
Bundle: Chemistry in Focus, Loose-leaf Version, 7th + OWLv2, 1 term (6 months) Printed Access Card
7th Edition
ISBN: 9781337812269
Author: Nivaldo J. Tro
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 5, Problem 5.9YT
Interpretation Introduction
Interpretation:
Using Lewis structure and VSEPR theory, the molecular geometry of
Concept introduction:
The VSEPR(valence shell electron pair repulsion) theory is helpful in predicting the shapes of molecules from their Lewis structures.
The electron geometries of a molecule are determined on the basis of the total number of electron groups, the number of bonding groups, and the number of lone pairs.
To determine the molecular geometry of the molecule, the Lewis structure is drawn and the electron groups are counted. On the basis of bonding groups, the molecular geometry is predicted.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Draw the Fischer projection for a D-aldo-pentose. (aldehyde pentose). How many total
stereoisomers are there? Name the sugar you drew.
Draw the Fischer projection for a L-keto-hexose. (ketone pentose). How many total
stereoisomers are there? Draw the enantiomer.
Draw a structure using wedges and dashes for the following compound:
H-
Et
OH
HO-
H
H-
Me
OH
Which of the following molecules are NOT typical carbohydrates? For the molecules that are
carbohydrates, label them as an aldose or ketose.
HO
Он
ОН ОН
Он
ОН
но
ΤΗ
HO
ОН
HO
eve
Он он
ОН
ОН
ОН
If polyethylene has an average molecular weight of 25,000 g/mol, how many repeat units
are present?
Chapter 5 Solutions
Bundle: Chemistry in Focus, Loose-leaf Version, 7th + OWLv2, 1 term (6 months) Printed Access Card
Ch. 5 - Drawing Lewis Structures for Ionic Compounds Draw...Ch. 5 - Using Lewis Structures to Determine the Correct...Ch. 5 - Prob. 5.3YTCh. 5 - Prob. 5.4YTCh. 5 - Drawing Lewis Structures for Covalent Compounds...Ch. 5 - Prob. 5.6YTCh. 5 - Prob. 5.7YTCh. 5 - Prob. 5.8YTCh. 5 - Prob. 5.9YTCh. 5 - Determining if a Molecule Is Polar Is SCl2 a polar...
Ch. 5 - Based on the Lewis structures for hydrogen and...Ch. 5 - Prob. 2SCCh. 5 - Prob. 3SCCh. 5 - Prob. 4SCCh. 5 - Which one of the following bonds is polar? a. a...Ch. 5 - Prob. 6SCCh. 5 - Why is salt, NaCl, relatively harmless even though...Ch. 5 - If sodium is dropped into water, a loud fizzing...Ch. 5 - Explain ionic bonding according to Lewis theory.Ch. 5 - Prob. 4ECh. 5 - Prob. 5ECh. 5 - Prob. 6ECh. 5 - Draw electron dot structures for the following...Ch. 5 - Explain VSEPR theory. According to this theory,...Ch. 5 - Prob. 9ECh. 5 - Prob. 10ECh. 5 - In what ways is water unique? What about the water...Ch. 5 - What is the difference between a polar and a...Ch. 5 - Why do polar molecules have a greater tendency to...Ch. 5 - Prob. 14ECh. 5 - Lewis Structures for Atoms Draw Lewis structures...Ch. 5 - Draw Lewis structures for each of the following...Ch. 5 - Ionic Lewis Structures Draw a Lewis structure for...Ch. 5 - Draw a Lewis structure for each of the following...Ch. 5 - Draw a Lewis structure for each of the following...Ch. 5 - Draw a Lewis structure for each of the following...Ch. 5 - Covalent Lewis Structures Draw a Lewis structure...Ch. 5 - Draw a Lewis structure for each molecular...Ch. 5 - General Lewis Structures Determine whether each...Ch. 5 - Determine whether each compound is ionic or...Ch. 5 - What is wrong with each Lewis structure? Fix the...Ch. 5 - What is wrong with each Lewis structure? Fix the...Ch. 5 - Predicting the Shapes of Molecules Use VSEPR...Ch. 5 - Use VSEPR theory to determine the geometry of the...Ch. 5 - Draw a Lewis structure and use VSEPR theory to...Ch. 5 - Draw a Lewis structure and use VSEPR theory to...Ch. 5 - CF2Cl2 is a chlorofluorocarbon implicated in ozone...Ch. 5 - Chlorofluorocarbons have been banned because they...Ch. 5 - Determining Molecular Polarity Determine whether...Ch. 5 - Determine whether each molecule is polar:...Ch. 5 - Determine whether each molecule is polar:...Ch. 5 - Determine whether each molecule is polar:...Ch. 5 - Explain why water would be a gas at room...Ch. 5 - Prob. 38ECh. 5 - Prob. 39ECh. 5 - One of the observations that led G. N. Lewis to...Ch. 5 - G. N. Lewis developed a model for chemical bonding...Ch. 5 - The opening quote of this chapter states that Man...Ch. 5 - Draw a Lewis structure of the H2 molecule. If you...Ch. 5 - Prob. 44ECh. 5 - The Lewis structures for CH4,N2,andCO2, along with...Ch. 5 - CH3COCH3 (acetone) is a common laboratory solvent...
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
- Draw the a-anomer cyclized pyranose Haworth projection of the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. Assign R and S for each chiral center. HO CHO -H HO -H H- -OH H -OH CH₂OH Draw the ẞ-anomer cyclized furanose Haworth projection for the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. HO CHO -H H -OH HO -H H -OH CH₂OHarrow_forwardName the below disaccharide. Circle any hemiacetals. Identify the numbering of glycosidic linkage, and identify it as a or ẞ. OH HO HO OH HO HO HO OHarrow_forwardWhat are the monomers used to make the following polymers? F. а. b. с. d. Вецер хочому なarrow_forward
- 1. Propose a reasonable mechanism for the following transformation. I'm looking for curved mechanistic arrows and appropriate formal charges on intermediates. OMe MeO OMe Me2N NMe2 OTBS OH xylenes OMe 'OTBSarrow_forwardWhat is the polymer made from the following monomers? What type of polymerization is used for each? а. ОН H2N но b. ن -NH2 d. H₂N NH2 довarrow_forwardCondensation polymers are produced when monomers containing two different functional groups link together with the loss of a small molecule such as H2O. The difunctional monomer H2N(CH2)6COOH forms a condensation polymer. Draw the carbon-skeleton structure of the dimer that forms from this monomer.arrow_forward
- What is the structure of the monomer?arrow_forward→ BINDERIYA GANBO... BINDERIYA GANBO. AP Biology Notes Gamino acid chart - G... 36:22 司 10 ☐ Mark for Review Q 1 Hide 80 8 2 =HA O=A¯ = H₂O Acid HIO HBrO HCIO Question 10 of 35 ^ Σ DELL □ 3 % Λ & 6 7 * ∞ 8 do 5 $ 4 # m 3 ° ( 9 Highlights & Notes AXC Sign out Carrow_forwardWhich representation(s) show polymer structures that are likely to result in rigid, hard materials and those that are likely to result in flexible, stretchable, soft materials?arrow_forward
- 3. Enter the molecular weight of the product obtained from the Williamson Ether Synthesis? OH OH & OH excess CH3l Ag₂Oarrow_forwardPlease answer 1, 2 and 3 on the endarrow_forwardIn the box below, specify which of the given compounds are very soluble in polar aprotic solvents. You may select more than one compound. Choose one or more: NaCl NH4Cl CH3CH2CH2CH2CH2CN CH3CH2OH hexan-2-one NaOH CH3SCH3arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
- Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning


General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:Cengage Learning

World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning

Chemistry for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning

Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Types of bonds; Author: Edspira;https://www.youtube.com/watch?v=Jj0V01Arebk;License: Standard YouTube License, CC-BY