Concept explainers
The (aq) designation listed after a solute indicates the process of hydration. Using KBr(aq) and C2H5OH(aq) as your examples, explain the process of hydration for soluble ionic compounds and for soluble covalent compounds.

Interpretation: The process of hydration for soluble ionic compounds and soluble covalent compounds with
Concept Introduction: When an ionic compound is dissolved in water, the positive ends of the water molecules are attracted to the negative charged ions and that negative ends are attracted to the positive charged ions. This process is called as hydration.
Answer to Problem 1RQ
Answer
Soluble ionic compounds have to tendency to breakup into their positive and negatively charged ions when they are dissolved into solution.
In
In the hydration process for ions, the partial negative end of the polar water molecules surrounds and stabilizes the cations in the solution. The water molecules present here would align themselves in such a way that the oxygen end of water aligns with the
In the case of
This is assumption when an aqueous solution (aq) is placed after an ionic compound.
Soluble covalent compounds are that compound that doesn’t have to tendency to break into ions when they are dissolved in solution.
Consider,
The hydration process for polar covalent solutes takes place when the covalent solutes and solvents align themselves such that their opposite charged parts attract each other.
The partial negative end of
This is the hydration process for polar covalent compounds. This is assumption when an aqueous solution (aq) is placed after an ionic compound.
It is difficult to predict the partial negative ends and partial positive ends of polar covalent compounds.
Explanation of Solution
Explanation
To explain the process of hydration in soluble ionic compounds
The process of hydration can be defined as dissolution of ionic compound in water, where
the positive ends of the water molecules are attracted to the negative charged ions and that negative ends are attracted to the positive charged ions.
When an ionic compound that is soluble in water can break apart into their ions upon dissolution such ionic compounds are called as soluble ionic compounds.
Taking the example of
The dissolution of
The equation can be given as,
In the hydration process for ions, the partial negative end of the polar water molecules surrounds and stabilizes the cations in the solution. The water molecules present here would align themselves in such a way that the oxygen end of water aligns with the
In the case of
This is assumption when an aqueous solution (aq) is placed after an ionic compound.
The separation of ions that are placed in solution is surrounded by the water that is permitable. There is an enthalpy change. The enthalpy change for this process is called as hydration enthalpy.
When a compound is made to get soluble in water, there is no break apart into their ions upon dissolution such ionic compounds are called as soluble covalent compounds.
To explain the process of hydration in soluble covalent compound
Soluble covalent compounds are that compound that doesn’t have to tendency to break into ions when they are dissolved in solution.
Consider,
The hydration process for polar covalent solutes takes place when the covalent solutes and solvents align themselves such that their opposite charged parts attract each other.
The partial negative end of
This is the hydration process for polar covalent compounds. This is assumption when an aqueous solution (aq) is placed after an ionic compound.
It is difficult to predict the partial negative ends and partial positive ends of polar covalent compounds.
The concept of hydration of soluble ionic and covalent compounds were explained with
Want to see more full solutions like this?
Chapter 4 Solutions
Chemistry-Stud. Solution Guide
- Show by chemical equation the reaction of [HCN] and [CH3MgBr] with any alarrow_forwardGive the chemical equation for the preparation of: -Any aldehyde -Any keytonearrow_forward+ C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forward
- → Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Aarrow_forwardFor each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forward
- Identifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardAssign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
- World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningIntroductory Chemistry: A FoundationChemistryISBN:9781337399425Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningIntroduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning





