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Concept explainers
(a)
Interpretation:
The given molecule is chiral or not is to be identified.
Concept introduction:
The absence of chiral centers does not guarantee that a molecule is achiral. For a molecule to be chiral, it must not be superimposable on its mirror image. Allenes are the cumulated dienes in which one carbon atom is attached with each of its two neighbouring carbon atoms by double bonds. Disubstituted allenes are the ones in which the two hydrogen atoms on the same carbon or on adjacent carbon atoms are replaced by two non-hydrogen substituents.
Examine both “ends” of the allene. If either of those ends is attached to two identical substituents, it is achiral – because it will have a mirror plane. If neither of the ends are attached to two identical substituents, then it is chiral.
(b)
Interpretation:
The given molecule is chiral or not is to be identified.
Concept introduction:
The absence of chiral centers does not guarantee that a molecule is achiral. For a molecule to be chiral, it must not be superimposable on its mirror image. Allenes are the cumulated dienes in which one carbon atom is attached with each of its two neighbouring carbon atoms by double bonds. Disubstituted allenes are the ones in which the two hydrogen atoms on the same carbon or on adjacent carbon atoms are replaced by two non-hydrogen substituents.
Examine both “ends” of the allene. If either of those ends is attached to two identical substituents, it is achiral – because it will have a mirror plane. If neither of the ends are attached to two identical substituents, then it is chiral.
(c)
Interpretation:
The given molecule is chiral or not is to be identified.
Concept introduction:
The absence of chiral centers does not guarantee that a molecule is achiral. For a molecule to be chiral, it must not be superimposable on its mirror image. Allenes are the cumulated dienes in which one carbon atom is attached with each of its two neighbouring carbon atoms by double bonds. Disubstituted allenes are the ones in which the two hydrogen atoms on the same carbon or on adjacent carbon atoms are replaced by two non-hydrogen substituents.
Examine both “ends” of the allene. If either of those ends is attached to two identical substituents, it is achiral – because it will have a mirror plane. If neither of the ends are attached to two identical substituents, then it is chiral.
(d)
Interpretation:
The given molecule is chiral or not is to be identified.
Concept introduction:
The absence of chiral centers does not guarantee that a molecule is achiral. For a molecule to be chiral, it must not be superimposable on its mirror image. Allenes are the cumulated dienes in which one carbon atom is attached with each of its two neighbouring carbon atoms by double bonds. Disubstituted allenes are the ones in which the two hydrogen atoms on the same carbon or on adjacent carbon atoms are replaced by two non-hydrogen substituents.
Examine both “ends” of the allene. If either of those ends is attached to two identical substituents, it is achiral – because it will have a mirror plane. If neither of the ends are attached to two identical substituents, then it is chiral.
(e)
Interpretation:
The given molecule is chiral or not is to be identified.
Concept introduction:
The absence of chiral centers does not guarantee that a molecule is achiral. For a molecule to be chiral, it must not be superimposable on its mirror image. Allenes are the cumulated dienes in which one carbon atom is attached with each of its two neighbouring carbon atoms by double bonds. Disubstituted allenes are the ones in which the two hydrogen atoms on the same carbon or on adjacent carbon atoms are replaced by two non-hydrogen substituents.
Examine both “ends” of the allene. If either of those ends is attached to two identical substituents, it is achiral – because it will have a mirror plane. If neither of the ends are attached to two identical substituents, then it is chiral.
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Chapter 5 Solutions
EBK GET READY FOR ORGANIC CHEMISTRY
- 2. 200 LOD For an unknown compound with a molecular ion of 101 m/z: a. Use the molecular ion to propose at least two molecular formulas. (show your work) b. What is the DU for each of your possible formulas? (show your work) C. Solve the structure and assign each of the following spectra. 8 6 4 2 (ppm) 150 100 50 ō (ppm) 4000 3000 2000 1500 1000 500 HAVENUMBERI-11arrow_forwardComplete the spectroscopy with structurearrow_forwardComplete the spectroscopy with structurearrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage LearningMacroscale and Microscale Organic ExperimentsChemistryISBN:9781305577190Author:Kenneth L. Williamson, Katherine M. MastersPublisher:Brooks Cole
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