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Concept explainers
(a)
Interpretation: The IUPAC name of the following 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 IUPAC name of the following 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 IUPAC name of the following 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.
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Chapter 17 Solutions
EBK BASIC CHEMISTRY
- The emission data in cps displayed in Table 1 is reported to two decimal places by the chemist. However, the instrument output is shown in Table 2. Table 2. Iron emission from ICP-AES Sample Blank Standard Emission, cps 579.503252562 9308340.13122 Unknown Sample 343.232365741 Did the chemist make the correct choice in how they choose to display the data up in Table 1? Choose the best explanation from the choices below. No. Since the instrument calculates 12 digits for all values, they should all be kept and not truncated. Doing so would eliminate significant information. No. Since the instrument calculates 5 decimal places for the standard, all of the values should be limited to the same number. The other decimal places are not significant for the blank and unknown sample. Yes. The way Saman made the standards was limited by the 250-mL volumetric flask. This glassware can report values to 2 decimal places, and this establishes our number of significant figures. Yes. Instrumental data…arrow_forwardSteps and explanation pleasearrow_forwardSteps and explanation to undertand concepts.arrow_forward
- Nonearrow_forward7. Draw a curved arrow mechanism for the following reaction. HO cat. HCI OH in dioxane with 4A molecular sievesarrow_forwardTry: Convert the given 3D perspective structure to Newman projection about C2 - C3 bond (C2 carbon in the front). Also, show Newman projection of other possible staggered conformers and circle the most stable conformation. Use the template shown. F H3C Br Harrow_forward
- Nonearrow_forward16. Consider the probability distribution p(x) = ax", 0 ≤ x ≤ 1 for a positive integer n. A. Derive an expression for the constant a, to normalize p(x). B. Compute the average (x) as a function of n. C. Compute σ2 = (x²) - (x)², the variance of x, as a function of n.arrow_forward451. Use the diffusion model from lecture that showed the likelihood of mixing occurring in a lattice model with eight lattice sites: Case Left Right A B C Permeable Barrier → and show that with 2V lattice sites on each side of the permeable barrier and a total of 2V white particles and 2V black particles, that perfect de-mixing (all one color on each side of the barrier) becomes increasingly unlikely as V increases.arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
- Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStaxChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
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