Chemistry: The Central Science (14th Edition)
14th Edition
ISBN: 9780134414232
Author: Theodore E. Brown, H. Eugene LeMay, Bruce E. Bursten, Catherine Murphy, Patrick Woodward, Matthew E. Stoltzfus
Publisher: PEARSON
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Chapter 9, Problem 43E
(a)
Interpretation Introduction
To determine: The Lewis structures of three isomers of 
(b)
Interpretation Introduction
To determine: The isomer which has zero dipole moment out of three isomers of 
(c)
Interpretation Introduction
To determine: The isomeric forms of 
Also they have dipole moments or not.
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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
Resonance Effects
Overall Electron-Density
×
NO2
○ donating
O donating
O withdrawing
O withdrawing
O electron-rich
electron-deficient
no inductive effects
O no resonance effects
O similar to benzene
E
[
CI
O donating
withdrawing
O no inductive effects
Explanation
Check
○ donating
withdrawing
no resonance effects
electron-rich
electron-deficient
O similar to benzene
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Chapter 9 Solutions
Chemistry: The Central Science (14th Edition)
Ch. 9.2 - Consider the following AB3 molecules and ions-...Ch. 9.2 - Prob. 9.1.2PECh. 9.2 - Prob. 9.2.1PECh. 9.2 - Prob. 9.2.2PECh. 9.2 - Prob. 9.3.1PECh. 9.2 - Prob. 9.3.2PECh. 9.3 - Prob. 9.4.1PECh. 9.3 - Determine whether the following molecules are...Ch. 9.5 - Prob. 9.5.1PECh. 9.5 - Prob. 9.5.2PE
Ch. 9.6 - Prob. 9.6.1PECh. 9.6 - Prob. 9.6.2PECh. 9.6 - Prob. 9.7.1PECh. 9.6 - Prob. 9.7.2PECh. 9.7 - Prob. 9.8.1PECh. 9.7 - Prob. 9.8.2PECh. 9.8 - Prob. 9.9.1PECh. 9.8 - Prob. 9.9.2PECh. 9 - Prob. 1DECh. 9 - 9.1 A certain AB4, molecule has a "seesaw" shape...Ch. 9 - Prob. 2ECh. 9 - Prob. 3ECh. 9 - Prob. 4ECh. 9 - Prob. 5ECh. 9 - Prob. 6ECh. 9 - In the hydrocarbon a. What is the hybridization at...Ch. 9 - The drawing below shows the overlap of two hybrid...Ch. 9 - Prob. 9ECh. 9 -
9.10 The following is part of a molecular...Ch. 9 - Prob. 11ECh. 9 - Prob. 12ECh. 9 -
9.13
a. An AB2 molecule is linear. How...Ch. 9 - a. Methane (CH4) and the perchlorate ion (C104-)...Ch. 9 - Prob. 15ECh. 9 - Prob. 16ECh. 9 - Prob. 17ECh. 9 - Prob. 18ECh. 9 - In which of these molecules or ions does the...Ch. 9 - Prob. 20ECh. 9 - How many nonbonding electron pairs are there in...Ch. 9 - Prob. 22ECh. 9 - Prob. 23ECh. 9 - Prob. 24ECh. 9 - Give the electron-domain and molecular geometries...Ch. 9 - Prob. 26ECh. 9 - Prob. 27ECh. 9 - Prob. 28ECh. 9 - Prob. 29ECh. 9 - Prob. 30ECh. 9 - Ammonia, NH3 reacts with incredibly strong bases...Ch. 9 - In which of the following AFn molecules or ions is...Ch. 9 - a. Explain why BrF4 is square planar, whereas...Ch. 9 -
9.34 Name the proper three-dimensional molecule...Ch. 9 - Prob. 35ECh. 9 - Prob. 36ECh. 9 - Prob. 37ECh. 9 - Prob. 38ECh. 9 - a. (a) Is the molecule BF3 polar or nonpolar? b....Ch. 9 - Prob. 40ECh. 9 - Predict whether each of the following molecules is...Ch. 9 - Prob. 42ECh. 9 - Prob. 43ECh. 9 - Prob. 44ECh. 9 - For each statement, irldicate whether it is true...Ch. 9 - Draw sketches illustrating the overlap between the...Ch. 9 - For each statement, indicate whether it is true or...Ch. 9 - Prob. 48ECh. 9 - Prob. 49ECh. 9 - Consider the SC12 molecule. a. What IS the...Ch. 9 - Indicate the hybridization of the central atom in...Ch. 9 - Prob. 52ECh. 9 - Prob. 53ECh. 9 - Prob. 54ECh. 9 - Prob. 55ECh. 9 - Prob. 56ECh. 9 - a. Draw Lewis structures for ethane (C2He),...Ch. 9 - a. Draw Lewis structures for ethane (C2He),...Ch. 9 - Prob. 59ECh. 9 - Ethyl acetate. C4H802, is a fragrant substance...Ch. 9 - Prob. 61ECh. 9 - Prob. 62ECh. 9 - Prob. 63ECh. 9 - Prob. 64ECh. 9 - In the formate ion, HC02- , the carbon atom is the...Ch. 9 - Prob. 66ECh. 9 - Prob. 67ECh. 9 - Prob. 68ECh. 9 - Prob. 69ECh. 9 - a. If you combine two atomic orbitals on two...Ch. 9 - Prob. 71ECh. 9 - Prob. 72ECh. 9 - Prob. 73ECh. 9 - Indicate whether each statement is true or false....Ch. 9 - Prob. 75ECh. 9 - Prob. 76ECh. 9 - Prob. 77ECh. 9 - Prob. 78ECh. 9 - Prob. 79ECh. 9 - Prob. 80ECh. 9 - Determine the electron configurations for CN+, CN,...Ch. 9 - Prob. 82ECh. 9 - Consider the molecular orbitals of the P2...Ch. 9 - The iodine bromide molecule, IBr, is an...Ch. 9 - Prob. 85AECh. 9 - Prob. 86AECh. 9 - Consider the following XF4 ions: PF4, BrF4-,...Ch. 9 -
9.88 Consider the molecule PF4Cl....Ch. 9 - Prob. 89AECh. 9 - Fill in the blank spaces in the following chart....Ch. 9 - Prob. 91AECh. 9 - Prob. 92AECh. 9 - Prob. 93AECh. 9 - Prob. 94AECh. 9 - Prob. 95AECh. 9 - Prob. 96AECh. 9 - Prob. 97AECh. 9 - Prob. 98AECh. 9 - Prob. 99AECh. 9 - Prob. 100AECh. 9 - In ozone, 03, the two oxygen atoms on the ends Of...Ch. 9 - Butadiene, C4H6, is a planar molecule that has the...Ch. 9 - The structure of borazine, B3N3H6, is a...Ch. 9 - Prob. 104AECh. 9 - Prob. 105AECh. 9 - Prob. 106AECh. 9 - Prob. 107AECh. 9 - Prob. 108AECh. 9 - Azo dyes are organic dyes that are used for many...Ch. 9 - a. Using only the valence atomic orbitals of a...Ch. 9 - Carbon monoxide, CO, is isoelectronic to N2. a....Ch. 9 - The energy-level diagram in Figure 9.36 shows that...Ch. 9 - A compound composed of 2.1 29.8%N, and 68.1%O has...Ch. 9 -
9.114 Sulfur tetrafluoride (SR4) reacts slowly...Ch. 9 - Prob. 115IECh. 9 - The molecule 2-butene, C4Hs, can undergo a...Ch. 9 - Prob. 117IECh. 9 - Use average bond enthalpies (Table 8.3 ) to...Ch. 9 - Prob. 119IECh. 9 - Prob. 120IECh. 9 - Prob. 121IECh. 9 - Prob. 122IE
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- Understanding how substituents activate Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation HN NH2 Check X (Choose one) (Choose one) (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Aarrow_forwardIdentifying electron-donating and electron-withdrawing effects on benzene 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. Inductive Effects Resonance Effects Overall Electron-Density Molecule CF3 O donating O donating O withdrawing O withdrawing O no inductive effects O no resonance effects electron-rich electron-deficient O similar to benzene CH3 O donating O withdrawing O no inductive effects O donating O withdrawing Ono resonance effects O electron-rich O electron-deficient O similar to benzene Explanation Check Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward* Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forward
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- → 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
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