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Unless under pressure, carbonic acid \(\left(\mathrm{H}_{2} \mathrm{CO}_{3}\right)\) in aqueous solution breaks down into carbon dioxide and water and carbon dioxide is evolved as bubbles of gas. Write an equation for the conversion of carbonic acid to carbon dioxide and water.

Short Answer

Expert verified
Answer: The balanced chemical equation for the breakdown of carbonic acid into carbon dioxide and water is H2CO3 → CO2 + H2O.

Step by step solution

01

Write the unbalanced equation

First, write down the molecular formulas for the reactants and products. Carbonic acid (H2CO3) decomposes into carbon dioxide (CO2) and water (H2O). The unbalanced equation is: H2CO3 → CO2 + H2O
02

Balance the chemical equation

Now, we need to balance the equation by ensuring the number of atoms for each element is equal on both sides. In this case, the equation is already balanced: H2CO3 → CO2 + H2O There are two hydrogen atoms, one carbon atom, and three oxygen atoms on each side of the reaction. Thus, the balanced equation for the conversion of carbonic acid to carbon dioxide and water is: H2CO3 → CO2 + H2O

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Most popular questions from this chapter

Alcohols (Chapter 10) are weak organic acids, \(\mathrm{p} K_{\mathrm{a}} 15-18\). The \(\mathrm{p} K_{\mathrm{a}}\) of ethanol, \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{OH}\), is \(15.9\). Write equations for the equilibrium reactions of ethanol with each base. Which equilibria lie considerably toward the right? Which lie considerably toward the left? (a) \(\mathrm{NaHCO}_{3}\) (b) \(\mathrm{NaOH}\) (c) \(\mathrm{NaNH}_{2}\) (d) \(\mathrm{NH}_{3}\)

For each conjugate acid-base pair, identify the first species as an acid or a base and the second species as its conjugate acid or conjugate base. In addition, draw Lewis structures for each species, showing all valence electrons and any formal charges. (a) \(\mathrm{H}_{2} \mathrm{SO}_{4}, \mathrm{HSO}_{4}^{-}\) (b) \(\mathrm{NH}_{3^{\prime}} \mathrm{NH}_{2}^{-}\) (c) \(\mathrm{CH}_{3} \mathrm{OH}, \mathrm{CH}_{3} \mathrm{O}^{-}\)

The sec-butyl cation can react as both a Brønsted-Lowry acid (a proton donor) and a Lewis acid (an electron pair acceptor) in the presence of a water- sulfuric acid mixture. In each case, however, the product is different. The two reactions are as follows: (1) $\mathrm{CH}_{3}-\stackrel{+}{\mathrm{CH}}-\mathrm{CH}_{2}-\mathrm{CH}_{3}+\mathrm{H}_{2} \mathrm{O} \rightleftharpoons \mathrm{CH}_{3}-\stackrel{\mathrm{CH}}{+}-\mathrm{CH}_{2}-\mathrm{CH}_{3}$ sec-Butyl cation (2) $\mathrm{CH}_{3}-\mathrm{CH}_{-}^{+}-\mathrm{CH}_{2}-\mathrm{CH}_{3}+\mathrm{H}_{2} \mathrm{O} \rightleftharpoons \mathrm{CH}_{3}-\mathrm{CH}^{2} \mathrm{CH}-\mathrm{CH}_{3}+\mathrm{H}_{3} \mathrm{O}^{+}$ sec-Butyl cation (a) In which reaction(s) does this cation react as a Lewis acid? In which reaction(s) does it react as a Bronsted-Lowry acid? (b) Write Lewis structures for reactants and products and show by the use of curved arrows how each reaction occurs.

For each conjugate acid-base pair, identify the first species as an acid or a base and the second species as its conjugate acid or base. In addition, draw Lewis structures for each species, showing all valence electrons and any formal charge. (a) \(\mathrm{HCOOH} \mathrm{HCOO}^{-}\) (b) \(\mathrm{NH}_{4}{ }^{+} \mathrm{NH}_{3}\) (d) \(\mathrm{HCO}_{3}^{-} \quad \mathrm{CO}_{3}^{2-}\) (e) \(\mathrm{H}_{2} \mathrm{PO}_{4}^{-} \quad \mathrm{HPO}_{4}{ }^{2-}\) (c) \(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{O}^{-} \mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{OH}\) (g) \(\mathrm{CH}_{3} \mathrm{~S}^{-} \mathrm{CH}_{3} \mathrm{SH}\) (f) \(\mathrm{CH}_{3} \mathrm{CH}_{3} \mathrm{CH}_{3} \mathrm{CH}_{2}^{-}\)

Methyl isocyanate, \(\mathrm{CH}_{3}-\mathrm{N}=\mathrm{C}=\mathrm{O}\), is used in the industrial synthesis of a type of pesticide and herbicide known as a carbamate. As a historical note, an industrial accident in Bhopal, India, in 1984 resulted in leakage of an unknown quantity of this chemical into the air. An estimated 200,000 people were exposed to its vapors, and over 2000 of these people died. (a) Write a Lewis structure for methyl isocyanate and predict its bond angles. What is the hybridization of its carbonyl carbon? Of its nitrogen atom? (b) Methyl isocyanate reacts with strong acids, such as sulfuric acid, to form a cation. Will this molecule undergo protonation more readily on its oxygen or nitrogen atom? In considering contributing structures to each hybrid, do not consider structures in which more than one atom has an incomplete octet.

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