
Chemistry: The Molecular Nature of Matter and Change
9th Edition
ISBN: 9781260477467
Author: Martin Silberberg
Publisher: Mcgraw-hill Higher Education (us)
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Question
Chapter 10, Problem 10.30P
Interpretation Introduction
Interpretation:
The name of all the molecular shapes that have a tetrahedral electron-group arrangement is to be determined.
Concept introduction:
VSEPR theory is based on the repulsions between the electrons pair in the valence shell. According to VSEPR theory, the shape of a molecule depends on the position of the electron pairs to minimize the repulsion, and maximize the stability.
According to VSEPR theory, the table for molecular geometries when the central atom has no lone pair is as follows:
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+
C8H16O2 (Fatty acid) +
11 02 → 8 CO2
a. Which of the above are the reactants?
b. Which of the above are the products?
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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
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2
h. Where were the electrons initially in this chemical reaction and where is it now that it is
finished?
→
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?
Rank 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)
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Chapter 10 Solutions
Chemistry: The Molecular Nature of Matter and Change
Ch. 10.1 - Write a Lewis structure for
H2S;
;
SOCl2.
Ch. 10.1 - Prob. 10.1BFPCh. 10.1 - Prob. 10.2AFPCh. 10.1 - Prob. 10.2BFPCh. 10.1 - Prob. 10.3AFPCh. 10.1 - Prob. 10.3BFPCh. 10.1 - Prob. 10.4AFPCh. 10.1 - Prob. 10.4BFPCh. 10.1 - Write a Lewis structure with minimal formal...Ch. 10.1 - Prob. 10.5BFP
Ch. 10.2 - Prob. 10.6AFPCh. 10.2 - Prob. 10.6BFPCh. 10.2 - Prob. 10.7AFPCh. 10.2 - Prob. 10.7BFPCh. 10.2 - Prob. 10.8AFPCh. 10.2 - Prob. 10.8BFPCh. 10.3 - Prob. 10.9AFPCh. 10.3 - Prob. 10.9BFPCh. 10 - Prob. 10.1PCh. 10 - When is a resonance hybrid needed to adequately...Ch. 10 - Prob. 10.3PCh. 10 - Prob. 10.4PCh. 10 - Draw a Lewis structure for (a) SiF4; (b) SeCl2;...Ch. 10 - Draw a Lewis structure for (a) ; (b) C2F4; (c)...Ch. 10 - Prob. 10.7PCh. 10 - Prob. 10.8PCh. 10 - Prob. 10.9PCh. 10 - Draw Lewis structures of all the important...Ch. 10 - Prob. 10.11PCh. 10 - Draw Lewis structures of all the important...Ch. 10 - Prob. 10.13PCh. 10 - Prob. 10.14PCh. 10 - Draw the Lewis structure with lowest formal...Ch. 10 - Draw the Lewis structure with lowest formal...Ch. 10 - Prob. 10.17PCh. 10 - Prob. 10.18PCh. 10 - Prob. 10.19PCh. 10 - Prob. 10.20PCh. 10 - These species do not obey the octet rule. Draw a...Ch. 10 - These species do not obey the octet rule. Draw a...Ch. 10 - Molten beryllium chloride reacts with chloride ion...Ch. 10 - Prob. 10.24PCh. 10 - Prob. 10.25PCh. 10 - Phosgene is a colorless, highly toxic gas that was...Ch. 10 - If you know the formula of a molecule or ion, what...Ch. 10 - In what situation is the name of the molecular...Ch. 10 - Prob. 10.29PCh. 10 - Prob. 10.30PCh. 10 - Consider the following molecular shapes. (a) Which...Ch. 10 - Use wedge-bond perspective drawings (if necessary)...Ch. 10 - Prob. 10.33PCh. 10 - Determine the electron-group arrangement,...Ch. 10 - Determine the electron-group arrangement,...Ch. 10 - Prob. 10.36PCh. 10 - Prob. 10.37PCh. 10 - Prob. 10.38PCh. 10 - Prob. 10.39PCh. 10 - Determine the shape, ideal bond angle(s), and the...Ch. 10 - Prob. 10.41PCh. 10 - Determine the shape around each central atom in...Ch. 10 - Prob. 10.43PCh. 10 - Prob. 10.44PCh. 10 - Prob. 10.45PCh. 10 - Prob. 10.46PCh. 10 - Arrange the following ACln species in order of...Ch. 10 - State an ideal value for each of the bond angles...Ch. 10 - Prob. 10.49PCh. 10 - Prob. 10.50PCh. 10 - Prob. 10.51PCh. 10 - Prob. 10.52PCh. 10 - How can a molecule with polar covalent bonds not...Ch. 10 - Prob. 10.54PCh. 10 - Consider the molecules SCl2, F2, CS2, CF4, and...Ch. 10 - Consider the molecules BF3, PF3, BrF3, SF4, and...Ch. 10 - Prob. 10.57PCh. 10 - Prob. 10.58PCh. 10 - Prob. 10.59PCh. 10 - Prob. 10.60PCh. 10 - Prob. 10.61PCh. 10 - Prob. 10.62PCh. 10 - Prob. 10.63PCh. 10 - Prob. 10.64PCh. 10 - Prob. 10.65PCh. 10 - Prob. 10.66PCh. 10 - When SO3 gains two electrons, forms. (a) Which...Ch. 10 - The actual bond angle in NO2 is 134.3°, and in it...Ch. 10 - Prob. 10.69PCh. 10 - Propylene oxide is used to make many products,...Ch. 10 - Prob. 10.71PCh. 10 - Prob. 10.72PCh. 10 - Prob. 10.73PCh. 10 - Prob. 10.74PCh. 10 - Prob. 10.75PCh. 10 - Prob. 10.76PCh. 10 - Prob. 10.77PCh. 10 - A gaseous compound has a composition by mass of...Ch. 10 - Prob. 10.79PCh. 10 - Prob. 10.80PCh. 10 - Prob. 10.81PCh. 10 - Prob. 10.82PCh. 10 - Pure HN3 (atom sequence HNNN) is explosive. In...Ch. 10 - Prob. 10.84PCh. 10 - Prob. 10.85PCh. 10 - Oxalic acid (H2C2O4) is found in toxic...Ch. 10 - Prob. 10.87PCh. 10 - Hydrazine (N2H4) is used as a rocket fuel because...Ch. 10 - Prob. 10.89PCh. 10 - Prob. 10.90PCh. 10 - Prob. 10.91PCh. 10 - Consider the following molecular shapes:
Match...Ch. 10 - Prob. 10.93PCh. 10 - Prob. 10.94PCh. 10 - Prob. 10.95PCh. 10 - Phosphorus pentachloride, a key industrial...
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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 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_forwardIdentifying 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_forward
- Assign R or S to all the chiral centers in each compound drawn below porat bg 9 Br Brarrow_forwarddescrive the energy levels of an atom and howan electron moces between themarrow_forwardRank each set of substituents using the Cahn-Ingold-Perlog sequence rules (priority) by numbering the highest priority substituent 1.arrow_forward
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