Organic Chemistry
9th Edition
ISBN: 9781305080485
Author: John E. McMurry
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 2.SE, Problem 22VC
cis-l, 2-Dichloroethylene and trans-1, 2-dichloroethylene are isomers, compounds with the same formula but different chemical structures. Look at the following electrostatic potential maps, and tell whether either compound has a dipole moment.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
Draw the Lewis structure of chlorine pentafluoride. Identify BOTH its electron pair and molecular geometries. If an overall dipole moment is present, draw the arrow.
Illustrate the Electrostatic potential plot of ethylene ?
2) Explain (use resonance structures) why this molecule has a measurable dipole
moment.
Chapter 2 Solutions
Organic Chemistry
Ch. 2.1 - Prob. 1PCh. 2.1 - Prob. 2PCh. 2.1 - Use the electronegativity values shown in Figure...Ch. 2.1 - Look at the following electrostatic potential map...Ch. 2.2 - Ethylene glycol, HOCH2CH2OH, may look nonpolar...Ch. 2.2 - Make three-dimensional drawings of the following...Ch. 2.3 - Calculate formal charges for the nonhydrogen atoms...Ch. 2.3 - Organic phosphate groups occur commonly in...Ch. 2.6 - Which of the following pairs of structures...Ch. 2.6 - Draw the indicated number of resonance forms for...
Ch. 2.7 - Nitric acid (HNO3) reacts with ammonia (NH3) to...Ch. 2.8 - Prob. 12PCh. 2.8 - Amide ion, H2N-, is a much stronger base than...Ch. 2.9 - Prob. 14PCh. 2.9 - Prob. 15PCh. 2.9 - Prob. 16PCh. 2.11 - Using curved arrows, show how the species in part...Ch. 2.11 - Prob. 18PCh. 2.12 - Of the two vitamins A and C, one is hydrophilic...Ch. 2.SE - Prob. 20VCCh. 2.SE - The following model is a representation of...Ch. 2.SE - cis-l, 2-Dichloroethylene and trans-1,...Ch. 2.SE - The following molecular models are representations...Ch. 2.SE - Predict the product(s) of the acid/base reactions...Ch. 2.SE - Use curved arrows to draw the protonated form of...Ch. 2.SE - Prob. 26MPCh. 2.SE - Double bonds can also act like Lewis bases,...Ch. 2.SE - Prob. 28APCh. 2.SE - Use the electronegativity table given in Figure...Ch. 2.SE - Which of the following molecules has a dipole...Ch. 2.SE - Prob. 31APCh. 2.SE - Phosgene, C12C=O, has a smaller dipole moment than...Ch. 2.SE - Prob. 33APCh. 2.SE - Methanethiol, CH3SH, has a substantial dipole...Ch. 2.SE - Calculate the formal charges on the atoms shown in...Ch. 2.SE - Assign formal charges to the atoms in each of the...Ch. 2.SE - Which of the following pairs of structures...Ch. 2.SE - Prob. 38APCh. 2.SE - 1, 3-Cyclobutadiene is a rectangular molecule with...Ch. 2.SE - Alcohols can act either as weak acids or as weak...Ch. 2.SE - The O-H hydrogen in acetic acid is more acidic...Ch. 2.SE - Draw electron-dot structures for the following...Ch. 2.SE - Write the products of the following acid-base...Ch. 2.SE - Rank the following substances in order of...Ch. 2.SE - Which, if any, of the substances in Problem 2-44...Ch. 2.SE - The ammonium ion (NH4+, pKa = 9.25) has a lower...Ch. 2.SE - Prob. 47APCh. 2.SE - Prob. 48APCh. 2.SE - Calculate Ka values from the following pka’s:...Ch. 2.SE - Calculate pKa values from the following Ka’s:...Ch. 2.SE - What is the pH of a 0.050 M solution of formic...Ch. 2.SE - Prob. 52APCh. 2.SE - Maleic acid has a dipole moment, but the closely...Ch. 2.SE - Assume that you have two unlabeled bottles, one of...Ch. 2.SE - Identify the acids and bases in the following...Ch. 2.SE - Which of the following pairs represent resonance...Ch. 2.SE - Draw as many resonance structures as you can for...Ch. 2.SE - Carbocations, which contain a trivalent,...Ch. 2.SE - We’ll see in the next chapter that organic...Ch. 2.SE - The azide functional group, which occurs in...Ch. 2.SE - Phenol, C6H5OH, is a stronger acid than methanol,...Ch. 2.SE - Thiamin diphosphate (TPP), a derivative of vitamin...Ch. 2.SE - Determine if each compound or ion below has a...Ch. 2.SE - Prob. 64APCh. 2.SE - Prob. 65APCh. 2.SE - Draw the conjugate base for each compound below...Ch. 2.SE - 1, 1, 1-Trichloroethanol is an acid more than 1000...
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
- Consider the molecule of furan. Its Lewis structure is shown. H X Is furan polar? If yes, consider which side of the molecule has partial negative charge and which - partial positive. Then, indicate the direction of the dipole moment relative to the molecule as shown. Non-polar, zero dipole moment. Polar, the dipole vector points along one of the C-O bonds. Polar, the dipole vector points along one of the C-H bonds. Polar, the dipole vector points along the vertical axis. Polar, the dipole vector points along the horizontal axis.arrow_forward(a) How does a polar molecule differ from a nonpolar one? (b) Atoms X and Y have different electronegativities. Will the diatomic molecule X—Y necessarily be polar? Explain. (c) What factors affect the size of the dipole moment of a diatomic molecule?arrow_forwardDraw the Lewis dot structure of the conjugate base of cyclopentane by assuming all the atoms in the molecule obey the octet rule. Show all lone pairs and formal charges. Do no draw resonance structures.arrow_forward
- Chlorine monofluoride, ClF, and iodine monofluoride, IF, are interhalogencompounds—compounds that contain bonds between different halogen elements.Which of these molecules has the larger dipole moment?arrow_forwardDoes COS have a dipole moment? Explain.arrow_forwarda) Determine the shape around each of the central atoms in acetone (CH,),C=O by writing its Lewis structure. Show the bond angles and find the electron group arrangement of each central atom. (Explanation should be made in detail)arrow_forward
- Draw the Lewis Structures for boron trifluoride (BF3), phosphorous trichloride (PCI3), oxygen difluroide (OF2), nitrogen trichloride (NCI3) and meth (CH4). Which do you expect to be the most polar? (Hint: which will have the greatest molecular dipole?) O boron trifluoride O phosphorous trichloride O methane O oxygen difluroide O nitrogen trichloridearrow_forward) Bean hexene is an odor compound used in cosmetics and cleaners. It is also known as leguminal. Its formula is: CH3CH2CHCHCH2CH2OCHCH2CH3 | OCH3 Please draw a Lewis structure for this compound with CORRECT GEOMETRY (use dashes and wedges!) Label all pi bonds in the molecule (if there are any) Indicate the bond angles for the red highlighted section of the molecule. (hint: you may want to keep the main carbon chain in-plane with the page for clarity) For this question, you don’t need to draw out the orbitals.arrow_forwardwhich of the following statement is not true? 1)Nitrogen s relative inertness is due to formation of strong and stable bond between 2 nitrogens atom. 2)the bond energy of N2 is relatively higher that makes it relatively inert. 3)the bond energy of an O-H bond is always the same in all compounds that contain an O-H bond 4)carbon-carbon single bond is the longest among all sorts of carbon-carbon bonds 5)a shorter bond in general ,is a stronger bond than a longer bondarrow_forward
- Propylene, C3H6, is a gas that is used to form the importantpolymer called polypropylene. Its Lewis structure is given. (a) What is the total number of valence electrons in the propylenemolecule? (b) How many valence electrons are usedto make σ bonds in the molecule? (c) How many valenceelectrons are used to make π bonds in the molecule? (d) Howmany valence electrons remain in nonbonding pairs in themolecule? (e) What is the hybridization at each carbon atomin the molecule?arrow_forwardVarious forces of attraction are encountered in strontium and in ammonium chloride. Identify the forces present in: Strontium Ammonium Chloride Hence, complete the table below giving the shapes and bond angles of the species given.arrow_forwardA resonance hybrid is a structure that can be depicted by more than one valid Lewis structure. part1: Draw the major resonance form of fulminic acid, HCNO, with the atoms connected as indicated in the formula. Your structure should have nonzero formal charges minimized, and it should include all nonzero formal charges and all nonbonding electrons. part2: Draw the second most important resonance form of fulminic acid, HCNO, with the atoms connected as indicated in the formula. Your structure should have nonzero formal charges minimized, and it should include all nonzero formal charges and all nonbonding electrons. part3: Draw the least important resonance contributor for fulminic acid, HCNO, with the atoms connected as indicated in the formula. Your structure should have nonzero formal charges minimized and should include all nonzero formal charges and all nonbonding electrons.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
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
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
INTRODUCTION TO MOLECULAR QUANTUM MECHANICS -Valence bond theory - 1; Author: AGK Chemistry;https://www.youtube.com/watch?v=U8kPBPqDIwM;License: Standard YouTube License, CC-BY