Concept explainers
(a)
Interpretation:
The correct structure is to be drawn from the given IUPAC name of the molecule.
Concept introduction:
The structure of a compound can be drawn on the basis of its IUPAC name. The IUPAC name is made of three parts, prefix, root, and suffix. The suffix indicates the highest priority group present. Its location is written as a prefix for the functional group name unless redundant. The root is the longest continuous carbon chain that also 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 prefix di, tri, etc., before a prefix or suffix indicates the number of instances of that functional group.
Answer to Problem F.6P
The correct structure of
Explanation of Solution
The compound is a
The methyl groups are then attached to the next ring carbon.
Therefore, the structure of
The structure of the compound can be drawn from its IUPAC name, which lists the functional groups attached to an alkyl/aryl root (parent).
(b)
Interpretation:
The correct structure is to be drawn from the given IUPAC name of molecule.
Concept introduction:
The structure of a compound can be drawn on the basis of its IUPAC name. The IUPAC name is made of three parts, prefix, root, and suffix. The suffix indicates the highest priority group present. Its location is written as a prefix for the functional group name unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. Any other functional groups present are listed alphabetically as prefixes along with their locants.
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 prefix di, tri, etc., before a prefix or suffix indicates the number of instances of that functional group.
Answer to Problem F.6P
The structure of
Explanation of Solution
The name shows that the root is a seven carbon ring with two double bonds. The root name is, therefore, cycloheptadiene. The only functional group is an amide (
Thus, the structure of
The structure of the compound can be drawn from its IUPAC name, which lists the functional groups attached to an alkyl/aryl root (parent).
(c)
Interpretation:
The correct structure of
Concept introduction:
The structure of a compound can be drawn on the basis of its IUPAC name. The IUPAC name is made of three parts, prefix, root, and suffix. The suffix indicates the highest priority group present. Its location is written as a prefix for the functional group name unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. Any other functional groups present are listed alphabetically as prefixes along with their locants.
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 prefix di, tri, etc., before a prefix or suffix indicates the number of instances of that functional group.
Answer to Problem F.6P
The structure of
Explanation of Solution
The name shows that the root is an eight carbon ring with two functional groups directly attached to ring carbons. The highest priority group is a carboxylic acid group, and the corresponding ring carbon is numbered 1. The second, nitrile group, is then on C4.
Both C1 and C4 are chiral carbons with R and S configurations respectively. According to Cahn-Ingold-Prelog rules, this means the priority groups 1 to 3 attached to C1 are arranged clockwise if the lowest priority group H is pointing away from the observer, or counterclockwise if H is pointing toward the observer. The priority groups 1 to 3 attached to C4 are arranged conterclockwise if the lowest priority H is pointing away, or clockwise if it is pointing toward the observer.
The structure of the compound can, therefore, be drawn as:
The structure of the compound can be drawn from its IUPAC name, which lists the functional groups attached to an alkyl/aryl root (parent).
(d)
Interpretation:
The structure of
Concept introduction:
The structure of a compound can be drawn on the basis of its IUPAC name. The IUPAC name is made of three parts, prefix, root, and suffix. The suffix indicates the highest priority group present. Its location is written as a prefix for the functional group name unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. Any other functional groups present are listed alphabetically as prefixes along with their locants.
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 prefix di, tri, etc., before a prefix or suffix indicates the number of instances of that functional group.
Answer to Problem F.6P
The correct structure of
Explanation of Solution
The name shows that the root is a cyclobutane ring. Two functional groups are attached to the ring, a secondary amide and a hydroxyl group. The amide is the higher priority group, so the ring atoms are numbered from the carbon to which it is attached. The hydroxyl group is then attached to the adjacent carbon C2.
C1 and C2 are both chiral carbons with an absolute configuration of S. This means on each of these carbons, the priority 1 to 3 groups are arranged counterclockwise with the lowest priority H pointing away from the observer, or clockwise with the H pointing toward the observer.
The complete structure, using dash-wedge representation, for the two functional groups, can then be drawn as
The structure of the compound can be drawn from its IUPAC name, which lists the functional groups attached to an alkyl/aryl root (parent).
(e)
Interpretation:
The structure of
Concept introduction:
The structure of a compound can be drawn on the basis of its IUPAC name. The IUPAC name is made of three parts, prefix, root, and suffix. The suffix indicates the highest priority group present. Its location is written as a prefix for the functional group name unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. Any other functional groups present are listed alphabetically as prefixes along with their locants.
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 prefix di, tri, etc., before a prefix or suffix indicates the number of instances of that functional group.
Answer to Problem F.6P
The structure of
Explanation of Solution
The name shows that the root is a six carbon ring, with two double bonds. The root name is, therefore, cyclohexadiene. One functional group, nitrile, is attached to the ring. The ring
C1 is a chiral carbon with an absolute configuration of R. Therefore, the priority groups 1 to 3 attached to it must be arranged clockwise with the lowest priority hydrogen pointing away from the observer.
Thus, the structure of the compound can be drawn as
The structure of the compound can be drawn from its IUPAC name, which lists the functional groups attached to an alkyl/aryl root (parent).
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Chapter F Solutions
ORGANIC CHEMISTRY PRINCIPLES & MECHANISM
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- Give detailed Solution with explanation needed .give answer all sub parts if you not then don't give answer..I will give you upvote for answering all..arrow_forwardGive a clear detailed Solution with explanation..give the mechanismarrow_forwardGive detailed Solution with explanation needed..don't give Handwritten answer..explain each steps..,,??)*arrow_forward
- Give detailed Solution with explanation needed..give answer both sub parts..if you not then don't give answer...give correct answerarrow_forwardQ.2 Give the structure(s) of the major organic produc(s) of I-L and O-P, Show stereochemistry if appropriate. H20, H2SO4 H2 I J H9SO4 Pd/CaCO3/Pb 1. BH3 Li, NH3 K L 2. NaOH, H202 H2, Pd/C H2 Pd/CaCO3/Pb H20, H2SO4 H9SO4 2 equiv HBrarrow_forwardDraw the structure(s) of the major organic product(s) of the following reaction. 1. NaOCH3 / CH3OH H3C CH3 2. 1 eq. 2-bromo-2-methylpropane • You do not have to consider stereochemistry. • Omit products derived from the acidic or basic reagent itself, e.g. HN(i-Pr)2 derived from N(i-Pr),. • If no reaction occurs, draw the organic starting material. • If substantial starting material is present at the end of the reaction, include it in the products. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. Draw the structure(s) of the major organic product(s) of the following reaction. Aqueous NaHCO3 0° C 1 eq. Cl2 • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If the reaction produces a racemic mixture, draw both stereoisomers. • If no reaction occurs, draw the organic starting material. • Draw one structure per sketcher. Add additional…arrow_forward
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