13. Redox active species can be quantitated using electrogravimetric analysis. d. For a colored species like Cu (ag), why might you choose to use electrogravimetric analysis over something like UV-vis spectroscopy? e. Cu²* is reduced to Cu, using a current of 0.607 A. If 0.2035 g of Cu is collected, how long was the current applied? f. For electrolysis, full consideration of the potential required to drive the reaction may be E=Ecathode-Eanode-IR-overpotentials. Would you need to consider IR and overpotentials for this analysis? Why or why not?

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13. Redox active species can be quantitated using electrogravimetric analysis.
d. For a colored species like Cu (aq), why might you choose to use
electrogravimetric analysis over something like UV-vis spectroscopy?
e. Cu²* is reduced to Cu using a current of 0.607 A. If 0.2035 g of Cu is
collected, how long was the current applied?
f. For electrolysis, full consideration of the potential required to drive
the reaction may be E=Ecathode-Eanode"IR-overpotentials. Would you
need to consider IR and overpotentials for this analysis? Why or why
not?
Transcribed Image Text:13. Redox active species can be quantitated using electrogravimetric analysis. d. For a colored species like Cu (aq), why might you choose to use electrogravimetric analysis over something like UV-vis spectroscopy? e. Cu²* is reduced to Cu using a current of 0.607 A. If 0.2035 g of Cu is collected, how long was the current applied? f. For electrolysis, full consideration of the potential required to drive the reaction may be E=Ecathode-Eanode"IR-overpotentials. Would you need to consider IR and overpotentials for this analysis? Why or why not?
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