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What is the maximum number of hydrogen bonds that can form between two acetic acid molecules?

Short Answer

Expert verified
Two acetic acid molecules can form a maximum of two hydrogen bonds with each other.

Step by step solution

01

Identify Active Groups in Acetic Acid

The acetic acid molecule has one Carboxyl group (-COOH), which includes a Hydroxyl (-OH) group capable of forming Hydrogen bonds.
02

Determining Hydrogen Bond Formation

The Hydrogen in the Hydroxyl group of one molecule can form a Hydrogen bond with the Oxygen of the Carboxyl group in another acetic acid molecule, as Oxygen is electronegative and hydrogen has a partial positive charge. Similarly, Hydrogen in the Hydroxyl group of the second acetic acid molecule can form a Hydrogen bond with the Oxygen of the Carboxyl group in the first acetic acid molecule.
03

Counting the Maximum Number of Hydrogen Bonds

Hence, two acetic acid molecules can form two hydrogen bonds with each other.

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Key Concepts

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

Acetic Acid
Acetic acid is a simple carboxylic acid that is well-known for its characteristic sour taste and pungent smell. It is commonly found in vinegar, where it acts as the main chemical component. This molecule consists of a methyl group \((-CH_3)\) attached to a carboxyl group \((-COOH)\). The presence of this carboxyl group makes acetic acid a weak acid. Despite being a weak acid, acetic acid can easily participate in hydrogen bonding, which plays a crucial role in its physical properties, like boiling point and solubility.
Hydrogen bonding occurs due to the interaction between the hydrogen atom, which is slightly positive, and an electronegative atom such as oxygen or nitrogen in acetic acid. This enables acetic acid molecules to intermingle and create a network of hydrogen bonds that significantly impact their behavior in solutions.
Carboxyl Group
The carboxyl group is a functional group extensively found in organic chemistry. It is represented by the formula \((-COOH)\). This group consists of a carbonyl group \((-C=O)\) and a hydroxyl group \((-OH)\), both attached to the same carbon atom. The unique structure of the carboxyl group makes it highly polar, which facilitates the formation of hydrogen bonds with other molecules.
In acetic acid, the carboxyl group is the site of reactivity allowing hydrogen bonding. This group can donate a hydrogen atom to another electronegative atom, or accept a hydrogen from another polar molecule, thus enabling two separate acetic acid molecules to form hydrogen bonds with each other. This property not only influences how acetic acid molecules interact but also explains its acidity and reactivity in chemical reactions.
Hydroxyl Group
The hydroxyl group \((-OH)\) is an important functional group in many organic compounds, including acetic acid. This group consists of an oxygen atom bound to a hydrogen atom, creating a polar unit that is capable of forming hydrogen bonds with adjacent molecules.
In acetic acid, the hydroxyl group can both donate and accept hydrogen bonds. The hydrogen atom of the hydroxyl group is slightly positive, allowing it to bond with a more electronegative atom, such as the oxygen in another acetic acid molecule's carboxyl group. This dual capability plays a vital role in the molecular interaction of acetic acid, making it possible to form two hydrogen bonds between two molecules.
  • The hydroxyl group contributes to the acidity of acetic acid by allowing deprotonation, which is the release of its hydrogen ion \((H^+)\).
  • It also enhances solubility in water due to its ability to form multiple hydrogen bonds with water molecules.
The versatile nature of the hydroxyl group in forming hydrogen bonds is key to many of the properties exhibited by molecules like acetic acid.

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Most popular questions from this chapter

Explain the important distinctions between each pair of terms: (a) adhesive and cohesive forces; (b) vaporization and condensation; (c) triple point and critical point; (d) face-centered and body-centered cubic unit cell; (e) tetrahedral and octahedral hole.

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 \(\mathrm{NaH}(\mathrm{s})\)

When a wax candle is burned, the fuel consists of gaseous hydrocarbons appearing at the end of the candle wick. Describe the phase changes and processes by which the solid wax is ultimately consumed.

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?

Of the compounds \(\mathrm{HF}, \mathrm{CH}_{4}, \mathrm{CH}_{3} \mathrm{OH}, \mathrm{N}_{2} \mathrm{H}_{4},\) and \(\mathrm{CHCl}_{3},\) hydrogen bonding is an important intermolecular force in (a) none of these; (b) two of these; (c) three of these; (d) all but one of these; (e) all of these.

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