EBK CHEMISTRY: THE MOLECULAR SCIENCE
EBK CHEMISTRY: THE MOLECULAR SCIENCE
5th Edition
ISBN: 9780100478640
Author: STANITSKI
Publisher: YUZU
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 10, Problem 121QRT

(a)

Interpretation Introduction

Interpretation:

The chemical equation of hydrogenation reaction of 4-octyne has to by state with help of Lewis structures.

Concept Introduction:

The addition of H2 in presence of catalyst is known as catalytic hydrogenation reaction. This is a syn addition.  Alkyne is reduced to alkane.  In this reaction two weak pi bond of alkyne and sigma bond between H2 is broken and four CH bonds are formed.

(a)

Expert Solution
Check Mark

Explanation of Solution

The hydrogenation reaction of 4-octyne gives an alkene, 4-octene, in the first step.  The alkyne has two π bond in it.  One π bond of cis-4-octyne gets brake to form 4-octene. The corresponding chemical reaction is shown below.

EBK CHEMISTRY: THE MOLECULAR SCIENCE, Chapter 10, Problem 121QRT , additional homework tip  1

Figure 1

The hydrogenation reaction of cis-4-octyne gives an alkene, octane, in the second step.  The alkene has a π bond in it.  The π bond of cis-4-octyne gets brake to form octane. The corresponding chemical reaction is shown below.

EBK CHEMISTRY: THE MOLECULAR SCIENCE, Chapter 10, Problem 121QRT , additional homework tip  2

Figure 2

(b)

Interpretation Introduction

Interpretation:

The standard enthalpy change for the overall hydrogenation reaction of 4-octyne has to be calculated.

Concept Introduction:

The amount of energy which is produced or absorbed during the reaction is the enthalpy change of a chemical reaction.  When bonds get break, some amount of energy is absorbed by the system.  When bonds are formed, some amount of energy is produced by the system.

(b)

Expert Solution
Check Mark

Explanation of Solution

The overall reaction hydrogenation reaction of 4-octyne is shown below.

EBK CHEMISTRY: THE MOLECULAR SCIENCE, Chapter 10, Problem 121QRT , additional homework tip  3

Figure 3

The reactant 4-octyne has 14 CH bonds, 6 CC bonds and a CC bond.

The reactant hydrogen gas has a HH bond.

The product octane has 18 CH bonds and 7 CC bonds.

The bond enthalpy for CH is 416kJ/mol.

The bond enthalpy for CC is 813kJ/mol.

The bond enthalpy for CC is 356kJ/mol.

The bond enthalpy for HH is 436kJ/mol.

The standard enthalpy change for the overall reaction is calculated by the formula as shown below.

  ΔH°=([(numberofbonds)×D(bondsbroken)][(numberofbonds)×D(bondsformed)])

Where,

  • ΔH° is standard enthalpy change for the overall reaction.
  • D is the bond enthalpy.

The above equation can rewritten for hydrogenation reaction of 4-octyne as shown below.

  ΔH°=[(14×D(CH)+6×D(CC)+D(CC))+2×D(HH)(18×D(CH)+7×D(CC))]

Substitute the value of bond enthalpy for CH, bond enthalpy for CC, bond enthalpy for CC, and bond enthalpy for HH in the above equation.

  ΔH°=[(14×(416kJ/mol)+6×(356kJ/mol)+(813kJ/mol))+2×(436kJ/mol)((18×(416kJ/mol)+7×(356kJ/mol)))]=[5824+2136+813+87274882492]kJ/mol=[96459980]kJ/mol=335kJ/mol_

The standard enthalpy change for the overall hydrogenation reaction of 4-octyne is 335kJ/mol_.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Draw all the structural and geometric isomers of pentene, C5H10, that have an unbranched hydrocarbon chain.
Give the molecular formula of a hydrocarbon containingsix carbon atoms that is (a) a cyclic alkane, (b) a cyclicalkene, (c) a linear alkyne, (d) an aromatic hydrocarbon.
write the structure formulas of alkanes with molecular formula C6H14, which with chlorine give: a) three monochlorinated isomers? b) five monochlorinated isomers c) only two monochlorinated isomers

Chapter 10 Solutions

EBK CHEMISTRY: THE MOLECULAR SCIENCE

Ch. 10.4 - Prob. 10.8CECh. 10.4 - Prob. 10.9CECh. 10.4 - Prob. 10.10CECh. 10.4 - Prob. 10.11ECh. 10.5 - Prob. 10.12ECh. 10.5 - Prob. 10.4PSPCh. 10.5 - Prob. 10.13ECh. 10.6 - Prob. 10.14CECh. 10.6 - Prob. 10.5PSPCh. 10.6 - Prob. 10.6PSPCh. 10.6 - Prob. 10.7PSPCh. 10.6 - Prob. 10.8PSPCh. 10.6 - Prob. 10.9PSPCh. 10.6 - Prob. 10.15CECh. 10.6 - Prob. 10.16ECh. 10.7 - Prob. 10.17CECh. 10.7 - Prob. 10.18CECh. 10.7 - Prob. 10.19CECh. 10.7 - Prob. 10.20CECh. 10.7 - Prob. 10.10PSPCh. 10.7 - Prob. 10.21ECh. 10 - Prob. ISPCh. 10 - Prob. IISPCh. 10 - Prob. IIISPCh. 10 - Prob. 1QRTCh. 10 - Prob. 2QRTCh. 10 - Prob. 3QRTCh. 10 - Prob. 4QRTCh. 10 - Prob. 5QRTCh. 10 - Prob. 6QRTCh. 10 - Prob. 7QRTCh. 10 - Give two reasons why ethylene glycol has a higher...Ch. 10 - Prob. 9QRTCh. 10 - Prob. 10QRTCh. 10 - Prob. 11QRTCh. 10 - Prob. 12QRTCh. 10 - Prob. 13QRTCh. 10 - Prob. 14QRTCh. 10 - Prob. 15QRTCh. 10 - Prob. 16QRTCh. 10 - Prob. 17QRTCh. 10 - Prob. 18QRTCh. 10 - Prob. 19QRTCh. 10 - Prob. 20QRTCh. 10 - Prob. 21QRTCh. 10 - Prob. 22QRTCh. 10 - Prob. 23QRTCh. 10 - Prob. 24QRTCh. 10 - Prob. 25QRTCh. 10 - Prob. 26QRTCh. 10 - Prob. 27QRTCh. 10 - Prob. 28QRTCh. 10 - Prob. 29QRTCh. 10 - Prob. 30QRTCh. 10 - Prob. 31QRTCh. 10 - Prob. 32QRTCh. 10 - Prob. 33QRTCh. 10 - Prob. 34QRTCh. 10 - Prob. 35QRTCh. 10 - Prob. 36QRTCh. 10 - Prob. 37QRTCh. 10 - Prob. 38QRTCh. 10 - Prob. 39QRTCh. 10 - Prob. 40QRTCh. 10 - Prob. 41QRTCh. 10 - Prob. 42QRTCh. 10 - Prob. 43QRTCh. 10 - Prob. 44QRTCh. 10 - Prob. 45QRTCh. 10 - Prob. 46QRTCh. 10 - Prob. 47QRTCh. 10 - Beeswax contains this compound: Identify what...Ch. 10 - Prob. 49QRTCh. 10 - Prob. 50QRTCh. 10 - Prob. 51QRTCh. 10 - Prob. 52QRTCh. 10 - Prob. 53QRTCh. 10 - Prob. 54QRTCh. 10 - Prob. 55QRTCh. 10 - Prob. 56QRTCh. 10 - Prob. 57QRTCh. 10 - Prob. 58QRTCh. 10 - Prob. 59QRTCh. 10 - Prob. 60QRTCh. 10 - Prob. 61QRTCh. 10 - Prob. 62QRTCh. 10 - Prob. 63QRTCh. 10 - Prob. 64QRTCh. 10 - Prob. 65QRTCh. 10 - Prob. 66QRTCh. 10 - Prob. 67QRTCh. 10 - Prob. 68QRTCh. 10 - Prob. 69QRTCh. 10 - Prob. 70QRTCh. 10 - Prob. 71QRTCh. 10 - Prob. 72QRTCh. 10 - Prob. 73QRTCh. 10 - Prob. 74QRTCh. 10 - Prob. 75QRTCh. 10 - Prob. 76QRTCh. 10 - Prob. 77QRTCh. 10 - Prob. 78QRTCh. 10 - Prob. 79QRTCh. 10 - Identify and name all the functional groups in...Ch. 10 - Prob. 81QRTCh. 10 - Prob. 82QRTCh. 10 - Prob. 83QRTCh. 10 - Prob. 84QRTCh. 10 - Prob. 85QRTCh. 10 - Prob. 86QRTCh. 10 - Prob. 87QRTCh. 10 - Prob. 88QRTCh. 10 - Prob. 89QRTCh. 10 - Prob. 90QRTCh. 10 - Prob. 91QRTCh. 10 - Prob. 92QRTCh. 10 - Prob. 93QRTCh. 10 - Prob. 94QRTCh. 10 - Prob. 95QRTCh. 10 - Prob. 96QRTCh. 10 - Assume that a car burns pure octane. C8H18 (d =...Ch. 10 - Prob. 98QRTCh. 10 - Prob. 99QRTCh. 10 - Prob. 100QRTCh. 10 - Prob. 101QRTCh. 10 - Prob. 102QRTCh. 10 - Prob. 103QRTCh. 10 - Prob. 104QRTCh. 10 - Prob. 105QRTCh. 10 - Prob. 106QRTCh. 10 - Prob. 107QRTCh. 10 - Prob. 108QRTCh. 10 - Prob. 109QRTCh. 10 - Prob. 110QRTCh. 10 - Prob. 111QRTCh. 10 - Prob. 112QRTCh. 10 - Prob. 113QRTCh. 10 - Prob. 114QRTCh. 10 - Prob. 115QRTCh. 10 - Prob. 116QRTCh. 10 - Prob. 118QRTCh. 10 - Prob. 119QRTCh. 10 - Prob. 120QRTCh. 10 - Prob. 121QRTCh. 10 - Prob. 122QRTCh. 10 - Prob. 123QRTCh. 10 - Prob. 124QRTCh. 10 - Prob. 125QRTCh. 10 - Prob. 126QRTCh. 10 - Prob. 127QRTCh. 10 - Prob. 10.ACPCh. 10 - Prob. 10.BCPCh. 10 - Prob. 10.CCP
Knowledge Booster
Background pattern image
Chemistry
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
Text book image
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Text book image
Introductory Chemistry For Today
Chemistry
ISBN:9781285644561
Author:Seager
Publisher:Cengage
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Chapter 4 Alkanes and Cycloalkanes Lesson 2; Author: Linda Hanson;https://www.youtube.com/watch?v=AL_CM_Btef4;License: Standard YouTube License, CC-BY
Chapter 4 Alkanes and Cycloalkanes Lesson 1; Author: Linda Hanson;https://www.youtube.com/watch?v=PPIa6EHJMJw;License: Standard Youtube License