Chemistry
Chemistry
4th Edition
ISBN: 9780078021527
Author: Julia Burdge
Publisher: McGraw-Hill Education
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 9, Problem 36QP
Interpretation Introduction

Interpretation:

The hybrid orbitals of carbon atoms in the given molecules are to be determined.

Concept introduction:

Hybridization is the combining of atomic orbitals to form hybrid orbitals.

To determine hybridization of an atom, first draw the Lewis structure of the molecule.

Find the number of electron domains around an atom so as to get the number of hybrid orbitals used by the atom for bonding.

When atomic orbitals combine, they form equal number of hybrid orbitals.

The s orbital combines with one, two, or three p orbitals to form sp,sp2, or sp3 hybrid orbitals, respectively.

Expert Solution & Answer
Check Mark

Answer to Problem 36QP

Solution:

a) sp3,sp3

b) sp3,sp2,sp2

c) sp3,sp,sp,sp3

d) sp3,sp2

e) sp3,sp2

a)

Explanation of Solution

The Lewis structure of CH3CH3 molecule is as follows:

Chemistry, Chapter 9, Problem 36QP , additional homework tip  1

In this, the two carbon atoms are bonded to each other and the three hydrogen atoms by single bonds. Thus, there are four electron domains around each carbon atom. Four electron domainsdepict thepresence of four hybrid orbitals. Thus, in both carbon atoms sp3 hybrid orbitals are present.

b)

The Lewis structure of CH3CH=CH2 molecule is as follows:

Chemistry, Chapter 9, Problem 36QP , additional homework tip  2

The carbon on the left is bonded to three hydrogen atoms by single bonds and to a carbon atom by a single bond. Thus, there are four electron domains around each carbon atom. Four electron domainsdepict thepresence of four hybrid orbitals. Thus, in this carbon sp3 hybrid orbitals are present.

The central carbon is bonded to one carbon atom by a single bond, to another by double bond and to a hydrogen by a single bond. Thus, there are three electron domains around this carbon atom. Three electron domainsdepict thepresence of three hybrid orbitals. Thus, hybridization of the central carbon is sp2.

The carbon on the right is bonded to two hydrogen atoms by a single bond and to a carbon by a double bond. Thus, there are three electron domains around this carbon atom. Three electron domainsdepict thepresence of three hybrid orbitals. Thus, hybridization of the carbon on the right is sp2.

Thus, the hybridizations of the carbon atoms, from left to right in the molecule, are sp3,sp2, and sp2.

c)

The Lewis structure of CH3-C=C-CH2OH molecule is as follows:

Chemistry, Chapter 9, Problem 36QP , additional homework tip  3

The carbon on left is bonded to three hydrogen atoms by single bonds and to a carbon atom by single bond. Thus, there are four electron domains around each carbon atom. Four electron domainsdepict thepresence of four hybrid orbitals. Thus, in this carbon, sp3 hybrid orbitals are present.

The two carbon atoms in the center are bonded to each other by double bonds and to a carbon by a single bond. Thus, there are two electron domains around each carbon atom. Two electron domains depict the presence of two hybrid orbitals. Thus, in these two carbons, sp hybrid orbitals are present.

The carbon on the right is bonded to two hydrogen atoms by single bonds, to a carbon atom by a single bond and to an oxygen by a single bond. Thus, there are four electron domains around this carbon atom. Four electron domainsdepict the presence of four hybrid orbitals. Thus, in this carbon, sp3 hybrid orbitals are present.

Thus, the hybridizations of the carbon atoms from left to right in the molecule are sp3, sp, sp, and sp3.

d)

The Lewis structure of CH3CH=O molecule is as follows:

Chemistry, Chapter 9, Problem 36QP , additional homework tip  4

The carbon on the left is bonded to three hydrogen atoms by single bonds and to a carbon atom by a single bond. Thus, there are four electron domains around each carbon atom. Four electron domainsdepict the presence of four hybrid orbitals. Thus, in this carbon sp3 hybrid orbitals are present.

The carbon on the right is bonded to a hydrogen atom by a single bond and to an oxygen atom by a double bond. Thus, there are three electron domains around this carbon atom. Three electron domainsdepict the presence of three hybrid orbitals. Thus, the hybridization of the carbon atom on the right is sp2.

Thus, the hybridizations of carbon atoms from left to right in the molecule are sp3 and sp2.

e)

The Lewis structure of CH3COOH molecule is as follows:

Chemistry, Chapter 9, Problem 36QP , additional homework tip  5

The carbon on left is bonded to three hydrogen atoms by single bonds and to carbon atom by single bond. Thus, there are four electron domains around each carbon atom. Four electron domainsdepict the presence of four hybrid orbitals. Thus, in this carbon sp3 hybrid orbitals are present.

The carbon on the right is bonded to an oxygen atom by a double bond and to another oxygen atom by a single bond. Thus, there are three electron domains around this carbon atom. Three electron domainsdepict the presence of three hybrid orbitals. Thus, the hybridization of the carbonatomon the right is sp2.

Thus, the hybridizations of carbon atoms from left to right in the molecule are sp3 and sp2.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
Allene (1,2-propadiene), H2C=C=CH2, has two adjacent double bonds. What kind of hybridization must the central carbon have? Sketch the bonding π orbitals in allene.What shape do you predict for allene?
What are the hybridizations of carbons 1 and 2 respectively in the following structure?
What is the hybridization of the central iodine atom in I3 -?

Chapter 9 Solutions

Chemistry

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
Background pattern image
Chemistry
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
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Chemistry
    Chemistry
    ISBN:9781133611097
    Author:Steven S. Zumdahl
    Publisher:Cengage Learning
    Text book image
    Chemistry
    Chemistry
    ISBN:9781305957404
    Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
    Publisher:Cengage Learning
    Text book image
    Chemistry: An Atoms First Approach
    Chemistry
    ISBN:9781305079243
    Author:Steven S. Zumdahl, Susan A. Zumdahl
    Publisher:Cengage Learning
  • Text book image
    Chemistry: Principles and Practice
    Chemistry
    ISBN:9780534420123
    Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
    Publisher:Cengage Learning
    Text book image
    Chemistry: Principles and Reactions
    Chemistry
    ISBN:9781305079373
    Author:William L. Masterton, Cecile N. Hurley
    Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781133611097
Author:Steven S. Zumdahl
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
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