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Concept explainers
(a)
Interpretation:
The IUPAC name for the structure is to be given.
Concept introduction:
In the
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Answer to Problem A.30P
The correct IUPAC name for the structure is
Explanation of Solution
The given structure is
In the structure above, the ring has more carbon atoms than any of the straight chain groups. Hence, the root name of this structure is “cyclopentane.” The carbon atom of this ring, which is attached to two methyl groups, will be numbered as
The correct IUPAC name for the given structure is
(b)
Interpretation:
The IUPAC name for the structure is to be given.
Concept introduction:
In the IUPAC nomenclature, the longest continuous carbon chain or the largest carbon ring is considered as the parent chain. The name of this corresponding parent chain/ring will be the root of the molecule’s name. Identify the substituents and add the name of the substituent as a prefix to the left of the root. The number assigned to the carbon that is bonded to the substituent is called the locator number or locant. In case of two or more different substituents, the alphabetical order is considered. Number each carbon atom of the chain sequentially, beginning with
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Answer to Problem A.30P
The correct IUPAC name for the structure is
Explanation of Solution
The given structure is
In the above structure, the ring has more carbon atoms than any of the straight chain groups. Hence, the root name of this structure is “cyclobutane.” The carbon atom of this ring, which is attached to two substituents, will be numbered as
The correct IUPAC name for the given structure is
(c)
Interpretation:
The IUPAC name for the structure is to be given.
Concept introduction:
In the IUPAC nomenclature, the longest continuous carbon chain or the largest carbon ring is considered as the parent chain. The name of this corresponding parent chain/ring will be the root of the molecule’s name. Identify the substituents and add the name of the substituent as a prefix to the left of the root. The number assigned to the carbon that is bonded to the substituent is called the locator number or locant. In case of two or more different substituents, the alphabetical order is considered. Number each carbon atom of the chain sequentially, beginning with
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Answer to Problem A.30P
The correct IUPAC name for the structure is
Explanation of Solution
The given structure is
In the structure above, two rings are present. The ring on the left has more number of carbon atoms than the ring on the right; hence the root name of this compound is “cyclopentane.” The carbon atom of this cyclopentane ring to which the cyclobutane ring is attached will be numbered as
The correct IUPAC name for the given structure is
(d)
Interpretation:
The IUPAC name for the structure is to be given.
Concept introduction:
In the IUPAC nomenclature, the longest continuous carbon chain or the largest carbon ring is considered as the parent chain. The name of this corresponding parent chain/ring will be the root of the molecule’s name. Identify the substituents and add the name of the substituent as a prefix to the left of the root. The number assigned to the carbon that is bonded to the substituent is called the locator number or locant. In case of two or more different substituents, the alphabetical order is considered. Number each carbon atom of the chain sequentially, beginning with
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Answer to Problem A.30P
The correct IUPAC name for the structure is
Explanation of Solution
The given structure is
In the structure above, there are two rings and a straight chain of carbon atoms. Out of these, the straight continuous carbon chain has more atoms than any of the rings. Hence, the straight chain carbon will serve as the parent, and the two rings will serve as substituents. Thus, the root name of this structure is “pentane.” The numbering of this parent chain should start from the left as the substituent encountered receives the lowest possible locator number. The two substituents are attached on the
The correct IUPAC name for the given structure is
(e)
Interpretation:
The IUPAC name for the structure is to be given.
Concept introduction:
In the IUPAC nomenclature, the longest continuous carbon chain or the largest carbon ring is considered as the parent chain. The name of this corresponding parent chain/ring will be the root of the molecule’s name. Identify the substituents and add the name of the substituent as a prefix to the left of the root. The number assigned to the carbon that is bonded to the substituent is called the locator number or locant. In case of two or more different substituents, the alphabetical order is considered. Number each carbon atom of the chain sequentially, beginning with
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Answer to Problem A.30P
The correct IUPAC name for the structure is
Explanation of Solution
The given structure is
In the structure above, the straight continuous chain of carbon atoms will serve as the parent as it contains the highest number of carbon atoms than the rings. Hence, the root name of this structure is “butane.” There are two types of substituents attached- cyclopropyl and methyl. As the prefix “cyclo” is considered while naming, it will appear first in the IUPAC name. Thus, the numbering will also start from the left so that the carbon atom with two cyclopropyl rings will get the lowest possible locator numbers. The prefix di will be used for both the substituents as they appear twice. Thus, the IUPAC name for this structure is
The correct IUPAC name for the given structure is
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Chapter A Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_forward
- H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- 1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forwardhere is my question can u help me please!arrow_forward
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