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Concept explainers
(a)
Interpretation:
For the given cycloalkane, cis‑trans isomerism is possible or not has to be determined and if it is possible, the structural formula has to be drawn.
Concept Introduction:
Organic compounds are represented shortly by the molecular formula and structural formula. Each and every compound has its own molecular formula. Compounds can have same molecular formula but not same structural formula.
Isomers are the compounds that have same molecular formula but different structural formula. The main difference lies in the way the atoms are arranged in the structure. Isomers have different chemical and physical properties even when they have same molecular formula. This is known as Isomerism.
If there is difference only in the connectivity of the atoms in the molecule, then it is known as constitutional isomerism. The isomers are known as constitutional isomers. They will have same molecular formula and same
For constitutional isomers to be present in cycloalkane, a minimum of four carbon atoms has to be present.
Cycloalkanes can also exhibit stereoisomerism. The difference between constitutional isomerism and stereoisomerism is that, the result of difference in connectivity of carbon atoms is known as constitutional isomerism and the result of differences in configuration is known as stereoisomerism. Stereoisomers are compounds that possess same molecular formula and connectivity of atoms but different orientations of atoms in space. Cis isomers are the one where the two substituted groups on different carbon atom are present above or below the plane or the ring of carbon atoms. Trans isomers are the one where the two substituted groups on different carbon atom are present one above and one below the plane or the ring of carbon atoms.
(b)
Interpretation:
For the given cycloalkane, cis‑trans isomerism is possible or not has to be determined and if it is possible, the structural formula has to be drawn.
Concept Introduction:
Organic compounds are represented shortly by the molecular formula and structural formula. Each and every compound has its own molecular formula. Compounds can have same molecular formula but not same structural formula.
Isomers are the compounds that have same molecular formula but different structural formula. The main difference lies in the way the atoms are arranged in the structure. Isomers have different chemical and physical properties even when they have same molecular formula. This is known as Isomerism.
If there is difference only in the connectivity of the atoms in the molecule, then it is known as constitutional isomerism. The isomers are known as constitutional isomers. They will have same molecular formula and same functional group, but they differ in the connectivity between the atoms in the molecule.
For constitutional isomers to be present in cycloalkane, a minimum of four carbon atoms has to be present.
Cycloalkanes can also exhibit stereoisomerism. The difference between constitutional isomerism and stereoisomerism is that, the result of difference in connectivity of carbon atoms is known as constitutional isomerism and the result of differences in configuration is known as stereoisomerism. Stereoisomers are compounds that possess same molecular formula and connectivity of atoms but different orientations of atoms in space. Cis isomers are the one where the two substituted groups on different carbon atom are present above or below the plane or the ring of carbon atoms. Trans isomers are the one where the two substituted groups on different carbon atom are present one above and one below the plane or the ring of carbon atoms.
(c)
Interpretation:
For the given cycloalkane, cis‑trans isomerism is possible or not has to be determined and if it is possible, the structural formula has to be drawn.
Concept Introduction:
Organic compounds are represented shortly by the molecular formula and structural formula. Each and every compound has its own molecular formula. Compounds can have same molecular formula but not same structural formula.
Isomers are the compounds that have same molecular formula but different structural formula. The main difference lies in the way the atoms are arranged in the structure. Isomers have different chemical and physical properties even when they have same molecular formula. This is known as Isomerism.
If there is difference only in the connectivity of the atoms in the molecule, then it is known as constitutional isomerism. The isomers are known as constitutional isomers. They will have same molecular formula and same functional group, but they differ in the connectivity between the atoms in the molecule.
For constitutional isomers to be present in cycloalkane, a minimum of four carbon atoms has to be present.
Cycloalkanes can also exhibit stereoisomerism. The difference between constitutional isomerism and stereoisomerism is that, the result of difference in connectivity of carbon atoms is known as constitutional isomerism and the result of differences in configuration is known as stereoisomerism. Stereoisomers are compounds that possess same molecular formula and connectivity of atoms but different orientations of atoms in space. Cis isomers are the one where the two substituted groups on different carbon atom are present above or below the plane or the ring of carbon atoms. Trans isomers are the one where the two substituted groups on different carbon atom are present one above and one below the plane or the ring of carbon atoms.
(d)
Interpretation:
For the given cycloalkane, cis‑trans isomerism is possible or not has to be determined and if it is possible, the structural formula has to be drawn.
Concept Introduction:
Organic compounds are represented shortly by the molecular formula and structural formula. Each and every compound has its own molecular formula. Compounds can have same molecular formula but not same structural formula.
Isomers are the compounds that have same molecular formula but different structural formula. The main difference lies in the way the atoms are arranged in the structure. Isomers have different chemical and physical properties even when they have same molecular formula. This is known as Isomerism.
If there is difference only in the connectivity of the atoms in the molecule, then it is known as constitutional isomerism. The isomers are known as constitutional isomers. They will have same molecular formula and same functional group, but they differ in the connectivity between the atoms in the molecule.
For constitutional isomers to be present in cycloalkane, a minimum of four carbon atoms has to be present.
Cycloalkanes can also exhibit stereoisomerism. The difference between constitutional isomerism and stereoisomerism is that, the result of difference in connectivity of carbon atoms is known as constitutional isomerism and the result of differences in configuration is known as stereoisomerism. Stereoisomers are compounds that possess same molecular formula and connectivity of atoms but different orientations of atoms in space. Cis isomers are the one where the two substituted groups on different carbon atom are present above or below the plane or the ring of carbon atoms. Trans isomers are the one where the two substituted groups on different carbon atom are present one above and one below the plane or the ring of carbon atoms.
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Chapter 12 Solutions
General, Organic, and Biological Chemistry
- Provide steps and explanation please.arrow_forwardDraw a structural formula for the major product of the acid-base reaction shown. H 0 N + HCI (1 mole) CH3 N' (1 mole) CH3 You do not have to consider stereochemistry. ● • Do not include counter-ions, e.g., Na+, I, in your answer. . In those cases in which there are two reactants, draw only the product from 989 CH3 344 ? [Farrow_forwardQuestion 15 What is the major neutral organic product for the following sequence? 1. POCI₂ pyridine ? 2. OsO4 OH 3. NaHSO Major Organic Product ✓ OH OH 'OH OH 'OH 'CIarrow_forward
- Could you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forwardCould you please solve the first problem in this way and present it similarly but color-coded or step by step so I can understand it better? Thank you!arrow_forwardCould you please solve the first problem in this way and present it similarly but (color-coded) and step by step so I can understand it better? Thank you! I want to see what they are doingarrow_forward
- Can you please help mne with this problem. Im a visual person, so can you redraw it, potentislly color code and then as well explain it. I know im given CO2 use that to explain to me, as well as maybe give me a second example just to clarify even more with drawings (visuals) and explanations.arrow_forwardPart 1. Aqueous 0.010M AgNO 3 is slowly added to a 50-ml solution containing both carbonate [co32-] = 0.105 M and sulfate [soy] = 0.164 M anions. Given the ksp of Ag2CO3 and Ag₂ soy below. Answer the ff: Ag₂ CO3 = 2 Ag+ caq) + co} (aq) ksp = 8.10 × 10-12 Ag₂SO4 = 2Ag+(aq) + soy² (aq) ksp = 1.20 × 10-5 a) which salt will precipitate first? (b) What % of the first anion precipitated will remain in the solution. by the time the second anion starts to precipitate? (c) What is the effect of low pH (more acidic) condition on the separate of the carbonate and sulfate anions via silver precipitation? What is the effect of high pH (more basic)? Provide appropriate explanation per answerarrow_forwardPart 4. Butanoic acid (ka= 1.52× 10-5) has a partition coefficient of 3.0 (favors benzene) when distributed bet. water and benzene. What is the formal concentration of butanoic acid in each phase when 0.10M aqueous butanoic acid is extracted w❘ 25 mL of benzene 100 mL of a) at pit 5.00 b) at pH 9.00arrow_forward
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