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(a)
Interpretation:
The structure of the given molecule is to be drawn.
Concept introduction:
The structure of a compound is drawn from its IUPAC name. The IUPAC name is made up of three parts, prefix, root, and suffix. The suffix indicates the highest priority functional group present in the structure. Its location is written as a prefix for the functional group name, unless redundant. The root is the longest continuous carbon chain or the largest ring that includes the highest priority functional group. Any other
If any chiral carbons are present, their absolute configurations are specified at the start, along with the carbon number, if necessary. Similarly, the stereochemistry (E/Z) of any double bond is also specified at the start. A di, tri, etc., before a prefix or suffix, indicates the number of instances of that functional group.
(b)
Interpretation:
The structure of the given molecule is to be drawn.
Concept introduction:
The structure of a compound is drawn from its IUPAC name. The IUPAC name is made up of three parts, prefix, root, and suffix. The suffix indicates the highest priority functional group present in the structure. Its location is written as a prefix for the functional group name, unless redundant. The root is the longest continuous carbon chain or the largest ring that includes the highest priority functional group. Any other functional groups present are listed alphabetically as prefixes along with their locants. For cyclic compounds, the numbering starts from that carbon where the highest priority group is attached. If any chiral carbons are present, their absolute configurations are specified at the start, along with the carbon number, if necessary. Similarly, the stereochemistry (E/Z) of any double bond is also specified at the start. A di, tri, etc., before a prefix or suffix, indicates the number of instances of that functional group.
(c)
Interpretation:
The structure of the given molecule is to be drawn.
Concept introduction:
The structure of a compound is drawn from its IUPAC name. The IUPAC name is made up of three parts, prefix, root, and suffix. The suffix indicates the highest priority functional group present in the structure. Its location is written as a prefix for the functional group name, unless redundant. The root is the longest continuous carbon chain or the largest ring that includes the highest priority functional group. Any other functional groups present are listed alphabetically as prefixes along with their locants. For cyclic compounds, the numbering starts from that carbon where the highest priority group is attached.
If any chiral carbons are present, their absolute configurations are specified at the start, along with the carbon number, if necessary. Similarly, the stereochemistry (E/Z) of any double bond is also specified at the start. A di, tri, etc., before a prefix or suffix, indicates the number of instances of that functional group.
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Chapter F Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
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- Given each of the IUPAC names provided, draw the corresponding structure. (a) 1-ethoxy-3-methoxyhexane;(b) 1,5-dipropoxypentane; (c) 4-butoxy-1,2-dimethoxyheptanearrow_forwardGiven each of the IUPAC names provided, draw the corresponding structure. (a) 4-(1-methylethyl)heptane;(b) 3-(1,1-dimethylethyl)-4-(1,2-dimethylpropyl)decanearrow_forwardDraw the structure of the following compounds which parent names have been traced to a common name; (a)5-methyl-4-nitroimidazole (b)2-chloro-4-methoxythiazole.arrow_forward
- Given each of the IUPAC names provided, draw the corresponding structure. (a) 1-(1,1-dimethylethyl)-2,4-diethylcyclohexane; (b) 1,4-dibutyl-2-(1-methylpropyl)cyclooctane; (c) 1,1-dicyclopropyl-3-(1,1-dimethylethyl)cycloheptanearrow_forwardDraw condensed formulas for the following compounds:(a) 3-ethyl-3-methyloctane; (b) 1-ethyl-3-propylcyclohexane (also draw a carbon-skeleton formula for this compound); (c) 3,3-diethyl-1-hexyne; (d) trans-3-methyl-3-heptene.arrow_forwardWhich of the following compounds, is the most acidic: (a) 2-methylhex-3-yne, (b) 2,5-dimethylhex-3-yne or (c) 2,2,5-trimethylhex-3-yne?arrow_forward
- Draw the structures of the following compounds. (a) trans-1-chloro-2-methylcyclohexanearrow_forwardDraw the molecule that corresponds to each IUPAC name. (a) 3,3-dipropoxypentan-1-amine; (b) 2,3,4-trichlorocyclohexanol; (c) 3-cyclopropylpentan-1-ol; (d) 3-(1-methylethyl)cycloheptanaminearrow_forwardDraw the structures for each of the following molecules. (a) 2-fluorotoluene; (b) 4-ethoxytoluene; (c) 2-ethoxyanisole;(d) 1,3-diphenylheptane; (e) 4,4-diphenyl-1-octene; (f) benzylbenzenearrow_forward
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