Organic Chemistry-Package(Custom)
Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
Question
Book Icon
Chapter 1, Problem 1.74P
Interpretation Introduction

(a)

Interpretation: The shortest CC single bond is to be labeled.

Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order, shorter is the bond length.

Expert Solution
Check Mark

Answer to Problem 1.74P

The shortest CC single bond is [2].

Explanation of Solution

In hybridization, one 2s orbital is always used, but the number of 2p orbitals varies with the type of hybridization. The percent s-character gives the fraction of 2s orbital which is present in a hybrid orbital. As the percent s-character increases, the bond becomes shorter and stronger. This due to the fact that a 2s orbital keeps electron density closer to a nucleus as compared to a 2p orbital.

Organic Chemistry-Package(Custom), Chapter 1, Problem 1.74P

Figure 1

Both [1] and [2] are single CC bond as shown above. Bond [1] is formed by Csp3Csp3 hybrid orbitals and bond [2] is formed by Csp3Csp2 hybrid orbitals. Thus, bond [2] has more percent s-character. Hence, the shortest CC single bond is [2].

Conclusion

The shortest CC single bond is [2].

Interpretation Introduction

(b)

Interpretation: The longest CC single bond is to be labeled.

Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.

Expert Solution
Check Mark

Answer to Problem 1.74P

The longest CC single bond is [1].

Explanation of Solution

In hybridization, one 2s orbital is always used, but the number of 2p orbitals varies with the type of hybridization. The percent s-character gives the fraction of 2s orbital which is present in a hybrid orbital. As the percent s-character increases, the bond becomes shorter and stronger. This due to the fact that a 2s orbital keeps electron density closer to a nucleus as compared to a 2p orbital. Both [1] and [2] are single bond as shown in Figure 1. Bondbut [1] is formed by Csp3Csp3 hybrid orbitals and bond [2] is formed by Csp3Csp2 hybrid orbitals. Thus, bond [1] has less percent s-character. Hence the longest CC single bond is [1].

Conclusion

The longest CC single bond is [1].

Interpretation Introduction

(c)

Interpretation: The shortest CC bond is to be labeled.

Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.

Expert Solution
Check Mark

Answer to Problem 1.74P

The shortest CC bond is triple bond between two carbon atoms.

Explanation of Solution

In hybridization, one 2s orbital is always used, but the number of 2p orbitals varies with the type of hybridization. The percent s-character gives the fraction of 2s orbital which is present in a hybrid orbital. As the percent s-character increases, the bond becomes shorter and stronger. This due to the fact that a 2s orbital keeps electron density closer to a nucleus as compared to a 2p orbital. Triple bond is formed by CspCsp hybrid orbitals it has highest percent s-character among other CC bond. Hence, the shortest CC bond is triple bond.

Conclusion

The shortest CC bond is triple bond between two carbon atoms.

Interpretation Introduction

(d)

Interpretation: The weakest CC bond is to be labeled.

Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.

Expert Solution
Check Mark

Answer to Problem 1.74P

The weakest CC bond is [1].

Explanation of Solution

In hybridization, one 2s orbital is always used, but the number of 2p orbitals varies with the type of hybridization. The percent s-character gives the fraction of 2s orbital which is present in a hybrid orbital. As the percent s-character increases, the bond becomes shorter and stronger. This due to the fact that a 2s orbital keeps electron density closer to a nucleus as compared to a 2p orbital..

Both [1] and [2] are single bond as shown in Figure 1. Bond [1] is formed by Csp3Csp3 hybrid orbitals and bond [2] is formed by Csp3Csp2 hybrid orbitals. Bond [1] has less percent s-character. Hence, the weakest CC bond is [1].

Conclusion

The weakest CC bond is [1].

Interpretation Introduction

(e)

Interpretation: The strongest CH bond is to be labeled.

Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.

Expert Solution
Check Mark

Answer to Problem 1.74P

The strongest CH bond is with triple CC bond.

Explanation of Solution

The length and strength of a CH bond depends on the hybridization of the carbon atom. In hybridization, one 2s orbital is always used, but the number of 2p orbitals varies with the type of hybridization. The percent s-character gives the fraction of 2s orbital which is present in a hybrid orbital. As the percent s-character increases, the bond becomes shorter and stronger. This due to the fact that a 2s orbital keeps electron density closer to a nucleus as compared to a 2p orbital.

Triple bond is formed by CspCsp it has highest percent s-character among other CC bond. Hence, CH with triple CC bond has highest percent s character and is the strongest bond.

Conclusion

The strongest CH bond is with triple CC bond.

Interpretation Introduction

(f)

Interpretation: Bond [1] and [2] are of different length, even though they are both CC single bond reason is to be explained.

Concept introduction: There is an inverse relationship between bond length and bond strength. Shorter bonds are stronger bonds or higher the bond order shorter is the bond length.

Expert Solution
Check Mark

Answer to Problem 1.74P

Bond [1] and [2] are of different length, even though they are both CC single bond due to the difference in percent-s character.

Explanation of Solution

In hybridization, one 2s orbital is always used, but the number of 2p orbitals varies with the type of hybridization. The percent s-character gives the fraction of 2s orbital which is present in a hybrid orbital. As the percent s-character increases, the bond becomes shorter and stronger. This due to the fact that a 2s orbital keeps electron density closer to a nucleus as compared to a 2p orbital. Both [1] and [2] are single bond as shown in Figure 1. Bond [1] is formed by Csp3Csp3 hybrid orbitals and bond [2] is formed by Csp3Csp2 hybrid orbitals. Hence, bond [2] has more percent s character and is shorter in length than bond [1].

Conclusion

Bond [1] and [2] are of different length, even though they are both CC single bond due to the difference in percent-s character.

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
Answer the following questions about compound A. a. Label the shortest C-C single bond. b. Label the longest C-C single bond. c. Considering all the bonds, label the shortest C-C bond. d. Label the weakest C-C bond. e. Label the strongest C-H bond. f. Explain why bond (1) and bond (2) are different in length, even though they are both C-C single bonds. (2)
Draw the Lewis structure for a ClO- ion on a separate piece of paper. a. How many lone pairs of electrons are of the Cl atom? b. How many lone pairs of electrons are on the O atom? c. Is the bond between chlorine and oxygen a single, double, or triple bond?
The element sulphur has atomic number 16. Sulphur forms a molecular compound with chloride with a molecular formula SCl2. The atomic number of chlorine is 17. a. Write down the electronic configuration of a sulphur atom and a chlorine atom. b. Draw a Lewis structure of an SCl2 molecule, by showing the electrons in the outer shells of the atoms. c. State how many bond pairs and lone pairs of electrons are arranged around the sulphur atoms in SCl2 molecule. d. Sketch the shape and state the molecular geometry of SCl2 molecule. e. Explain the hybridisation of the central atom in SCl2 molecule. f.Explain the intermolecular forces exists in SCl2 molecule.

Chapter 1 Solutions

Organic Chemistry-Package(Custom)

Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Draw a second resonance structure for each...Ch. 1 - Prob. 1.14PCh. 1 - Draw a second resonance structure for nitrous...Ch. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Prob. 1.19PCh. 1 - Prob. 1.20PCh. 1 - Simplify each condensed structure by using...Ch. 1 - Prob. 1.22PCh. 1 - Prob. 1.23PCh. 1 - Convert each skeletal structure to a complete...Ch. 1 - Draw in all hydrogens and lone pairs on the...Ch. 1 - Prob. 1.26PCh. 1 - What orbitals are used to form each of the CC, and...Ch. 1 - What orbitals are used to form each bond in the...Ch. 1 - Determine the hybridization around the highlighted...Ch. 1 - Classify each bond in the following molecules as ...Ch. 1 - Prob. 1.31PCh. 1 - Rank the following atoms in order of increasing...Ch. 1 - Prob. 1.33PCh. 1 - Prob. 1.34PCh. 1 - Provide the following information about...Ch. 1 - Use the ball-and-stick model to answer each...Ch. 1 - Citric acid is responsible for the tartness of...Ch. 1 - Zingerone gives ginger its pungent taste. a.What...Ch. 1 - Two radioactive isotopes of iodine used for the...Ch. 1 - Prob. 1.40PCh. 1 - Assign formal charges to each carbon atom in the...Ch. 1 - Assign formal charges to each N and O atom in the...Ch. 1 - Draw one valid Lewis structure for each compound....Ch. 1 - Prob. 1.44PCh. 1 - Prob. 1.45PCh. 1 - Prob. 1.46PCh. 1 - Draw all possible isomers for each molecular...Ch. 1 - 1.45 Draw Lewis structures for the nine isomers...Ch. 1 - Prob. 1.49PCh. 1 - Prob. 1.50PCh. 1 - Prob. 1.51PCh. 1 - Prob. 1.52PCh. 1 - Prob. 1.53PCh. 1 - Prob. 1.54PCh. 1 - Draw all reasonable resonance structures for each...Ch. 1 - Prob. 1.56PCh. 1 - Rank the resonance structures in each group in...Ch. 1 - 1.56 Consider the compounds and ions with curved...Ch. 1 - 1.57 Predict all bond angles in each...Ch. 1 - Predict the geometry around each indicated atom....Ch. 1 - Prob. 1.61PCh. 1 - Prob. 1.62PCh. 1 - Draw in all the carbon and hydrogen atoms in each...Ch. 1 - Prob. 1.64PCh. 1 - Prob. 1.65PCh. 1 - Prob. 1.66PCh. 1 - Prob. 1.67PCh. 1 - Each of the following condensed or skeletal...Ch. 1 - Prob. 1.69PCh. 1 - Prob. 1.70PCh. 1 - Prob. 1.71PCh. 1 - Prob. 1.72PCh. 1 - Prob. 1.73PCh. 1 - Prob. 1.74PCh. 1 - Two useful organic compounds that contain Cl atoms...Ch. 1 - Use the symbols + and to indicate the polarity of...Ch. 1 - Label the polar bonds in each molecule. Indicate...Ch. 1 - Answer the following questions about acetonitrile...Ch. 1 - Prob. 1.79PCh. 1 - The principles of this chapter can be applied to...Ch. 1 - a. What is the hybridization of each N atom in...Ch. 1 - 1.77 Stalevo is the trade name for a medication...Ch. 1 - 1.78 and are two highly reactive carbon...Ch. 1 - 1.79 The N atom in (acetamide) is hybridized,...Ch. 1 - Prob. 1.85PCh. 1 - Prob. 1.86PCh. 1 - Prob. 1.87PCh. 1 - Prob. 1.88PCh. 1 - Prob. 1.89PCh. 1 - Prob. 1.90P
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
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
Living by Chemistry
Chemistry
ISBN:9781464142314
Author:Angelica M. Stacy
Publisher:W. H. Freeman
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
Text book image
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry In Focus
Chemistry
ISBN:9781337399692
Author:Tro, Nivaldo J.
Publisher:Cengage Learning,
Text book image
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning