(a)
Interpretation:
The structure for the molecule corresponding to the given IUPAC name, is to be drawn.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the
(b)
Interpretation:
The structure for the molecule is to be drawn that corresponds to the given IUPAC name.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group. The locator numbers which are written immediately before the name of substituents indicate the carbon atoms of the root to which they are attached.
(c)
Interpretation:
The structure for the molecule corresponding to the given IUPAC name is to be drawn.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group. The locator numbers which are written immediately before the name of substituents indicate the carbon atoms of the root to which they are attached.
(d)
Interpretation:
The structure for the molecule corresponding to the given IUPAC name is to be drawn.
Concept introduction:
In the given IUPAC name, the end part of the name indicates the longest continuous carbon chain or largest ring that is established as the root. The suffix ‘ol’ refers to the alcohol functional group. The suffix ‘amino’ refers to the amine functional group. The locator numbers which are written immediately before the name of substituents indicate the carbon atoms of the root to which they are attached.
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ORGANIC CHEMISTRY E-BOOK W/SMARTWORK5
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- Draw the following compounds: A) (2S,5R)-chloro-2-ethylhexanoic acid B) (1R,2R,4R)-4-ethylcyclohexane-1,2-diol C) (2S,3R)-3-amino-2-phenylbutanal D) (1S,2S,3R)-2-fluoro-3-propylcyclobutanol E) (2E,7Z)-5-bromo-2,7-nonadienearrow_forwardLook up the structure of lisdexamfetamine (Vyvanse), a drug used in the treatment of attention deficit hyperactivity disorder (ADHD). Redraw it and identify all the functional groups present. What is known about itstherapeutic properties?arrow_forwardAssume for the purposes of this problem that to be an alcohol (-ol) or an amine (-amine), the hydroxyl or amino group must be bonded to a tetrahedral (sp3 hybridized) carbon atom. Write the structural formula of a compound with an unbranched chain of four carbon atoms that is an: Q. Alkynoic acidarrow_forward
- What is the functional group of each ring in Erythromycin? There are 3 rings( a, b, and c) starting from the top working clockwise).arrow_forwardDraw the following structures: a) N-cyclopropyl-3-methylhexanamide b) phenylpropanoate c) 3-chloro-2-isopropoxynonanearrow_forward(a)(2R,3S)-2,3-dibromohexane, draw any diastereomers.arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning