
CHEMISTRY-TEXT
8th Edition
ISBN: 9780134856230
Author: Robinson
Publisher: PEARSON
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Textbook Question
Chapter 7, Problem 7.95SP
Assign formal charges to the atoms in the following structures
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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 7 Solutions
CHEMISTRY-TEXT
Ch. 7 - Use the electro negativity values in Figure 7.4...Ch. 7 - Conceptual APPLY 7.2 An electrostatic potential...Ch. 7 - The dipole moment of AgCI in the gas phaseis...Ch. 7 - Predict which bond has greater percent ionic...Ch. 7 - Select the correct electron-dot structure for H2S...Ch. 7 - Use the octet rule to predict the molecular...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Select the correct electron-dot structure for...Ch. 7 - Identify the correct electron-dot structure(s) for...
Ch. 7 - Prob. 7.11PCh. 7 - Which oxygen species do you predict to be most...Ch. 7 - Draw an electron-dot structure for the following...Ch. 7 - There are two molecules with the formula C2H6O...Ch. 7 - The following structure is a representation of...Ch. 7 - Draw two possible electron-dot structures for the...Ch. 7 - Called “laughing gas, nitrous oxide (N2O) is...Ch. 7 - Draw as many resonance structures as possible for...Ch. 7 - Prob. 7.19PCh. 7 - Prob. 7.20ACh. 7 - Calculate the formal charge on each atom in the...Ch. 7 - Start with the electron-dot structure for the...Ch. 7 - Calculate formal charges on the C and O atoms in...Ch. 7 - Three resonance structures for anisole (Problem...Ch. 7 - The toxicity of the organophosphate insecticides...Ch. 7 - Prob. 7.26PCh. 7 - Prob. 7.27PCh. 7 - The following structure is a representation of the...Ch. 7 - The electron-dot structure for the nerve a gentsar...Ch. 7 - Draw the new electron-dot structures indicated by...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - Two electrostatic potential maps are shown, one of...Ch. 7 - Prob. 7.34CPCh. 7 - Which of the following drawings is most likely to...Ch. 7 - The following ball-and-stick molecular model is a...Ch. 7 - The following hall-and-stick molecular model is a...Ch. 7 - Sinapaldehyde, a compound present in the toasted...Ch. 7 - Vitamin C (ascorbic acid) has the following...Ch. 7 - Match the following descriptions with the type of...Ch. 7 - Why do two atoms come together to form a covalent...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Predict which of the following bonds should be...Ch. 7 - Prob. 7.45SPCh. 7 - What general trends in electro negativity occur in...Ch. 7 - Predict the electro negativity of the undiscovered...Ch. 7 - Order the following elements according to...Ch. 7 - Order the following elements according to...Ch. 7 - Which of the following substances contain bonds...Ch. 7 - Use the electro negativity data in Figure 7.4 to...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Which of the substances...Ch. 7 - Which of the substances...Ch. 7 - Order the following compounds according to the...Ch. 7 - Order the following compounds according to the...Ch. 7 - Prob. 7.58SPCh. 7 - Using only the elements Ca, Cl, and Si, give...Ch. 7 - The dipole moment of BrCl is 0.518 D, and the...Ch. 7 - Prob. 7.61SPCh. 7 - Prob. 7.62SPCh. 7 - Prob. 7.63SPCh. 7 - Why does the octet rule apply primarily to...Ch. 7 - Which of the following substances contains an atom...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron.dot structure for the hydronium...Ch. 7 - Oxalic acid, H2C2O4 , is a mildly poisonous...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Prob. 7.72SPCh. 7 - Identify the fourth-row elements, X, that form the...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Prob. 7.79SPCh. 7 - Methylphenidate (C14H19NO2) , marketed as Ritalin,...Ch. 7 - Pregabalin (C8H17NO2) , marketed as Lyric a, is an...Ch. 7 - The following molecular model is that of...Ch. 7 - Ibuprofen C 13 H 18 O 2 marketed under such brand...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can for...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Benzene has the following structural formula. Use...Ch. 7 - Draw three resonance structures for sulfur...Ch. 7 - Some mothballs used when storing clothes are made...Ch. 7 - Four different structures (a), (b), (c), and (d)...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Calculate formal charges for the C and O atoms in...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Prob. 7.102SPCh. 7 - Prob. 7.103SPCh. 7 - Boron trifluoride reacts with dimethyl ether to...Ch. 7 - Thiofulminic acid, HCNS, has recently been...Ch. 7 - Draw two rcsonancc strutur for methyl isocyanate,...Ch. 7 - In the cyanatc ion. OCN , carbon is the central...Ch. 7 - Prob. 7.108MPCh. 7 - Prob. 7.109MPCh. 7 - Prob. 7.110MPCh. 7 - The neutral OH molecule has been implicated in...Ch. 7 - Prob. 7.112MPCh. 7 - Prob. 7.113MP
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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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