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For each of the following substances describe the importance of dispersion (London) forces, dipoledipole interactions, and hydrogen bonding: (a) \(HCl;\) (b) \(\mathrm{Br}_{2} ;\) (c) ICl; (d) \(\mathrm{HF} ;\)\ (e) \(\mathrm{CH}_{4}\)

Short Answer

Expert verified
HCl exhibits dispersion forces and dipole-dipole interactions. Br2 and CH4 only exhibit dispersion forces. ICl exhibits dispersion forces and dipole-dipole interactions. HF exhibits all three forces: dispersion, dipole-dipole, and hydrogen bonding.

Step by step solution

01

Identify the Type of Substance in HCl

HCl is a polar covalent compound and hence, it exhibits dipole-dipole forces and dispersion forces. Hydrogen bonding is not observed in HCl, as it does not contain a hydrogen atom bonded to F, O, or N.
02

Identify the Type of Substance in Br2

Br2 is a nonpolar covalent compound. In nonpolar compounds, only dispersion forces exist. Thus, Br2 exhibits dispersion (London) forces.
03

Identify the Type of Substance in ICl

ICl is a polar covalent compound, thus it exhibits dipole-dipole forces and dispersion forces. Just like HCl, ICl does not present hydrogen bonding since it lacks a hydrogen atom that is directly bonded to F, O or N.
04

Identify the Type of Substance in HF

HF is a polar covalent compound that contains a hydrogen atom bonded to F. Thus, apart from dispersion forces and dipole-dipole forces, HF also exhibits hydrogen bonding.
05

Identify the Type of Substance in CH4

Finally, CH4 is a nonpolar covalent compound, just as Br2. Therefore, it only exhibits dispersion (London) forces.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Dispersion Forces
Dispersion forces, also known as London forces, are the weakest intermolecular forces present in all molecules, regardless of their polarity. These forces arise due to temporary fluctuations in electron distribution within atoms and molecules, leading to a fleeting dipole effect. This temporary dipole can induce a similar dipole in neighboring atoms, resulting in a weak attraction between them.

Key points about dispersion forces include:
  • Present in all molecules, polar and nonpolar.
  • Strength increases with the size and number of electrons in a molecule.
  • More significant in larger, heavier atoms like bromine (\( ext{Br}_2\)) or methane (\( ext{CH}_4\)).
These forces are crucial in nonpolar substances like \( ext{Br}_2\) where they are the primary type of intermolecular force.
Dipole-Dipole Interactions
Dipole-dipole interactions occur between polar molecules that have a permanent dipole moment. A dipole moment arises due to the difference in electronegativity between atoms forming a molecule, resulting in partial positive and negative charges at opposite ends. These interactions are stronger than dispersion forces but weaker than hydrogen bonds.

Some central aspects of dipole-dipole interactions include:
  • Only occur in polar molecules, like HCl and ICl.
  • The strength of the interaction depends on the magnitude of the dipole moment.
  • Higher boiling points in polar substances indicate stronger dipole-dipole interactions.
In substances like \( ext{ICl}\) and HCl, these forces lead to a greater attraction than what dispersion forces alone would offer.
Hydrogen Bonding
Hydrogen bonding is a particularly strong type of dipole-dipole interaction that occurs when a hydrogen atom is directly bonded to a highly electronegative element such as fluorine, oxygen, or nitrogen. This bond plays a crucial role in determining the structure and properties of compounds.

Key features of hydrogen bonding are:
  • Strongest type of intermolecular force after ionic and covalent bonds.
  • Significantly affects boiling and melting points, solubility, and viscosity.
  • Commonly seen in water, alcohols, and HF molecules.
Hydrogen fluoride (\( ext{HF}\)) is a prime example where hydrogen bonding leads to high boiling points and unique properties when compared to other hydrogen halides.

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Most popular questions from this chapter

A supplier of cylinder gases warns customers to determine how much gas remains in a cylinder by weighing the cylinder and comparing this mass to the original mass of the full cylinder. In particular, the customer is told not to try to estimate the mass of gas available from the measured gas pressure. Explain the basis of this warning. Are there cases where a measurement of the gas pressure can be used as a measure of the remaining available gas? If so, what are they?

A 25.0 L volume of \(\mathrm{He}(\mathrm{g})\) at \(30.0^{\circ} \mathrm{C}\) is passed through \(6.220 \mathrm{g}\) of liquid aniline \(\left(\mathrm{C}_{6} \mathrm{H}_{5} \mathrm{NH}_{2}\right)\) at \(30.0^{\circ} \mathrm{C} .\) The liquid remaining after the experiment weighs \(6.108 \mathrm{g}\) Assume that the He(g) becomes saturated with aniline vapor and that the total gas volume and temperature remain constant. What is the vapor pressure of aniline at \(30.0^{\circ} \mathrm{C} ?\)

How many liters of \(\mathrm{CH}_{4}(\mathrm{g}),\) measured at \(23.4^{\circ} \mathrm{C}\) and \(768 \mathrm{mmHg},\) must be burned to provide the heat needed to vaporize 3.78 L of water at \(100^{\circ} \mathrm{C}\) ? \(\Delta \mathrm{H}_{\text {combustion }}=\) \(-8.90 \times 10^{2} \mathrm{kJmol}^{-1} \mathrm{CH}_{4} \quad\) For \(\quad \mathrm{H}_{2} \mathrm{O}(\mathrm{l}) \quad\) at \(\quad 100^{\circ} \mathrm{C}\) \(d=0.958 \mathrm{g} \mathrm{cm}^{-3},\) and \(\Delta H_{\mathrm{vap}}=40.7 \mathrm{kJmol}^{-1}\)

In ionic compounds with certain metals, hydrogen exists as the hydride ion, \(\mathrm{H}^{-}\). Determine the electron affinity of hydrogen; that is, \(\Delta H\) for the process \(\mathrm{H}(\mathrm{g})+e^{-} \rightarrow \mathrm{H}^{-}(\mathrm{g}) .\) To do so, use data from Section \(12-7 ;\) the bond energy of \(\mathrm{H}_{2}(\mathrm{g})\) from table 10.3 \(-812 \mathrm{kJmol}^{-1} \mathrm{NaH}\) for the lattice energy of \(\mathrm{NaH}(\mathrm{s})\) and \(-57 \mathrm{kJmol}^{-1}\) NaH for the enthalpy of formation of \(\mathrm{NaH}(\mathrm{s})\)

All solids contain defects or imperfections of structure or composition. Defects are important because they influence properties, such as mechanical strength. Two common types of defects are a missing ion in an otherwise perfect lattice, and the slipping of an ion from its normal site to a hole in the lattice. The holes discussed in this chapter are often called interstitial sites, since the holes are in fact interstices in the array of spheres. The two types of defects described here are called point de kcts because they occur within specific sites. In the 1930 s, two solidstate physicists, W. Schottky and J. Fraenkel, studied the two types of point defects: A Schottky defect corresponds to a missing ion in a lattice, while a Fraenkel defect corresponds to an ion that is displaced into an interstitial site. (a) An example of a Schottky defect is the absence of a \(\mathrm{Na}^{+}\) ion in the NaCl structure. The absence of a \(\mathrm{Na}^{+}\) ion means that a \(\mathrm{Cl}^{-}\) ion must also be absent to preserve electrical neutrality. If one NaCl unit is missing per unit cell, does the overall stoichiometry change, and what is the change in density? (b) An example of a Fraenkel defect is the movement of \(a \mathrm{Ag}^{+}\) ion to a tetrahedral interstitial site from its normal octahedral site in \(\mathrm{AgCl}\), which has a structure like \(\mathrm{NaCl}\). Does the overall stoichiometry of the compound change, and do you expect the density to change? (c) Titanium monoxide (TiO) has a sodium chloridelike structure. X-ray diffraction data show that the edge length of the unit cell is \(418 \mathrm{pm}\). The density of the crystal is \(4.92 \mathrm{g} / \mathrm{cm}^{3}\) Do the data indicate the presence of vacancies? If so, what type of vacancies?

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