
Concept explainers
Interpretation : Whether hydrogen is always partially positive when bonded to another atom has to be explained.
Concept Introduction :
In a polar covalent bond, atom with higher electronegativity value attracts more electrons than atom with low electronegativity value. Atoms that are less electronegative will have positive charge. Atomwith higher electronegativity value will have partial negative charge.

Answer to Problem 5E
No, hydrogen will not always have partial positive charge when bonded to other atoms. When it bonds with atoms having low electronegativity value such as boron, it will have partial negative charge.
Explanation of Solution
Given information:
Hydrogen is partially positive when bonded to some atoms.
Atoms that are more electronegative have partial negative charge and atoms that are less electronegative have partial positive charge.
For example in compound HCl hydrogen and chlorine atomsform a covalent bond. The difference between electronegativity value of hydrogen (2.10) and of chlorine (3.16) is 1.06. Here hydrogen has less electronegativityvalue than chlorine so it will have partial positive charge and chlorine will have partial negative charge.
Another example is hydrogen bonding with boron forming HF-From the electronegativity scale, electronegativity value of hydrogen is 2.10 and boron is 2.04. Hence, hydrogen will attract the bonded electrons more strongly than boron. So here hydrogen has a partial negative charge and boron has a partial positive charge.
In case of compounds where hydrogen bonds with atoms having less electronegativity value than 2.01, it will have a partial negative charge. In all other cases it will have a partial positive charge.
Chapter U2 Solutions
Living By Chemistry: First Edition Textbook
Additional Science Textbook Solutions
Campbell Essential Biology (7th Edition)
Organic Chemistry (8th Edition)
Campbell Biology: Concepts & Connections (9th Edition)
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
Cosmic Perspective Fundamentals
Genetic Analysis: An Integrated Approach (3rd Edition)
- Stereochemistry Identifying the enantiomer of a simple organic molecule 1/5 Check 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 t above box under the table. Br ま HO H 0 Molecule 1 Molecule 2 Molecule 3 OH H Br H H" Br OH Br Molecule 4 Br H OH + + OH Molecule 5 Br H OH none of the above Molecule 6 Br H... OHarrow_forwardPlease answer the questions and provide detailed explanations.arrow_forwardQuestion 16 0/1 pts Choose the correct option for the following cycloaddition reaction. C CF3 CF3 CF3 CF3 The reaction is suprafacial/surafacial and forbidden The reaction is antarafacial/antarafacial and forbidden The reaction is antarafacial/antarafacial and allowed The reaction is suprafacial/surafacial and allowedarrow_forward
- 1. Give the structures of the products obtained when the following are heated. Include stereochemistry where relevant. A NO2 + NO2 B + C N=C CEN + { 2. Which compounds would you heat together in order to synthesize the following?arrow_forwardExplain how myo-inositol is different from D-chiro-inositol. use scholarly sources and please hyperlink.arrow_forwardWhat is the molarisuty of a 0.396 m glucose solution if its density is 1.16 g/mL? MM glucose 180.2 /mol.arrow_forward
- Provide the proper IUPAC or common name for the following compound. Dashes, commas, and spaces must be used correctly. Br ......Im OHarrow_forwardCan you please help me solve this problems. The top one is just drawing out the skeletal correct and then the bottom one is just very confusing to me and its quite small in the images. Can you enlarge it and explain it to me please. Thank You much (ME EX1) Prblm #33arrow_forwardI'm trying to memorize VESPR Shapes to solve problems like those. I need help making circles like the second image in blue or using an x- and y-axis plane to memorize these and solve those types of problems, especially the ones given in the top/first image (180, 120, 109.5). Can you help me with this? or is their any other efficient method do soarrow_forward
- Can you please explain this problems to me? I'm very confused about it. Please provide a detailed, step-by-step explanation for me! (ME EX1) Prblm 27arrow_forwardQuestion 6 of 7 (1 point) | Question Attempt: 1 of 1 = 1 ✓2 ✓ 3 ✓ 4 ✓ 5 6 ✓ 7 This organic molecule is dissolved in a basic aqueous solution: Jen ✓ ? A short time later sensitive infrared spectroscopy reveals the presence of a new C-OH stretch absorption. That is, must now be a new molecule present with at least one C- OH bond. there 18 In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule Ar © + Click and drag to start drawing a structure. Add/Remove step Click and drawing Save For Later Submit Assignmentarrow_forwardCan you please explain this problem to me? I'm very confused about it. Please provide a detailed, step-by-step explanation for me! (ME EX1) Prblm 22arrow_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





