Interpretation:
The mechanism of the radical halogenation of ethane, including the initiation step, propagation steps, and three termination steps is to be drawn.
Concept introduction:
Halogen molecules undergo homolysis when irradiated with UV light to produce two radical atoms. Homolysis is the type of bond dissociation where each atom gets one of the bond electrons. The radical is an molecule or atom with an unpaired electron. It is highly highly reactive and unstable species. This homolytic dissociation is called initiation.
Being reactive, a radical will react with other species present. This produces another radical, which can continue the reaction is a step called propagation. The reaction is generally branched as each initiation step produces two radicals. The propagation steps continue as long as radicals are present, and may be terminated by a reaction between two radicals.
The reaction generally results in substitution, often of a hydrogen atom from the hydrocarbon skeleton. When there are distinct types of hydrogen atoms in the reactant, the hydrogen removed is one that will lead to the formation of the most stable radical. The relative stability of radicals changes in the same was as the stability of carbocation. This decides the major product of the reaction.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 25 Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
- Write the equilibrium constant expression for the following system at equilibrium: I2 (g) ⇌ 2 I (g)arrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardWe learned four factors (ARIO) for comparing the relative acidity of compounds. When two of these factors are in competition, the order of priority is the order in which these factors were covered ("atom" being the most important factor and "orbital" being the least important). However, we also mentioned that there are exceptions to this order of priority. Compare the two compounds and identify the exception. OH PK-4.75 SH PK-10.6 5. "Resonance" is more important than "atom" because the conjugate base of first compound is more stable than the second. "Atom" is more important than "resonance" because the conjugate base of first compound is more stable than the second. "Resonance" is more important than "atom" because the conjugate base of second compound is more stable than the first. "Atom" is more important than "resonance" because the conjugate base of second compound is more stable than the first.arrow_forward
- The relative fitnesses of three genotypes are WA/A= 1.0, WA/a = 0.7, and Wa/a = 0.3. If the population starts at the allele frequency p = 0.5, what is the value of p in the next generation? (3 pts) 12pt v Paragraph V BIU ALarrow_forwardIdentify the most acidic proton in the compound: a d b Оа Ob Ос ○ darrow_forwardA Standard Reference Material is certified to contain 94.6 ppm of an organic contaminant in soil. Your analysis gives values of 98.6, 98.4, 97.2, 94.6, and 96.2. Do your results differ from the expected results at the 95% confidence interval?arrow_forward
- The percentage of an additive in gasoline was measured six times with the following results: 0.13, 0.12, 0.16, 0.17, 0.20, and 0.11%. Find the 95% confidence interval for the percentage of additive.arrow_forwardExplain why this data led Rayleigh to look for and to discover Ar.arrow_forward5) Confidence interval. Berglund and Wichardt investigated the quantitative determination of Cr in high-alloy steels using a potentiometric titration of Cr(VI). Before the titration, samples of the steel were dissolved in acid and the chromium oxidized to Cr(VI) using peroxydisulfate. Shown here are the results (as %w/w Cr) for the analysis of a reference steel. 16.968, 16.922, 16.840, 16.883, 16.887, 16.977, 16.857, 16.728 Calculate the mean, the standard deviation, and the 95% confidence interval about the mean. What does this confidence interval mean?arrow_forward
- In the Nitrous Acid Test for Amines, what is the observable result for primary amines? Group of answer choices nitrogen gas bubbles form a soluble nitrite salt yellow oily layer of nitrosoaminearrow_forward3. a. Use the MS to propose at least two possible molecular formulas. For an unknown compound: 101. 27.0 29.0 41.0 50.0 52.0 55.0 57.0 100 57.5 58.0 58.5 62.0 63.0 64.0 65.0 74.0 40 75.0 76.0 20 20 40 60 80 100 120 140 160 180 200 220 m/z 99.5 68564810898409581251883040 115.0 116.0 77404799 17417M 117.0 12.9 118.0 33.5 119.0 36 133 0 1.2 157.0 2.1 159.0 16 169.0 219 170.0 17 171.0 21.6 172.0 17 181.0 1.3 183.0 197.0 100.0 198.0 200. 784 Relative Intensity 2 2 8 ō (ppm) 6 2arrow_forwardSolve the structure and assign each of the following spectra (IR and C-NMR)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)