ORGANIC CHEMISTRY PRINCIPLES & MECHANISM
ORGANIC CHEMISTRY PRINCIPLES & MECHANISM
2nd Edition
ISBN: 9780393681826
Author: KARTY
Publisher: NORTON
bartleby

Concept explainers

Question
Book Icon
Chapter 2, Problem 2.33P
Interpretation Introduction

Interpretation:

The electron geometry for each indicated atom in the structure of Falcarinol is to be identified. Where applicable, the atom’s molecular geometry and bond angles are estimated.

Concept introduction:

According to the VSEPR theory, the geometry is identified based on groups attached to the central atom. The electron geometry depends on the total number of electrons groups attached to the central atoms. The molecular geometry is decided by the total number of bonded atoms or groups to the central atom. The bond angle is calculated based on the electron geometry of the molecule.

Expert Solution & Answer
Check Mark

Answer to Problem 2.33P

ORGANIC CHEMISTRY PRINCIPLES & MECHANISM, Chapter 2, Problem 2.33P , additional homework tip  1

Type Atom Electron Geometry Molecular Geometry Bond Angle
(a) C Trigonal Planar Trigonal Planar 1200
(b) C Trigonal Planar Trigonal Planar 1200
(c) O Tetrahedral Bent 104.50
(d) C Linear Linear 1800
(e) C Tetrahedral Tetrahedral 109.50

Explanation of Solution

The Lewis structure is drawn based on the total valence electrons in the structure. Carbon atom has four valence electrons, hydrogen has one valence electrons and oxygen has six valence electrons. Hydrogen atoms completed its duet. We need to add lone pairs on the oxygen atom to completes octet.

The atoms are shown with alphabets. The electron geometry and molecular geometry based on a number of electrons groups and bonding groups attached to it respectively is to be written.

ORGANIC CHEMISTRY PRINCIPLES & MECHANISM, Chapter 2, Problem 2.33P , additional homework tip  2

  1. The electron geometry and molecular geometry of Carbon

    There are three groups of electrons around the carbon atom, two single bonds with hydrogen and one double bond with carbon. For central carbon atom, no lone pair is present on it. According to VSEPR theory, its electron geometry and its molecular geometry is trigonal planar. The bond angle for tetrahedral geometry is 1200.

  2. The electron geometry and molecular geometry of Carbon

    There are three groups of electrons around the carbon atom, one single bond with hydrogen and one single bond with carbon and one double bond with another carbon. For central carbon atom, no lone pair is present on it. According to VSEPR theory, its electron geometry is trigonal planar and its molecular geometry is trigonal planar. The bond angle of tetrahedral geometry is 1200.

  3. The electron geometry and molecular geometry of O in -OH group.

    There are four groups of electrons around the oxygen atom, one single bond with hydrogen, one single bond with carbon and two lone pairs on it. According to VSEPR theory, its electron geometry is tetrahedral while its molecular geometry is bent. The bond angle for tetrahedral geometry is 104.50

  4. The electron geometry and molecular geometry of Carbon atom.

    There are two groups of electrons around the carbon atom, one single bond with carbon and a triple bond with another carbon. For central carbon atom, no lone pair is present on it. According to VSEPR theory, its electron geometry is linear and its molecular geometry is linear. The bond angle for tetrahedral geometry is 1800.

  5. The electron geometry and molecular geometry of C in -CH3 group.

    There are four groups of electrons around the carbon atom, one single bond with carbon and three single bonds with hydrogen atoms. For central carbon atom, no lone pair is present on it. According to VSEPR theory, its electron geometry is tetrahedral and its molecular geometry is tetrahedral. The bond angle of tetrahedral geometry is 109.50.

Conclusion

According to VSEPR theory, the electron geometry and molecular geometry is identified.

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
Blocking Group are use to put 2 large sterically repulsive group ortho. Show the correct sequence toconnect the reagent to product with the highest yield possible. * see image **NOTE: The compound on the left is the starting point, and the compound on the right is the final product. Please show the steps in between to get from start to final, please. These are not two different compounds that need to be worked.
I dont understand this.
Can you please explain this prooblem to me, show me how the conjugation is added, did I add them in the correct places and if so please show me. Thanks!

Chapter 2 Solutions

ORGANIC CHEMISTRY PRINCIPLES & MECHANISM

Ch. 2 - Prob. 2.11PCh. 2 - Prob. 2.12PCh. 2 - Prob. 2.13PCh. 2 - Prob. 2.14PCh. 2 - Prob. 2.15PCh. 2 - Prob. 2.16PCh. 2 - Prob. 2.17PCh. 2 - Prob. 2.18PCh. 2 - Prob. 2.19PCh. 2 - Prob. 2.20PCh. 2 - Prob. 2.21PCh. 2 - Prob. 2.22PCh. 2 - Prob. 2.23PCh. 2 - Prob. 2.24PCh. 2 - Prob. 2.25PCh. 2 - Prob. 2.26PCh. 2 - Prob. 2.27PCh. 2 - Prob. 2.28PCh. 2 - Prob. 2.29PCh. 2 - Prob. 2.30PCh. 2 - Prob. 2.31PCh. 2 - Prob. 2.32PCh. 2 - Prob. 2.33PCh. 2 - Prob. 2.34PCh. 2 - Prob. 2.35PCh. 2 - Prob. 2.36PCh. 2 - Prob. 2.37PCh. 2 - Prob. 2.38PCh. 2 - Prob. 2.39PCh. 2 - Prob. 2.40PCh. 2 - Prob. 2.41PCh. 2 - Prob. 2.42PCh. 2 - Prob. 2.43PCh. 2 - Prob. 2.44PCh. 2 - Prob. 2.45PCh. 2 - Prob. 2.46PCh. 2 - Prob. 2.47PCh. 2 - Prob. 2.48PCh. 2 - Prob. 2.49PCh. 2 - Prob. 2.50PCh. 2 - Prob. 2.51PCh. 2 - Prob. 2.52PCh. 2 - Prob. 2.53PCh. 2 - Prob. 2.54PCh. 2 - Prob. 2.55PCh. 2 - Prob. 2.56PCh. 2 - Prob. 2.57PCh. 2 - Prob. 2.58PCh. 2 - Prob. 2.59PCh. 2 - Prob. 2.60PCh. 2 - Prob. 2.61PCh. 2 - Prob. 2.62PCh. 2 - Prob. 2.63PCh. 2 - Prob. 2.64PCh. 2 - Prob. 2.65PCh. 2 - Prob. 2.66PCh. 2 - Prob. 2.67PCh. 2 - Prob. 2.68PCh. 2 - Prob. 2.69PCh. 2 - Prob. 2.70PCh. 2 - Prob. 2.71PCh. 2 - Prob. 2.72PCh. 2 - Prob. 2.1YTCh. 2 - Prob. 2.2YTCh. 2 - Prob. 2.3YTCh. 2 - Prob. 2.4YTCh. 2 - Prob. 2.5YTCh. 2 - Prob. 2.6YTCh. 2 - Prob. 2.7YTCh. 2 - Prob. 2.8YTCh. 2 - Prob. 2.9YTCh. 2 - Prob. 2.10YTCh. 2 - Prob. 2.11YTCh. 2 - Prob. 2.12YTCh. 2 - Prob. 2.13YTCh. 2 - Prob. 2.14YTCh. 2 - Prob. 2.15YTCh. 2 - Prob. 2.16YTCh. 2 - Prob. 2.17YTCh. 2 - Prob. 2.18YTCh. 2 - Prob. 2.19YTCh. 2 - Prob. 2.20YT
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: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
Text book image
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Text book image
Introductory Chemistry: A Foundation
Chemistry
ISBN:9781337399425
Author:Steven S. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Introductory Chemistry: An Active Learning Approa...
Chemistry
ISBN:9781305079250
Author:Mark S. Cracolice, Ed Peters
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
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning