
EBK CHEMISTRY
4th Edition
ISBN: 8220102797864
Author: Burdge
Publisher: YUZU
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 9.6, Problem 1PPC
Interpretation Introduction
Interpretation: The reason as to why hybrid orbitals are used to explain bonding in
and
or
is to be explained.
Concept introduction: Hybrid orbital theory is based upon the formation of hybrid orbitals by mixing of atomic orbitals.
To explain bonding by hybrid orbitals, the number of electrons around the central atom are determined by drawing the Lewis structure of the molecule.
Excitation of electrons to higher orbitals occurs to get the highest number of unpaired electrons.
The required number of hybrid orbitals are combined to obtain the hybridization of the central atom.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
A student proposes the transformation below in one step of an organic synthesis. There may be one or more reactants missing from the left-hand side, but there
are no products missing from the right-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 reactants to the left-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.
+
T
X
O
O
лет-ле
HO
OH
HO
OH
This transformation can't be done in one step.
Determine the structures of the missing organic molecules in the following reaction:
X+H₂O
H*
H+
Y
OH
OH
Note: Molecules that share the same letter have the exact same structure.
In the drawing area below, draw the skeletal ("line") structures of the missing organic molecules X and Y. You may draw the structures in any arrangement
that you like, so long as they aren't touching.
Click and drag to start drawing a structure.
X
S
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.
HO.
O
:☐
+
G
Na O.H
Click and drag to start
drawing a structure.
XS
xs H₂O
Chapter 9 Solutions
EBK CHEMISTRY
Ch. 9.1 - Practice Problem ATTEMPT
Determine the shapes of...Ch. 9.1 - Prob. 1PPBCh. 9.1 - Prob. 1PPCCh. 9.1 - 9.1.1 What are the electron-domain geometry and...Ch. 9.1 - What are the electron-domain geometry and...Ch. 9.1 - Prob. 3CPCh. 9.1 - Prob. 4CPCh. 9.1 - Prob. 5CPCh. 9.2 - Practice Problem ATTEMPT
Ethanolamine has a...Ch. 9.2 - Practice Problem BUILD
The bond angle in is...
Ch. 9.2 - Practice ProblemCONCEPTUALIZE Which of these...Ch. 9.2 - 9.2.1 Identify the polar molecules in the...Ch. 9.2 - Identify the nonpolar molecules in the following...Ch. 9.3 - Practice ProblemATTEMPT Use valence bond theory to...Ch. 9.3 - Practice ProblemBUILD For which molecule(s) can we...Ch. 9.3 - Practice ProblemCONCEPTUALIZE Which of these...Ch. 9.3 - Which of the following atoms, in its ground state,...Ch. 9.3 - According to valence bond theory, how many bonds...Ch. 9.4 - Practice Problem ATTEMPT Use hybrid orbital theory...Ch. 9.4 - Practice ProblemBUILD Use hybrid orbital theory to...Ch. 9.4 - Prob. 1PPCCh. 9.4 - How many orbitals does a set of s p 2 hybrid...Ch. 9.4 - How many p atomic orbitals are required to...Ch. 9.5 - Practice Problem ATTEMPT
The active ingredient in...Ch. 9.5 - Practice ProblemBUILD Determine the total number...Ch. 9.5 - Practice ProblemCONCEPTUALIZE In terms of valence...Ch. 9.5 - Which of the following molecules contain one or...Ch. 9.5 - 9.5.2 From left to right, give the hybridization...Ch. 9.5 - Which of the following pairs of atomic orbitals on...Ch. 9.5 - 9.5.4 Which of the following pairs of atomic...Ch. 9.6 - Practice ProblemATTEMPT Use valence bond theory...Ch. 9.6 - Prob. 1PPBCh. 9.6 - Prob. 1PPCCh. 9.6 - Prob. 1CPCh. 9.6 - Prob. 2CPCh. 9.6 - Prob. 3CPCh. 9.6 - Prob. 4CPCh. 9.7 - Prob. 1PPACh. 9.7 - Prob. 1PPBCh. 9.7 - Prob. 1PPCCh. 9.7 - Prob. 1CPCh. 9.7 - Prob. 2CPCh. 9.7 - Prob. 3CPCh. 9.7 - Prob. 4CPCh. 9.8 - Practice ProblemATTEMPT Use a combination of...Ch. 9.8 - Practice ProblemBUILD Use a combination of valence...Ch. 9.8 - Prob. 1PPCCh. 9 - Prob. 1KSPCh. 9 - Which of the following species does not have...Ch. 9 - 9.3
Which of the following species is polar?
Ch. 9 - Which of the following species is nonpolar (a) IC1...Ch. 9 - How is the geometry of a molecule defined, and why...Ch. 9 - 9.2 Sketch the shape of a linear triatomic...Ch. 9 - How many atoms are directly bonded to the central...Ch. 9 - Discuss the basic features of the VSEPR model....Ch. 9 - In the trigonal bipyramidal arrangement, why does...Ch. 9 - 9.6 Explain why the molecule is not square...Ch. 9 - Predict the geometries of the following species...Ch. 9 - Predict the geometries of the following species: (...Ch. 9 - Predict the geometry of the following molecules...Ch. 9 - Predict the geometry of the following molecules...Ch. 9 - Predict the geometry of the following ions using...Ch. 9 - 9.12 Predict the geometries of the following ions:...Ch. 9 - Describe the geometry around each of the three...Ch. 9 - 9.14 Which of the following species are...Ch. 9 - Prob. 15QPCh. 9 - The bonds in beryllium hydride ( BeH 2 ) molecules...Ch. 9 - Determine whether (a) BrF 5 and (b) BCl 3 are...Ch. 9 - Determine whether (a) OCS and (b) XeF 4 are polar.Ch. 9 - Prob. 19QPCh. 9 - Prob. 20QPCh. 9 - Prob. 21QPCh. 9 - Use valence bond theory to explain the bonding in...Ch. 9 - Prob. 23QPCh. 9 - Prob. 24QPCh. 9 - 9.25 What is the hybridization of atomic orbitals?...Ch. 9 - Prob. 26QPCh. 9 - 9.27 What is the angle between the following two...Ch. 9 - Prob. 28QPCh. 9 - Prob. 29QPCh. 9 - Prob. 30QPCh. 9 - Prob. 31QPCh. 9 - Prob. 32QPCh. 9 - Prob. 33QPCh. 9 - Prob. 34QPCh. 9 - Which of the following pairs of atomic orbitals of...Ch. 9 - Prob. 36QPCh. 9 - 9.37 Specify which hybrid orbitals are used by...Ch. 9 - The allene molecule ( H 2 C=C=CH 2 ) is linear...Ch. 9 - Prob. 39QPCh. 9 - Prob. 40QPCh. 9 - How many pi bonds and sigma bonds are there in the...Ch. 9 - Prob. 42QPCh. 9 - Benzo(a)pyrene is a potent carcinogen found in...Ch. 9 - What is molecular orbital theory? How does it...Ch. 9 - 9.45 Define the following terms: bonding molecular...Ch. 9 - Sketch the shapes of the following molecular...Ch. 9 - Explain the significance of bond order. Can bond...Ch. 9 - Explain in molecular orbital terms the changes in...Ch. 9 - 9.49 The formation of from two atoms is an...Ch. 9 - 9.50 Draw a molecular orbital energy level diagram...Ch. 9 - Prob. 51QPCh. 9 - Prob. 52QPCh. 9 - Which of these species has a longer bond, B 2 or B...Ch. 9 - Prob. 54QPCh. 9 - 9.55 Compare the Lewis and molecular orbital...Ch. 9 - Prob. 56QPCh. 9 - Prob. 57QPCh. 9 - Prob. 58QPCh. 9 - A single bond is almost always a sigma bond, and a...Ch. 9 - Prob. 60QPCh. 9 - In Chapter 8, we saw that the resonance concept is...Ch. 9 - Prob. 62QPCh. 9 - Prob. 63QPCh. 9 - Prob. 64QPCh. 9 - Nitryl fluoride ( FNO 2 ) is very reactive...Ch. 9 - Prob. 66QPCh. 9 - Prob. 67QPCh. 9 - Which of the following species is not likely to...Ch. 9 - Prob. 69APCh. 9 - Although both carbon and silicon are in Group 4A,...Ch. 9 - Predict the geometry of sulfur dichloride ( SCl 2...Ch. 9 - Antimony pentafluoride ( sbF 5 ) reacts with XeF 4...Ch. 9 - Prob. 73APCh. 9 - Prob. 74APCh. 9 - Predict the bond angles for the following...Ch. 9 - Briefly compare the VSEPR and hybridization...Ch. 9 - 9.77 Draw Lewis structures and give the other...Ch. 9 - Prob. 78APCh. 9 - Determine whether (a) PCl 5 and (b) H 2 CO (C...Ch. 9 - Prob. 80APCh. 9 - 9.81 Which of the following molecules are linear:...Ch. 9 - Prob. 82APCh. 9 - 9.83 The molecule can exist in either of the...Ch. 9 - Cyclopropane ( C 3 H 6 ) has the shape of a...Ch. 9 - Determine whether (a) CH 2 Cl 2 and (b) XeF 4 are...Ch. 9 - 9.86 Does the following molecule have a dipole...Ch. 9 - For which molecular geometries (linear, bent,...Ch. 9 - Prob. 88APCh. 9 - 9.89 Carbon suboxide is a colorless...Ch. 9 - The following molecules ( AX 4 Y 2 ) all have an...Ch. 9 - Prob. 91APCh. 9 - Write the ground-state electron configuration for...Ch. 9 - 9.93 What is the hybridization of C and of N in...Ch. 9 - The stable allotropic form of phosphorus is P 4 ,...Ch. 9 - Prob. 95APCh. 9 - Use molecular orbital theory to explain the...Ch. 9 - Carbon dioxide has a linear geometry and is...Ch. 9 - Draw three Lewis structures for compounds with the...Ch. 9 - Prob. 99APCh. 9 - Prob. 100APCh. 9 - Prob. 101APCh. 9 - Draw the Lewis structure of ketene ( C 2 H 2 O )...Ch. 9 - Prob. 103APCh. 9 - Which of the following ions possess a dipole...Ch. 9 - Prob. 105APCh. 9 - Prob. 106APCh. 9 - The compound TCDD, or...Ch. 9 - Progesterone is a hormone responsible for female...Ch. 9 - 9.109 Carbon monoxide is a poisonous compound due...Ch. 9 - Prob. 110APCh. 9 - Prob. 111APCh. 9 - Prob. 112APCh. 9 - 9.113 The compound 1,2-dichloroethane is...Ch. 9 - Consider an N 2 molecule in its first excited...Ch. 9 - Prob. 115APCh. 9 - Prob. 1SEPPCh. 9 - Prob. 2SEPPCh. 9 - These questions are not based on a descriptive...Ch. 9 - These questions are not based on a descriptive...
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
- What are the angles a and b in the actual molecule of which this is a Lewis structure? H H C H- a -H b H Note for advanced students: give the ideal angles, and don't worry about small differences from the ideal groups may have slightly different sizes. a = b = 0 °arrow_forwardWhat are the angles a and b in the actual molecule of which this is a Lewis structure? :0: HCOH a Note for advanced students: give the ideal angles, and don't worry about small differences from the ideal that might be caused by the fact that different electron groups may have slightly different sizes. a = 0 b=0° Sarrow_forwardDetermine the structures of the missing organic molecules in the following reaction: + H₂O +H OH O OH +H OH X Note: Molecules that share the same letter have the exact same structure. In the drawing area below, draw the skeletal ("line") structure of the missing organic molecule X. Click and drag to start drawing a structure.arrow_forward
- Identify the missing organic reactant in the following reaction: x + x O OH H* + ☑- X H+ O O Х 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") structure of the missing organic reactant X. Click and drag to start drawing a structure. Carrow_forwardCH3O OH OH O hemiacetal O acetal O neither O 0 O hemiacetal acetal neither OH hemiacetal O acetal O neither CH2 O-CH2-CH3 CH3-C-OH O hemiacetal O acetal CH3-CH2-CH2-0-c-O-CH2-CH2-CH3 O neither HO-CH2 ? 000 Ar Barrow_forwardWhat would be the best choices for the missing reagents 1 and 3 in this synthesis? 1. PPh3 2 2. n-BuLi 3 Draw the missing reagents in the drawing area below. You can draw them in any arrangement you like. • Do not draw the missing reagent 2. If you draw 1 correctly, we'll know what it is. • Note: if one of your reagents needs to contain a halogen, use bromine. Explanation Check Click and drag to start drawing a structure.arrow_forward
- Predict the products of this organic reaction: NaBH3CN + NH2 ? H+ Click and drag to start drawing a structure. ×arrow_forwardPredict the organic products that form in the reaction below: + OH +H H+ ➤ ☑ X - Y Note: You may assume you have an excess of either reactant if the reaction requires more than one of those molecules to form the products. In the drawing area below, draw the skeletal ("line") structures of the missing organic products X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Garrow_forwardPredict the organic products that form in the reaction below: OH H+ H+ + ☑ Y Note: You may assume you have an excess of either reactant if the reaction requires more than one of those molecules to form the products. In the drawing area below, draw the skeletal ("line") structures of the missing organic products X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. ✓ marrow_forward
- Determine the structures of the missing organic molecules in the following reaction: + H₂O +H H+ Y Z ☑ ☑ Note: Molecules that share the same letter have the exact same structure. In the drawing area below, draw the skeletal ("line") structures of the missing organic molecules X, Y, and Z. You may draw the structures in any arrangement that you like, so long as they aren't touching. Molecule X shows up in multiple steps, but you only have to draw its structure once. Click and drag to start drawing a structure. AP +arrow_forwardPlease help, this is all the calculations i got!!! I will rate!!!Approx mass of KMnO in vial: 3.464 4 Moss of beaker 3×~0. z Nax200: = 29.9219 Massof weacerv after remosimgain N2C2O4. Need to fill in all the missing blanks. ง ง Approx mass of KMnO4 in vials 3.464 Mass of beaker + 3x ~0-304: 29.9219 2~0.20 Miss of beaker + 2x- 29.7239 Mass of beaker + 1x~0.2g Naz (204 29-5249 Mass of beaver after removing as qa Na₂ C₂O T1 T2 T3 Final Buiet reading Initial butet reading (int)) Hass of NaOr used for Titration -reading (mL) calculation Results: 8.5ml 17mL 27.4mL Oml Om Oml T1 T2 T3 Moles of No CO Moles of KMO used LOF KM. O used Molenty of KMNO Averagem Of KMOWLarrow_forwardDraw the skeletal ("line") structure of 2-hydroxy-4-methylpentanal. Click and drag to start drawing a structure. Xarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningGeneral Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage Learning

Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning

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

Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning

Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
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

General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning
Types of bonds; Author: Edspira;https://www.youtube.com/watch?v=Jj0V01Arebk;License: Standard YouTube License, CC-BY