Concept explainers
Give the IUPAC name for each compound, including any R, S designation.
a. b.

(a)
Interpretation: The IUPAC name of the given compound, including any R,S designation, is to be stated.
Concept introduction: One should follow the given four steps to give the IUPAC name of a compound. The first step is naming of longest parent chain. The second step is numbering of chain. The third step is naming and numbering of substituents. The fourth step is combining the all parts.
Answer to Problem 39P
The IUPAC name of the given compound is (R)-
Explanation of Solution
The black balls of the given structure represent carbon atoms, the white balls represent hydrogen atoms and the brown ball represent bromine atom. Hence, the complete structure of the compound is,
Figure 1
The carbon atom at which bromine atom is attached is chiral in nature. The lowest priority
Figure 2
Hence, the configuration of stereogenic center is R.
Bromine group and ethyl group are present on the second and fifth carbon atom, respectively, of a chain of seven carbon atoms as shown in Figure 3.
Figure 3
Therefore, the IUPAC name of the given compound is (R)-
The IUPAC name of the given compound is (R)-

(b)
Interpretation: The IUPAC name of the given compound, including any R,S designation, is to be stated.
Concept introduction: One should follow the given four steps to give the IUPAC name of a compound. The first step is naming of longest parent chain. The second step is numbering of chain. The third step is naming and numbering of substituents. The fourth step is combining the all parts.
Answer to Problem 39P
The IUPAC name of the given compound is (1R)-
Explanation of Solution
The black balls of the given structure represent carbon atoms, the white balls represent hydrogen atoms and the green ball represent chlorine atom. Hence, the complete structure of the compound is,
Figure 4
The carbon atom at which chlorine atom is attached is chiral in nature. The lowest priority
Figure 5
Hence, the configuration of stereogenic center is R.
Chlorine group and isopropyl group are present on the first and third carbon atom, respectively, of a cyclopentane ring as shown in Figure 6.
Figure 6
Therefore, the IUPAC name of the given compound is (1R)-
The IUPAC name of the given compound is (1R)-
Want to see more full solutions like this?
Chapter 7 Solutions
Organic Chemistry (6th Edition)
Additional Science Textbook Solutions
Applications and Investigations in Earth Science (9th Edition)
Physical Science
Biology: Concepts and Investigations
General, Organic, and Biological Chemistry - 4th edition
- Consider this reaction (molecular weights are under each compound): HC=CH + 2 HCI --> C2H4Cl 2 MW = 26 36.5 99 If 4.4 g of HC=CH are reacted with 110 mL of a 2.3 M HCI solution, and 6.0 g of product are actually produced, what is the percent yield?arrow_forwardWhat is the name of the major product of this reaction? OH CH3 H₂SO4, heat 1-methylcyclohexene O2-methyl-1-cyclohexene O 3-mthylcyclohexene 1-methyl-2-cyclohexenearrow_forwardWe added a brown solution of Br2 to one of our products, and the brown color disappeared. This indicated that our product wasarrow_forward
- Rank the following according to reactivity toward nitration: a) benzene b) bromobenzene c) nitrobenzene d) phenol Od) greatest, c) least Od) greatest, b) least Od) greatest, a) least a) greatest, b) least a) greatest, c) least Oa) greatest, d) least Ob) greatest, a) least O b) greatest, c) least Ob) greatest, d) least O c) greatest, a) least O c) greatest, b) least O c) greatest, d) leastarrow_forwardO-Nitrophenol was distilled over with the steam in our experiment while the other isomer did not. This is due to: O intramolecular hydrogen bonding in the ortho isomer O intermolecular hydrogen bonding in the the ortho isomer O the ortho isomer has a lower density O the ortho isomer has a lower molecular weightarrow_forwardK 44% Problem 68 of 15 Submit Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. :6: :: :CI: CI CI: :0:0 Select to Add Arrows Select to Add Arrows H H Cl CI: CI CI: Select to Add Arrows Select to Add Arrows H :CI: Alarrow_forward
- I I H :0: Submit Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. 0:0 :0: CI ΑΙ :CI: :CI: :0: CI Select to Add Arrows Select to Add Arrows cl. :0: Cl © ハ CI:: CI H CO Select to Add Arrows Select to Add Arrows 10: AI ::arrow_forwardOrder the following compounds from slowest to fastest in a nucleophilic acyl substitution reaction. ii 요 OB D A E C OCE Darrow_forwardI need the most help figuring out how to find [I^-] mol/ L, [S2O8^2-] mol/L. 1st and 2nd Blank columns.arrow_forwardCan someone help me whats the issue?arrow_forwarda. The change in the Gibbs energy of a certain constant pressure process is found to fit the expression: AG-85.1 J mol −1 +36.5 J mol ¹K-1 × T A. Calculate the value of AS for the process. B. Next, use the Gibbs-Helmholtz equation: (a(AG/T)) ΔΗ - T2 to calculate the value of AH for the process.arrow_forwardNonearrow_forwardarrow_back_iosSEE MORE QUESTIONSarrow_forward_ios
- 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





