
Chemistry: Atoms First
2nd Edition
ISBN: 9780073511184
Author: Julia Burdge, Jason Overby Professor
Publisher: McGraw-Hill Education
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 7, Problem 7.22QP
(a) Dipole-dipole interaction
Interpretation Introduction
Interpretation:
For the given set of each type of intermolecular forces have to give examples
Concept introduction:
- When two dipolar molecules interact with each other, through space, there occurs a dipole-dipole interaction.
- While this interaction partially negative charge of the one end of the dipolar molecule will attract the partially positive charge of the other end of the dipolar molecule.
(b) Ion-dipole interaction
Interpretation Introduction
Interpretation:
For the given set of each type of ion-dipole interaction have to give examples
Concept introduction:
- Ion-dipole interaction occurs when there is an electrostatic interaction between charged ion and the polar molecule.
- It is very common between ionic compounds and in polar liquids.
- It becomes stronger when the charge on the ion increases or when the magnitude of the dipole of the polar molecule increases.
- A cation attracts the partially negative end of the polar molecule and anion attracts the partially positive end of the polar molecule.
(c) Dispersion force
Interpretation Introduction
Interpretation:
For the given set of each type dispersion force interaction have to give examples
Concept introduction:
- Electrons in one molecule are always free to move. So at any point they can move disorderly.
- While electrons moving disorderly they can make temporary dipole.
- This temporary dipole in one molecule can induce dipoles to the neighboring molecules, which leaves the molecules with temporary partially positive charge and partially negative charge.
- This attractive force is called as dispersion force or London dispersion force.
- Dispersion force is present between all molecules even in polar molecules.
(d)
Interpretation Introduction
Interpretation:
For the given set of each type van der Waals force have to give examples
Concept introduction:
- The intermolecular forces between the molecules are called as van der Waals force.
- Basically van der Waals force attracts the molecules and holds it close together.
- It exists between separate same molecules but not within the molecule.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Highlight each glycosidic bond in the molecule below. Then answer the questions in the table under the drawing area.
HO-
HO-
-0
OH
OH
HO
NG
HO-
HO-
OH
OH
OH
OH
NG
OH
€
+
Suppose the molecule in the drawing area below were reacted with H₂ over a platinum catalyst. Edit the molecule to show what would happen to it. That is, turn
it into the product of the reaction.
Also, write the name of the product molecule under the drawing area.
Name: ☐
H
C=0
X
H-
OH
HO-
H
HO-
-H
CH₂OH
×
Draw the Haworth projection of the disaccharide made by joining D-glucose and D-mannose with a ẞ(1-4) glycosidic bond. If the disaccharide has more than
one anomer, you can draw any of them.
Click and drag to start drawing a
structure.
X
Chapter 7 Solutions
Chemistry: Atoms First
Ch. 7.1 - Determine the shapes of (a) SO3 and (b) ICl4.Ch. 7.1 - Determine the shapes of (a) CO2 and (b) SCl2.Ch. 7.1 - (a) From what group must the terminal atoms come...Ch. 7.1 - These four models may represent molecules or...Ch. 7.1 - Acetic acid, the substance that gives vinegar its...Ch. 7.1 - Ethanolamine (HOCH2CH2NH2) has a smell similar to...Ch. 7.1 - The bond angle in NH3 is significantly smaller...Ch. 7.1 - Which of these models represents a species in...Ch. 7.1 - Prob. 7.1.1SRCh. 7.1 - Prob. 7.1.2SR
Ch. 7.1 - Prob. 7.1.3SRCh. 7.1 - Prob. 7.1.4SRCh. 7.2 - Prob. 7.3WECh. 7.2 - Prob. 3PPACh. 7.2 - For each of the following hypothetical molecules,...Ch. 7.2 - Which of these models could represent a polar...Ch. 7.2 - Prob. 7.2.1SRCh. 7.2 - Prob. 7.2.2SRCh. 7.3 - Prob. 7.4WECh. 7.3 - Prob. 4PPACh. 7.3 - Prob. 4PPBCh. 7.3 - Prob. 4PPCCh. 7.3 - Prob. 7.3.1SRCh. 7.3 - Prob. 7.3.2SRCh. 7.4 - Hydrogen selenide (H2Se) is a foul-smelling gas...Ch. 7.4 - Prob. 5PPACh. 7.4 - For which molecule(s) can we not use valence bond...Ch. 7.4 - Which of these models could represent a species...Ch. 7.4 - Prob. 7.4.1SRCh. 7.4 - Prob. 7.4.2SRCh. 7.5 - Prob. 7.6WECh. 7.5 - Use hybrid orbital theory to describe the bonding...Ch. 7.5 - Prob. 6PPBCh. 7.5 - Prob. 6PPCCh. 7.5 - Prob. 7.5.1SRCh. 7.5 - Prob. 7.5.2SRCh. 7.6 - Thalidomide (C13H10N2O4) is a sedative and...Ch. 7.6 - The active ingredient in Tylenol and a host of...Ch. 7.6 - Determine the total number of sigma and pi bonds...Ch. 7.6 - In terms of valence bond theory and hybrid...Ch. 7.6 - In addition to its rise in aqueous solution as a...Ch. 7.6 - Use valence bond theory and hybrid orbitals to...Ch. 7.6 - Use valence bond theory and hybrid orbitals to...Ch. 7.6 - Explain why hybrid orbitals are necessary to...Ch. 7.6 - Prob. 7.6.1SRCh. 7.6 - Prob. 7.6.2SRCh. 7.6 - Prob. 7.6.3SRCh. 7.6 - Prob. 7.6.4SRCh. 7.7 - Prob. 7.9WECh. 7.7 - Use molecular orbital theory to determine whether...Ch. 7.7 - Use molecular orbital theory to determine whether...Ch. 7.7 - For most of the homonuclear diatomic species shown...Ch. 7.7 - Prob. 7.7.1SRCh. 7.7 - Prob. 7.7.2SRCh. 7.7 - Prob. 7.7.3SRCh. 7.7 - Prob. 7.7.4SRCh. 7.8 - It takes three resonance structures to represent...Ch. 7.8 - Use a combination of valence bond theory and...Ch. 7.8 - Use a combination of valence bond theory and...Ch. 7.8 - Prob. 10PPCCh. 7.8 - Prob. 7.8.1SRCh. 7.8 - Prob. 7.8.2SRCh. 7.8 - Prob. 7.8.3SRCh. 7.8 - Prob. 7.8.4SRCh. 7 - Prob. 7.1QPCh. 7 - Sketch the shape of a linear triatomic molecule, a...Ch. 7 - Prob. 7.3QPCh. 7 - Prob. 7.4QPCh. 7 - In the trigonal bipyramidal arrangement, why does...Ch. 7 - Prob. 7.6QPCh. 7 - Predict the geometry of the following molecules...Ch. 7 - Prob. 7.8QPCh. 7 - Predict the geometries of the following species...Ch. 7 - Predict the geometries of the following ions: (a)...Ch. 7 - Prob. 7.11QPCh. 7 - Prob. 7.12QPCh. 7 - Prob. 7.13QPCh. 7 - Describe the geometry about each of the central...Ch. 7 - Prob. 7.15QPCh. 7 - Prob. 7.16QPCh. 7 - Prob. 7.17QPCh. 7 - Prob. 7.18QPCh. 7 - Prob. 7.19QPCh. 7 - Prob. 7.20QPCh. 7 - Prob. 7.21QPCh. 7 - Prob. 7.22QPCh. 7 - Explain the term polarizability. What kind of...Ch. 7 - Prob. 7.24QPCh. 7 - What physical properties are determined by the...Ch. 7 - Prob. 7.26QPCh. 7 - Describe the types of intermolecular forces that...Ch. 7 - The compounds Br2 and ICl are isoelectronic (have...Ch. 7 - If you lived in Alaska, which of the following...Ch. 7 - The binary hydrogen compounds of the Group 4A...Ch. 7 - List the types of intermolecular forces that exist...Ch. 7 - Prob. 7.32QPCh. 7 - Prob. 7.33QPCh. 7 - Prob. 7.34QPCh. 7 - Diethyl ether has a boiling point of 34.5C, and...Ch. 7 - Prob. 7.36QPCh. 7 - Which substance in each of the following pairs...Ch. 7 - Prob. 7.38QPCh. 7 - What kind of attractive forces must be overcome to...Ch. 7 - Prob. 7.40QPCh. 7 - Prob. 7.41QPCh. 7 - The following compounds have the same molecular...Ch. 7 - Prob. 7.43QPCh. 7 - Prob. 7.44QPCh. 7 - Use valence bond theory to explain the bonding in...Ch. 7 - Prob. 7.46QPCh. 7 - Prob. 7.47QPCh. 7 - Prob. 7.48QPCh. 7 - Prob. 7.49QPCh. 7 - What is the hybridization of atomic orbitals? Why...Ch. 7 - Prob. 7.51QPCh. 7 - Prob. 7.52QPCh. 7 - Prob. 7.53QPCh. 7 - Describe the bonding scheme of the AsH3 molecule...Ch. 7 - Prob. 7.55QPCh. 7 - Prob. 7.56QPCh. 7 - Describe the hybridization of phosphorus in PF5.Ch. 7 - Prob. 7.58QPCh. 7 - Prob. 7.59QPCh. 7 - Prob. 7.1VCCh. 7 - Prob. 7.2VCCh. 7 - Prob. 7.3VCCh. 7 - Prob. 7.4VCCh. 7 - Prob. 7.60QPCh. 7 - Which of the following pairs of atomic orbitals of...Ch. 7 - Prob. 7.62QPCh. 7 - Prob. 7.63QPCh. 7 - Prob. 7.64QPCh. 7 - Prob. 7.65QPCh. 7 - Prob. 7.66QPCh. 7 - Prob. 7.67QPCh. 7 - Prob. 7.68QPCh. 7 - Benzo[a]pyrene is a potent carcinogen found in...Ch. 7 - What is molecular orbital theory? How does it...Ch. 7 - Define the following terms: bonding molecular...Ch. 7 - Prob. 7.72QPCh. 7 - Prob. 7.73QPCh. 7 - Prob. 7.74QPCh. 7 - Prob. 7.75QPCh. 7 - Draw a molecular orbital energy level diagram for...Ch. 7 - Prob. 7.77QPCh. 7 - Prob. 7.78QPCh. 7 - Prob. 7.79QPCh. 7 - Acetylene (C2H2) has a tendency to lose two...Ch. 7 - Compare the Lewis and molecular orbital treatments...Ch. 7 - Prob. 7.82QPCh. 7 - Prob. 7.83QPCh. 7 - Prob. 7.84QPCh. 7 - Prob. 7.85QPCh. 7 - Draw the molecular orbital diagram for the cyanide...Ch. 7 - Given that BeO is diamagnetic, use a molecular...Ch. 7 - Prob. 7.88QPCh. 7 - Prob. 7.89QPCh. 7 - Both ethylene (C2H4) and benzene (C6H6) contain...Ch. 7 - Chemists often represent benzene with the...Ch. 7 - Determine which of these molecules has a more...Ch. 7 - Nitryl fluoride (FNO2) is used in rocket...Ch. 7 - Describe the bonding in the nitrate ion NO3 in...Ch. 7 - Prob. 7.95QPCh. 7 - Prob. 7.96QPCh. 7 - Prob. 7.97QPCh. 7 - Prob. 7.98QPCh. 7 - Prob. 7.99QPCh. 7 - Antimony pentafluoride (SbF5) combines with XeF4...Ch. 7 - Prob. 7.101QPCh. 7 - The molecular model of nicotine (a stimulant) is...Ch. 7 - Predict the bond angles for the following...Ch. 7 - The germanium pentafluoride anion (GeF5) has been...Ch. 7 - Draw Lewis structures and give the other...Ch. 7 - Which figure best illustrates the hybridization of...Ch. 7 - Prob. 7.107QPCh. 7 - Prob. 7.108QPCh. 7 - Prob. 7.109QPCh. 7 - Prob. 7.110QPCh. 7 - Prob. 7.111QPCh. 7 - Cyclopropane (C3H6) has the shape of a triangle in...Ch. 7 - The compound 1,2-dichloroethane (C2H4Cl2) is...Ch. 7 - Prob. 7.114QPCh. 7 - Prob. 7.115QPCh. 7 - Prob. 7.116QPCh. 7 - Prob. 7.117QPCh. 7 - Prob. 7.118QPCh. 7 - The amino acid selenocysteine is one of the...Ch. 7 - Prob. 7.120QPCh. 7 - Prob. 7.121QPCh. 7 - Prob. 7.122QPCh. 7 - Gaseous or highly volatile liquid anesthetics are...Ch. 7 - Prob. 7.124QPCh. 7 - Prob. 7.125QPCh. 7 - Two of the drugs that are prescribed for the...Ch. 7 - Prob. 7.127QPCh. 7 - Prob. 7.128QPCh. 7 - The BO+ ion is paramagnetic. Determine (a) whether...Ch. 7 - Use molecular orbital theory to explain the...Ch. 7 - Which best illustrates the change in geometry...Ch. 7 - Prob. 7.132QPCh. 7 - Prob. 7.133QPCh. 7 - Aluminum trichloride (AlCl3) is an...Ch. 7 - Prob. 7.135QPCh. 7 - Prob. 7.136QPCh. 7 - Prob. 7.137QPCh. 7 - Consider an N2 molecule in its first excited...Ch. 7 - The Lewis structure for O2 is Use molecular...Ch. 7 - Draw the Lewis structure of ketene (C2H2O) and...Ch. 7 - The compound TCDD, or...Ch. 7 - Name the kinds of attractive forces that must be...Ch. 7 - Carbon monoxide (CO) is a poisonous compound due...Ch. 7 - Prob. 7.144QPCh. 7 - Prob. 7.145QPCh. 7 - Prob. 7.146QPCh. 7 - Prob. 7.147QPCh. 7 - Prob. 7.148QPCh. 7 - Prob. 7.1KSPCh. 7 - Which of the following species does not have...Ch. 7 - Prob. 7.3KSPCh. 7 - Prob. 7.4KSP
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
- Epoxides can be opened in aqueous acid or aqueous base to produce diols (molecules with two OH groups). In this question, you'll explore the mechanism of epoxide opening in aqueous acid. 2nd attempt Be sure to show all four bonds at stereocenters using hash and wedge lines. 0 0 Draw curved arrows to show how the epoxide reacts with hydronium ion. 100 +1: 1st attempt Feedback Be sure to show all four bonds at stereocenters using hash and wedge lines. See Periodic Table See Hint H A 5 F F Hr See Periodic Table See Hintarrow_forward03 Question (1 point) For the reaction below, draw both of the major organic products. Be sure to consider stereochemistry. > 1. CH₂CH₂MgBr 2. H₂O 3rd attempt Draw all four bonds at chiral centers. Draw all stereoisomers formed. Draw the structures here. e 130 AN H See Periodic Table See Hint P C Brarrow_forwardYou may wish to address the following issues in your response if they are pertinent to the reaction(s) you propose to employ:1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Please make it in detail and draw it out too in what step what happens. Thank you for helping me!arrow_forward
- 1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Everything in detail and draw out and write it.arrow_forwardCalculating the pH at equivalence of a titration 3/5 Izabella A chemist titrates 120.0 mL of a 0.7191M dimethylamine ((CH3)2NH) solution with 0.5501 M HBr solution at 25 °C. Calculate the pH at equivalence. The pk of dimethylamine is 3.27. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of HBr solution added. pH = ☐ ✓ 18 Ar Boarrow_forwardAlcohols can be synthesized using an acid-catalyzed hydration of an alkene. An alkene is combined with aqueous acid (e.. sulfuric acid in water). The reaction mechanism typically involves a carbocation intermediate. > 3rd attempt 3343 10 8 Draw arrows to show the reaction between the alkene and hydronium ion. that 2nd attempt Feedback 1st attempt تعمال Ju See Periodic Table See Hint F D Ju See Periodic Table See Hintarrow_forward
- Draw the simplified curved arrow mechanism for the reaction of acetone and CHgLi to give the major product. 4th attempt Π Draw the simplified curved arrow mechanism T 3rd attempt Feedback Ju See Periodic Table See Hint H -H H -I H F See Periodic Table See Hintarrow_forwardSelect the correct reagent to accomplish the first step of this reaction. Then draw a mechanism on the Grignard reagent using curved arrow notation to show how it is converted to the final product. 4th attempt Part 1 (0.5 point) Select the correct reagent to accomplish the first step of this reaction. Choose one: OA Mg in ethanol (EtOH) OB. 2 Li in THF O C. Li in THF D. Mg in THF O E Mg in H2O Part 2 (0.5 point) Br Part 1 Bri Mg CH B CH, 1 Draw intermediate here, but no arrows. © TE See Periodic Table See Hint See Hint ין Harrow_forwardSelect the product for the following reaction. HO HO PCC OH ○ OH O HO ○ HO HO HOarrow_forward
- 5:45 Х Select the final product for the following reaction sequence. O O 1. Mg. ether 2.D.Oarrow_forwardBased on the chart Two similarities between the molecule with alpha glycosidic linkages. Two similarities between the molecules with beta glycosidtic linkages. Two differences between the alpha and beta glycosidic linkages.arrow_forwardplease help fill in the tablearrow_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 LearningPhysical ChemistryChemistryISBN:9781133958437Author:Ball, David W. (david Warren), BAER, TomasPublisher:Wadsworth Cengage Learning,Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Introductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. 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

Physical Chemistry
Chemistry
ISBN:9781133958437
Author:Ball, David W. (david Warren), BAER, Tomas
Publisher:Wadsworth Cengage Learning,

Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning

Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. 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
Types of bonds; Author: Edspira;https://www.youtube.com/watch?v=Jj0V01Arebk;License: Standard YouTube License, CC-BY