EBK CHEMISTRY: AN ATOMS FIRST APPROACH
2nd Edition
ISBN: 8220100552236
Author: ZUMDAHL
Publisher: CENGAGE L
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Chapter 4, Problem 108CWP
Interpretation Introduction
Interpretation: The given statements are to be analyzed with respect to the
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You are trying to decide if there is a single reagent you can add that will make the following synthesis possible without any other major side products:
xi
1. ☑
2. H₂O
хе
i
Draw the missing reagent X you think will make this synthesis work in the drawing area below.
If there is no reagent that will make your desired product in good yield or without complications, just check the box under the drawing area and leave it blank.
Click and drag to start drawing a
structure.
There is no reagent that will make this synthesis work without complications.
: ☐
S
☐
Predict the major products of this organic reaction:
H
OH
1. LiAlH4
2. H₂O
?
Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry.
Click and drag to start drawing a
structure.
G
C
टे
For each reaction below, decide if the first stable organic product that forms in solution will create a new C-C bond, and check the appropriate box.
Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below.
Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first
stable product you expect to form in solution.
NH2
CI
MgCl
?
Will the first product that forms in this reaction
create a new CC bond?
Yes
No
MgBr
?
Will the first product that forms in this reaction
create a new CC bond?
Yes
No
G
टे
Chapter 4 Solutions
EBK CHEMISTRY: AN ATOMS FIRST APPROACH
Ch. 4 - Explain the main postulate of the VSEPR model....Ch. 4 - Explain why CF4 and Xef4 are nonpolar compounds...Ch. 4 - Consider the following compounds: CO2, SO2, KrF2,...Ch. 4 - Prob. 4RQCh. 4 - What hybridization is required for central atoms...Ch. 4 - Prob. 6RQCh. 4 - Prob. 7RQCh. 4 - What are molecular orbitals? How do they compare...Ch. 4 - Explain the difference between the and MOs for...Ch. 4 - Prob. 3ALQ
Ch. 4 - Which of the following would you expect to be more...Ch. 4 - Arrange the following molecules from most to least...Ch. 4 - Which is the more correct statement: The methane...Ch. 4 - Prob. 7ALQCh. 4 - Prob. 8ALQCh. 4 - Which of the following statements is/are true?...Ch. 4 - Give one example of a compound having a linear...Ch. 4 - In the hybrid orbital model, compare and contrast ...Ch. 4 - Prob. 13QCh. 4 - Prob. 14QCh. 4 - Prob. 15QCh. 4 - Prob. 16QCh. 4 - Compare and contrast bonding molecular orbitals...Ch. 4 - Prob. 18QCh. 4 - Why does the molecular orbital model do a better...Ch. 4 - The three NO bonds in NO3 are all equivalent in...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure and bond angles...Ch. 4 - Prob. 24ECh. 4 - Prob. 25ECh. 4 - Two variations of the octahedral geometry (see...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - Predict the molecular structure (including bond...Ch. 4 - State whether or not each of the following has a...Ch. 4 - The following electrostatic potential diagrams...Ch. 4 - Which of the molecules in Exercises 21 and 22 have...Ch. 4 - Which of the molecules in Exercises 27 and 28 have...Ch. 4 - Write Lewis structures and predict the molecular...Ch. 4 - Write Lewis structures and predict whether each of...Ch. 4 - Consider the following Lewis structure where E is...Ch. 4 - Consider the following Lewis structure where E is...Ch. 4 - The molecules BF3, CF4, CO2, PF5, and SF6 are all...Ch. 4 - Two different compounds have the formula XeF2Cl2....Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - Use the localized electron model to describe the...Ch. 4 - The space-filling models of ethane and ethanol are...Ch. 4 - The space-filling models of hydrogen cyanide and...Ch. 4 - Prob. 45ECh. 4 - Prob. 46ECh. 4 - Prob. 47ECh. 4 - Give the expected hybridization of the central...Ch. 4 - For each of the following molecules, write the...Ch. 4 - For each of the following molecules or ions that...Ch. 4 - Prob. 51ECh. 4 - The allene molecule has the following Lewis...Ch. 4 - Indigo is the dye used in coloring blue jeans. The...Ch. 4 - Prob. 54ECh. 4 - Prob. 55ECh. 4 - Many important compounds in the chemical industry...Ch. 4 - Two molecules used in the polymer industry are...Ch. 4 - Hot and spicy foods contain molecules that...Ch. 4 - One of the first drugs to be approved for use in...Ch. 4 - The antibiotic thiarubin-A was discovered by...Ch. 4 - Prob. 61ECh. 4 - Sketch the molecular orbital and label its type (...Ch. 4 - Prob. 63ECh. 4 - Which of the following are predicted by the...Ch. 4 - Prob. 65ECh. 4 - Prob. 66ECh. 4 - Prob. 67ECh. 4 - Using the molecular orbital model to describe the...Ch. 4 - Prob. 69ECh. 4 - A Lewis structure obeying the octet rule can be...Ch. 4 - Using the molecular orbital model, write electron...Ch. 4 - Using the molecular orbital model, write electron...Ch. 4 - In which of the following diatomic molecules would...Ch. 4 - In terms of the molecular orbital model, which...Ch. 4 - Prob. 75ECh. 4 - Show how a hydrogen 1s atomic orbital and a...Ch. 4 - Use Figs. 4-54 and 4-55 to answer the following...Ch. 4 - The diatomic molecule OH exists in the gas phase....Ch. 4 - Prob. 79ECh. 4 - Describe the bonding in NO+, NO, and NO, using...Ch. 4 - Describe the bonding in the O3 molecule and the...Ch. 4 - Prob. 82ECh. 4 - Prob. 83AECh. 4 - Vitamin B6 is an organic compound whose deficiency...Ch. 4 - Two structures can be drawn for cyanuric acid: a....Ch. 4 - Prob. 86AECh. 4 - What do each of the following sets of...Ch. 4 - Aspartame is an artificial sweetener marketed...Ch. 4 - Prob. 89AECh. 4 - The three most stable oxides of carbon are carbon...Ch. 4 - Prob. 91AECh. 4 - Which of the following molecules have net dipole...Ch. 4 - The strucrure of TeF5 is Draw a complete Lewis...Ch. 4 - Complete the following resonance structures for...Ch. 4 - Prob. 95AECh. 4 - Describe the bonding in the first excited state of...Ch. 4 - Using an MO energy-level diagram, would you expect...Ch. 4 - Show how a dxz. atomic orbital and a pz, atomic...Ch. 4 - What type of molecular orbital would result from...Ch. 4 - Consider three molecules: A, B, and C. Molecule A...Ch. 4 - Prob. 101CWPCh. 4 - Predict the molecular structure, bond angles, and...Ch. 4 - Draw the Lewis structures for SO2, PCl3, NNO, COS,...Ch. 4 - Draw the Lewis structures for TeCl4, ICl5, PCl5,...Ch. 4 - A variety of chlorine oxide fluorides and related...Ch. 4 - Pelargondin is the molecule responsible for the...Ch. 4 - Complete a Lewis structure for the compound shown...Ch. 4 - Prob. 108CWPCh. 4 - Consider the molecular orbital electron...Ch. 4 - Place the species B2+ , B2, and B2 in order of...Ch. 4 - The compound NF3 is quite stable, but NCl3 is very...Ch. 4 - Predict the molecular structure for each of the...Ch. 4 - Prob. 113CPCh. 4 - Cholesterol (C27liu;O) has the following...Ch. 4 - Cyanamide (H2NCN), an important industrial...Ch. 4 - As compared with CO and O2, CS and S2 are very...Ch. 4 - Prob. 117CPCh. 4 - Use the MO model to explain the bonding in BeH2....Ch. 4 - Prob. 119CPCh. 4 - Arrange the following from lowest to highest...Ch. 4 - Prob. 121CPCh. 4 - Prob. 122CPCh. 4 - Carbon monoxide (CO) forms bonds to a variety of...Ch. 4 - The space-filling model for benzoic acid, a food...Ch. 4 - As the bead engineer of your starship in charge of...Ch. 4 - A flask containing gaseous N2 is irradiated with...Ch. 4 - Determine the molecular structure and...
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- For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. དྲ。 ✗MgBr ? O CI Will the first product that forms in this reaction create a new C-C bond? Yes No • ? Will the first product that forms in this reaction create a new CC bond? Yes No × : ☐ Xarrow_forwardPredict the major products of this organic reaction: OH NaBH4 H ? CH3OH Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. ☐ : Sarrow_forwardPredict the major products of this organic reaction: 1. LIAIHA 2. H₂O ? Note: be sure you use dash and wedge bonds when necessary, for example to distinguish between major products with different stereochemistry. Click and drag to start drawing a structure. X : ☐arrow_forward
- For each reaction below, decide if the first stable organic product that forms in solution will create a new C - C bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. NH2 tu ? ? OH Will the first product that forms in this reaction create a new CC bond? Yes No Will the first product that forms in this reaction create a new CC bond? Yes No C $ ©arrow_forwardAs the lead product manager at OrganometALEKS Industries, you are trying to decide if the following reaction will make a molecule with a new C-C bond as its major product: 1. MgCl ? 2. H₂O* If this reaction will work, draw the major organic product or products you would expect in the drawing area below. If there's more than one major product, you can draw them in any arrangement you like. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry. If the major products of this reaction won't have a new CC bond, just check the box under the drawing area and leave it blank. Click and drag to start drawing a structure. This reaction will not make a product with a new CC bond. G marrow_forwardIncluding activity coefficients, find [Hg22+] in saturated Hg2Br2 in 0.00100 M NH4 Ksp Hg2Br2 = 5.6×10-23.arrow_forward
- give example for the following(by equation) a. Converting a water insoluble compound to a soluble one. b. Diazotization reaction form diazonium salt c. coupling reaction of a diazonium salt d. indacator properties of MO e. Diazotization ( diazonium salt of bromobenzene)arrow_forward2-Propanone and ethyllithium are mixed and subsequently acid hydrolyzed. Draw and name the structures of the products.arrow_forward(Methanesulfinyl)methane is reacted with NaH, and then with acetophenone. Draw and name the structures of the products.arrow_forward
- 3-Oxo-butanenitrile and (E)-2-butenal are mixed with sodium ethoxide in ethanol. Draw and name the structures of the products.arrow_forwardWhat is the reason of the following(use equations if possible) a.) In MO preperation through diazotization: Addition of sodium nitrite in acidfied solution in order to form diazonium salt b.) in MO experiment: addition of sodium hydroxide solution in the last step to isolate the product MO. What is the color of MO at low pH c.) In MO experiment: addition of sodium hydroxide solution in the last step to isolate the product MO. What is the color of MO at pH 4.5 d.) Avoiding not cooling down the reaction mixture when preparing the diazonium salt e.) Cbvcarrow_forwardA 0.552-g sample of an unknown acid was dissolved in water to a total volume of 20.0 mL. This sample was titrated with 0.1103 M KOH. The equivalence point occurred at 29.42 mL base added. The pH of the solution at 10.0 mL base added was 3.72. Determine the molar mass of the acid. Determine the Ka of the acid.arrow_forward
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