Chemistry: An Atoms-Focused Approach
14th Edition
ISBN: 9780393912340
Author: Thomas R. Gilbert, Rein V. Kirss, Natalie Foster
Publisher: W. W. Norton & Company
expand_more
expand_more
format_list_bulleted
Concept explainers
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
For example, alanine is a chiral amino acid that has two enantiomers: (+)-alanine and (-)-alanine.
These two are optical isomers.
NH2
NH2
4.
One of the most important properties of chiral
molecules in solution is their effect on plane-
polarized light, this effect is called optical activity.
-C H
2
COOH
HOOC
CH
When an enantiomer rotates a plane-polarized light
in the positive direction or clockwise, it is
dextrorotary (+ or d), while for a negative direction
or counterclockwise, it is levorotary (- or l)
(+)-Alanine
(-)-Alanine
Alanine is a chiral amino acid that has two
enantiomers: (+)-alanine and ()-alanine. These two are
optical isomers.
On a blank sheet of paper, draw the constitutional isomers of C6H14?
The (R,R) isomer of methylphenidate (Ritalin) is used to treat attention deficit hyperactivity disorder (ADHD). The (S,S) isomer is an antidepressant. Identify the two chiral carbons in the structure below. Is this the (R,R) or the (S,S) isomer? Draw the other isomer.
Chapter 19 Solutions
Chemistry: An Atoms-Focused Approach
Ch. 19 - Prob. 19.1VPCh. 19 - Prob. 19.2VPCh. 19 - Prob. 19.3VPCh. 19 - Prob. 19.4VPCh. 19 - Prob. 19.5VPCh. 19 - Prob. 19.6VPCh. 19 - Prob. 19.7VPCh. 19 - Prob. 19.8VPCh. 19 - Prob. 19.9VPCh. 19 - Prob. 19.10VP
Ch. 19 - Prob. 19.11VPCh. 19 - Prob. 19.12VPCh. 19 - Prob. 19.13QACh. 19 - Prob. 19.14QACh. 19 - Prob. 19.15QACh. 19 - Prob. 19.16QACh. 19 - Prob. 19.17QACh. 19 - Prob. 19.18QACh. 19 - Prob. 19.19QACh. 19 - Prob. 19.20QACh. 19 - Prob. 19.21QACh. 19 - Prob. 19.22QACh. 19 - Prob. 19.23QACh. 19 - Prob. 19.24QACh. 19 - Prob. 19.25QACh. 19 - Prob. 19.26QACh. 19 - Prob. 19.27QACh. 19 - Prob. 19.28QACh. 19 - Prob. 19.29QACh. 19 - Prob. 19.30QACh. 19 - Prob. 19.31QACh. 19 - Prob. 19.32QACh. 19 - Prob. 19.33QACh. 19 - Prob. 19.34QACh. 19 - Prob. 19.35QACh. 19 - Prob. 19.36QACh. 19 - Prob. 19.37QACh. 19 - Prob. 19.38QACh. 19 - Prob. 19.39QACh. 19 - Prob. 19.40QACh. 19 - Prob. 19.41QACh. 19 - Prob. 19.42QACh. 19 - Prob. 19.43QACh. 19 - Prob. 19.44QACh. 19 - Prob. 19.45QACh. 19 - Prob. 19.46QACh. 19 - Prob. 19.47QACh. 19 - Prob. 19.48QACh. 19 - Prob. 19.49QACh. 19 - Prob. 19.50QACh. 19 - Prob. 19.51QACh. 19 - Prob. 19.52QACh. 19 - Prob. 19.53QACh. 19 - Prob. 19.54QACh. 19 - Prob. 19.55QACh. 19 - Prob. 19.56QACh. 19 - Prob. 19.57QACh. 19 - Prob. 19.58QACh. 19 - Prob. 19.59QACh. 19 - Prob. 19.60QACh. 19 - Prob. 19.61QACh. 19 - Prob. 19.62QACh. 19 - Prob. 19.63QACh. 19 - Prob. 19.64QACh. 19 - Prob. 19.65QACh. 19 - Prob. 19.66QACh. 19 - Prob. 19.67QACh. 19 - Prob. 19.68QACh. 19 - Prob. 19.69QACh. 19 - Prob. 19.70QACh. 19 - Prob. 19.71QACh. 19 - Prob. 19.72QACh. 19 - Prob. 19.73QACh. 19 - Prob. 19.74QACh. 19 - Prob. 19.75QACh. 19 - Prob. 19.76QACh. 19 - Prob. 19.77QACh. 19 - Prob. 19.78QACh. 19 - Prob. 19.79QACh. 19 - Prob. 19.80QACh. 19 - Prob. 19.81QACh. 19 - Prob. 19.82QACh. 19 - Prob. 19.83QACh. 19 - Prob. 19.84QACh. 19 - Prob. 19.85QACh. 19 - Prob. 19.86QACh. 19 - Prob. 19.87QACh. 19 - Prob. 19.88QACh. 19 - Prob. 19.89QACh. 19 - Prob. 19.90QACh. 19 - Prob. 19.91QACh. 19 - Prob. 19.92QACh. 19 - Prob. 19.93QACh. 19 - Prob. 19.94QACh. 19 - Prob. 19.95QACh. 19 - Prob. 19.96QACh. 19 - Prob. 19.97QACh. 19 - Prob. 19.98QACh. 19 - Prob. 19.99QACh. 19 - Prob. 19.100QACh. 19 - Prob. 19.101QACh. 19 - Prob. 19.102QACh. 19 - Prob. 19.103QACh. 19 - Prob. 19.104QACh. 19 - Prob. 19.105QACh. 19 - Prob. 19.106QACh. 19 - Prob. 19.107QACh. 19 - Prob. 19.108QACh. 19 - Prob. 19.109QACh. 19 - Prob. 19.110QACh. 19 - Prob. 19.111QACh. 19 - Prob. 19.112QACh. 19 - Prob. 19.113QACh. 19 - Prob. 19.114QACh. 19 - Prob. 19.115QACh. 19 - Prob. 19.116QACh. 19 - Prob. 19.117QACh. 19 - Prob. 19.118QACh. 19 - Prob. 19.119QACh. 19 - Prob. 19.120QACh. 19 - Prob. 19.121QACh. 19 - Prob. 19.122QACh. 19 - Prob. 19.123QACh. 19 - Prob. 19.124QACh. 19 - Prob. 19.125QACh. 19 - Prob. 19.126QACh. 19 - Prob. 19.127QACh. 19 - Prob. 19.128QACh. 19 - Prob. 19.129QACh. 19 - Prob. 19.130QACh. 19 - Prob. 19.131QACh. 19 - Prob. 19.132QACh. 19 - Prob. 19.133QACh. 19 - Prob. 19.134QACh. 19 - Prob. 19.135QACh. 19 - Prob. 19.136QACh. 19 - Prob. 19.137QACh. 19 - Prob. 19.138QACh. 19 - Prob. 19.139QACh. 19 - Prob. 19.140QACh. 19 - Prob. 19.141QACh. 19 - Prob. 19.142QA
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
- a. Use bond energies (see Table 3-3) to estimate H for the reaction of two molecules of glycine to form a peptide linkage. b. Would you predict S to favor the formation of peptide linkages between two molecules of glycine? c. Would you predict the formation of proteins to be a spontaneous process?arrow_forwardWhat is the structure of SeF5NF2?arrow_forwardWhat is an isomer? Name the isomers of the compound with the closed formula C4H9CI. Which of these isomers can have a chiral structure? Examine it from a stereochemical point of viewarrow_forward
- 3. Sketch the cis and trans isomers formed when the anion of the amino acid glycine, H2NCH2CO2 (gly), reacts with CoCl2.arrow_forwardConsider the compound C₂H₃N. Which one of the structures in Figure 4 is the best representation of this compound based on your current knowledge? * A B C D All these structures are good representations of the compound.arrow_forwardHow many chiral centers are in the following molecule? 03 02 05 04 R OHarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningWorld of ChemistryChemistryISBN:9780618562763Author:Steven S. ZumdahlPublisher:Houghton Mifflin College DivWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
- General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
World of Chemistry
Chemistry
ISBN:9780618562763
Author:Steven S. Zumdahl
Publisher:Houghton Mifflin College Div
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Lipids - Fatty Acids, Triglycerides, Phospholipids, Terpenes, Waxes, Eicosanoids; Author: The Organic Chemistry Tutor;https://www.youtube.com/watch?v=7dmoH5dAvpY;License: Standard YouTube License, CC-BY