Selected Solutions Manual For General Chemistry: Principles And Modern Applications
11th Edition
ISBN: 9780133387902
Author: Ralph H. Petrucci, F. Geoffrey Herring, Jeffry D. Madura, Carey Bissonnette
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 11, Problem 61IAE
Interpretation Introduction
Interpretation:
The bonding scheme in ethyl cyanoacetate needs to be explained.
Concept introduction:
Ethyl cyanoacetate is a compound by used to synthesis of a large number of the compounds. It is also a flavoring for food and used to synthesize dyes and pharmaceuticals.
- Dyes are water-soluble cationic compound. Uses of dyes = acrylic fibers use to wool and silk, cotton, paper.
- Pharmaceuticals: uses − (1) drugs production two types of drugs generic or medical. The synthesis of dyes and pharmaceuticals has used to molecular orbital theory.
Molecular orbital theory to explain the electronic structure of molecules also used covalent bond theory. When atomic orbital overlap to form sigma and pi bond respectively.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionChapter 11 Solutions
Selected Solutions Manual For General Chemistry: Principles And Modern Applications
Ch. 11 - Prob. 1ECh. 11 - Explain why it is necessary to hybridize atomic...Ch. 11 - Describe the molecular geometry of H2O suggested...Ch. 11 - Describe the molecular geometry of NH2 suggested...Ch. 11 - In which of the following, CO32-,SO2,CCl4,CO,NO3-...Ch. 11 - In the manner of Example 11-1, describe the...Ch. 11 - For each of the following species, identify the...Ch. 11 - Propose a plausible Lewis structure, geometric...Ch. 11 - Describe a hybridization scheme for the central Cl...Ch. 11 - Describe a hybridization scheme for the central S...
Ch. 11 - Match each of the following species with one of...Ch. 11 - Propose a hybridization scheme to account for...Ch. 11 - Indicate which of the following molecules and ions...Ch. 11 - In the manner of Figure 11-18, indicate the...Ch. 11 - Write Lewis structures for the following...Ch. 11 - Represent bonding in the carbon dioxide molecule,...Ch. 11 - Use the method of Figure 11-19 to represent...Ch. 11 - Use the method of Figure 11-19 to represent...Ch. 11 - The molecular model below represents citric acid,...Ch. 11 - Malic is e common organic acid found in unripe...Ch. 11 - Shown below are ball-and-stick models. Describe...Ch. 11 - Shown below are ban-and-stick models. Describe...Ch. 11 - Prob. 23ECh. 11 - The structure of the molecule allene, CH2CCH2 , is...Ch. 11 - Angelic acid, shown below, occurs in symbol root,...Ch. 11 - Dimethylolpropionic acid, shown below, is used in...Ch. 11 - Explain the essential difference in how the...Ch. 11 - Describe the bond order of diatomic carbon, C2 ,...Ch. 11 - Prob. 29ECh. 11 - The paramagnetism of gaseous B2 has been...Ch. 11 - Prob. 31ECh. 11 - Is it correct to say that when a diatomic molecule...Ch. 11 - For the following pairs of molecular orbitals,...Ch. 11 - For each of the species C2+,O2,F2+ , and NO+ ; a....Ch. 11 - Write plausible molecular orbital occupancy...Ch. 11 - We have used the term “isoelectronic” to refer to...Ch. 11 - Consider the molecules NO+ and N2+ and use...Ch. 11 - Consider the molecules CO+ and CN- and use...Ch. 11 - Construct the molecular orbital diagram for CF....Ch. 11 - Construct the molecular orbital diagram for SrCl....Ch. 11 - Explain why the concept of delocalized molecular...Ch. 11 - Explain how it is possible to avoid the concept of...Ch. 11 - In which of the following molecules would you...Ch. 11 - In which of the following ions would you expect to...Ch. 11 - The Lewis structure of N2 indicates that the...Ch. 11 - Show that both the valence bond method and...Ch. 11 - A group of spectroscopists believe that they have...Ch. 11 - Lewis theory is satisfactory to explain bonding in...Ch. 11 - The compound potassium sesquoxide has the...Ch. 11 - Draw a Lewis structure for the urea molecule, CO(...Ch. 11 - Methyl nitrate, CH2NO2 , is used as a rocket...Ch. 11 - Fluorine nitrate, FONO2 , is an oxidizing agent...Ch. 11 - Draw a Lewis structure(s) for the nitrite ion, NO2...Ch. 11 - Think of the reaction shown here as involving the...Ch. 11 - Prob. 55IAECh. 11 - Prob. 56IAECh. 11 - The molecule formamide, HCONH2 , has the...Ch. 11 - Pyridine, C2H2N , is used in the synthesis of...Ch. 11 - Prob. 59IAECh. 11 - The ion F2Cl is linear, but the ion F2Cl+ is bent....Ch. 11 - Prob. 61IAECh. 11 - Prob. 62IAECh. 11 - Prob. 63IAECh. 11 - Prob. 64IAECh. 11 - Histidine, an essential amino acid, serves as a...Ch. 11 - The anion I42 is linear, and the anion I5 is...Ch. 11 - Prob. 67IAECh. 11 - A conjugated hydrocarbon has an alternation of...Ch. 11 - An elusive intermediate of atmospheric reactions...Ch. 11 - Resonance energy is the difference in energy...Ch. 11 - Furan, C4H4O , is a substance derivable from oat...Ch. 11 - As discussed in Are You Wondering 11-1, the sp...Ch. 11 - In Chapter 10, we saw that electronegativity...Ch. 11 - Borazine, B2N2H2 is often referred to as inorganic...Ch. 11 - Which of the following combinations of orbitals...Ch. 11 - Prob. 76FPCh. 11 - Prob. 77SAECh. 11 - Prob. 78SAECh. 11 - Explain the important distinctions between the...Ch. 11 - A molecule in which sp2 hybrid orbitals are used...Ch. 11 - Prob. 81SAECh. 11 - The hybridization scheme for the central atom...Ch. 11 - Of the following, the species with a bond order of...Ch. 11 - The hybridization scheme for Xe in XeF2 is (a) sp;...Ch. 11 - Delocalized molecular orbitals are found in (a)...Ch. 11 - Prob. 86SAECh. 11 - Why does the hybridization sp2d not account for...Ch. 11 - What is the total number of (a) bonds and (b) p...Ch. 11 - Which of the following species are paramagnetic?...Ch. 11 - Use the valence molecular orbital configuration to...Ch. 11 - Use the valence molecular orbital configuration to...Ch. 11 - Which of these diatomic molecules do you think has...Ch. 11 - For each of the following ions or molecules,...Ch. 11 - Draw Lewis structures for the NO2 and NO2+ ions,...Ch. 11 - In which of the following is the central atom sp...Ch. 11 - Prob. 96SAECh. 11 - According to molecular orbital theory, the O22 ion...Ch. 11 - What is the angle between the hybrid orbitals...Ch. 11 - Consider the molecule with the Lewis structure...Ch. 11 - Construct a concept map that embodies the ideas of...Ch. 11 - Prob. 101SAECh. 11 - Construct a concept map that describes the...
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
- The structure of amphetamine, a stimulant, is shown below. (Replacing one H atom on the NH2, or amino, group with CH3 gives methamphetamine a particularly dangerous drug commonly known as speed.) (a) What are the hybrid orbitals used by the C atoms of the C6 ring. by the C atoms of the side chain, and by the N atom? (b) Give approximate values for the bond angles A, B, and C. (c) How many bonds and bonds are in the molerule? (d) Is the molecule polar or nonpolar? (e) Amphetamine reacts readily with a proton (H+) in aqueous solution. Where does this proton attach to the molecule? Explain how the electrostatic potential map predicts this site of protonation.arrow_forwardMinoxidil (C9H15N15O) is a compound produced by the Pharmacia Upjohn Company that has been approved as a treatment for some types of male pattern baldness. Note that in such shorthand ring structures, each point where lines meet is a carbon atom and that the hydrogen atoms bonded to the carbon atoms in the rings have been omitted. There will be four bonds to each carbon atom. a. Give the hybridization of the five nitrogen atoms in minoxidil. b. Give the hybridization of each of the nine carbon atoms in minoxidil. c. Give the approximate values for the bond angles marked a, b, c, d, e, and f. d. Including all the hydrogen atoms, how many bonds exist in minoxidil? e. How many bonds exist in minoxidil?arrow_forwardAcetic acid, the sour constituent of vinegar, has the following structure: Indicate what geometry iiv is expected to be found about each of the atoms labeled a, b, and c.arrow_forward
- What are the bond angles predicted by the VSEPR model about the carbon atom in the formate ion, HCO2? Considering that the bonds to this atom are not identical, would you expect the experimental values to agree precisely with the VSEPR values? How might they differ?arrow_forwardExplain in terms of bonding theory why all four hydrogen atoms of allene, H2CCCH2, cannot lie in the same plane.arrow_forwardAspirin, or acetylsalicylic acid, has the formula C9H8O4 and the skeleton structure (a) Complete the Lewis structure and give the number of bonds and bonds in aspirin. (b) What is the hybridization about the CO2H carbon atom (colored blue)? (c) What is the hybridization about the carbon atom in the benzene-like ring that is bonded to an oxygen atom (colored red)? Also, what is the hybridization of the oxygen atom bonded to this carbon atom?arrow_forward
- A compound of chlorine and fluorine, CIFx, reacts at about 75C with uranium to produce uranium hexafluoride and chlorine fluoride, CIF. A certain amount of uranium produced 5.63 g of uranium hexafluoride and 457 mL of chlorine fluoride at 75C and 3.00 atm. What is x? Describe the geometry, polarity, and bond angles of the compound and the hybridization of chlorine. How many sigma and pi bonds are there?arrow_forwardThe bond length in C2 is 131 pm. Compare this with the bond lengths in C2H2 (120 pm), C2H4 (134 pm), and C2H6 (153 pm). What bond order would you predict for C2 from its bond length? Does this agree with the molecular orbital configuration you would predict for C2?arrow_forwardThe sulfamate ion, H2NSO3, can be thought of as having been formed from the amide ion, NH2, and sulphur trioxide, SO3. (a) What are the electron-pair and molecular geometries or the amide ion and or SO3? What are the hybridizations of the N and S atoms, respectively? (b) Sketch a structure for the sulfamate ion, and estimate the bond angles. (c) What changes in hybridization do you expect for N and S in the course of the reaction NH2 + SO3 H2NSO3? (d) Is SO3 the donor of an electron pair or the acceptor of an electron pair in the reaction with amide ion? Does the electrostatic potential map shown below confirm your prediction?arrow_forward
arrow_back_ios
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningGeneral Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry & 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 LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY