Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 4.3B, Problem 4.2P
- a. Write the propagation steps leading to the formation of dichloromethane (CH2Cl2) from chloromethane.
- b. Explain why free-radical halogenation usually gives mixtures of products.
- c. How could an industrial plant control the proportions of methane and chlorine to favor production of CCl4? To favor production of CH3Cl?
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
2. Describe the mechanism of hydrocarbon cracking
for production of hydrogen and write the reactions
that takes place during methane cracking for
hydrogen production.
Consider the complete combustion of octane. Calculate the bond energies (in kJ/mol) for the:
Combustion of methane
CH₂(g) +20₂(g) →CO₂(g)+2H₂O(g)
a. bonds broken
b. bonds formed
c. overall reaction
How could an industrial plant control the proportions of methane and chlorine to favor the production of CCl4? To favor the production of CH3Cl?
Chapter 4 Solutions
Organic Chemistry (9th Edition)
Ch. 4.3A - Draw Lewis structures for the following free...Ch. 4.3B - a. Write the propagation steps leading to the...Ch. 4.3C - Prob. 4.3PCh. 4.3C - Prob. 4.4PCh. 4.4 - The following reaction has a value of G =...Ch. 4.4 - Under base-catalyzed conditions two molecules of...Ch. 4.5B - When ethene is mixed with hydrogen in the presence...Ch. 4.5B - For each reaction, estimate whether S for the...Ch. 4.7 - a. Propose a mechanism for the free radical...Ch. 4.7 - a. Using bond-dissociation enthalpies from...
Ch. 4.8 - The reaction of tert-butyl chloride with methanol...Ch. 4.8 - Under certain conditions, the bromination of...Ch. 4.8 - When a small piece of plat num is added to a...Ch. 4.10 - Prob. 4.14PCh. 4.10 - Prob. 4.15PCh. 4.12 - The bromination of methane proceeds through the...Ch. 4.12 - a. Using me BDEs in Table4-2 (page 167 ), compute...Ch. 4.13A - What would be the product ratio in the...Ch. 4.13A - Classify each hydrogen atom in the following...Ch. 4.13B - Use the bond-dissociation enthalpies in Tabte4-2...Ch. 4.13B - Prob. 4.21PCh. 4.13B - Prob. 4.22PCh. 4.14 - a. Compute the heats of reaction for abstraction...Ch. 4.14 - 2,3-Dimethylbutane reacts with bromine in the...Ch. 4.14 - Prob. 4.25PCh. 4.15 - Prob. 4.26PCh. 4.15 - Prob. 4.27PCh. 4.16A - Prob. 4.28PCh. 4.16A - Prob. 4.29PCh. 4.16B - Prob. 4.30PCh. 4.16C - Prob. 4.31PCh. 4.16C - Acetonitrile (CH3C N) is deprotonated by very...Ch. 4.16D - Prob. 4.33PCh. 4 - The following reaction is a common synthesis used...Ch. 4 - Consider the following reaction-energy diagram. a....Ch. 4 - Draw a reaction-energy diagram for a one-step...Ch. 4 - Draw a reaction-energy diagram for a two-step...Ch. 4 - Prob. 4.38SPCh. 4 - Treatment of tert-butyl alcohol with concentrated...Ch. 4 - Label each hydrogen atom in the following...Ch. 4 - Prob. 4.41SPCh. 4 - Prob. 4.42SPCh. 4 - Prob. 4.43SPCh. 4 - Prob. 4.44SPCh. 4 - Prob. 4.45SPCh. 4 - Prob. 4.46SPCh. 4 - For each compound, predict the major product of...Ch. 4 - When exactly 1 mole of methane is mixed with...Ch. 4 - Prob. 4.49SPCh. 4 - Prob. 4.50SPCh. 4 - Prob. 4.51SPCh. 4 - When dichloromethane is treated with strong NaOH,...Ch. 4 - Prob. 4.53SPCh. 4 - When a small amount of iodine is added to a...Ch. 4 - Prob. 4.55SPCh. 4 - When healthy, Earths stratosphere contains a low...Ch. 4 - Prob. 4.57SPCh. 4 - lodination of alkanes using iodine (I2) is usually...
Knowledge Booster
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
- Write the steps for formation of tetrachloromethane (CCl4) from the reaction of methane with Cl2 + hn.arrow_forwardplease answer asaparrow_forwardthe analysis of a mixture of hydrocarbon cracking products, all of which are able to be distilled, but distillation is unable to separate them cleanly. A. a pharmaceutical product containing 2 stereoisomers of the active ingredient, both of which are fairly polar, aromatic, water soluble, and decompose rather than boil. B. C. The separation of a mixture of water-soluble globular proteins of various sizes. The analysis of a mixture of reactor gases that includes methane, hydrogen, carbon dioxide, carbon monoxide, and nitrogen. D.arrow_forward
- Methane is oxidized in the atmosphere by photochemical reaction. Write the chemical equation of this reaction?_CH4 + O2 CH2O + H2OCH4 + O H3C. + H. + O.CH4 + O CH3C. + HO.CH4 + O .CH3 + HO.arrow_forwardComplete and balance the following combustion reactions. Assume that each hydrocarbon is converted completely to carbon dioxide and water. (a) Propane + O2 (b) Octane + O2 (c) Cyclohexane + O2 (d) 2-Methylpentane + O2arrow_forwardWhat is a hydrocarbon? What is the difference between a saturated hydrocarbon and an unsaturated hydrocarbon? Distinguish between normal and branched hydrocarbons. What is an alkane? What is a cyclic alkane? What are the two general formulas for alkanes? What is the hybridization of carbon atoms in alkanes? What are the bond angles in alkanes? Why are cyclopropane and cyclobutane so reactive? The normal (unbranched) hydrocarbons are often referred to as straight-chain hydrocarbons. What does this name refer to? Does it mean that the carbon atoms in a straight-chain hydrocarbon really have a linear arrangement? Explain. In the shorthand notation for cyclic alkanes, the hydrogens are usually omitted. How do you determine the number of hydrogens bonded to each carbon in a ring structure?arrow_forward
- How Isotopes of carbon and hydrogen are used in organic chemistry ?arrow_forwardCombustion requires three primary components: fuel, energy, and an oxidizer. The fuel is the organic starting material and once the activation energy is achieved, large amounts of energy are rapidly released fragmenting reactants into individual atoms. The components quickly rearrange into smaller and more stable molecules. Oxygen serves as an oxidizer, due to its electronegativity, accepting electrons and forming products including water and carbon dioxide. Nitroguanidine (CH4N4O2) is used in select fertilizers and more commonly as a component to propel munitions. Suppose a field artillery soldier was calculating how much nitroguanidine was needed to propel a round. The soldier would need to consider the desired volume of gas to displace along the gun tube and the ambient operating conditions. a. Predict the reaction products for the detonation of 1 mole of nitroguanidine. b. Calculate the amount of explosive needed (in pounds) to produce 1500.0 liters of gas at standard temperature…arrow_forwardSKIP IF YOU ALREADY DID THISarrow_forward
- 3. Like polymers, dendrimers are macromolecules (large molecules). Some dendrimers have been used in applications like drug delivery and waste water reclamation. What is the result of the following reaction producing a "first generation" dendrimer? NH2 H2N. (-HCI) ???? 4 NH2arrow_forward(Picture attached) Functional Groups: 1. Benzene 2. Halogen 3. Carboxyl 4. Hydroxyl Identify the functional groups that the 2 molecules contain. Note: each functional group can be used more than once. Put in numerical order with no space. Sucarlose = Ibuprofen =arrow_forwardUsed widely prior to the end of the 20th Century, chlorofluorocarbons (CFCS for short) were widely used as refrigerants for both industrial and household applications. One CFC, called Freon-11 (fluorotrichloromethane) is an organic compound that has been classified as an ozone depleting substance owing to its propensity to break down via a free radical process. It has a chemical formula of CFCl. Carefully examine the structural diagram of Freon-11 then click on its MOST polar bond. F C. CI CI CI Selected Coordinates Clear «< Question 20 of 29 8 9. 11 delete U 11 K Marrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
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