![Basic Chemistry](https://www.bartleby.com/isbn_cover_images/9780134878119/9780134878119_smallCoverImage.jpg)
(a)
Interpretation: The name of the following aromatic compound should be determined:
Concept Introduction: The ring structures of the compound having uncommon stability due to delocalized pi electron density shared in between all the carbon atoms of the ring is said to be an aromatic compound.
In order to give the name to the multiple substituted
- For single substituted aromatic compound (when the substituent contains six or fewer carbons), the name of the substituted group is written first followed by the name of the aromatic compound.
- For single substituted aromatic compound (when the substituent contains more than six carbons), the name of the aromatic compound is written first followed by the name of the substituted group.
- For single substituted aromatic compound, the numbering on the ring is done in such a way that the multiple substituents get the lowest number.
(b)
Interpretation: The name of the following aromatic compound should be determined:
Concept Introduction: The ring structures of the compound having uncommon stability due to delocalized pi electron density shared in between all the carbon atoms of the ring is said to be an aromatic compound.
In order to give the name to the multiple substituted aromatic compounds, the following steps are followed:
- For single substituted aromatic compound (when the substituent contains six or fewer carbons), the name of the substituted group is written first followed by the name of the aromatic compound.
- For single substituted aromatic compound (when the substituent contains more than six carbons), the name of the aromatic compound is written first followed by the name of the substituted group.
- For single substituted aromatic compound, the numbering on the ring is done in such a way that the multiple substituents get the lowest number.
(c)
Interpretation: The name of the following aromatic compound should be determined:
Concept Introduction: The ring structures of the compound having uncommon stability due to delocalized pi electron density shared in between all the carbon atoms of the ring is said to be an aromatic compound.
In order to give the name to the multiple substituted aromatic compounds, the following steps are followed:
- For single substituted aromatic compound (when the substituent contains six or fewer carbons), the name of the substituted group is written first followed by the name of the aromatic compound.
- For single substituted aromatic compound (when the substituent contains more than six carbons), the name of the aromatic compound is written first followed by the name of the substituted group.
- For single substituted aromatic compound, the numbering on the ring is done in such a way that the multiple substituents get the lowest number.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 17 Solutions
Basic Chemistry
- Highlight in red each acidic location on the organic molecule at left. Highlight in blue each basic location on the organic molecule at right. Note for advanced students: we mean acidic or basic in the Brønsted-Lowry sense only. Cl N شیخ x Garrow_forwardQ4: Draw the mirror image of the following molecules. Are the molecules chiral? C/ F LL CI CH3 CI CH3 0 CI CH3 CI CH3 CH3arrow_forwardComplete combustion of a 0.6250 g sample of the unknown crystal with excess O2 produced 1.8546 g of CO2 and 0.5243 g of H2O. A separate analysis of a 0.8500 g sample of the blue crystal was found to produce 0.0465 g NH3. The molar mass of the substance was found to be about 310 g/mol. What is the molecular formula of the unknown crystal?arrow_forward
- 4. C6H100 5 I peak 3 2 PPM Integration values: 1.79ppm (2), 4.43ppm (1.33) Ipeakarrow_forwardNonearrow_forward3. Consider the compounds below and determine if they are aromatic, antiaromatic, or non-aromatic. In case of aromatic or anti-aromatic, please indicate number of I electrons in the respective systems. (Hint: 1. Not all lone pair electrons were explicitly drawn and you should be able to tell that the bonding electrons and lone pair electrons should reside in which hybridized atomic orbital 2. You should consider ring strain- flexibility and steric repulsion that facilitates adoption of aromaticity or avoidance of anti- aromaticity) H H N N: NH2 N Aromaticity (Circle) Aromatic Aromatic Aromatic Aromatic Aromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic nonaromatic nonaromatic nonaromatic nonaromatic nonaromatic aromatic TT electrons Me H Me Aromaticity (Circle) Aromatic Aromatic Aromatic Aromatic Aromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic Antiaromatic nonaromatic nonaromatic nonaromatic nonaromatic nonaromatic aromatic πT electrons H HH…arrow_forward
- A chemistry graduate student is studying the rate of this reaction: 2 HI (g) →H2(g) +12(g) She fills a reaction vessel with HI and measures its concentration as the reaction proceeds: time (minutes) [IH] 0 0.800M 1.0 0.301 M 2.0 0.185 M 3.0 0.134M 4.0 0.105 M Use this data to answer the following questions. Write the rate law for this reaction. rate = 0 Calculate the value of the rate constant k. k = Round your answer to 2 significant digits. Also be sure your answer has the correct unit symbol.arrow_forwardNonearrow_forwardNonearrow_forward
- Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781337399074/9781337399074_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781133949640/9781133949640_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305580350/9781305580350_smallCoverImage.gif)