Concept explainers
(a)
Interpretation:
The Lewis structures of
Concept Introduction:
- Lewis theory is about how electrons are arranged in the outer most valence shell of an atom so as to bond with the other atom in a molecule. Thus, the Lewis dot structure represents the bonding as well as the lone pairs and bond pairs of electrons.
- Planarity: The given molecules is said to be planar, only when all its atoms or ions lie on the same plane. If not so, then the molecule is said to be non-planar.
(b)
Interpretation:
The Lewis structures of
Concept Introduction:
- Lewis theory is about how electrons are arranged in the outer most valence shell of an atom so as to bond with the other atom in a molecule. Thus, the Lewis dot structure represents the bonding as well as the lone pairs and bond pairs of electrons.
- Planarity: The given molecules is said to be planar, only when all its atoms or ions lie on the same plane. If not so, then the molecule is said to be non-planar.
(c)
Interpretation:
The Lewis structure has to be drawn for
Concept Introduction:
Lewis structure:
Lewis theory is about how electrons are arranged in the outer most valence shell of an atom so as to bond with the other atom in a molecule. Thus, the Lewis dot structure represents the bonding as well as the lone pairs and bond pairs of electrons.
Bond moment:
In polar molecules, there will be a bond between a high electronegative atom and a least electronegative atom. The high electronegative atom pulls the shared pair of electrons towards itself and acquires a partial negative charge on it and creates a partial positive charge on the least electronegative atom. This is known as charge separation and the overall phenomenon is known as bond moment. It is a vector quantity which means it has both magnitude and direction.
Resultant dipole moment:
If all possible bond moments of a polar molecule are with different magnitudes, then a net dipole moment will be resulted which is known as the resultant dipole moment. If the bond moments are with same magnitudes, then there won’t be a resultant dipole moment since all the bond moments cancel with each other. So, the resultant dipole moment depends on the magnitude of bond moments. It is independent of the directions of bond moments.
(d)
Interpretation:
The Lewis structure has to be drawn for
Concept Introduction:
Lewis structure:
Lewis theory is about how electrons are arranged in the outer most valence shell of an atom so as to bond with the other atom in a molecule. Thus, the Lewis dot structure represents the bonding as well as the lone pairs and bond pairs of electrons.
Polarity:
In a molecule, if a covalent bond is existing between two different electronegative atoms, then there will be charge separation between the two atoms. One atom acquires a partial positive charge and the other atom acquires a partial negative charge. This phenomenon is known as polarity. So, if a molecule is said to be polar then there will be charge separation in the molecule which can have dipole moment whereas if a molecule is said to be non-polar then there will not be any charge separation in the molecule and hence do not have dipole moment in it.
(e)
Interpretation:
The Lewis structure has to be drawn for
Concept Introduction:
Lewis structure:
Lewis theory is about how electrons are arranged in the outer most valence shell of an atom so as to bond with the other atom in a molecule. Thus, the Lewis dot structure represents the bonding as well as the lone pairs and bond pairs of electrons.
Bond angle:
In a particular geometry, the angle formed between two adjacent bonds of a same atom is known as the bond angle. The bond angle between two bonds differs with respect to a particular geometry.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 10 Solutions
EBK GENERAL CHEMISTRY: THE ESSENTIAL CO
- Question 7 (10 points) Identify the carboxylic acid present in each of the following items and draw their structures: Food Vinegar Oranges Yogurt Sour Milk Pickles Acid Structure Paragraph ✓ BI UAE 0118 + v Task: 1. Identify the carboxylic acid 2. Provide Name 3. Draw structure 4. Take a picture of your table and insert Add a File Record Audio Record Video 11.arrow_forwardCheck the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. Molecule 1 Molecule 2 IZ IN Molecule 4 Molecule 5 ZI none of the above ☐ Molecule 3 Х IN www Molecule 6 NH Garrow_forwardHighlight each chiral center in the following molecule. If there are none, then check the box under the drawing area. There are no chiral centers. Cl Cl Highlightarrow_forward
- A student proposes the following two-step synthesis of an ether from an alcohol A: 1. strong base A 2. R Is the student's proposed synthesis likely to work? If you said the proposed synthesis would work, enter the chemical formula or common abbreviation for an appropriate strong base to use in Step 1: If you said the synthesis would work, draw the structure of an alcohol A, and the structure of the additional reagent R needed in Step 2, in the drawing area below. If there's more than one reasonable choice for a good reaction yield, you can draw any of them. ☐ Click and drag to start drawing a structure. Yes No ロ→ロ 0|0 G Х D : ☐ பarrow_forwardटे Predict the major products of this organic reaction. Be sure to use wedge and dash bonds when necessary, for example to distinguish between different major products. ☐ ☐ : ☐ + NaOH HO 2 Click and drag to start drawing a structure.arrow_forwardShown below are five NMR spectra for five different C6H10O2 compounds. For each spectrum, draw the structure of the compound, and assign the spectrum by labeling H's in your structure (or in a second drawing of the structure) with the chemical shifts of the corresponding signals (which can be estimated to nearest 0.1 ppm). IR information is also provided. As a reminder, a peak near 1700 cm-1 is consistent with the presence of a carbonyl (C=O), and a peak near 3300 cm-1 is consistent with the presence of an O–H. Extra information: For C6H10O2 , there must be either 2 double bonds, or 1 triple bond, or two rings to account for the unsaturation. There is no two rings for this problem. A strong band was observed in the IR at 1717 cm-1arrow_forward
- Predict the major products of the organic reaction below. : ☐ + Х ك OH 1. NaH 2. CH₂Br Click and drag to start drawing a structure.arrow_forwardNG NC 15Show all the steps you would use to synthesize the following products shown below using benzene and any organic reagent 4 carbons or less as your starting material in addition to any inorganic reagents that you have learned. NO 2 NC SO3H NO2 OHarrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)