
Basic Chemistry (5th Edition)
5th Edition
ISBN: 9780134138046
Author: Karen C. Timberlake
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 10.5, Problem 10.33QAP
Interpretation Introduction
Interpretation:
Interpret the reason for non polar nature of F2 while HF is polar molecule.
Concept Introduction:
The atom present in a molecule having large difference in their electronegativity results in polar nature of the molecule.
If the difference in electronegativity is lower or approching to 0 then the molecule having non polar nature.
The range of non polar bond is 0 to 0.4 while for polar covalent bond the range is 0.4 to 1.8 and for ionic bond the range is 1.8 to 3.3.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
The acid-base chemistry of both EDTA and EBT are important to ensuring that the reactions proceed as desired, thus the pH is controlled using a buffer. What percent of the EBT indicator will be in the desired HIn2- state at pH = 10.5. pKa1 = 6.2 and pKa2 = 11.6 of EBT
What does the phrase 'fit for purpose' mean in relation to analytical chemistry? Please provide examples too.
For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Molecule
Inductive Effects
Resonance Effects
Overall Electron-Density
×
NO2
○ donating
O donating
O withdrawing
O withdrawing
O electron-rich
electron-deficient
no inductive effects
O no resonance effects
O similar to benzene
E
[
CI
O donating
withdrawing
O no inductive effects
Explanation
Check
○ donating
withdrawing
no resonance effects
electron-rich
electron-deficient
O similar to benzene
© 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Acces
Chapter 10 Solutions
Basic Chemistry (5th Edition)
Ch. 10.1 - Prob. 10.1QAPCh. 10.1 - Determine the total number of valence electrons...Ch. 10.1 - Prob. 10.3QAPCh. 10.1 - Draw the Lewis structure for each of the following...Ch. 10.1 - Prob. 10.5QAPCh. 10.1 - If the available number of valence electrons for a...Ch. 10.1 - Prob. 10.7QAPCh. 10.1 - Draw the Lewis structure for each of the following...Ch. 10.2 - What is resonance?Ch. 10.2 - Prob. 10.10QAP
Ch. 10.2 - Draw resonance structures for each of the...Ch. 10.2 - Prob. 10.12QAPCh. 10.3 - Prob. 10.13QAPCh. 10.3 - 10.14 Choose the shape (1 to 6) that matches each...Ch. 10.3 - Prob. 10.15QAPCh. 10.3 - Prob. 10.16QAPCh. 10.3 - Prob. 10.17QAPCh. 10.3 - Prob. 10.18QAPCh. 10.3 - Use VSEPR theory to predict the shape of each of...Ch. 10.3 - Prob. 10.20QAPCh. 10.3 - Prob. 10.21QAPCh. 10.3 - Draw the Lewis structure and predict the shape for...Ch. 10.4 - Describe the trend in electronegativity as...Ch. 10.4 - Prob. 10.24QAPCh. 10.4 - Prob. 10.25QAPCh. 10.4 - Prob. 10.26QAPCh. 10.4 - Prob. 10.27QAPCh. 10.4 - Prob. 10.28QAPCh. 10.4 - Prob. 10.29QAPCh. 10.4 - Prob. 10.30QAPCh. 10.4 - Prob. 10.31QAPCh. 10.4 - Prob. 10.32QAPCh. 10.5 - Prob. 10.33QAPCh. 10.5 - Prob. 10.34QAPCh. 10.5 - Prob. 10.35QAPCh. 10.5 - Prob. 10.36QAPCh. 10.5 - Prob. 10.37QAPCh. 10.5 - Prob. 10.38QAPCh. 10.6 - Prob. 10.39QAPCh. 10.6 - Prob. 10.40QAPCh. 10.6 - Prob. 10.41QAPCh. 10.6 - Prob. 10.42QAPCh. 10.6 - Prob. 10.43QAPCh. 10.6 - Prob. 10.44QAPCh. 10.7 - 10.45 Using Figure 10.6, calculate the heat change...Ch. 10.7 - 10.46 Using Figure 10.6, calculate the heat change...Ch. 10.7 - 10.47 Using Figure 10.6. calculate the heat change...Ch. 10.7 - 10.48 Using Figure 10.6. calculate the heat change...Ch. 10.7 - 10.49 Using Figure 10.6 and the specific heat of...Ch. 10.7 - 10.50 Using Figure 10.6 and the specific heal of...Ch. 10.7 - 10.51 An ice bag containing 275 g of ice at 0°C...Ch. 10.7 - Prob. 10.52QAPCh. 10 - Prob. 10.53FUCh. 10 - Prob. 10.54FUCh. 10 - Prob. 10.55FUCh. 10 - Prob. 10.56FUCh. 10 - Prob. 10.57FUCh. 10 - Prob. 10.58FUCh. 10 - Prob. 10.59UTCCh. 10 - Prob. 10.60UTCCh. 10 - Prob. 10.61UTCCh. 10 - Prob. 10.62UTCCh. 10 - Prob. 10.63UTCCh. 10 - Prob. 10.64UTCCh. 10 - Prob. 10.65UTCCh. 10 - Prob. 10.66UTCCh. 10 - 10.67 Use your knowledge of changes of state to...Ch. 10 - Prob. 10.68UTCCh. 10 - Prob. 10.69UTCCh. 10 - Prob. 10.70UTCCh. 10 - Prob. 10.71UTCCh. 10 - Prob. 10.72UTCCh. 10 - Prob. 10.73AQAPCh. 10 - Prob. 10.74AQAPCh. 10 - Prob. 10.75AQAPCh. 10 - Prob. 10.76AQAPCh. 10 - Prob. 10.77AQAPCh. 10 - Prob. 10.78AQAPCh. 10 - Prob. 10.79AQAPCh. 10 - Prob. 10.80AQAPCh. 10 - Prob. 10.81AQAPCh. 10 - Prob. 10.82AQAPCh. 10 - Prob. 10.83AQAPCh. 10 - Prob. 10.84AQAPCh. 10 - Prob. 10.85AQAPCh. 10 - Prob. 10.86AQAPCh. 10 - Prob. 10.87AQAPCh. 10 - Prob. 10.88AQAPCh. 10 - Prob. 10.89AQAPCh. 10 - Prob. 10.90AQAPCh. 10 - Prob. 10.91AQAPCh. 10 - Prob. 10.92AQAPCh. 10 - Prob. 10.93AQAPCh. 10 - Prob. 10.94AQAPCh. 10 - Indicate the major type of intermolecular...Ch. 10 - Prob. 10.96AQAPCh. 10 - Prob. 10.97AQAPCh. 10 - Prob. 10.98AQAPCh. 10 - Prob. 10.99AQAPCh. 10 - Prob. 10.100AQAPCh. 10 - Prob. 10.101AQAPCh. 10 - Prob. 10.102AQAPCh. 10 - Prob. 10.103CQCh. 10 - Prob. 10.104CQCh. 10 - Prob. 10.105CQCh. 10 - Prob. 10.106CQCh. 10 - Prob. 10.107CQCh. 10 - Prob. 10.108CQCh. 10 - Prob. 10.109CQCh. 10 - Prob. 10.110CQCh. 10 - Prob. 10.111CQCh. 10 - Prob. 10.112CQCh. 10 - Prob. 13CICh. 10 - Prob. 14CICh. 10 - Prob. 15CICh. 10 - Prob. 16CI
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
- Understanding how substituents activate Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation HN NH2 Check X (Choose one) (Choose one) (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Aarrow_forwardIdentifying electron-donating and electron-withdrawing effects on benzene For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Inductive Effects Resonance Effects Overall Electron-Density Molecule CF3 O donating O donating O withdrawing O withdrawing O no inductive effects O no resonance effects electron-rich electron-deficient O similar to benzene CH3 O donating O withdrawing O no inductive effects O donating O withdrawing Ono resonance effects O electron-rich O electron-deficient O similar to benzene Explanation Check Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward* Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forward
- Draw TWO general chemical equation to prepare Symmetrical and non-Symmetrical ethers Draw 1 chemical reaction of an etherarrow_forwardPlease help me with the following questions for chemistry.arrow_forwardDraw the chemical structure [OR IUPAC name] of the following: a- m-chloromethoxybenzene b.arrow_forward
- Show by chemical equation the reaction of [HCN] and [CH3MgBr] with any alarrow_forwardGive the chemical equation for the preparation of: -Any aldehyde -Any keytonearrow_forward+ C8H16O2 (Fatty acid) + 11 02 → 8 CO2 a. Which of the above are the reactants? b. Which of the above are the products? H2o CO₂ c. Which reactant is the electron donor? Futty acid d. Which reactant is the electron acceptor? e. Which of the product is now reduced? f. Which of the products is now oxidized? 02 #20 102 8 H₂O g. Where was the carbon initially in this chemical reaction and where is it now that it is finished? 2 h. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forward
- → Acetyl-CoA + 3NAD+ + 1FAD + 1ADP 2CO2 + CoA + 3NADH + 1FADH2 + 1ATP a. Which of the above are the reactants? b. Which of the above are the products? c. Which reactant is the electron donor? d. Which reactants are the electron acceptors? e. Which of the products are now reduced? f. Which product is now oxidized? g. Which process was used to produce the ATP? h. Where was the energy initially in this chemical reaction and where is it now that it is finished? i. Where was the carbon initially in this chemical reaction and where is it now that it is finished? j. Where were the electrons initially in this chemical reaction and where is it now that it is finished?arrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Aarrow_forwardFor each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_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 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

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
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY