
Interpretation:
The type of intermolecular forces that can exist when water,
Concept Introduction:
There are three major types of intermolecular forces:
London dispersion force also called an induced dipole-induced dipole attraction is a temporary attractive force that results when the electrons in two adjacent atoms occupy positions that make the atoms form temporary dipoles.
Dipole-dipole interaction results when two dipolar molecules interact with each other through space, there occurs a partially negative charge of one of the polar molecules is attracted to the partially positive charge of the second polar molecule.
Ion-dipole interaction results of an electrostatic interaction between a charged ion and a molecule that has a dipole. It is an attractive force that is commonly found in solutions, especially ionic compounds dissolved in polar liquids.

Trending nowThis is a popular solution!

Chapter 11 Solutions
Chemistry & Chemical Reactivity
- Answer by equation pleasearrow_forwardSome of the theories used to describe interface structure can be distinguished by:1. the measured potential difference.2. the distribution of ions in solution.3. the calculation of charge density.4. the external Helmoltz plane.arrow_forwardWhen talking about the acidity of carboxylic acids, is it the same thing to say higher or stronger acidity?arrow_forward
- Using the following two half-reactions, determine the pH range in which $NO_2^-\ (aq)$ cannot be found as the predominant chemical species in water.* $NO_3^-(aq)+10H^+(aq)+8e^-\rightarrow NH_4^+(aq)+3H_2O(l),\ pE^{\circ}=14.88$* $NO_2^-(aq)+8H^+(aq)+6e^-\rightarrow NH_4^+(aq)+2H_2O(l),\ pE^{\circ}=15.08$arrow_forwardIndicate characteristics of oxodec acid.arrow_forwardWhat is the final product when hexanedioic acid reacts with 1º PCl5 and 2º NH3.arrow_forward
- What is the final product when D-galactose reacts with hydroxylamine?arrow_forwardIndicate the formula of the product obtained by reacting methyl 5-chloro-5-oxopentanoate with 1 mole of 4-penten-1-ylmagnesium bromide.arrow_forwardIn the two chair conformations of glucose, the most stable is the one with all the OH groups in the equatorial position. Is this correct?arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
- World of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College DivChemistry & 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





