
General Chemistry: Principles and Modern Applications, Loose Leaf Version (11th Edition)
11th Edition
ISBN: 9780133897319
Author: Ralph H. Petrucci, F. Geoffrey Herring, Jeffry D. Madura, Carey Bissonnette
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 10, Problem 151SAE
Interpretation Introduction
Interpretation:
Difference between molecular − geometry and electron group geometry should be explained using NH3 as the structure.
Concept introduction:
For molecular geometry consider only the bonded atoms and for the determination of the electron − group geometry considers all bonded and lone pair electrons.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
can someone draw out the reaction mechanism for this reaction showing all the curly arrows and 2. Draw the GPNA molecule and identify the phenylalanine portion. 3. Draw L-phenylalanine with the correct stereochemistry
What is the reaction mechanism for this?
Predict the major products of both organic reactions.
Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major
products.
esc
esc
Explanation
Check
2
:
+
+
X
H₁₂O
+
Х
ง
WW
E
R
Y
qab
Ccaps lock
shift
$
P
X
Click and drag to start
drawing a structure.
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility
Bil
T
FR
F18
9
G
t
K
L
Z
X
V
B
N
M
control
opption
command
command
T
C
d
Chapter 10 Solutions
General Chemistry: Principles and Modern Applications, Loose Leaf Version (11th Edition)
Ch. 10 - Write Lewis symbols for the following atoms. (a)...Ch. 10 - Write Lewis symbols for the following ions. (a)...Ch. 10 - Write plausible Lewis structures for the following...Ch. 10 - Each of the following molecules contains at least...Ch. 10 - By means of Lewis structures, represent bonding...Ch. 10 - Which of the following have Lewis structures that...Ch. 10 - Prob. 7ECh. 10 - Suggest reasons why the following do not exist as...Ch. 10 - Describe what is wrong with each of the following...Ch. 10 - Describe what is wrong with each of the following...
Ch. 10 - Prob. 11ECh. 10 - Indicate what is wrong with each of the following...Ch. 10 - Write Lewis structures for the following ionic...Ch. 10 - Under appropriate conditions, both hydrogen and...Ch. 10 - Derive the correct formulas for the following...Ch. 10 - Each of the following ionic compounds consists of...Ch. 10 - Assign formal charges to each of the atoms in the...Ch. 10 - Assign formal charges to each of the atoms in the...Ch. 10 - Both oxidation state and formal charge involve...Ch. 10 - Prob. 20ECh. 10 - Prob. 21ECh. 10 - Assign formal charges to the atoms in the...Ch. 10 - Prob. 23ECh. 10 - Show that the idea of minimizing the formal...Ch. 10 - Write acceptable Lewis structures for the...Ch. 10 - Two molecules that have the same formulas but...Ch. 10 - The following polyatomic anions involve covalent...Ch. 10 - Represent the following ionic compounds by Lewis...Ch. 10 - Write a plausible Lewis structure for...Ch. 10 - Prob. 30ECh. 10 - Write Lewis structures for the molecules...Ch. 10 - Write Lewis structures for the molecules...Ch. 10 - Write Lewis structures for the molecules...Ch. 10 - Write Lewis structures for the molecules...Ch. 10 - Identify the main group that the element X belongs...Ch. 10 - Prob. 36ECh. 10 - Use your knowledge of electronegativities, but do...Ch. 10 - Which of the blowing molecules would you expect to...Ch. 10 - What is the percent ionic character of each of the...Ch. 10 - Prob. 40ECh. 10 - Prob. 41ECh. 10 - Use a cross-base arrow () to represent the...Ch. 10 - Which electrostatic potential map corresponds to...Ch. 10 - Prob. 44ECh. 10 - Two electrostatic potential maps are shown, one...Ch. 10 - Prob. 46ECh. 10 - Prob. 47ECh. 10 - Which of the following species requires a...Ch. 10 - Dinitrogen oxide (nitrous oxide, or "laughing...Ch. 10 - The Lewis structure of nitric acid, HONO2, is a...Ch. 10 - Draw Lewis structures for the following species,...Ch. 10 - Draw Lewis structures for the following species,...Ch. 10 - Write plausible Lewis structures for the following...Ch. 10 - Write plausible Lewis structures for the following...Ch. 10 - Which of the following species would you expect to...Ch. 10 - Write a plausible Lewis structure for NO2 , and...Ch. 10 - In which of the following species is it necessary...Ch. 10 - Prob. 58ECh. 10 - Use VSEPR theory to predict the geometric shapes...Ch. 10 - Use VSEPR theory to predict the geometric shapes...Ch. 10 - Each of the following is either linear, angular...Ch. 10 - Predict the geometric shapes of (a) CO ; (b)...Ch. 10 - One of the following ions has a trigonal-planer...Ch. 10 - Two of the following have the same shape. Which...Ch. 10 - Prob. 65ECh. 10 - Sketch the probable geometric shape of molecule of...Ch. 10 - Use the VSEPR theory to predict the shapes of the...Ch. 10 - Use the VSEPR theory to predict the shape of (a)...Ch. 10 - The molecular shape of BF2 is planar (see Table...Ch. 10 - Explain why it is not necessary to find the Lewis...Ch. 10 - Comment on the similarities and differences in the...Ch. 10 - Comment on the similarities and differences in the...Ch. 10 - Draw a plausible Lewis structure for the following...Ch. 10 - Draw a plausible Lewis structure for the following...Ch. 10 - Sketch the propyne molecule, CH2CCH. Indicate the...Ch. 10 - Sketch the propene molecule, CH2CHCH2. Indicate...Ch. 10 - Lactic acid has the formula CH2CH(OH)COOH. Sketch...Ch. 10 - Levulinic acid has the formula CH2(CO)CH2CH2COOH....Ch. 10 - Prob. 79ECh. 10 - Prob. 80ECh. 10 - Predict the shapes of the following molecules, and...Ch. 10 - Which of the blowing molecules would you expect to...Ch. 10 - The molecule H2O2 has a resultant dipole moment of...Ch. 10 - Prob. 84ECh. 10 - Without referring to tables in the text, indicate...Ch. 10 - Estimate the lengths of the blowing bonds and...Ch. 10 - A relationship between bond lengths and...Ch. 10 - In which of the following molecules would you...Ch. 10 - Prob. 89ECh. 10 - Prob. 90ECh. 10 - A reaction involved in the formation of ozone the...Ch. 10 - Use data from Table 10.3, but without performing...Ch. 10 - Use data from Table 10.3 to estimate the enthalpy...Ch. 10 - One of the chemical reactions that occurs in the...Ch. 10 - Estimate the standard enthalpies of formation at...Ch. 10 - Prob. 96ECh. 10 - Use bond energies from Table 10.3 to estimate rH...Ch. 10 - Equations (1) end (2) can be combined to yield the...Ch. 10 - One reaction involved in the sequence of reactions...Ch. 10 - Prob. 100ECh. 10 - Given the bond-dissociation energies:...Ch. 10 - Prob. 102IAECh. 10 - Prob. 103IAECh. 10 - Prob. 104IAECh. 10 - Prob. 105IAECh. 10 - Draw Lewis structures for two different molecules...Ch. 10 - Sodium azide, NaN2 is the nitrogen gas-forming...Ch. 10 - Prob. 108IAECh. 10 - Prob. 109IAECh. 10 - A few years ago the synthesis of a salt containing...Ch. 10 - Prob. 111IAECh. 10 - In certain polar solvents, PCI, undergoes an...Ch. 10 - Prob. 113IAECh. 10 - Prob. 114IAECh. 10 - Use the VSEPR theory to predict a probable shape...Ch. 10 - The standard enthalpy of formation of...Ch. 10 - Prob. 117IAECh. 10 - Prob. 118IAECh. 10 - Prob. 119IAECh. 10 - R. S. Mulliken proposed that the electronegativity...Ch. 10 - When molten sulfur reacts with chlorine gas, a...Ch. 10 - Hydrogen azide, HN2 , can exist in two forms. One...Ch. 10 - Prob. 123IAECh. 10 - Prob. 124IAECh. 10 - Prob. 125IAECh. 10 - One of the allotropes of sulfur is a ring of eight...Ch. 10 - One of the allotropes of phosphorus consists of...Ch. 10 - In this problem, we examine the basis of three...Ch. 10 - Prob. 129FPCh. 10 - Prob. 130FPCh. 10 - Prob. 131SAECh. 10 - Briefly describe each of the following ideas: (a)...Ch. 10 - Explain the important distinctions between (a)...Ch. 10 - Prob. 134SAECh. 10 - The formal charges on the O atoms in the ion...Ch. 10 - Which molecule is nonlinear?...Ch. 10 - Which molecule is nonpolar?...Ch. 10 - The highest bond-dissociation energy is found in...Ch. 10 - The greatest bond length is found in...Ch. 10 - Draw plausible Lewis structures for the blowing...Ch. 10 - Predict the shapes of the following...Ch. 10 - Which of the following ionic compounds is composed...Ch. 10 - Which of the following molecules does not obey the...Ch. 10 - Which of the following molecules has no polar...Ch. 10 - The electron-group geometry of H2O is (a)...Ch. 10 - For each of the following compounds, give the...Ch. 10 - Use bond enthalpies from Table 10.3 to determine...Ch. 10 - Prob. 148SAECh. 10 - Prob. 149SAECh. 10 - What is the VSEPR theory? On what physical basis...Ch. 10 - Prob. 151SAECh. 10 - Prob. 152SAECh. 10 - Prob. 153SAECh. 10 - Prob. 154SAE
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
- Draw the Markovnikov product of the hydrohalogenation of this alkene. this problem. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for caps lock Explanation Check 2 W E R + X 5 HCI Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bil Y F G H K L ZZ X C V B N M control opption command F10 F10 command 4 BA Ar Carrow_forwardI don't understand why the amide on the top left, with the R attached to one side, doesn't get substituted with OH to form a carboxylic acid. And if only one can be substituted, why did it choose the amide it chose rather than the other amide?arrow_forwardesc Draw the Markovnikov product of the hydration of this alkene. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for this problem. Explanation Check BBB + X 0 1. Hg (OAc)2, H₂O 2. Na BH 5 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bl P 豆 28 2 28 N 9 W E R T Y A S aps lock G H K L Z X C V B N M T central H command #e commandarrow_forward
- C A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. . If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. (X) This transformation can't be done in one step. + Tarrow_forwardく Predict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. No reaction. Explanation Check OH + + ✓ 2 H₂SO 4 O xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardDraw the skeletal ("line") structure of 1,3-dihydroxy-2-pentanone. Click and drag to start drawing a structure. X Parrow_forward
- Predicting edict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. + No reaction. Explanation Check HO Na O H xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Iarrow_forwardChoosing reagents and conditions for acetal formation or hydrolysis 0/5 A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. + This transformation can't be done in one step. 5 I H Autumn alo 值 Ar Barrow_forwardA block of copper of mass 2.00kg(cp = 0.3851 .K) and g temperature 0°C is introduced into an insulated container in which there is 1.00molH, O(g) at 100°C and 1.00 2 atm. Note that C P = 4.184. K for liquid water, and g that A H = 2260 for water. vap g Assuming all the steam is condensed to water, and that the pressure remains constant: (a) What will be the final temperature of the system? (b) What is the heat transferred from the water to the copper? (c) What is the entropy change of the water, the copper, and the total system?arrow_forward
- Identify the missing organic reactants in the following reaction: H+ X + Y OH H+ O O Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H₂O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Explanation Check Click and drag to start drawing a structure. X G 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Cente ? Earrow_forwardCalculate the solubility of CaF2 in g/L (Kp = 4.0 x 10-8). sparrow_forwardFor the following reaction with excess reagent, predict the product. Be sure your answer accounts for stereochemistry. If multiple stereocenters are formed, be sure to draw all products using appropriate wedges and dashes. 1. EtLi, Et₂O CH₁ ? 2. H₂O*arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Introductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage LearningChemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning

Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
Publisher:Cengage Learning

Chemistry for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning

Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning

Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning


Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY