
Concept explainers
Interpretation:
The optical isomer from the following should be identified:
Concept introduction:
Two mirror image representations are possible for a molecule having chiral center in its structure. If the mirror images are non-superimposable to each other then, they are said to be optical isomers.

Answer to Problem 73A
The correct option is (a):
Explanation of Solution
A molecule is said to be chiral molecule when all the attached groups to central carbon atom are different and lacks in plane of symmetry in the molecule. The molecules having chiral centres show optical isomerism as there are two mirror image representations possible for a molecule having chiral center in its structure and if the mirror images are non-superimposable to each other then, they are said to be optical isomers.
In order to find the same molecules, let (b) be the reference molecule to which other structures are compared as:
For structure (c), on rotating the structure in such a way that T comes at top like:
Thus, the obtained structure is same as that of (b).
For structure (d), on rotating and moving the structure in such a way that T comes at top and R at bottom like:
Thus, the obtained structure is same as that of (b).
Since, in (a) structure the orientation of atoms around carbon is different so, it is an optical isomer.
Hence, structure (b), (c) and (d) are same and (a) is the optical isomer.
Chapter 21 Solutions
Glencoe Chemistry: Matter and Change, Student Edition
Additional Science Textbook Solutions
Introductory Chemistry (6th Edition)
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
Microbiology: An Introduction
Campbell Biology (11th Edition)
Human Physiology: An Integrated Approach (8th Edition)
Biology: Life on Earth (11th Edition)
- Design experiments in UV-Vis to figure the optimal mole ratio of copper (1:1, 2:1, 3:1 and etc)versus ethambutol using all necessary chemicals including dihydrochloride and copper nitrate hemipentahydrate and sodium hydroxide. Show how UV-Vis absorbance and maximum wavelength would change in responsearrow_forwardCorrect each molecule in the drawing area below so that it has the condensed structure it would have if it were dissolv a 0.1 M aqueous solution of HCI. If there are no changes to be made, check the No changes box under the drawing area. No changes. HO—CH,—C—CH,—OH X 5 2 2 2 HO–CH,—CH,—C—CH,—OH Explanation Check Center Accessi ©2025 on 5 Carrow_forwardMake the calculations to prepare 2M H2SO4, from concentrated H2SO4 (98%; density: 1.84 g/mL).arrow_forward
- H CH3 CH3 b) Write the products of your compound and the following reagents. If the reaction would not work for your compound, write "no reaction" and explain the problem. NaCN H* H₂NNHCH5 H* -à NaBH -à CH2MgBr Cro₁₂ --à H3O+ -à c) Would your compound give a positive Tollen's test? Why or why not?arrow_forwardHomework 4 Chem 204 Dr. Hellwig Consider this compound, which will be referred to as "your compound". a) Name your compound according to the IUPAC system. Include stereochemistry (E/Z/R/S) H CH3 CH3arrow_forwardWhat is the mechanism for this?arrow_forward
- 21.50 Determine the combinations of haloalkane(s) and alkoxide(s) that could be used to synthesize the following ethers through Williamson ether synthesis. (a) (c) (d) (e) (f) H₂COarrow_forward1. Arrange the following in order of increasing bond energy (lowest bond energy first, highest bond energy last). Provide your rationale. C=C, C-F, C=C, C-N, C-C List the bond order for each example.arrow_forwardWhat is the major enolate formed when treated with LDA? And why that one?arrow_forward
- 4. Calculate the total number of sigma bonds and total number of pi bonds in each of the following compounds. a. HH :D: +1 I H-N-C-C-O-H I H b. HH H Н :N=C-C-C=C-CEC-H :0: total o H-C-H H-C = `C-H I H. 11 H-C = C= CH H total o total π total π 1 Harrow_forwardIn the following reaction, what quantity in moles of CH₃OH are required to give off 4111 kJ of heat? 2 CH₃OH (l) + 3 O₂ (g) → 2 CO₂ (g) + 4 H₂O(g) ∆H° = -1280. kJarrow_forwardIndicate the processes in the dismutation of Cu2O.arrow_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





