EBK GET READY FOR ORGANIC CHEMISTRY
EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 9780321830555
Author: KARTY
Publisher: VST
bartleby

Videos

Question
Book Icon
Chapter 6, Problem 6.46P
Interpretation Introduction

(a)

Interpretation:

It is to be determined whether the given reactant is suitable for a reaction involving ethanamine (CH3CH2NH2) as a solvent with respect to leveling effect.

Concept introduction:

Leveling effect refers to the effect of a solvent on the properties of acids and bases. For an acid-base reaction, the strength of the strong acid is limited or leveled by the basicity of the solvent. Similarly, the strength of the strong base is leveled by the acidity of the solvent. With respect to the leveling effect, a solvent is unsuitable for a particular reactant R if R is a stronger acid that the solvent’s conjugate acid (i.e., R has the lower pKa) or if R is a stronger base than the solvent’s conjugate base (i.e., the conjugate acid of R has a higher pKa than the solvent).

Expert Solution
Check Mark

Answer to Problem 6.46P

With respect to the leveling effect, ethanamine is a suitable solvent for a reaction involving the chloride ion ClΘ as a reactant.

Explanation of Solution

The reaction of chloride ion ClΘ with ethanamine is shown below:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 6, Problem 6.46P , additional homework tip  1

Hydrochloric acid, HCl (pKa = -7), is a stronger acid than ethanamine, CH3CH2NH2 (pKa = 10.8). The reactant side of the reaction is most favored because the stronger acid, HCl, is on the product side. Chloride ion ClΘ changes the properties of ethanamine. Therefore, ethanamine (CH3CH2NH2) is a suitable solvent for ClΘ because the equilibrium lies to the reactant side.

Conclusion

The solvent effect on the reactant is determined with respect to the leveling effect.

Interpretation Introduction

(b)

Interpretation:

It is to be determined whether the given reactant is suitable for a reaction involving ethanamine (CH3CH2NH2) as a solvent with respect to leveling effect.

Concept introduction:

Leveling effect refers to the effect of a solvent on the properties of acids and bases. For an acid-base reaction, the strength of the strong acid is limited or leveled by the basicity of the solvent. Similarly, the strength of the strong base is leveled by the acidity of the solvent. With respect to the leveling effect, a solvent is unsuitable for a particular reactant R if R is a stronger acid that the solvent’s conjugate acid (i.e., R has the lower pKa) or if R is a stronger base than the solvent’s conjugate base (i.e., the conjugate acid of R has a higher pKa than the solvent).

Expert Solution
Check Mark

Answer to Problem 6.46P

With respect to the leveling effect, ethanamine is a not suitable solvent for a reaction involving HCl as a reactant.

Explanation of Solution

The reaction of HCC:Θ with ethanamine is shown below:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 6, Problem 6.46P , additional homework tip  2

Hydrochloric acid, HCl (pKa = -7), is a stronger acid than ethanamine, CH3CH2NH2 (pKa = 10.8). The product side of the reaction is most favored because the stronger acid, HCl, is on the reactant side. HCl changes the properties of ethanamine. Therefore, ethanamine (CH3CH2NH2) is not a suitable solvent for HCl because the equilibrium lies to the product side.

Conclusion

The solvent effect on the reactant is determined with respect to the leveling effect.

Interpretation Introduction

(c)

Interpretation:

It is to be determined whether the given reactant is suitable for a reaction involving ethanamine (CH3CH2NH2) as a solvent with respect to leveling effect.

Concept introduction:

Leveling effect refers to the effect of a solvent on the properties of acids and bases. For an acid-base reaction, the strength of the strong acid is limited or leveled by the basicity of the solvent. Similarly, the strength of the strong base is leveled by the acidity of the solvent. With respect to the leveling effect, a solvent is unsuitable for a particular reactant R if R is a stronger acid that the solvent’s conjugate acid (i.e., R has the lower pKa) or if R is a stronger base than the solvent’s conjugate base (i.e., the conjugate acid of R has a higher pKa than the solvent).

Expert Solution
Check Mark

Answer to Problem 6.46P

With respect to the leveling effect, ethanamine is not a suitable solvent for a reaction involving H3C:Θ as a reactant.

Explanation of Solution

The reaction of H3C:Θ with ethanamine is shown below:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 6, Problem 6.46P , additional homework tip  3

Ethanamine, CH3CH2NH2 (pKa = 10.8), is a stronger acid than methane, CH4 (pKa = 48). The product side of the reaction is most favored because the stronger acid, CH3CH2NH2, is on the reactant side. H3C:Θ does not change the properties of ethanamine. Therefore, ethanamine (CH3CH2NH2) is not a suitable solvent for H3C:Θ because the equilibrium lies to the product side.

Conclusion

The solvent effect on the reactant is determined with respect to the leveling effect.

Interpretation Introduction

(d)

Interpretation:

It is to be determined whether the given reactant is suitable for a reaction involving ethanamine (CH3CH2NH2) as a solvent with respect to leveling effect.

Concept introduction:

Leveling effect refers to the effect of a solvent on the properties of acids and bases. For an acid-base reaction, the strength of the strong acid is limited or leveled by the basicity of the solvent. Similarly, the strength of the strong base is leveled by the acidity of the solvent. With respect to the leveling effect, a solvent is unsuitable for a particular reactant R if R is a stronger acid that the solvent’s conjugate acid (i.e., R has the lower pKa) or if R is a stronger base than the solvent’s conjugate base (i.e., the conjugate acid of R has a higher pKa than the solvent).

Expert Solution
Check Mark

Answer to Problem 6.46P

With respect to the leveling effect, ethanamine is not a suitable solvent for a reaction involving ΘNH2 as a reactant.

Explanation of Solution

The reaction of ΘNH2 with ethanamine is shown below:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 6, Problem 6.46P , additional homework tip  4

Ethanamine, CH3CH2NH2 (pKa = 10.8), is a stronger acid than ammonia, NH3 (pKa = 36). The product side of the reaction is most favored because the stronger acid, CH3CH2NH2, is on the reactant side. ΘNH2 does not change the properties of ethanamine. Therefore, ethanamine (CH3CH2NH2) is not a suitable solvent for ΘNH2 because the equilibrium lies to the product side.

Conclusion

The solvent effect on the reactant is determined with respect to the leveling effect.

Interpretation Introduction

(e)

Interpretation:

It is to be determined whether the given reactant is suitable for a reaction involving ethanamine (CH3CH2NH2) as a solvent with respect to leveling effect.

Concept introduction:

Leveling effect refers to the effect of a solvent on the properties of acids and bases. For an acid-base reaction, the strength of the strong acid is limited or leveled by the basicity of the solvent. Similarly, the strength of the strong base is leveled by the acidity of the solvent. With respect to the leveling effect, a solvent is unsuitable for a particular reactant R if R is a stronger acid that the solvent’s conjugate acid (i.e., R has the lower pKa) or if R is a stronger base than the solvent’s conjugate base (i.e., the conjugate acid of R has a higher pKa than the solvent).

Expert Solution
Check Mark

Answer to Problem 6.46P

With respect to the leveling effect, ethanamine is not a suitable solvent for a reaction involving NH4 as a reactant.

Explanation of Solution

The reaction of NH4 with ethanamine is shown below:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 6, Problem 6.46P , additional homework tip  5

Ethanamine, CH3CH2NH2 (pKa = 10.8), is a stronger acid than ammonia, NH3 (pKa = 36). The product side of the reaction is most favored because the stronger acid, CH3CH2NH2, is on the reactant side. NH4 does not change the properties of ethanamine. Therefore, ethanamine (CH3CH2NH2) is not a suitable solvent for NH4 because the equilibrium lies to the product side.

Conclusion

The solvent effect on the reactant is determined with respect to the leveling effect.

Interpretation Introduction

(f)

Interpretation:

It is to be determined whether the given reactant is suitable for a reaction involving ethanamine ( ) as a solvent with respect to leveling effect.

Concept introduction:

Leveling effect refers to the effect of a solvent on the properties of acids and bases. For an acid-base reaction, the strength of the strong acid is limited or leveled by the basicity of the solvent. Similarly, the strength of the strong base is leveled by the acidity of the solvent. With respect to the leveling effect, a solvent is unsuitable for a particular reactant R if R is a stronger acid that the solvent’s conjugate acid (i.e., R has the lower pKa) or if R is a stronger base than the solvent’s conjugate base (i.e., the conjugate acid of R has a higher pKa than the solvent).

Expert Solution
Check Mark

Answer to Problem 6.46P

With respect to the leveling effect, ethanamine is not a suitable solvent for a reaction involving ΘOH as a reactant.

Explanation of Solution

The reaction of hydroxide ion ΘOH with ethanamine is shown below:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 6, Problem 6.46P , additional homework tip  6

Ethanamine, CH3CH2NH2 (pKa = 10.8), is a stronger acid than water, H2O (pKa = 15.7). The product side of the reaction is most favored because the stronger acid, CH3CH2NH2, is on the reactant side. ΘOH does not change the properties of ethanamine. Therefore, ethanamine (CH3CH2NH2) is not a suitable solvent for ΘOH because the equilibrium lies to the product side.

Conclusion

The solvent effect on the reactant is determined with respect to the leveling effect.

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
Part VII. Below are the 'HNMR, 13 C-NMR, COSY 2D- NMR, and HSQC 2D-NMR (similar with HETCOR but axes are reversed) spectra of an organic compound with molecular formula C6H1003 - Assign chemical shift values to the H and c atoms of the compound. Find the structure. Show complete solutions. Predicted 1H NMR Spectrum 4.7 4.6 4.5 4.4 4.3 4.2 4.1 4.0 3.9 3.8 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1 f1 (ppm) Predicted 13C NMR Spectrum 100 f1 (ppm) 30 220 210 200 190 180 170 160 150 140 130 120 110 90 80 70 -26 60 50 40 46 30 20 115 10 1.0 0.9 0.8 0 -10
Q: Arrange BCC and Fec metals, in sequence from the Fable (Dr. R's slides) and Calculate Volume and Density. Aa BCC V 52 5 SFCC
None

Chapter 6 Solutions

EBK GET READY FOR ORGANIC CHEMISTRY

Ch. 6 - Prob. 6.11PCh. 6 - Prob. 6.12PCh. 6 - Prob. 6.13PCh. 6 - Prob. 6.14PCh. 6 - Prob. 6.15PCh. 6 - Prob. 6.16PCh. 6 - Prob. 6.17PCh. 6 - Prob. 6.18PCh. 6 - Prob. 6.19PCh. 6 - Prob. 6.20PCh. 6 - Prob. 6.21PCh. 6 - Prob. 6.22PCh. 6 - Prob. 6.23PCh. 6 - Prob. 6.24PCh. 6 - Prob. 6.25PCh. 6 - Prob. 6.26PCh. 6 - Prob. 6.27PCh. 6 - Prob. 6.28PCh. 6 - Prob. 6.29PCh. 6 - Prob. 6.30PCh. 6 - Prob. 6.31PCh. 6 - Prob. 6.32PCh. 6 - Prob. 6.33PCh. 6 - Prob. 6.34PCh. 6 - Prob. 6.35PCh. 6 - Prob. 6.36PCh. 6 - Prob. 6.37PCh. 6 - Prob. 6.38PCh. 6 - Prob. 6.39PCh. 6 - Prob. 6.40PCh. 6 - Prob. 6.41PCh. 6 - Prob. 6.42PCh. 6 - Prob. 6.43PCh. 6 - Prob. 6.44PCh. 6 - Prob. 6.45PCh. 6 - Prob. 6.46PCh. 6 - Prob. 6.47PCh. 6 - Prob. 6.48PCh. 6 - Prob. 6.49PCh. 6 - Prob. 6.50PCh. 6 - Prob. 6.51PCh. 6 - Prob. 6.52PCh. 6 - Prob. 6.53PCh. 6 - Prob. 6.54PCh. 6 - Prob. 6.55PCh. 6 - Prob. 6.56PCh. 6 - Prob. 6.57PCh. 6 - Prob. 6.58PCh. 6 - Prob. 6.59PCh. 6 - Prob. 6.60PCh. 6 - Prob. 6.61PCh. 6 - Prob. 6.62PCh. 6 - Prob. 6.63PCh. 6 - Prob. 6.64PCh. 6 - Prob. 6.65PCh. 6 - Prob. 6.66PCh. 6 - Prob. 6.67PCh. 6 - Prob. 6.68PCh. 6 - Prob. 6.69PCh. 6 - Prob. 6.70PCh. 6 - Prob. 6.71PCh. 6 - Prob. 6.72PCh. 6 - Prob. 6.73PCh. 6 - Prob. 6.74PCh. 6 - Prob. 6.75PCh. 6 - Prob. 6.76PCh. 6 - Prob. 6.77PCh. 6 - Prob. 6.78PCh. 6 - Prob. 6.79PCh. 6 - Prob. 6.80PCh. 6 - Prob. 6.81PCh. 6 - Prob. 6.82PCh. 6 - Prob. 6.83PCh. 6 - Prob. 6.84PCh. 6 - Prob. 6.85PCh. 6 - Prob. 6.86PCh. 6 - Prob. 6.87PCh. 6 - Prob. 6.88PCh. 6 - Prob. 6.1YTCh. 6 - Prob. 6.2YTCh. 6 - Prob. 6.3YTCh. 6 - Prob. 6.4YTCh. 6 - Prob. 6.5YTCh. 6 - Prob. 6.6YTCh. 6 - Prob. 6.7YTCh. 6 - Prob. 6.8YTCh. 6 - Prob. 6.9YTCh. 6 - Prob. 6.10YTCh. 6 - Prob. 6.11YTCh. 6 - Prob. 6.12YTCh. 6 - Prob. 6.13YTCh. 6 - Prob. 6.14YTCh. 6 - Prob. 6.15YTCh. 6 - Prob. 6.16YTCh. 6 - Prob. 6.17YTCh. 6 - Prob. 6.18YTCh. 6 - Prob. 6.19YTCh. 6 - Prob. 6.20YT
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.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Chemistry: Principles and Reactions
    Chemistry
    ISBN:9781305079373
    Author:William L. Masterton, Cecile N. Hurley
    Publisher:Cengage Learning
    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
    Chemistry & Chemical Reactivity
    Chemistry
    ISBN:9781337399074
    Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
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
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Seven Name Reactions in One - Palladium Catalysed Reaction (047 - 053); Author: Rasayan Academy - Jagriti Sharma;https://www.youtube.com/watch?v=5HEKTpDFkqI;License: Standard YouTube License, CC-BY