Chemistry & Chemical Reactivity
Chemistry & Chemical Reactivity
9th Edition
ISBN: 9781305176461
Author: Kotz
Publisher: Cengage
Question
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Chapter 11, Problem 51SCQ

(a)

Interpretation Introduction

Interpretation:

Among the given hydrogen halide, the one with largest  total intermolecular forces has to be identified.

Concept Introduction:

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.

A hydrogen bonding is partially an electrostatic attraction between H atom which is bonded to more electronegative atom such as N, O, orF and another adjacent atom bearing a lone pair of electron

(b)

Interpretation Introduction

Interpretation:

Reason for the dispersion forces greater for HI than HCl has to be identified.

Concept Introduction:

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.

A hydrogen bonding is partially an electrostatic attraction between H atom which is bonded to more electronegative atom such as N, O, orF and another adjacent atom bearing a lone pair of electron

(c)

Interpretation Introduction

Interpretation:

Reason for dipole-dipole forces greater for HCl than for HI has to be identified.

Concept Introduction:

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.

A hydrogen bonding is partially an electrostatic attraction between H atom which is bonded to more electronegative atom such as N, O, orF and another adjacent atom bearing a lone pair of electron

(d)

Interpretation Introduction

Interpretation:

Hydrogen halide that has largest dispersion forces has to be identified.

Concept Introduction:

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.

A hydrogen bonding is partially an electrostatic attraction between H atom which is bonded to more electronegative atom such as N, O, orF and another adjacent atom bearing a lone pair of electron

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2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled** Peak Chemical Shift (d) 5.7 1 Multiplicity multiplate .......... 5.04 double of doublet 2 4.98 double of doublet 3 4.05 doublet of quartet 4 5 LO 3.80 quartet 1.3 doublet 6 Peak Chemical Shift (d) Multiplicity
Interpreting NMR spectra is a skill that often requires some amount of practice, which, in turn, necessitates access to a collection of NMR spectra. Beyond Labz Organic Synthesis and Organic Qualitative Analysis have spectral libraries containing over 700 1H NMR spectra. In this assignment, you will take advantage of this by first predicting the NMR spectra for two closely related compounds and then checking your predictions by looking up the actual spectra in the spectra library. After completing this assignment, you may wish to select other compounds for additional practice. 1. Write the IUPAC names for the following two structures: Question 2 Question 3 2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled**
11:14 ... worksheets.beyondlabz.com 3. To check your predictions, click this link for Interpreting NMR Spectra 1. You will see a list of all the - compounds in the spectra library in alphabetical order by IUPAC name. Hovering over a name in the list will show the structure on the chalkboard. The four buttons on the top of the Spectra tab in the tray are used to select the different spectroscopic techniques for the selected compound. Make sure the NMR button has been selected. 4. Scroll through the list of names to find the names for the two compounds you have been given and click on the name to display the NMR spectrum for each. In the NMR tables below, list the chemical shift, the splitting, and the number of hydrogens associated with each peak for each compound. Compare your answers to your predictions. **Not all slots must be filled** Peak Chemical Shift (d) Multiplicity 1 2 3 4 5

Chapter 11 Solutions

Chemistry & Chemical Reactivity

Ch. 11.6 - The molar enthalpy of vaporization of methanol,...Ch. 11.6 - Prob. 2CYUCh. 11.6 - Prob. 1RCCh. 11.6 - Prob. 2RCCh. 11.6 - Prob. 3RCCh. 11.6 - Prob. 1QCh. 11.6 - Prob. 2QCh. 11.A - Prob. 1QCh. 11.A - Prob. 2QCh. 11 - Prob. 1PSCh. 11 - Intermolecular forces: What type of forces must be...Ch. 11 - Prob. 3PSCh. 11 - Prob. 4PSCh. 11 - Considering intermolecular forces in the pure...Ch. 11 - Considering intermolecular forces in the pure...Ch. 11 - Prob. 7PSCh. 11 - Which of the following compounds would be expected...Ch. 11 - Prob. 9PSCh. 11 - When salts of Mg2+, Na+, and Cs+ are placed in...Ch. 11 - Prob. 11PSCh. 11 - The enthalpy of vaporization of liquid mercury is...Ch. 11 - Answer the following questions using Figure 11.12:...Ch. 11 - Answer the following questions using Figure 11.12:...Ch. 11 - Prob. 15PSCh. 11 - Refer to Figure 11.12 to answer these questions:...Ch. 11 - Which member of each of the following pairs of...Ch. 11 - Place the following four compounds in order of...Ch. 11 - Prob. 19PSCh. 11 - You are comparing three different substances, A,...Ch. 11 - Equilibrium vapor pressures of benzene, C6H6, at...Ch. 11 - Prob. 22PSCh. 11 - Can carbon monoxide (Tc = 132.9 K; Pc = 34.5 atm...Ch. 11 - Methane (CH4) cannot be liquefied at room...Ch. 11 - What is surface tension? Give an example...Ch. 11 - What factors affect the viscosity of a substance?...Ch. 11 - If a piece of filter paper (an absorbent paper...Ch. 11 - When water is placed in a buret it forms a concave...Ch. 11 - Prob. 29GQCh. 11 - What types of intermolecular forces are important...Ch. 11 - Which of the following salts, Li2SO4 or Cs2SO4, is...Ch. 11 - Prob. 32GQCh. 11 - Prob. 33GQCh. 11 - Prob. 34GQCh. 11 - Rank the following compounds in order of...Ch. 11 - Prob. 36GQCh. 11 - Prob. 37GQCh. 11 - The following data are the equilibrium vapor...Ch. 11 - Prob. 39ILCh. 11 - A hand boiler can be purchased in toy stores or at...Ch. 11 - Prob. 41ILCh. 11 - Prob. 42ILCh. 11 - Acetone, CH3COCH3, is a common laboratory solvent....Ch. 11 - Cooking oil floats on top of water. From this...Ch. 11 - Liquid ethylene glycol, HOCH2CH2OH, is one of the...Ch. 11 - Liquid methanol, CH3OH, is placed in a glass tube....Ch. 11 - Account for these facts: (a) Although ethanol...Ch. 11 - Prob. 48SCQCh. 11 - Prob. 49SCQCh. 11 - Prob. 50SCQCh. 11 - Prob. 51SCQCh. 11 - Prob. 52SCQCh. 11 - A fluorocarbon, CF4, has a critical temperature of...Ch. 11 - Prob. 55SCQCh. 11 - List four properties of liquids that are directly...Ch. 11 - List the following ions in order of hydration...Ch. 11 - Prob. 59SCQCh. 11 - An 8.82-g sample of Br2 is placed in an evacuated...Ch. 11 - Polarizability is defined as the extent to which...Ch. 11 - Prob. 62SCQCh. 11 - A pressure cooker (a kitchen appliance) is a pot...Ch. 11 - Vapor pressures of NH3() at several temperatures...Ch. 11 - Prob. 65SCQCh. 11 - Prob. 66SCQCh. 11 - Prob. 67SCQ
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