OWLv2 with MindTap Reader, 4 terms (24 months) Printed Access Card for Zumdahl/Zumdahl's Chemistry, 9th
9th Edition
ISBN: 9781285185446
Author: Steven S. Zumdahl, Susan A. Zumdahl
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 8, Problem 152CP
Think of forming an ionic compound as three steps (this is a simplification, as with all models): (I) removing an electron from the metal; (2) adding an electron to the nonmetal; and (3) allowing the metal cation and nonmetal anion to come together.
a. What is the sign of the energy change for each of these three processes?
b. In general, what is the sign of the sum of the first two processes? Use examples to support your answer.
c. What must be the sign of the sum of the three process
d. Given your answer to part c, why do ionic bonds occur?
e. Given your above explanations, why is NaCl stable but not Na2Cl? NaCl2? What about MgO compared to MgO2? Mg2O?
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Complete the following table. The only density needed is already given. Show your
calculations in a neat and easy-to-follow manner in the space below the table. All units
should be included and significant figures should be given close attention. Be sure to notice
that the amount of material should be in millimoles rather than moles, and the theoretical
mass of the product should in milligrams rather than grams.
LOCH 3
+
H2SO4
HNO 3
O=C-OCH 3
NO2
x
H₂O
F.W.
4.0 mL 1.3 M
amount
0.50 mL
in H2SO4
mg Theoretical
Theoretical
mmoles
density
1.09
Kumada Coupling:
1. m-Diisobutylbenzene below could hypothetically be synthesized by Friedel-Crafts reaction. Write out the reaction with a
mechanism and give two reasons why you would NOT get the desired product.
Draw the reaction (NOT a mechanism) for a Kumada coupling to produce the molecule above from m-dichlorobenzene.
Calculate the theoretical yield for the reaction in question 2 using 1.5 g of p-dichlorobenzene and 3.0 mL isobutyl bromide.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Wintergreen from Aspirin:
1. In isolating the salicylic acid, why is it important to press out as much of the water as possible?
2. Write the mechanism of the esterification reaction you did.
3.
What characteristic absorption band changes would you expect in the IR spectrum on going from aspirin to salicyclic acid and
then to methyl salicylate as you did in the experiment today? Give approximate wavenumbers associated with each functional
group change.
What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What
other impurities are present in your product and how do you know?
Chapter 8 Solutions
OWLv2 with MindTap Reader, 4 terms (24 months) Printed Access Card for Zumdahl/Zumdahl's Chemistry, 9th
Ch. 8 - Distinguish between the terms electronegativity...Ch. 8 - When an element forms an anion, what happens to...Ch. 8 - Define the term lattice energy. Why,...Ch. 8 - Explain how bond energies can be used to estimate...Ch. 8 - Prob. 5RQCh. 8 - Explain the terms resonance and delocalized...Ch. 8 - Define formal charge and explain how to calculate...Ch. 8 - Give two requirements that should be satisfied for...Ch. 8 - Consider the following compounds: CO2, SO2, KrF2,...Ch. 8 - Explain the electronegativity trends across a row...
Ch. 8 - The ionic compound AB is formed. The charges on...Ch. 8 - Prob. 3ALQCh. 8 - The bond energy for a CH bond is about 413 kJ/mol...Ch. 8 - Prob. 5ALQCh. 8 - Which has the greater bond lengths: NO2 or NO3?...Ch. 8 - The following ions are best described with...Ch. 8 - The second electron affinity values for both...Ch. 8 - What is meant by a chemical bond? Why do atoms...Ch. 8 - Why are some bonds ionic and some covalent?Ch. 8 - How does a bond between Na and Cl differ from a...Ch. 8 - Arrange the following molecules from most to least...Ch. 8 - Does a Lewis structure tell which electron come...Ch. 8 - Describe the type of bonding that exists in die...Ch. 8 - Some plant fertilizer compounds are (NH4)2SO4,...Ch. 8 - Some of the important properties of ionic...Ch. 8 - What is the electronegativity trend? Where does...Ch. 8 - Give one example of a compound having a linear...Ch. 8 - When comparing the size of different ions, the...Ch. 8 - In general the higher the charge on the ions in an...Ch. 8 - Combustion reactions of fossil fuels provide most...Ch. 8 - Which of the following statements is/are true?...Ch. 8 - Three resonance structures can be drawn for CO2....Ch. 8 - Which of the following statements is(are) true?...Ch. 8 - Without using Fig. 3-4, predict the order of...Ch. 8 - Without using Fig. 3-4, predict the order of...Ch. 8 - Without using Fig. 3-4, predict which bond in each...Ch. 8 - Without using Fig. 3-4, predict which bond in each...Ch. 8 - Prob. 31ECh. 8 - Prob. 32ECh. 8 - Which of the following incorrectly shows the bond...Ch. 8 - Indicate the bond polarity (show the partial...Ch. 8 - Predict the type of bond (ionic, covalent, or...Ch. 8 - List all the possible bonds that can occur between...Ch. 8 - Hydrogen has an electronegativity value between...Ch. 8 - Rank the following bonds in order of increasing...Ch. 8 - State whether or not each of the following has a...Ch. 8 - The following electrostatic potential diagrams...Ch. 8 - Prob. 41ECh. 8 - Prob. 42ECh. 8 - Predict the empirical formulas of the ionic...Ch. 8 - Predict the empirical formulas of the ionic...Ch. 8 - Write electron configurations for a. the cations...Ch. 8 - Write electron configurations for a. the cations...Ch. 8 - Which of the following ions have noble gas...Ch. 8 - What noble gas has the same electron configuration...Ch. 8 - Give the formula of a negative ion that would have...Ch. 8 - Prob. 50ECh. 8 - Give three ions that are isoelectronic with neon....Ch. 8 - Consider the ions Sc3+, Cl, K+, Ca2+, and S2....Ch. 8 - Prob. 53ECh. 8 - For each of the following groups, place the atoms...Ch. 8 - Which compound in each of the following pairs of...Ch. 8 - Which compound in each of the following pairs of...Ch. 8 - Use the following data for potassium chloride to...Ch. 8 - Use the following data for magnesium fluoride to...Ch. 8 - Consider the following energy changes: E(kJ/mol)...Ch. 8 - Compare the electron affinity of fluorine to the...Ch. 8 - Prob. 61ECh. 8 - Use the following data (in kJ/mol) to estimate E...Ch. 8 - Rationalize the following lattice energy values:...Ch. 8 - The lattice energies of FeCl3, FeCl2, and Fe2O3...Ch. 8 - Use bond energy values (Table 3-3) to estimate E...Ch. 8 - Use bond energy values (Table 3-3) to estimate E...Ch. 8 - Prob. 67ECh. 8 - Acetic acid is responsible for the sour taste of...Ch. 8 - Use bond energies to predict E for the following...Ch. 8 - The major industrial source of hydrogen gas is by...Ch. 8 - Use bond energies to estimate E for the combustion...Ch. 8 - Prob. 72ECh. 8 - Prob. 73ECh. 8 - Consider the following reaction: A2+B22AB E =...Ch. 8 - Compare your answers from parts a and b of...Ch. 8 - Compare your answers from Exercise 72 to the H...Ch. 8 - The standard enthalpies of formation for S(g),...Ch. 8 - Use the following standard enthalpies of formation...Ch. 8 - The standard enthalpy of formation for N2H2(g) is...Ch. 8 - The standard enthalpy of formation for NO(g) is...Ch. 8 - Write Lewis structures that obey the octet rule...Ch. 8 - Write Lewis structures that obey the octet rule...Ch. 8 - Write Lewis structures that obey the octet rule...Ch. 8 - Write Lewis structures that obey the octet rule...Ch. 8 - One type of exception to the octet rule are...Ch. 8 - Lewis structures can be used to understand why...Ch. 8 - The most common exceptions to the octet rule are...Ch. 8 - Prob. 88ECh. 8 - Write Lewis structures for the following. Show all...Ch. 8 - Prob. 90ECh. 8 - Benzene (C6H6) consists of a six-membered ring of...Ch. 8 - Borazine (B3N3H6) has often been called inorganic...Ch. 8 - An important observation supporting the concept of...Ch. 8 - Consider the following bond lengths: CO143pmC9O123...Ch. 8 - A toxic cloud covered Bhopal, India, in December...Ch. 8 - Peroxyacetyl nitrate, or PAN, is present in...Ch. 8 - Prob. 99ECh. 8 - Use formal charge arguments to explain why CO has...Ch. 8 - Write Lewis structures that obey the octet rule...Ch. 8 - Write Lewis structures for the species in Exercise...Ch. 8 - Oxidation of the cyanide ion produces the stable...Ch. 8 - When molten sulfur reacts with chlorine gas, a...Ch. 8 - Prob. 106ECh. 8 - Prob. 108ECh. 8 - Predict the molecular structure and bond angles...Ch. 8 - Predict die molecular structure and bond angles...Ch. 8 - There are several molecular structures based on...Ch. 8 - Two variations of the octahedral geometry (see...Ch. 8 - Predict the molecular structure (including bond...Ch. 8 - Predict the molecular structure (including bond...Ch. 8 - Predict the molecular structure (including bond...Ch. 8 - Predict the molecular structure (including bond...Ch. 8 - Prob. 117ECh. 8 - Which of the molecules in Exercise 120 have net...Ch. 8 - Which of the molecules in Exercise 121 have net...Ch. 8 - Which of the molecules in Exercise 122 have net...Ch. 8 - Write Lewis structures and predict the molecular...Ch. 8 - Write Lewis structures and predict whether each of...Ch. 8 - Consider the following Lewis structure where E is...Ch. 8 - Consider the following Lewis structure where E is...Ch. 8 - Prob. 125ECh. 8 - Two different compounds have the formula XeF2Cl2....Ch. 8 - Arrange the following in order of increasing...Ch. 8 - For each of the following, write an equation that...Ch. 8 - Use bond energies (table 3-3), values of electron...Ch. 8 - Write Lewis structures for CO32, HCO3, and H2CO3....Ch. 8 - Which member of the following pairs would you...Ch. 8 - What do each of the following sets of...Ch. 8 - Prob. 133AECh. 8 - Although both Br3 and I3 ions are known, the F3...Ch. 8 - Which of the following molecules have not dipole...Ch. 8 - Prob. 137AECh. 8 - Look up the energies for the bonds in CO and N2....Ch. 8 - Classify the bonding in each of the following...Ch. 8 - List the bonds PCl, PF, OF, and SiF from least...Ch. 8 - Arrange the atoms and/or ions in the following...Ch. 8 - Use the following data to estimate E for the...Ch. 8 - Use bond energy values to estimate E for the...Ch. 8 - Which of the following compounds or ions exhibit...Ch. 8 - The formulas of several chemical substances are...Ch. 8 - Predict the molecular structure, bond angles, and...Ch. 8 - Use Coulombs Jaw, V=Q1Q240r=2.311019Jnm(Q1Q2r) to...Ch. 8 - Prob. 148CPCh. 8 - Calculate the standard heat of formation of the...Ch. 8 - Given the following information: Energy of...Ch. 8 - Prob. 151CPCh. 8 - Think of forming an ionic compound as three steps...Ch. 8 - The compound NF3 is quite stable, but NCl3, is...Ch. 8 - Three processes that have been used for the...Ch. 8 - The compound hexaazaisowurtzitane is one of the...Ch. 8 - Many times extra stability is characteristic of a...Ch. 8 - The study of carbon-containing compounds and their...Ch. 8 - Draw a Lewis structure for the N,...Ch. 8 - Prob. 159CPCh. 8 - Consider the following computer-generated model of...Ch. 8 - A compound, XF5, is 42.81% fluorine by mass....Ch. 8 - Identify the following elements based on their...
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Synthesis of ZybanⓇ: 1. Write a mechanism for the bromination of m-chloropropiophenone. Br₂ CH2Cl2 Cl Br 2. Give the expected m/z (to a round number) for the molecular ion from the product above (including isotopic peaks). 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSynthesis of Ibuprofen-Part 2: 1. Some pain relievers including ibuprofen (MotrinⓇ) and naproxen (Aleve®) are "α-arylpropanoic acids." Look up the structure of naproxen (AleveⓇ), another a-arylpropionic acid. Using the same reactions that we used for making ibuprofen, show how to make naproxen from the compound below. Show all intermediates and reagents in your synthesis. Show how you would prepare ibuprofen starting from p-isobutylbenzene rather than p-isobutylacetophenenone. What reaction steps would need to change/add? 3. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAcid Catalyzed Aromatization of Carvone: 1. Starting with the ketone, below, draw a mechanism for the reaction to give the phenol as shown. H2SO4 HO- H₂O 2. Why do we use CDCl instead of CHCl, for acquiring our NMR spectra? 3. Why does it not matter which enantiomer of carvone is used for this reaction? What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Assign this H NMRarrow_forwardPlease complete these blanks need that asaparrow_forwardNitration of Methyl Benzoate: 1. Predict the major product for the reaction below AND provide a mechanism. Include ALL resonance structures for the intermediate. C(CH3)3 NO₂* ? 2. Assuming the stoichiometry is 1:1 for the reaction above, what volume of concentrated nitric acid would be required to mononitrate 0.50 grams of the compound above? What product(s) might you expect if you nitrated phenol instead of methyl benzoate? Explain your reasoning. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
- Sodium Borohydride Reduction (continued on the next page): 1. Draw the product of each of the reactions below and give the formula mass to the nearest whole number. ? (1) NaBH (2) acid (1) NaBD4 (2) acid ? 2. In mass spectra, alcohols typically break as shown in equation 8 in chapter 11 (refer to your lab manual). The larger group is generally lost and this gives rise to the base peak in the mass spectrum. For the products of each of the reactions in question # 1, draw the ion corresponding to the base peak for that product and give its mass to charge ratio (m/z). 3. Given the reaction below, calculate how many mg of 1-phenyl-1-butanol that can be produced using 31 mg NaBH4 and an excess of butyrophenone. 4. + NaBH4 OH (after workup with dilute HCI) What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardAspirin from Wintergreen: 1. In isolating the salicylic acid, why is it important to press out as much of the water as possible? Write a step-by-step mechanism for the esterification of salicylic acid with acetic anhydride catalyzed by concentrated H₂SO4. 3. Calculate the exact monoisotopic mass of aspirin showing your work. What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forwardSynthesis of Ibuprofen-Part 1: 1. What characteristic absorption band changes would you expect in the IR spectrum on going from p-isobutylacetophenone to 1-(4-isobutylphenyl)-ethanol and then to 1-(4-isobutylphenyl)-1-choroethane as you did in the experiment today? Give approximate wavenumbers associated with each functional group change. Given that the mechanism of the chlorination reaction today involves formation of a benzylic carbocation, explain why the following rearranged product is not formed. محرم محمد 3. Why do we use dilute HCl for the first step of the reaction today and concentrated HCI for the second step? What signals appeared/disappeared/shifted that indicate that you have your intended product and not starting material? What other impurities are present in your product and how do you know?arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage Learning
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry for Engineering StudentsChemistryISBN:9781285199023Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Chemistry for Engineering Students
Chemistry
ISBN:9781285199023
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Calorimetry Concept, Examples and Thermochemistry | How to Pass Chemistry; Author: Melissa Maribel;https://www.youtube.com/watch?v=nSh29lUGj00;License: Standard YouTube License, CC-BY