
Interpretation:
Temperature condition is needed to be explained in the given dehydrogenation reaction.
Concept introduction:
Dehydrogenation: dehydrogenation is a process of elimination of hydrogen molecule from the substrate at high temperature condition.
Free energy: reaction is feasible when free energy is negative.

Answer to Problem 41PP
Reaction is feasible at higher temperature conditions only since
Explanation of Solution
To explain: the conditions for the given reaction.
Given reaction is shown below.
Clear from the reaction that the ethane molecule converted ethylene molecule at high temperature condition by releasing hydrogen gas.
Given reaction refers the dehydrogenation process at high temperatures. Given substrate is ethane and this ethane molecule heated at high temperature (7500 C) to produce ethylene and hydrogen gas.
To give: the reason for high temperatures needed for the dehydrogenation process.
Given reaction is favorable when
At higher temperature condition, the given reaction is feasible since
Conclusion
At higher temperature conditions, value of free energy will be negative so the dehydrogenation reaction is feasible at higher temperature conditions.
Want to see more full solutions like this?
Chapter 8 Solutions
Organic Chemistry, Third Edition Binder Ready Version
- Can I get helpp drawing my arrowsarrow_forwardWhich of the m/z values corresponds to the base peak in the mass spectrum shown? 100 80 A. 45 B. 44 C. 29 D. 15 Intensity 20 0 10 20 30 40 B- m/z -8 50 E. 30 Which of the m/z values correspond to the molecular ion for the compound shown? A. 18 B. 82 OH C. 100 D. 102 E. 103arrow_forwardCan someone help me with drawing my arrows.arrow_forward
- I'm having trouble with converting lewis diagrams into VSEPR diagrams. I currently have this example of C2BrCl3 which I want to turn into a lewis structure, but I'm not sure what steps I need to do in order to do so. I have the table written down, however, there's two central atoms so what would I do? There seems to be 4 electron domains on the carbon atom and no lone pairs so it would seem like this shape would be tetrahedral. Here's what I have now. Thanks!arrow_forwardWe discussed the solid phase resin using in peptide synthesis. Provide a mechanism, for its formation. DRAW THE MECHANISM.arrow_forwardPlease help. Every time I've asked an expert in the past, it's been wrong :(arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





