Chemistry: Matter and Change
1st Edition
ISBN: 9780078746376
Author: Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher: Glencoe/McGraw-Hill School Pub Co
expand_more
expand_more
format_list_bulleted
Question
Chapter 8.4, Problem 62SSC
Interpretation Introduction
Interpretation:
The definition of bond angle needs to be given.
Concept introduction:
The covalent bonding in molecules can be explained on the basis of Lewis structure and Hybridization.
Bond angle, bond length and bond order are certain parameters, which are used to explain the bonding between atoms.
Expert Solution & Answer
Answer to Problem 62SSC
The bond angle represents the angle between three bonded atoms in any given molecule.
Explanation of Solution
Bond length can be defined as the distance between the nuclei of two bonded atoms in a molecule, whereas the bond angle represents the angle between three bonded atoms in any given molecule.
The bond angle determines the molecular geometry of the molecule such as 109°28’ is the bond angle of tetrahedral geometry.
Conclusion
The bond angle represents the angle between three bonded atoms in any given molecule.
Chapter 8 Solutions
Chemistry: Matter and Change
Ch. 8.1 - Prob. 1PPCh. 8.1 - Prob. 2PPCh. 8.1 - Prob. 3PPCh. 8.1 - Prob. 4PPCh. 8.1 - Prob. 5PPCh. 8.1 - Prob. 6PPCh. 8.1 - Prob. 7SSCCh. 8.1 - Prob. 8SSCCh. 8.1 - Prob. 9SSCCh. 8.1 - Prob. 10SSC
Ch. 8.1 - Prob. 11SSCCh. 8.1 - Prob. 12SSCCh. 8.1 - Prob. 13SSCCh. 8.2 - Prob. 14PPCh. 8.2 - Prob. 15PPCh. 8.2 - Prob. 16PPCh. 8.2 - Prob. 17PPCh. 8.2 - Prob. 18PPCh. 8.2 - Prob. 19PPCh. 8.2 - Prob. 20PPCh. 8.2 - Prob. 21PPCh. 8.2 - Prob. 22PPCh. 8.2 - Prob. 23PPCh. 8.2 - Prob. 24PPCh. 8.2 - Prob. 25PPCh. 8.2 - Prob. 26PPCh. 8.2 - Prob. 27PPCh. 8.2 - Prob. 28PPCh. 8.2 - Prob. 29PPCh. 8.2 - Prob. 30PPCh. 8.2 - Prob. 31SSCCh. 8.2 - Prob. 32SSCCh. 8.2 - Prob. 33SSCCh. 8.2 - Prob. 34SSCCh. 8.2 - Prob. 35SSCCh. 8.2 - Prob. 36SSCCh. 8.3 - Prob. 37PPCh. 8.3 - Prob. 38PPCh. 8.3 - Prob. 39PPCh. 8.3 - Prob. 40PPCh. 8.3 - Prob. 41PPCh. 8.3 - Prob. 42PPCh. 8.3 - Prob. 43PPCh. 8.3 - Prob. 44PPCh. 8.3 - Prob. 45PPCh. 8.3 - Prob. 46PPCh. 8.3 - Prob. 47PPCh. 8.3 - Prob. 48PPCh. 8.3 - Prob. 49PPCh. 8.3 - Prob. 50SSCCh. 8.3 - Prob. 51SSCCh. 8.3 - Prob. 52SSCCh. 8.3 - Prob. 53SSCCh. 8.3 - Prob. 54SSCCh. 8.3 - Prob. 55SSCCh. 8.4 - Prob. 56PPCh. 8.4 - Prob. 57PPCh. 8.4 - Prob. 58PPCh. 8.4 - Prob. 59PPCh. 8.4 - Prob. 60PPCh. 8.4 - Prob. 61SSCCh. 8.4 - Prob. 62SSCCh. 8.4 - Prob. 63SSCCh. 8.4 - Prob. 64SSCCh. 8.4 - Prob. 65SSCCh. 8.4 - Prob. 66SSCCh. 8.4 - Prob. 67SSCCh. 8.5 - Prob. 68SSCCh. 8.5 - Prob. 69SSCCh. 8.5 - Prob. 70SSCCh. 8.5 - Prob. 71SSCCh. 8.5 - Prob. 72SSCCh. 8.5 - Prob. 73SSCCh. 8.5 - Prob. 74SSCCh. 8.5 - Prob. 75SSCCh. 8.5 - Prob. 76SSCCh. 8.5 - Prob. 77SSCCh. 8 - Prob. 78ACh. 8 - Prob. 79ACh. 8 - Prob. 80ACh. 8 - Prob. 81ACh. 8 - Prob. 82ACh. 8 - Prob. 83ACh. 8 - Prob. 84ACh. 8 - Prob. 85ACh. 8 - Prob. 86ACh. 8 - Prob. 87ACh. 8 - Prob. 88ACh. 8 - Prob. 90ACh. 8 - Prob. 91ACh. 8 - Prob. 92ACh. 8 - Prob. 93ACh. 8 - Prob. 94ACh. 8 - Prob. 95ACh. 8 - Prob. 96ACh. 8 - Prob. 97ACh. 8 - Prob. 98ACh. 8 - Prob. 99ACh. 8 - Prob. 100ACh. 8 - Prob. 101ACh. 8 - Prob. 102ACh. 8 - Prob. 103ACh. 8 - Prob. 104ACh. 8 - Prob. 105ACh. 8 - Prob. 106ACh. 8 - Prob. 107ACh. 8 - Prob. 108ACh. 8 - Prob. 109ACh. 8 - Prob. 110ACh. 8 - Prob. 111ACh. 8 - Prob. 112ACh. 8 - Prob. 113ACh. 8 - Prob. 114ACh. 8 - Prob. 115ACh. 8 - Prob. 116ACh. 8 - Prob. 117ACh. 8 - Prob. 118ACh. 8 - Prob. 119ACh. 8 - Rank the bonds according to increasing polarity....Ch. 8 - Prob. 121ACh. 8 - Prob. 122ACh. 8 - Use Lewis structures to predict the molecular...Ch. 8 - Prob. 124ACh. 8 - Prob. 125ACh. 8 - Prob. 126ACh. 8 - Prob. 127ACh. 8 - Prob. 128ACh. 8 - Prob. 129ACh. 8 - Prob. 130ACh. 8 - Prob. 131ACh. 8 - Prob. 132ACh. 8 - Prob. 133ACh. 8 - Prob. 134ACh. 8 - Prob. 135ACh. 8 - Prob. 136ACh. 8 - Prob. 137ACh. 8 - Prob. 138ACh. 8 - Prob. 139ACh. 8 - Prob. 140ACh. 8 - Prob. 141ACh. 8 - Prob. 142ACh. 8 - Prob. 143ACh. 8 - Prob. 144ACh. 8 - Prob. 145ACh. 8 - Prob. 1STPCh. 8 - Prob. 2STPCh. 8 - Prob. 3STPCh. 8 - Prob. 4STPCh. 8 - Prob. 5STPCh. 8 - Prob. 6STPCh. 8 - Prob. 7STPCh. 8 - Prob. 8STPCh. 8 - Prob. 9STPCh. 8 - Prob. 10STPCh. 8 - Prob. 11STPCh. 8 - Prob. 12STPCh. 8 - Prob. 13STPCh. 8 - Prob. 14STPCh. 8 - Prob. 15STPCh. 8 - Prob. 16STPCh. 8 - Prob. 17STPCh. 8 - Prob. 18STPCh. 8 - Prob. 19STP
Additional Science Textbook Solutions
Find more solutions based on key concepts
Match the following examples of mutagens. Column A Column B ___a. A mutagen that is incorporated into DNA in pl...
Microbiology: An Introduction
2 Of the uterus, small intestine, spinal cord, and heart, which is/are in the dorsal body cavity?
Anatomy & Physiology (6th Edition)
10.71 Identify each of the following as an acid or a base: (10.1)
H2SO4
RbOH
Ca(OH)2
HI
...
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
Which of the following factors would tend to increase membrane fluidity? A. a greater proportion of unsaturated...
Campbell Biology in Focus (2nd Edition)
18. SCIENTIFIC THINKING By measuring the fossil remains of Homo floresiensis, scientists have estimated its wei...
Campbell Biology: Concepts & Connections (9th Edition)
Level 2: Application/Analysis 4. Nitrifying bactcria participatc in the nitrogen cycle mainly by (A) converting...
Campbell Biology (11th Edition)
Knowledge Booster
Similar questions
- What are is the organic molecule X and product Y of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forwardAt 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Without using graphs, calculate the order of the reaction. t/s [R]/(mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forwardPredict the organic products that form in the reaction below, and draw the skeletal ("line") structures of the missing organic products. Please include all steps & drawings & explanations.arrow_forward
- What are the missing reagents for the spots labeled 1 and 3? Please give a detailed explanation and include the drawings and show how the synthesis proceeds with the reagents.arrow_forwardWhat are the products of the following acetal hydrolysis? Please draw a skeletal line structure and include a detailed explanation and drawing of how the mechanism proceeds. Please include any relevant information that is needed to understand the process of acetal hydrolysis.arrow_forwardWhat would happen if you added the HCI to the Grignard reagent before adding benzophenone? Draw a reaction mechanism to support your answer.arrow_forward
- At 300 K, in the decomposition reaction of a reactant R into products, several measurements of the concentration of R over time have been made (see table). Calculate the order of the reaction. t/s [R]/ (mol L-1) 0 0,5 171 0,16 720 0,05 1400 0,027arrow_forwardWrite the correct IUPAC names of the molecules in the picturearrow_forwardHow many grams of solid NaCN have to be added to 1.5L of water to dissolve 0.18 mol of Fe(OH)3 in the form Fe(CN)63 - ? ( For simplicity, ignore the reaction of CN - ion with water) Ksp for Fe(OH)3 is 2.8E -39, and Kform for Fe(CN)63 - is 1.0E31arrow_forward
- Draw the most stable chair conformation of 1-ethyl-1-methylcyclohexane, clearly showing the axial and equatorial substituents. [4] Draw structures corresponding to the following IUPAC name for each of the following compounds; [5] i) 4-Isopropyl-2,4,5-trimethylheptane ii) trans-1-tert-butyl-4-ethylcyclohexane iii) Cyclobutylcycloheptane iv) cis-1,4-di-isopropylcyclohexane (chair conformation) v) 3-Ethyl-5-isobutylnonanearrow_forwardDraw and name molecules that meet the following descriptions; [4] a) An organic molecule containing 2 sp2 hybridised carbon and 1 sp-hybridised carbon atom. b) A cycloalkene, C7H12, with a tetrasubstituted double bond. Also answer question 2 from the imagearrow_forwardH 14. Draw the line angle form of the following molecule make sure you use the proper notation to indicate spatial positioning of atoms. F F H 15. Convert the following condensed form to line angle form: (CH3)3CCH2COCH2CON(CH2CH3)2arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
ChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill Education
Principles 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 Education
Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY