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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
![Check Mark](/static/check-mark.png)
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
![Check Mark](/static/check-mark.png)
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
![Check Mark](/static/check-mark.png)
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
![Check Mark](/static/check-mark.png)
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: Study Guide/solutions Manual (second)
- 5) Confidence interval. Berglund and Wichardt investigated the quantitative determination of Cr in high-alloy steels using a potentiometric titration of Cr(VI). Before the titration, samples of the steel were dissolved in acid and the chromium oxidized to Cr(VI) using peroxydisulfate. Shown here are the results (as %w/w Cr) for the analysis of a reference steel. 16.968, 16.922, 16.840, 16.883, 16.887, 16.977, 16.857, 16.728 Calculate the mean, the standard deviation, and the 95% confidence interval about the mean. What does this confidence interval mean?arrow_forwardIn the Nitrous Acid Test for Amines, what is the observable result for primary amines? Group of answer choices nitrogen gas bubbles form a soluble nitrite salt yellow oily layer of nitrosoaminearrow_forward3. a. Use the MS to propose at least two possible molecular formulas. For an unknown compound: 101. 27.0 29.0 41.0 50.0 52.0 55.0 57.0 100 57.5 58.0 58.5 62.0 63.0 64.0 65.0 74.0 40 75.0 76.0 20 20 40 60 80 100 120 140 160 180 200 220 m/z 99.5 68564810898409581251883040 115.0 116.0 77404799 17417M 117.0 12.9 118.0 33.5 119.0 36 133 0 1.2 157.0 2.1 159.0 16 169.0 219 170.0 17 171.0 21.6 172.0 17 181.0 1.3 183.0 197.0 100.0 198.0 200. 784 Relative Intensity 2 2 8 ō (ppm) 6 2arrow_forward
- Solve the structure and assign each of the following spectra (IR and C-NMR)arrow_forward1. For an unknown compound with a molecular formula of C8H100: a. What is the DU? (show your work) b. Solve the structure and assign each of the following spectra. 8 6 2 ō (ppm) 4 2 0 200 150 100 50 ō (ppm) LOD D 4000 3000 2000 1500 1000 500 HAVENUMBERI -11arrow_forward16. The proton NMR spectral information shown in this problem is for a compound with formula CioH,N. Expansions are shown for the region from 8.7 to 7.0 ppm. The normal carbon-13 spec- tral results, including DEPT-135 and DEPT-90 results, are tabulated: 7 J Normal Carbon DEPT-135 DEPT-90 19 ppm Positive No peak 122 Positive Positive cus и 124 Positive Positive 126 Positive Positive 128 No peak No peak 4° 129 Positive Positive 130 Positive Positive (144 No peak No peak 148 No peak No peak 150 Positive Positive してしarrow_forward
- 3. Propose a synthesis for the following transformation. Do not draw an arrow-pushing mechanism below, but make sure to draw the product of each proposed step (3 points). + En CN CNarrow_forwardShow work..don't give Ai generated solution...arrow_forwardLabel the spectrum with spectroscopyarrow_forward
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