When naming cycloalkynes that lack any other functional groups, the triple bond does not require a locant, because it is assumed to be between C1 and C2. Write the IUPAC name of the following structures. Specify (R) or (S) and (E) or (Z) as needed. Br i-Pr Br
When naming cycloalkynes that lack any other functional groups, the triple bond does not require a locant, because it is assumed to be between C1 and C2. Write the IUPAC name of the following structures. Specify (R) or (S) and (E) or (Z) as needed. Br i-Pr Br
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Transcribed Image Text:When naming cycloalkynes that lack any other functional groups, the triple bond does not require a locant, because it is assumed to be between C1 and C2. Write the IUPAC name of the following structures. Specify (R) or (S) and (E) or (Z) as needed.
**Diagram Explanation:**
The diagram shows a cyclic compound with a triple bond. It depicts a seven-membered ring with a triple bond assumed to be between the first and second carbon atoms. The molecule has two bromine (Br) atoms attached, one indicated by a wedge (representing a bond coming out of the plane) and the other by a dashed line (representing a bond going into the plane). An isopropyl (i-Pr) group is also attached to the ring. The spatial orientation suggests stereochemistry that may need (R)/(S) and (E)/(Z) specification for complete IUPAC naming.
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