ORGANIC CHEMISTRY-OWL V2 ACCESS
ORGANIC CHEMISTRY-OWL V2 ACCESS
8th Edition
ISBN: 9781305582422
Author: Brown
Publisher: CENGAGE L
bartleby

Concept explainers

Question
Book Icon
Chapter 5, Problem 5.10P

(a)

Interpretation Introduction

Interpretation:

Atomic orbitals which are used to form each σ and π bond have to be identified for the highlighted carbon atom of the given compound.

Concept Introduction:

Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.

Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.

Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.

  TypeofBondNo.ofσbondsNo.ofπbondsSingle10Double11Triple12

Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,

TypeofmoleculeHybridaizationAtomicorbitalsusedforhybridaizationGeometryAX2sp1s+1pLinearAX3,AX2Bsp21s+2pTrigonalplanarAX4,AX3B,AX2B2sp31s+3pTetrahedralAX5,AX4B,AX3B2,AX2B3sp3d1s+3p+1dTrigonalbipyramidalAX6,AX5B,AX4B2sp3d21s+3p+2dOctahedralACentralatomXAtomsbondedtoABNonbondingelectronpairsonA

(a)

Expert Solution
Check Mark

Explanation of Solution

In the marked carbon atom, one s and three p orbital hybridize forming four sp3 orbitals. Atomic orbitals are used to form each σ and π bond for the highlighted carbon atom can be given as,

ORGANIC CHEMISTRY-OWL V2 ACCESS, Chapter 5, Problem 5.10P , additional homework tip  1

In the marked carbon atom, one s and two p orbital hybridize forming three sp2 orbitals. Atomic orbitals are used to form each σ and π bond for the highlighted carbon atom can be given as,

ORGANIC CHEMISTRY-OWL V2 ACCESS, Chapter 5, Problem 5.10P , additional homework tip  2

(b)

Interpretation Introduction

Interpretation:

Atomic orbitals which are used to form each σ and π bond have to be identified for the highlighted carbon atom of the given compound.

Concept Introduction:

Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.

Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.

Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.

  TypeofBondNo.ofσbondsNo.ofπbondsSingle10Double11Triple12

Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,

TypeofmoleculeHybridaizationAtomicorbitalsusedforhybridaizationGeometryAX2sp1s+1pLinearAX3,AX2Bsp21s+2pTrigonalplanarAX4,AX3B,AX2B2sp31s+3pTetrahedralAX5,AX4B,AX3B2,AX2B3sp3d1s+3p+1dTrigonalbipyramidalAX6,AX5B,AX4B2sp3d21s+3p+2dOctahedralACentralatomXAtomsbondedtoABNonbondingelectronpairsonA

(b)

Expert Solution
Check Mark

Explanation of Solution

In the marked carbon atom, one s and two p orbital hybridize forming three sp2 orbitals. Atomic orbitals are used to form each σ and π bond for the highlighted carbon atom can be given as,

ORGANIC CHEMISTRY-OWL V2 ACCESS, Chapter 5, Problem 5.10P , additional homework tip  3

(c)

Interpretation Introduction

Interpretation:

Atomic orbitals which are used to form each σ and π bond has to be identified for the highlighted carbon atom of the given compound.

Concept Introduction:

Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.

Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.

Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.

  TypeofBondNo.ofσbondsNo.ofπbondsSingle10Double11Triple12

Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,

TypeofmoleculeHybridaizationAtomicorbitalsusedforhybridaizationGeometryAX2sp1s+1pLinearAX3,AX2Bsp21s+2pTrigonalplanarAX4,AX3B,AX2B2sp31s+3pTetrahedralAX5,AX4B,AX3B2,AX2B3sp3d1s+3p+1dTrigonalbipyramidalAX6,AX5B,AX4B2sp3d21s+3p+2dOctahedralACentralatomXAtomsbondedtoABNonbondingelectronpairsonA

(c)

Expert Solution
Check Mark

Explanation of Solution

In the marked carbon atom, one s and two p orbital hybridize forming three sp2 orbitals. Atomic orbitals are used to form each σ and π bond for the highlighted carbon atom can be given as,

ORGANIC CHEMISTRY-OWL V2 ACCESS, Chapter 5, Problem 5.10P , additional homework tip  4

(d)

Interpretation Introduction

Interpretation:

Atomic orbitals which are used to form each σ and π bond has to be identified for the highlighted carbon atom of the given compound.

Concept Introduction:

Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.

Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.

Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.

  TypeofBondNo.ofσbondsNo.ofπbondsSingle10Double11Triple12

Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,

TypeofmoleculeHybridaizationAtomicorbitalsusedforhybridaizationGeometryAX2sp1s+1pLinearAX3,AX2Bsp21s+2pTrigonalplanarAX4,AX3B,AX2B2sp31s+3pTetrahedralAX5,AX4B,AX3B2,AX2B3sp3d1s+3p+1dTrigonalbipyramidalAX6,AX5B,AX4B2sp3d21s+3p+2dOctahedralACentralatomXAtomsbondedtoABNonbondingelectronpairsonA

(d)

Expert Solution
Check Mark

Explanation of Solution

In the marked carbon atom, one s and two p orbital hybridize forming three sp2 orbitals. Atomic orbitals are used to form each σ and π bond for the highlighted carbon atom can be given as,

ORGANIC CHEMISTRY-OWL V2 ACCESS, Chapter 5, Problem 5.10P , additional homework tip  5

(e)

Interpretation Introduction

Interpretation:

Atomic orbitals which are used to form each σ and π bond has to be identified for the highlighted carbon atom of the given compound.

Concept Introduction:

Hybridization is the mixing of valence atomic orbitals to get equivalent hybridized orbitals that having similar characteristics and energy.

Sigma (σ) bonds are the bonds in which shared hybrid orbital’s electron density are concentrated along the internuclear axis.

Pi (π) bonds are the bonds in which shared unhybridized orbital’s (p, d, etc) electron density are concentrated in above and below of the plane of the molecule.

  TypeofBondNo.ofσbondsNo.ofπbondsSingle10Double11Triple12

Geometry of different types of molecule with respect to the hybridizations are mentioned are mentioned below,

TypeofmoleculeHybridaizationAtomicorbitalsusedforhybridaizationGeometryAX2sp1s+1pLinearAX3,AX2Bsp21s+2pTrigonalplanarAX4,AX3B,AX2B2sp31s+3pTetrahedralAX5,AX4B,AX3B2,AX2B3sp3d1s+3p+1dTrigonalbipyramidalAX6,AX5B,AX4B2sp3d21s+3p+2dOctahedralACentralatomXAtomsbondedtoABNonbondingelectronpairsonA

(e)

Expert Solution
Check Mark

Explanation of Solution

In the marked carbon atom, one s and one p orbital hybridize forming two sp2 orbitals. Atomic orbitals are used to form each σ and π bond for the highlighted carbon atom can be given as,

ORGANIC CHEMISTRY-OWL V2 ACCESS, Chapter 5, Problem 5.10P , additional homework tip  6

In the marked carbon atom, one s and two p orbital hybridize forming three sp2 orbitals. Atomic orbitals are used to form each σ and π bond for the highlighted carbon atom can be given as,

ORGANIC CHEMISTRY-OWL V2 ACCESS, Chapter 5, Problem 5.10P , additional homework tip  7

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
28. For each of the following species, add charges wherever required to give a complete, correct Lewis structure. All bonds and nonbonded valence electrons are shown. a. b. H H H H H :0-C-H H H H-C-H C. H H d. H-N-0: e. H H-O H-O H B=0 f. H—Ö—Ñ—Ö—H Norton Private B
At 0oC and 1 atm, the viscosity of hydrogen (gas) is 8.55x10-5 P. Calculate the viscosity of a gas, if possible, consisting of deuterium. Assume that the molecular sizes are equal.
Indicate the correct option for the velocity distribution function of gas molecules:a) its velocity cannot be measured in any other way due to the small size of the gas moleculesb) it is only used to describe the velocity of particles if their density is very high.c) it describes the probability that a gas particle has a velocity in a given interval of velocitiesd) it describes other magnitudes, such as pressure, energy, etc., but not the velocity of the molecules
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
    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
    Text book image
    Chemistry & Chemical Reactivity
    Chemistry
    ISBN:9781337399074
    Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
    Publisher:Cengage Learning
    Text book image
    Chemistry by OpenStax (2015-05-04)
    Chemistry
    ISBN:9781938168390
    Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
    Publisher:OpenStax
Text book image
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
Text book image
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Text book image
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax