
Concept explainers
Interpretation : The given pairs of atoms have to be arranged in order of increasing bond polarity and the reasoning has to be explained.
Concept Introduction :
The tendency of an atom to attract shared electrons is called electronegativity. Chemists have assigned each

Answer to Problem C8.2RE
Bond polarities of given pairs of atoms are:
H-I: 0.56
H-Cl:1.06
H-F:1.88
Based on the bond polarities, the given pairs can be arranged as:
H-I<H-Cl< H-F
Reason- The electronegativity value increases from bottom to top of the periodic table. So fluorine is more electronegative than chlorine and iodine is least electronegative. So the bond polarity of H-F is highest and H-I is lowest.
Explanation of Solution
Given information:
Three pairs of atoms are given:
H-I, H-Cl, H-F
The electronegativity scale is used to compare individual atoms. Atoms that are more electronegative attract bonded electrons more strongly than atoms with less electronegative values. This results in formation of a polar bond. As the difference in electronegativity increases, the bond polarity increases.
H-I- From the electronegativity scale, electronegativity value of hydrogen is 2.10 and iodine is 2.66. Difference in electronegativity value = 2.66-2.10=0.56.
H-Cl-From the electronegativity scale, electronegativity value of hydrogen is 2.10 and chlorine is 3.16. Difference in electronegativity value=3.16-2.10=1.06.
H-F- From the electronegativity scale, electronegativity value of hydrogen is 2.10 and fluorine is 3.98. Difference in electronegativity value=3.98-2.10=1.88.
Reason- From the electronegativity values of metals, one can see that the scale increase from bottom to top of the periodic table. Since all these nonmetals are bonding with hydrogen, the difference in their electronegativities increases from bottom to top. Hence the bond polarity of H-F is highest and that of H-I is lowest. This can be represented as:
H-I< H-Cl< H-F
By comparing the electronegativity values of atoms, one can compare the polarity of bonds.
Chapter U2 Solutions
Living by Chemistry
Additional Science Textbook Solutions
Applications and Investigations in Earth Science (9th Edition)
Genetic Analysis: An Integrated Approach (3rd Edition)
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
Introductory Chemistry (6th Edition)
Microbiology: An Introduction
Campbell Biology (11th Edition)
- Complete the reaction in the drawing area below by adding the major products to the right-hand side. If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead. Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule to represent each pair of enantiomers, using line bonds at the chiral center. More... No reaction. my ㄖˋ + 1. Na O Me Click and drag to start drawing a structure. 2. H +arrow_forwardPredict the intermediate 1 and final product 2 of this organic reaction: NaOMe H+ + 1 2 H H work up You can draw 1 and 2 in any arrangement you like. Note: if either 1 or 2 consists of a pair of enantiomers, just draw one structure using line bonds instead of 3D (dash and wedge) bonds at the chiral center. Click and drag to start drawing a structure. X $ dmarrow_forwardPredict the major products of this organic reaction: 1. NaH (20°C) 2. CH3Br ? Some notes: • Draw only the major product, or products. You can draw them in any arrangement you like. • Be sure to use wedge and dash bonds where necessary, for example to distinguish between major products that are enantiomers. • If there are no products, just check the box under the drawing area. No reaction. Click and drag to start drawing a structure. G Crarrow_forward
- Predict the major products of this organic reaction: 1. LDA (-78°C) ? 2. Br Some notes: • Draw only the major product, or products. You can draw them in any arrangement you like. . • Be sure to use wedge and dash bonds where necessary, for example to distinguish between major products that are enantiomers. • If there are no products, just check the box under the drawing area. No reaction. Click and drag to start drawing a structure. Xarrow_forwardPlease draw the structuresarrow_forwardDraw the missing intermediates 1 and 2, plus the final product 3, of this synthesis: 0 1. Eto 1. Eto- 1 2 2. MeBr 2. EtBr H3O+ A 3 You can draw the three structures in any arrangement you like. Explanation Check Click and drag to start drawing a structure.arrow_forward
- Draw the missing intermediate 1 and final product 2 of this synthesis: 1. MeO- H3O+ 1 2 2. PrBr Δ You can draw the two structures in any arrangement you like. Click and drag to start drawing a structure.arrow_forwardWhat is the differences between: Glyceride and phosphoglyceride Wax and Fat Soap and Fatty acid HDL and LDL cholesterol Phospho lipids and sphingosine What are the types of lipids? What are the main lipid components of membrane structures? How could lipids play important rules as signaling molecules and building units? The structure variety of lipids makes them to play significant rules in our body, conclude breifly on this statement.arrow_forwardWhat is the differences between DNA and RNA for the following: - structure - function - type What is the meaning of: - replication - transcription - translation show the base pair connection(hydrogen bond) in DNA and RNAarrow_forward
- What is the IP for a amino acid- give an example what are the types of amino acids What are the structures of proteins The N-Terminal analysis by the Edman method shows saralasin contains sarcosine at the N-terminus. Partial hydrolysis of saralasin with dilute hydrochloric acid yields the following fragments: Try-Val-His Sar-Arg-Val His-Pro-Ala Val- Tyr- Val Arg-Val-Tyr What is the structure of saralasin?arrow_forwardWhat is the IP for a amino acid- give an example what are the types of amino acids What are the structures of proteins The N-Terminal analysis by the Edman method shows saralasin contains sarcosine at the N-terminus. Partial hydrolysis of saralasin with dilute hydrochloric acid yields the following fragments: Try-Val-His Sar-Arg-Val His-Pro-Ala Val- Tyr- Val Arg-Val-Tyr What is the structure of saralasin?arrow_forward> aw the missing intermediates 1 and 2, plus the final product 3, of this synthesis: 1. Eto 1. EtO¯ H3O+ 1 2 2. PrBr 2. PrBr Δ You can draw the three structures in any arrangement you like. 3 Click and drag to start drawing a structure. Explanation Check 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use Privacarrow_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





