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The decreasing order of acidic nature of \(\mathrm{H}_{2} \mathrm{SO}_{4}\) (I), \(\mathrm{H}_{3} \mathrm{PO}_{4}(\mathrm{II})\), and \(\mathrm{HClO}_{4}(\mathrm{III})\) is (a) \(\mathrm{I}>\mathrm{II}>\mathrm{III}\) (b) \(\mathrm{I}>\mathrm{III}>\mathrm{II}\) (c) \(\mathrm{III}>\mathrm{I}>\mathrm{II}\) (d) \(\mathrm{III}>\mathrm{II}>\mathrm{I}\)

Short Answer

Expert verified
The correct order is (c) III > I > II.

Step by step solution

01

Understanding Acidic Strength

Acidic strength of an acid is determined by its ability to donate protons (H鈦 ions). The more easily an acid donates a proton, the stronger it is. Factors influencing acidic strength include the stability of the anion formed, the electronegativity of the atoms involved, and the oxidation state of the central atom.
02

Evaluating Perchloric Acid (HClO鈧)

HClO鈧 is known to be a very strong acid. The ClO鈧勨伝 ion is very stable due to resonance and the high electronegativity of chlorine. The significant electronegativity of oxygen in ClO鈧勨伝 also helps delocalize the negative charge, contributing to its strong acidic nature.
03

Evaluating Sulfuric Acid (H鈧係O鈧)

H鈧係O鈧 is a strong acid. When it dissociates, it forms HSO鈧勨伝, which is still a relatively strong acid. However, H鈧係O鈧 is not as strong as HClO鈧, because HSO鈧勨伝 holds its proton more tightly compared to ClO鈧勨伝, which doesn't hold its proton at all in solution.
04

Evaluating Phosphoric Acid (H鈧働O鈧)

H鈧働O鈧 is a weaker acid compared to both HClO鈧 and H鈧係O鈧. It partially ionizes in solution to form H鈧侾O鈧勨伝. The PO鈧劼斥伝 ion is also less stable compared to the sulfate or perchlorate ion, making H鈧働O鈧 a weaker acid.
05

Ranking the Acids by Strength

Considering the relative strengths calculated, the decreasing order of acidity would be: 1. HClO鈧 (strongest due to stable anion and high electronegativity)2. H鈧係O鈧 (strong but not as strong as HClO鈧)3. H鈧働O鈧 (weakest among the three). Thus, the correct order is \[ \text{III} > \text{I} > \text{II} \]

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Key Concepts

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

Perchloric Acid
Perchloric acid, represented chemically as HClO鈧, is renowned for being one of the strongest acids known. This potent acidic strength is due to several key reasons. Firstly, perchloric acid is capable of almost complete dissociation in solution, meaning it readily loses its proton
This characteristic is what defines a strong acid.
A significant factor contributing to this behavior is the stability of the perchlorate anion, ClO鈧勨伝. This anion benefits from extensive resonance.
  • The negative charge is well-distributed over the four oxygen atoms.
  • Chlorine is highly electronegative, facilitating the stability of the negative ion.
Additionally, oxygen itself has high electronegativity, which further helps in delocalizing the negative charge. This exceptional stability of ClO鈧勨伝 distills the need to hold onto the proton, enabling HClO鈧 to donate protons more readily and exhibit greater acidic strength compared to other acids, such as sulfuric and phosphoric acids.
Sulfuric Acid
Sulfuric acid, denoted as H鈧係O鈧, is another well-known strong acid and often used in a variety of industrial applications. Despite its strength, it is slightly less potent than perchloric acid.
When sulfuric acid dissociates in water, it primarily forms the bisulfate anion, HSO鈧勨伝.
  • HSO鈧勨伝 itself is a moderately strong acid.
  • The sulfur atom in sulfuric acid is in a high oxidation state, which affects the overall acidic strength.
While sulfuric acid is powerful, the anion HSO鈧勨伝 does not relinquish its hydrogen ion as readily compared to the intact release shown by perchlorate ions in HClO鈧. This means that sulfuric acid, although strong, holds onto its proton a little more tightly, rendering it slightly weaker than perchloric acid.
Phosphoric Acid
Phosphoric acid, expressed chemically as H鈧働O鈧, is significantly weaker when compared to both perchloric and sulfuric acids. Phosphoric acid is regarded as a triprotic acid, meaning it can lose up to three protons, but this does not happen readily all at once.
  • The anion formed initially when phosphoric acid ionizes is dihydrogen phosphate, H鈧侾O鈧勨伝.
  • The subsequent ions formed, HPO鈧劼测伝 and PO鈧劼斥伝, are even weaker.
A critical point in understanding the relative weakness of phosphoric acid lies in the lesser stability of its conjugate base, PO鈧劼斥伝. This instability contrasts sharply with the more stable conjugate bases of stronger acids like HClO鈧 and H鈧係O鈧. Hence, phosphoric acid does not donate its protons as easily, categorizing it as the weakest among these three acids.

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Most popular questions from this chapter

The percentage hydrolysis of \(\mathrm{NaCN}\) in \(\left(\frac{\mathrm{N}}{80}\right)\) aqueous solution [Dissociation constant of \(\mathrm{HCN}\) is \(1.3 \times 10^{-9}\) and \(\left.\mathrm{K}_{\mathrm{w}}=1.0 \times 10^{-14}\right]\) is (a) \(8.2\) (b) \(9.6\) (c) \(5.26\) (d) \(2.48\)

\(50 \mathrm{~mL}\) of \(0.2 \mathrm{M}\) aqueous \(\mathrm{CH}_{3} \mathrm{COOH}\) is mixed with \(50 \mathrm{~mL}\) of \(0.2 \mathrm{M}\) aqueous \(\mathrm{KOH}\) solution. The \(\mathrm{pH}\) of resulting solution is \(\left(\mathrm{pK}_{\mathrm{a}}\right.\) of acetic acid is \(4.7\) ) (a) \(7.0\) (b) \(9.35\) (c) \(8.85\) (d) \(6.05\)

Hydrolysis constant \(\mathrm{K}_{\mathrm{A}}\) and \(\mathrm{K}_{\mathrm{B}}\) of two salts of weak acids HA and \(\mathrm{HB}\) are \(10^{-8}\) and \(10^{-6}\) respectively. If the dissociation constant of third acid \(\mathrm{HC}\) is \(10^{-2}\). The order of acidic strengths of three acids will be (a) \(\mathrm{HA}>\mathrm{HB}>\mathrm{HC}\) (b) \(\mathrm{HB}>\mathrm{HA}>\mathrm{HC}\) (c) \(\mathrm{HC}>\mathrm{HA}>\mathrm{HB}\) (d) \(\mathrm{HA}=\mathrm{HB}=\mathrm{HC}\)

\(\mathrm{pH}\) of \(0.005 \mathrm{M}\) calcium acetate \(\left(\mathrm{pKa}\right.\) of \(\mathrm{CH}_{3} \mathrm{COOH}\) \(=4.74)\) is [2002] (a) \(7.37\) (b) \(9.37\) (c) \(9.26\) (d) \(8.37\)

Which of the following composition shows maximum buffer capacity? (a) \(0.1 \mathrm{M} \mathrm{CH}_{3} \mathrm{COOH}+0.2 \mathrm{M} \mathrm{CH}_{3} \mathrm{COONa}\) (b) \(0.1 \mathrm{M} \mathrm{CH}_{3} \mathrm{COOH}+0.15 \mathrm{M} \mathrm{CH}_{3} \mathrm{COONa}\) (c) \(0.05 \mathrm{M} \mathrm{CH}_{3} \mathrm{COOH}+0.15 \mathrm{M} \mathrm{CH}_{3} \mathrm{COONa}\) (d) \(0.1 \mathrm{M} \mathrm{CH}_{3} \mathrm{COOH}+0.12 \mathrm{M} \mathrm{CH}_{3} \mathrm{COONa}\)

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