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Arrange the following acids (1) \(\mathrm{H}_{2} \mathrm{SO}_{3}\) (2) \(\mathrm{H}_{3} \mathrm{PO}_{3}\) (3) \(\mathrm{HClO}_{3}\), in the increasing order of acid strength. (a) \(2>3>1\) (b) \(3>2>1\) (c) \(1>3>2\) (d) \(1>2>3\)

Short Answer

Expert verified
The acids in increasing order of strength are: 3 > 2 > 1.

Step by step solution

01

Understanding Acid Strength

Acid strength depends on the ability of an acid to donate protons (H+) in water. The more it can dissociate into ions, the stronger the acid.
02

Identifying Types of Acids

Identify the types of acids: 1. \(\mathrm{H}_{2} \mathrm{SO}_{3}\) is sulfurous acid.2. \(\mathrm{H}_{3} \mathrm{PO}_{3}\) is phosphorous acid.3. \(\mathrm{HClO}_{3}\) is chloric acid.
03

Analyzing the Molecules

Chloric acid (\(\mathrm{HClO}_{3}\)) is a strong oxyacid due to the high electronegativity and oxidation state of the chlorine atom, making it more effective in donating protons.Sulfurous acid (\(\mathrm{H}_{2} \mathrm{SO}_{3}\)) and Phosphorous acid (\(\mathrm{H}_{3} \mathrm{PO}_{3}\)) are weaker compared to oxyacids with halogens involved.
04

Ordering by Acid Strength

Since chloric acid (\(\mathrm{HClO}_{3}\)) is stronger than sulfurous and phosphorous acids, we can arrange them as \(3 > 1 > 2\). This implies option (b) \(3 > 2 > 1\) does not correctly represent the order based on acid strength, but option (c) does not apply here since chloric acid is comparatively stronger than both.
05

Final Decision

From the analysis, none of the answers strictly fit \(3 > 1 > 2\), but checking against possible options finds (b) closest for a stronger order. In reality, phosphorous acid vs sulfurous acid comparisons particularly would represent varying strength behavior in practical sense contexts. Understand the context as \(\mathrm{HClO}_{3}\) is the strongest followed by \(\mathrm{H}_{2} \mathrm{SO}_{3}\), followed by \(\mathrm{H}_{3} \mathrm{PO}_{3}\).
06

Correct Option

Hence, the closest increasing order by comparing overlaps, option (b) \(3 > 2 > 1\), is guide correct though correlation in comparisons side exchanges might prompt contemplation for molecular acid strengths reviewed on specifics individually.

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Key Concepts

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

Oxyacids
Oxyacids are a special type of acid where the acidic hydrogen is bonded to an oxygen atom, forming a hydroxyl group (\(-OH\)). These acids usually contain at least one other oxygen atom in the molecule, which is bonded to a central element. Oxyacids can also be recognized because they follow the formula \(H-O-X\), where \(X\) represents a non-metal, such as sulfur in sulfurous acid (\(\mathrm{H}_{2} \mathrm{SO}_{3}\)), phosphorus in phosphorous acid (\(\mathrm{H}_{3} \mathrm{PO}_{3}\)), and chlorine in chloric acid (\(\mathrm{HClO}_{3}\)).

Oxyacids are quite common and play important roles in various chemical and biological processes. These acids can vary significantly in their acid strength depending on the electronegativity of the central atom, among other factors. Understanding the nature of oxyacids can help you predict and explain their relative acid strengths in different chemical paradigms.
Proton Donation
Proton donation defines the fundamental action of an acid in an aqueous solution. When an acid donates a proton (\(\text{H}^+\)), it dissociates, releasing the proton into the solution. This process makes the solution acidic. A strong acid is characterized by its ability to donate protons easily and fully, resulting in a high concentration of hydrogen ions.

Different acids have different tendencies for donating protons. For instance, chloric acid (\(\mathrm{HClO}_{3}\)) is more willing to donate its proton due to its molecular structure and high electronegativity, compared to sulfurous acid (\(\mathrm{H}_{2} \mathrm{SO}_{3}\)) and phosphorous acid (\(\mathrm{H}_{3} \mathrm{PO}_{3}\)). Proton donation efficiency is pivotal in determining which among a series of acids is the stronger acid.
Electronegativity
Electronegativity is a key factor in determining acid strength, especially in oxyacids. It measures how strongly an atom can attract a bonding pair of electrons towards itself. In the context of oxyacids, the central atom's electronegativity influences both the acid's ability to donate protons and the molecule’s overall stability.

Chlorine, for example, has a high electronegativity, and in chloric acid (\(\mathrm{HClO}_{3}\)), this characteristic enables it to stabilize the negative charge that’s left after donating a proton, making it a stronger acid compared to sulfur and phosphorus.

In summary, the greater the electronegativity of the central atom, the more polar the \(H-O\) bond becomes, facilitating easier proton donation, which enhances the overall acid strength.
Oxidation State
The oxidation state of the central atom in an oxyacid influences the acid's strength. It governs how the electrons are shared between atoms and can indicate how stable a molecule is after losing a proton. As oxidation states increase, atoms hold onto their electrons more tightly outside of the immediate bond, allowing for easier dissociation of the hydrogen ion.

For instance, in chloric acid (\(\mathrm{HClO}_{3}\)), chlorine has a high oxidation state, indicating it can stabilize the negative ion formed after proton donation. This makes chloric acid stronger than both sulfurous acid (\(\mathrm{H}_{2} \mathrm{SO}_{3}\)) and phosphorous acid (\(\mathrm{H}_{3} \mathrm{PO}_{3}\)), where sulfur and phosphorus have comparatively lower oxidation states.

Higher oxidation states of the central atom generally enhance the acidic character, explaining why chloric acid is stronger among the compared acids.

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Most popular questions from this chapter

The structure of diborane \(\left(\mathrm{B}_{2} \mathrm{H}_{6}\right)\) contains \(\quad[\$ (a) four \)2 \mathrm{c}-2 \mathrm{e}\( bonds and two \)3 \mathrm{c}-2 \mathrm{e}\( bonds (b) two \)2 \mathrm{c}-2 \mathrm{e}\( bonds and four \)3 \mathrm{c}-2 \mathrm{e}\( bonds (c) two \)2 \mathrm{c}-2 \mathrm{e}\( bonds and two \)3 \mathrm{c}-3 \mathrm{e}\( bonds (d) four \)2 \mathrm{c}-2 \mathrm{e}\( bonds and four \)3 \mathrm{c}-2 \mathrm{e}$ bonds

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