At a potential of –1.0 V (versus SCE), carbon tetrachloride in methanol is reduced to chloroform at a Hg cathode: 2CCI, + 2H* + 2e¯+ 2Hg(1) → 2CHCI, + Hg,Cl,(s) At –1.80 V, the chloroform further reacts to give methane: 2CHCI, + 6H+ + 6e¯+ 6Hg(1) 2CH, + 3Hg,Cl,(s) Several 0.750-g samples containing CCl,, CHCI3, and inert organic species were dissolved in methanol and electrolyzed at –1.0 V until the current approached zero. A coulometer indicated the charge required to complete the reaction, as given in the second column of the following table. The potential of the cathode was then adjusted to –1.80 V. The additional charge required to complete the reaction at this potential is given in the third column of the table Calculate the percent CCI, and CHCI, in each mixture,
At a potential of –1.0 V (versus SCE), carbon tetrachloride in methanol is reduced to chloroform at a Hg cathode: 2CCI, + 2H* + 2e¯+ 2Hg(1) → 2CHCI, + Hg,Cl,(s) At –1.80 V, the chloroform further reacts to give methane: 2CHCI, + 6H+ + 6e¯+ 6Hg(1) 2CH, + 3Hg,Cl,(s) Several 0.750-g samples containing CCl,, CHCI3, and inert organic species were dissolved in methanol and electrolyzed at –1.0 V until the current approached zero. A coulometer indicated the charge required to complete the reaction, as given in the second column of the following table. The potential of the cathode was then adjusted to –1.80 V. The additional charge required to complete the reaction at this potential is given in the third column of the table Calculate the percent CCI, and CHCI, in each mixture,
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
Related questions
Question
![At a potential of –1.0 V (versus SCE), carbon tetrachloride in methanol is reduced to chloroform at a Hg
cathode:
2CCI, + 2H*+ 2e¯+ 2Hg(1)
→ 2CHCI, + Hg,Cl,(s)
At -1.80 V, the chloroform further reacts to give methane:
2CHCI, + 6H+ + 6e¯+ 6Hg(1)
→ 2CH, + 3Hg,Cl,(s)
Several 0.750-g samples containing CCL4, CHCI,, and inert organic species were dissolved in methanol and
electrolyzed at -1.0 V until the current approached zero. A coulometer indicated the charge required to
complete the reaction, as given in the second column of the following table. The potential of the cathode
was then adjusted to -1.80 V. The additional charge required to complete the reaction at this potential is
given in the third column of the table. Calculate the percent CCl, and CHCI, in each mixture.
Charge Required
at –1.0 V, C
Charge Required
at –1.8 V, C
Sample No.
1
10.84
69.20
2
20.52
88.50
3
6.22
45.98
4
11.60
68.62](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F82d2fac5-c3a7-402f-affb-f74ef4adf53b%2F1f6275d8-5452-46b5-93db-fc9ad3bc8056%2Fmc72etb_processed.png&w=3840&q=75)
Transcribed Image Text:At a potential of –1.0 V (versus SCE), carbon tetrachloride in methanol is reduced to chloroform at a Hg
cathode:
2CCI, + 2H*+ 2e¯+ 2Hg(1)
→ 2CHCI, + Hg,Cl,(s)
At -1.80 V, the chloroform further reacts to give methane:
2CHCI, + 6H+ + 6e¯+ 6Hg(1)
→ 2CH, + 3Hg,Cl,(s)
Several 0.750-g samples containing CCL4, CHCI,, and inert organic species were dissolved in methanol and
electrolyzed at -1.0 V until the current approached zero. A coulometer indicated the charge required to
complete the reaction, as given in the second column of the following table. The potential of the cathode
was then adjusted to -1.80 V. The additional charge required to complete the reaction at this potential is
given in the third column of the table. Calculate the percent CCl, and CHCI, in each mixture.
Charge Required
at –1.0 V, C
Charge Required
at –1.8 V, C
Sample No.
1
10.84
69.20
2
20.52
88.50
3
6.22
45.98
4
11.60
68.62
Expert Solution
![](/static/compass_v2/shared-icons/check-mark.png)
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution!
Trending now
This is a popular solution!
Step by step
Solved in 4 steps with 1 images
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Recommended textbooks for you
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
![Chemistry: Principles and Reactions](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
![Elementary Principles of Chemical Processes, Bind…](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY