" C0is the concentration of the electroactive species in bulk solution localid="1655441466748" (mol/m3,notmol/L) Consider the oxidation oflocalid="1655441474339" Fe(CN)64-in a solution of localid="1655441479067" 10.0mMK3Fe(CN)6+50.0mMK4Fe(CN)6at +0.90V(versus S.C.E.) at a rotation speed oflocalid="1655441490849" role="math" 2.00×103revolutions per minute. 27The diffusion coefficient oflocalid="1655441497131" Fe(CN)64-is2.5×10-9m2/sand the kinematic viscosity islocalid="1655441503345" 1.1×10-5m2/sCalculate the thickness of the diffusion layer and the current density. If you are careful, the current density should look like the value in Figure 17-16b.

Chemical oxygen demand by coulonetry. An electrochemical device incorporating photooxidation on a \({\rm{Ti}}{{\rm{O}}_2}\) surface could replace refluxing with \({{\rm{C}}_2}{\rm{O}}_7^{2 - }\) to measure chemical oxygen demand (Box 16-2). The diagram shows a working electrode beld at \( + 0.30\;{\rm{V}}\) versus \({\rm{Ag}}\mid {\rm{AgCl}}\) and coated with nanoparticles of 'TiO . Wltraviolet2inradiation generates electrons and holes in \({{\rm{T}}_1}{{\rm{O}}_2}\). Holes oxidize

organic matter at the surface. Electrons reduce \({{\rm{H}}_2}{\rm{O}}\) at the auxiliary electrode in a compartment connected to the working compartment by a salt bridge. The sample compartment is only 0.18 mm thick with a volume of \(13.5\mu \,{\rm{L}}\). It requires \(\~1\;\,{\rm{min}}\) for all organic matter to diffuse to the \({\rm{Ti}}{{\rm{O}}_2}\) surface and be exhaustively oxidized.

Left: Working electrode. Fight Photocument response for sample and blank Both solutions contain \(2{\rm{M}}\,{\rm{NaNO}}\). (Dst from H zhso, D. fisng. 5 . zhang K. Cutteral, and R. Jshn, "Development of a Drect Fhotselectrocherrical Method for Deterrination of Gherrical Ouygen Demand," And. Chan. 2004, 76 155.)

The blank curve in the graph shows the response when the sample compartment contains just electrolyte. Before inradiation, no current is observed. Ultraviolet radiation causes a spike in the current, followed by a decrease to a steady level near \(40\mu \). This current arises from oxidation of water at the \({\rm{Ti}}{{\rm{O}}_2}\)sufface under ultraviolet exposure. The upper curve sbows the same experiment, but with wastewater in the sample compartment. The increased current arises from oxidation of organic matter. When the organic matter is consumed, the cument decreases to the blank level. The area between the two curves tells us how many electrons flow from oxidation of organic matter in the sample.

  1. Balance the oxidation half-reaction that occurs in this cell:

\({{\rm{C}}_e}{{\rm{H}}_k}{{\rm{O}}_a}\;{{\rm{N}}_s}{{\rm{X}}_x} + {\rm{A}}{{\rm{H}}_2}{\rm{O}} \to {\rm{BC}}{{\rm{O}}_2} + {\rm{CX}} + {\rm{DN}}{{\rm{H}}_3} + {\rm{E}}{{\rm{H}}^ + } + {\rm{F}}{{\rm{e}}^ - }\)

where X is any halogen. Express the stoichiometry coefficients A, B, C, D, E, and F in terms of c, h, o, n, and x.

  1. How many molecules of \({{\rm{O}}_2}\)are required to balance the halfreaction in part (a) by reduction of oxygen (\({{\rm{O}}_2} + 4{{\rm{H}}^ + } + 4{{\rm{e}}^ - } \to 2{{\rm{H}}_2}{\rm{O}}\))?
  2. The area between the two curves in the graph is \(\int_0^\infty {({I_{{\rm{sample }}}}} - {I_{blank}})dt = 9.43\,{\rm{mC}}{\rm{.}}\) This is the number of electrons liberated by complete oxidation of the sample. How many moles of \({{\rm{O}}_2}\) would be required for the same oxidation?
  3. Chemical oxygen demand (COD) is expressed as mg of \({{\rm{O}}_2}\) required to oxidize 1 L of sample. Find the COD for this sample.
  4. If the only caidizable substance in the sample were \({{\rm{C}}_9}{{\rm{H}}_6}{\rm{N}}{{\rm{O}}_2}{\rm{CIB}}{{\rm{r}}_2}\). what is its concentration in molL?
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