Concept explainers
Interpretation:
The facts related to the resonance stabilization of benzene, heat of hydrogenation and fuel value of benzene and acetylene are to be determined; also the experiment to prove the existence of resonance in cyclooctatetraene is to be determined.
Concept Introduction:
The enthalpy change of the combustion reaction is calculated by the difference of sum of the enthalpy change of products and reactants.
(a)
To determine:
The comparison of heat of hydrogenation of benzene and acetylene and the greater fuel value out of
![Check Mark](/static/check-mark.png)
Explanation of Solution
The heat of hydrogenation of acetylene is
The heat of hydrogenation of benzene is
The fuel value of acetylene is higher than benzene which is consistent with the stability of benzene.
Step 1:
To determine:
The heat of hydrogenation and fuel value of
![Check Mark](/static/check-mark.png)
Answer to Problem 1DE
Solution:
The heat of hydrogenation of acetylene is
Explanation of Solution
The balanced chemical equation for the combustion of acetylene is,
The enthalpy change of the given reaction is calculated by the formula,
Substitute the values of
The fuel value of acetylene is calculated by dividing its standard enthalpy change by the mass.
Step 2:
To determine:
The heat of hydrogenation and fuel value of
![Check Mark](/static/check-mark.png)
Answer to Problem 1DE
Solution:
The heat of hydrogenation of benzene is
Explanation of Solution
The balanced chemical equation for the combustion of benzene is,
The enthalpy change of the given reaction is calculated by the formula,
Substitute the values of
The fuel value of benzene is calculated by dividing its standard enthalpy change by the mass.
Since, the fuel value of benzene is less than that of acetylene. Therefore, benzene ring is especially stable and not gets easily oxidized. Thus, the calculations of heat of hydrogenation and fuel value are consistent with the extra stabilization of benzene.
The heat of hydrogenation of acetylene is
The heat of hydrogenation of benzene is
The fuel value of acetylene is higher than benzene which is consistent with the stability of benzene.
(b)
To determine:
The heat of hydrogenation and fuel value of toluene.
![Check Mark](/static/check-mark.png)
Answer to Problem 1DE
Solution:
The heat of hydrogenation of toluene is
Explanation of Solution
The balanced chemical equation for the combustion of benzene is,
The enthalpy change of the given reaction is calculated by the formula,
Substitute the values of
The fuel value of benzene is calculated by dividing its standard enthalpy change by the mass.
The heat of hydrogenation of toluene is
(c)
To determine:
The explanation of stabilization of benzene by using the given values of heat of hydrogenation.
![Check Mark](/static/check-mark.png)
Answer to Problem 1DE
Solution:
The heat of hydrogenation for benzene is more than cyclohexane because benzene is more stable and it requires more energy to break its bonds.
Explanation of Solution
Given
The heat of hydrogenation of benzene to make cyclohexane is
The heat of hydrogenation of cyclohexene to make cyclohexane is
The heat of hydrogenation is the energy required to break the carbon-hydrogen bonds in the molecule. More is the heat of hydrogenation; more is the stability of the molecule. Since, the heat of hydrogenation of benzene is more than that of the cyclohexene. Therefore, the benzene is more stable than that of the cyclohexene.
The heat of hydrogenation for benzene is more than cyclohexane because benzene is more stable and it requires more energy to break its bonds.
(d)
To determine:
The explanation of resonance and stability of benzene on the basis of bond lengths and bond angles.
![Check Mark](/static/check-mark.png)
Answer to Problem 1DE
Solution:
The bond lengths and bond angle in benzene are all equal which confirms the existence of phenomenon of resonance in the molecule.
Explanation of Solution
The pi electrons present in the benzene ring is delocalized among all the carbon atoms of the ring. Due to this the bond lengths and bond angles of all carbon-carbon bonds are equal which proves the delocalized bonding in the ring. Therefore, the bond lengths and bond angles are sufficient to decide the existence of resonance and stability in the structure.
The bond lengths and bond angle in benzene are all equal which confirms the existence of phenomenon of resonance in the molecule.
(e)
To determine:
The experiment to prove the existence of resonance in cyclo octatetraene.
![Check Mark](/static/check-mark.png)
Answer to Problem 1DE
Solution:
The NMR spectrum of cyclo octatetraene proves that this molecule does not exhibit the phenomenon of resonance.
Explanation of Solution
The NMR spectrum of the given sample is the measure of number of hydrogen nuclei in the molecule. The number of peaks present in the NMR spectrum decides the types of nucleus present in the structure. The given structure of cyclooctatetraene contains two types of protons present in the structure having two different bond lengths. Therefore, the pheneomenon of resonance does not exhibit in this structure.
The NMR spectrum of cyclooctatetraene proves that this molecule does not exhibit the phenomenon of resonance.
Want to see more full solutions like this?
Chapter 8 Solutions
CHEMISTRY: THE CENTRAL SCIENCE
- NH2 1. CH3–MgCl 2. H3O+ ? As the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C - C bond as its major product: If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If the major products of this reaction won't have a new C - C bond, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. This reaction will not make a product with a new C - C bond. Х ☐: Carrow_forwardPredict the major products of this organic reaction. If there will be no major products, check the box under the drawing area instead. No reaction. : + Х è OH K Cr O 2 27 2 4' 2 Click and drag to start drawing a structure.arrow_forwardLaminar compounds are characterized by havinga) a high value of the internal surface of the solid.b) a high adsorption potential.arrow_forward
- Intercalation compounds have their sheetsa) negatively charged.b) positively charged.arrow_forwardIndicate whether the following two statements are correct or not:- Polythiazine, formed by N and S, does not conduct electricity- Carbon can have a specific surface area of 3000 m2/garrow_forwardIndicate whether the following two statements are correct or not:- The S8 heterocycle is the origin of a family of compounds- Most of the elements that give rise to stable heterocycles belong to group d.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
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)