World of Chemistry, 3rd edition
3rd Edition
ISBN: 9781133109655
Author: Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher: Brooks / Cole / Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Question
Chapter 11.3, Problem 3RQ
a.
Interpretation Introduction
Interpretation:The given orbital figure in part a. is to be labelled.
Concept Introduction:The shape of an orbital depends on the distribution of the electrons in free space.
a.
Expert Solution
Answer to Problem 3RQ
The given orbital is p orbital.
Explanation of Solution
p-orbitals are dumbbell shaped due to their
b.
Interpretation Introduction
Interpretation:The given orbital figure in part b. is to be labelled.
Concept Introduction:The shape of an orbital depends on the distribution of the electrons in free space.
b.
Expert Solution
Answer to Problem 3RQ
The given orbital is s orbital.
Explanation of Solution
Due to the absence of any angular momentum, the electrons are evenly spread in their probable locations in all directions. When mapped, these locations give the orbital a spherical shape due to the even spread in all directions.
c.
Interpretation Introduction
Interpretation:The given orbital figure in part c. is to be labelled and identified.
Concept Introduction:The shape of an orbital depends on the distribution of the electrons in free space.
c.
Expert Solution
Answer to Problem 3RQ
The given orbital is d orbital.
Explanation of Solution
d-orbitals are double dumbbell shaped due to their angular momentum number and spin number both being 2. Since both the numbers have value 2, the electrons’ movements in the three axes are restricted and on mapping the probable positions, the shape comes out to be somewhat flower-like arranged along the three axes of orientation.
Chapter 11 Solutions
World of Chemistry, 3rd edition
Ch. 11.1 - Prob. 1RQCh. 11.1 - Prob. 2RQCh. 11.1 - Prob. 3RQCh. 11.1 - Prob. 4RQCh. 11.1 - Prob. 5RQCh. 11.1 - Prob. 6RQCh. 11.1 - Prob. 7RQCh. 11.2 - Prob. 1RQCh. 11.2 - Prob. 2RQCh. 11.2 - Prob. 3RQ
Ch. 11.2 - Prob. 4RQCh. 11.2 - Prob. 5RQCh. 11.2 - Prob. 6RQCh. 11.3 - Prob. 1RQCh. 11.3 - Prob. 2RQCh. 11.3 - Prob. 3RQCh. 11.3 - Prob. 4RQCh. 11.3 - Prob. 5RQCh. 11.3 - Prob. 6RQCh. 11.4 - Prob. 1RQCh. 11.4 - Prob. 2RQCh. 11.4 - Prob. 3RQCh. 11.4 - Prob. 4RQCh. 11.4 - Prob. 5RQCh. 11.4 - Prob. 6RQCh. 11.4 - Prob. 7RQCh. 11 - Prob. 1ACh. 11 - Prob. 2ACh. 11 - Prob. 3ACh. 11 - Prob. 4ACh. 11 - Prob. 5ACh. 11 - Prob. 6ACh. 11 - Prob. 7ACh. 11 - Prob. 8ACh. 11 - Prob. 9ACh. 11 - Prob. 10ACh. 11 - Prob. 11ACh. 11 - Prob. 12ACh. 11 - Prob. 13ACh. 11 - Prob. 14ACh. 11 - Prob. 15ACh. 11 - Prob. 16ACh. 11 - Prob. 17ACh. 11 - Prob. 18ACh. 11 - Prob. 19ACh. 11 - Prob. 20ACh. 11 - Prob. 21ACh. 11 - Prob. 22ACh. 11 - Prob. 23ACh. 11 - Prob. 24ACh. 11 - Prob. 25ACh. 11 - Prob. 26ACh. 11 - Prob. 27ACh. 11 - Prob. 28ACh. 11 - Prob. 29ACh. 11 - Prob. 30ACh. 11 - Prob. 31ACh. 11 - Prob. 32ACh. 11 - Prob. 33ACh. 11 - Prob. 34ACh. 11 - Prob. 35ACh. 11 - Prob. 36ACh. 11 - Prob. 37ACh. 11 - Prob. 38ACh. 11 - Prob. 39ACh. 11 - Prob. 40ACh. 11 - Prob. 41ACh. 11 - Prob. 42ACh. 11 - Prob. 43ACh. 11 - Prob. 44ACh. 11 - Prob. 45ACh. 11 - Prob. 46ACh. 11 - Prob. 47ACh. 11 - Prob. 48ACh. 11 - Prob. 49ACh. 11 - Prob. 50ACh. 11 - Prob. 51ACh. 11 - Prob. 52ACh. 11 - Prob. 53ACh. 11 - Prob. 54ACh. 11 - Prob. 55ACh. 11 - Prob. 56ACh. 11 - Prob. 57ACh. 11 - Prob. 58ACh. 11 - Prob. 59ACh. 11 - Prob. 60ACh. 11 - Prob. 61ACh. 11 - Prob. 62ACh. 11 - Prob. 63ACh. 11 - Prob. 64ACh. 11 - Prob. 65ACh. 11 - Prob. 66ACh. 11 - Prob. 67ACh. 11 - Prob. 68ACh. 11 - Prob. 69ACh. 11 - Prob. 70ACh. 11 - Prob. 71ACh. 11 - Prob. 72ACh. 11 - Prob. 73ACh. 11 - Prob. 74ACh. 11 - Prob. 75ACh. 11 - Prob. 76ACh. 11 - Prob. 77ACh. 11 - Prob. 1STPCh. 11 - Prob. 2STPCh. 11 - Prob. 3STPCh. 11 - Prob. 4STPCh. 11 - Prob. 5STPCh. 11 - Prob. 6STPCh. 11 - Prob. 7STPCh. 11 - Prob. 8STPCh. 11 - Prob. 9STPCh. 11 - Prob. 10STPCh. 11 - Prob. 11STPCh. 11 - Prob. 12STP
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
- 03 Question (1 point) For the reaction below, draw both of the major organic products. Be sure to consider stereochemistry. > 1. CH₂CH₂MgBr 2. H₂O 3rd attempt Draw all four bonds at chiral centers. Draw all stereoisomers formed. Draw the structures here. e 130 AN H See Periodic Table See Hint P C Brarrow_forwardYou may wish to address the following issues in your response if they are pertinent to the reaction(s) you propose to employ:1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Please make it in detail and draw it out too in what step what happens. Thank you for helping me!arrow_forward1) Chemoselectivity (why this functional group and not another?) 2) Regioselectivity (why here and not there?) 3) Stereoselectivity (why this stereoisomer?) 4) Changes in oxidation state. Everything in detail and draw out and write it.arrow_forward
- Calculating the pH at equivalence of a titration 3/5 Izabella A chemist titrates 120.0 mL of a 0.7191M dimethylamine ((CH3)2NH) solution with 0.5501 M HBr solution at 25 °C. Calculate the pH at equivalence. The pk of dimethylamine is 3.27. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of HBr solution added. pH = ☐ ✓ 18 Ar Boarrow_forwardAlcohols can be synthesized using an acid-catalyzed hydration of an alkene. An alkene is combined with aqueous acid (e.. sulfuric acid in water). The reaction mechanism typically involves a carbocation intermediate. > 3rd attempt 3343 10 8 Draw arrows to show the reaction between the alkene and hydronium ion. that 2nd attempt Feedback 1st attempt تعمال Ju See Periodic Table See Hint F D Ju See Periodic Table See Hintarrow_forwardDraw the simplified curved arrow mechanism for the reaction of acetone and CHgLi to give the major product. 4th attempt Π Draw the simplified curved arrow mechanism T 3rd attempt Feedback Ju See Periodic Table See Hint H -H H -I H F See Periodic Table See Hintarrow_forward
- Select the correct reagent to accomplish the first step of this reaction. Then draw a mechanism on the Grignard reagent using curved arrow notation to show how it is converted to the final product. 4th attempt Part 1 (0.5 point) Select the correct reagent to accomplish the first step of this reaction. Choose one: OA Mg in ethanol (EtOH) OB. 2 Li in THF O C. Li in THF D. Mg in THF O E Mg in H2O Part 2 (0.5 point) Br Part 1 Bri Mg CH B CH, 1 Draw intermediate here, but no arrows. © TE See Periodic Table See Hint See Hint ין Harrow_forwardSelect the product for the following reaction. HO HO PCC OH ○ OH O HO ○ HO HO HOarrow_forward5:45 Х Select the final product for the following reaction sequence. O O 1. Mg. ether 2.D.Oarrow_forward
- Based on the chart Two similarities between the molecule with alpha glycosidic linkages. Two similarities between the molecules with beta glycosidtic linkages. Two differences between the alpha and beta glycosidic linkages.arrow_forwardplease help fill in the tablearrow_forwardAnswer F pleasearrow_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
Quantum Mechanics - Part 1: Crash Course Physics #43; Author: CrashCourse;https://www.youtube.com/watch?v=7kb1VT0J3DE;License: Standard YouTube License, CC-BY