Chapter 10: Problem 10
(a) Write equations for the reactions of KH with \(\mathrm{NH}_{3}\) and with ethanol. (b) Identify the conjugate acid-base pairs in each reaction.
Short Answer
Expert verified
KH reacts with NH₃ to form KNH₂ and H₂, and with ethanol to form C₂H₅OK and H₂. Conjugate pairs are KH/H₂ and NH₃/KNH₂ in the first reaction, and KH/H₂ and C₂H₅OH/C₂H₅O⁻ in the second.
Step by step solution
01
Write Equation for KH and NH3 Reaction
Potassium hydride (KH) reacts with ammonia (NH_3"). The reaction proceeds as follows: \(\mathrm{KH} + \mathrm{NH}_3 \rightarrow \mathrm{KNH}_2 + \mathrm{H}_2\).Here, hydrogen gas is released and potassium amide (KNH₂) is formed.
02
Identify Conjugate Acid-Base Pair in KH and NH3 Reaction
In the reaction \(\mathrm{KH} + \mathrm{NH}_3 \rightarrow \mathrm{KNH}_2 + \mathrm{H}_2\), the conjugate acid-base pairs are:1. Base: \(\mathrm{KH}\), which gives \(\mathrm{H}^-\) ion. Conjugate acid is \(\mathrm{H}_2\) after releasing \(\mathrm{H}^-\). 2. Acid: \(\mathrm{NH}_3\), which acts as a proton acceptor. Conjugate base is \(\mathrm{KNH}_2\) after donating a hydrogen ion.
03
Write Equation for KH and Ethanol Reaction
Potassium hydride reacts with ethanol (C₂H₅OH). The chemical equation is: \(\mathrm{KH} + \mathrm{C}_2\mathrm{H}_5\mathrm{OH} \rightarrow \mathrm{C}_2\mathrm{H}_5\mathrm{OK} + \mathrm{H}_2\).Hydrogen gas is again released, and potassium ethoxide (C₂H₅OK) is formed.
04
Identify Conjugate Acid-Base Pair in KH and Ethanol Reaction
In the reaction \(\mathrm{KH} + \mathrm{C}_2\mathrm{H}_5\mathrm{OH} \rightarrow \mathrm{C}_2\mathrm{H}_5\mathrm{OK} + \mathrm{H}_2\), the conjugate acid-base pairs are:1. Base: \(\mathrm{KH}\), providing \(\mathrm{H}^-\) ion, with \(\mathrm{H}_2 \) as the conjugate acid upon the release of \(\mathrm{H}^-\). 2. Acid: \(\mathrm{C}_2\mathrm{H}_5\mathrm{OH}\), which donates a proton to become \(\mathrm{C}_2\mathrm{H}_5\mathrm{O}^-\), the conjugate base.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Conjugate Acid-Base Pairs
In chemistry, a crucial aspect to understand in acid-base reactions is the concept of conjugate acid-base pairs. An acid-base pair includes an acid and a base that transform into each other by the gain or loss of a proton (H⁺ ion). Whenever an acid donates a proton, it becomes its conjugate base. Conversely, when a base accepts a proton, it becomes its conjugate acid.
- In the reaction between potassium hydride (KH) and ammonia (NH₃), KH functions as a base by releasing an H⁻ ion and ultimately forms molecular hydrogen (H₂) as its conjugate acid.
- Ammonia (NH₃) accepts a proton from KH, acting as an acid in this case, and transforms into potassium amide (KNH₂), which is the conjugate base.
- KH once again acts as a base, forming molecular hydrogen (H₂) as its conjugate acid.
- Ethanol (C₂H₅OH) donates a proton, acting as an acid, and becomes potassium ethoxide (C₂H₅O⁻), the conjugate base.
Chemical Equations
Chemical equations represent the substances involved in a chemical reaction, showcasing the reactants transforming into products. Understanding the symbols and structure of these equations helps explain what is happening at the molecular level. For instance, in the reaction \[\mathrm{KH} + \mathrm{NH}_3 \rightarrow \mathrm{KNH}_2 + \mathrm{H}_2\]we see that potassium hydride (KH) and ammonia (NH₃) are the reactants. They react to form potassium amide (KNH₂) and hydrogen gas (H₂), which are the products.
- The reactants are placed on the left side of the equation, and the products are shown on the right side, separated by an arrow (→) indicating the direction of the reaction.
- In a balanced equation, the number of atoms of each element is conserved, meaning they appear equally on both sides.
Reaction Mechanisms
Reaction mechanisms explain the step-by-step process through which a chemical reaction occurs. These mechanisms provide insight into the specific changes happening at the atomic or molecular level.
The reactions between potassium hydride (KH) and either ammonia (NH₃) or ethanol (C₂H₅OH) illustrate clear steps:
- In both reactions, KH acts as a hydride donor, releasing a hydrogen ion, which is a key proton exchange process.
- Ammonia or ethanol, acting as acids, readily accept this proton, facilitating the formation of new products such as potassium amide or potassium ethoxide, respectively.