EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
2nd Edition
ISBN: 9780393543971
Author: KARTY
Publisher: VST
Question
Book Icon
Chapter 15, Problem 15.19P
Interpretation Introduction

(a)

Interpretation:

The CN stretching mode that absorbs the higher-frequency IR photons is to be indicated for given pair of compounds. The reason for it is to be explained.

Concept introduction:

We simplify the picture of molecular vibrations by considering the ball-and-spring model, which treats bonds as simple springs that connect atoms together. According to Hooke’s law, the spring vibrates at a particular frequency (νspring) that depends on the mass (m) of the object connected to the spring (in this case, an atom) and the spring’s force constant (k), which is often thought of as the stiffness of the spring. The stiffer the spring, the more difficult it is to compress and extend it. A stronger and stiffer bond tends to lead to a higher vibrational frequency. A stiffer spring exerts a greater force on the attached atoms, causing them to move faster. Triple bonds tend to be stronger and stiffer than double bonds, just as double bonds tend to be stronger and stiffer than single bonds.

Expert Solution
Check Mark

Answer to Problem 15.19P

The CN stretching mode that absorbs the higher-frequency IR photons due to strong and stiffer bond is indicated below,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  1

Explanation of Solution

The given pair of compounds is,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  2

The triple bonds tend to be stronger and stiffer than double bonds. A stronger and stiffer bond tends to lead to a higher vibrational frequency. In given pair of compounds, with the faster vibration, the N stronger and stiffer than C = N bond. Therefore N bond absorbs the higher-frequency IR photons.

The CN stretching mode that absorbs the higher-frequency IR photons is shown below,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  3

Conclusion

The CN stretching mode that absorbs the higher-frequency IR photons is indicated on the basis of the relationship between strength and stiffness of the bond and vibrational frequency.

Interpretation Introduction

(b)

Interpretation:

The CN stretching mode that absorbs the higher-frequency IR photons is to be indicated for given pair of compounds. The reason for it is to be explained.

Concept introduction:

We simplify the picture of molecular vibrations by considering the ball-and-spring model, which treats bonds as simple springs that connect atoms together. According to Hooke’s law, the spring vibrates at a particular frequency (νspring) that depends on the mass (m) of the object connected to the spring (in this case, an atom) and the spring’s force constant (k), which is often thought of as the stiffness of the spring. The stiffer the spring, the more difficult it is to compress and extend it. A stronger and stiffer bond tends to lead to a higher vibrational frequency. A stiffer spring exerts a greater force on the attached atoms, causing them to move faster. Triple bonds tend to be stronger and stiffer than double bonds, just as double bonds tend to be stronger and stiffer than single bonds.

Expert Solution
Check Mark

Answer to Problem 15.19P

The CN stretching mode that absorbs the higher-frequency IR photons due to strong and stiffer bond is indicated below,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  4

Explanation of Solution

The given pair of compounds is,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  5

The double bonds tend to be stronger and stiffer than single bonds. A stronger and stiffer bond tends to lead to a higher vibrational frequency. In given pair of compounds, with the faster vibration, the =N stronger and stiffer than C - N bond. Therefore =N bond absorbs the higher-frequency IR photons.

The CN stretching mode that absorbs the higher-frequency IR photons is shown below,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  6

Conclusion

The CN stretching mode that absorbs the higher-frequency IR photons is indicated on the basis of the relationship between strength and stiffness of the bond and vibrational frequency.

Interpretation Introduction

(c)

Interpretation:

The CN stretching mode that absorbs the higher-frequency IR photons is to be indicated for given pair of compounds. The reason for it is to be explained.

Concept introduction:

We simplify the picture of molecular vibrations by considering the ball-and-spring model, which treats bonds as simple springs that connect atoms together. According to Hooke’s law, the spring vibrates at a particular frequency (νspring) that depends on the mass (m) of the object connected to the spring (in this case, an atom) and the spring’s force constant (k), which is often thought of as the stiffness of the spring. The stiffer the spring, the more difficult it is to compress and extend it. A decrease in the mass of an atom leads to an increase in vibrational frequency. A stronger and stiffer bond tends to lead to a higher vibrational frequency.

Expert Solution
Check Mark

Answer to Problem 15.19P

The CN stretching mode that absorbs the higher-frequency IR photons due to lower mass is indicated below,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  7

Explanation of Solution

The given pair of compounds is,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  8

In both compounds there is  N bond so both has essentially the same strength and therefore each bond’s spring stiffness must be about the same too. Therefore spring stiffness does not come into the play.

But 13C has higher mass than 12C so lower mass of 12C contributes to a higher frequency of vibration. Because the frequency of vibration is the same as the photon frequency, a 12 N stretch must absorb higher-frequency photons than 13 N stretch.

The CN stretching mode that absorbs the higher-frequency IR photons is shown below,

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M, Chapter 15, Problem 15.19P , additional homework tip  9

Conclusion

The vibrational mode that absorbs at a higher frequency in the IR region is determined on the basis of the relationship between mass and vibrational frequency.

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
Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check CF3 (Choose one) OH (Choose one) H (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy
Identifying electron-donating and electron-withdrawing effects For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects Resonance Effects Overall Electron-Density CF3 O donating O donating O electron-rich O withdrawing withdrawing O no inductive effects O no resonance effects O electron-deficient O similar to benzene OCH3 Explanation Check O donating O donating ○ withdrawing withdrawing O no inductive effects no resonance effects electron-rich electron-deficient O similar to benzene Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center
The acid-base chemistry of both EDTA and EBT are important to ensuring that the reactions proceed as desired, thus the pH is controlled using a buffer. What percent of the EBT indicator will be in the desired HIn2- state at pH = 10.5. pKa1 = 6.2 and pKa2 = 11.6 of EBT

Chapter 15 Solutions

EBK ORGANIC CHEMISTRY: PRINCIPLES AND M

Ch. 15 - Prob. 15.11PCh. 15 - Prob. 15.12PCh. 15 - Prob. 15.13PCh. 15 - Prob. 15.14PCh. 15 - Prob. 15.15PCh. 15 - Prob. 15.16PCh. 15 - Prob. 15.17PCh. 15 - Prob. 15.18PCh. 15 - Prob. 15.19PCh. 15 - Prob. 15.20PCh. 15 - Prob. 15.21PCh. 15 - Prob. 15.22PCh. 15 - Prob. 15.23PCh. 15 - Prob. 15.24PCh. 15 - Prob. 15.25PCh. 15 - Prob. 15.26PCh. 15 - Prob. 15.27PCh. 15 - Prob. 15.28PCh. 15 - Prob. 15.29PCh. 15 - Prob. 15.30PCh. 15 - Prob. 15.31PCh. 15 - Prob. 15.32PCh. 15 - Prob. 15.33PCh. 15 - Prob. 15.34PCh. 15 - Prob. 15.35PCh. 15 - Prob. 15.36PCh. 15 - Prob. 15.37PCh. 15 - Prob. 15.38PCh. 15 - Prob. 15.39PCh. 15 - Prob. 15.40PCh. 15 - Prob. 15.41PCh. 15 - Prob. 15.42PCh. 15 - Prob. 15.43PCh. 15 - Prob. 15.44PCh. 15 - Prob. 15.45PCh. 15 - Prob. 15.46PCh. 15 - Prob. 15.47PCh. 15 - Prob. 15.48PCh. 15 - Prob. 15.49PCh. 15 - Prob. 15.50PCh. 15 - Prob. 15.51PCh. 15 - Prob. 15.52PCh. 15 - Prob. 15.53PCh. 15 - Prob. 15.54PCh. 15 - Prob. 15.55PCh. 15 - Prob. 15.56PCh. 15 - Prob. 15.57PCh. 15 - Prob. 15.58PCh. 15 - Prob. 15.59PCh. 15 - Prob. 15.60PCh. 15 - Prob. 15.61PCh. 15 - Prob. 15.62PCh. 15 - Prob. 15.63PCh. 15 - Prob. 15.64PCh. 15 - Prob. 15.65PCh. 15 - Prob. 15.66PCh. 15 - Prob. 15.67PCh. 15 - Prob. 15.68PCh. 15 - Prob. 15.1YTCh. 15 - Prob. 15.2YTCh. 15 - Prob. 15.3YTCh. 15 - Prob. 15.4YTCh. 15 - Prob. 15.5YTCh. 15 - Prob. 15.6YTCh. 15 - Prob. 15.7YTCh. 15 - Prob. 15.8YTCh. 15 - Prob. 15.9YTCh. 15 - Prob. 15.10YTCh. 15 - Prob. 15.11YTCh. 15 - Prob. 15.12YTCh. 15 - Prob. 15.13YTCh. 15 - Prob. 15.14YTCh. 15 - Prob. 15.15YTCh. 15 - Prob. 15.16YTCh. 15 - Prob. 15.17YTCh. 15 - Prob. 15.18YTCh. 15 - Prob. 15.19YTCh. 15 - Prob. 15.20YTCh. 15 - Prob. 15.21YTCh. 15 - Prob. 15.22YTCh. 15 - Prob. 15.23YTCh. 15 - Prob. 15.24YTCh. 15 - Prob. 15.25YTCh. 15 - Prob. 15.26YTCh. 15 - Prob. 15.27YTCh. 15 - Prob. 15.28YTCh. 15 - Prob. 15.29YTCh. 15 - Prob. 15.30YT
Knowledge Booster
Background pattern image
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Text book image
Fundamentals Of Analytical Chemistry
Chemistry
ISBN:9781285640686
Author:Skoog
Publisher:Cengage