Concept explainers
(a)
Interpretation:
The structural formula of the given compound is to be predicted.
Concept introduction:
Those compounds which have the same molecular formula but have different arrangements of atoms are known as isomers. The phenomenon is called as isomerism. The isomers are generally classified as structural isomers and stereoisomers. Stereoisomers are further divided into two categories diastereomers and enantiomers.
Answer to Problem 11.55E
The structural formula of the given compound is shown below as,
Explanation of Solution
The given compound is
Figure 1
The structural formula of the given compound is shown in Figure 1.
(b)
Interpretation:
The structural formula of the given compound is to be predicted.
Concept introduction:
Those compounds which have the same molecular formula but have different arrangements of atoms are known as isomers. The phenomenon is called as isomerism. The isomers are generally classified as structural isomers and stereoisomers. Stereoisomers are further divided into two categories diastereomers and enantiomers.
Answer to Problem 11.55E
The structural formulas of the given compound are shown below as,
Explanation of Solution
The given compound is
Figure 2
The structural formulas of the given compound are shown in Figure 2.
(c)
Interpretation:
The structural formula of the given compound is to be predicted.
Concept introduction:
Those compounds which have the same molecular formula but have different arrangements of atoms are known as isomers. The phenomenon is called as isomerism. The isomers are generally classified as structural isomers and stereoisomers. Stereoisomers are further divided into two categories diastereomers and enantiomers.
Answer to Problem 11.55E
The structural formulas of the given compound are shown below as,
Explanation of Solution
Conformers are the type of isomers that can be interconverted into one other by simple rotation of bond.
The given compound is
Figure 3
The structural formulas of the given compound are shown in Figure 3.
(d)
Interpretation:
The structural formula of the given compound is to be predicted.
Concept introduction:
Those compounds which have the same molecular formula but have different arrangements of atoms are known as isomers. The phenomenon is called as isomerism. The isomers are generally classified as structural isomers and stereoisomers. Stereoisomers are further divided into two categories diastereomers and enantiomers.
Answer to Problem 11.55E
The structural formulas of the given compound are shown below as,
Explanation of Solution
The given compound,
Figure 4
The structural formulas of the given compound are shown in Figure 4.
(e)
Interpretation:
The structural formula of the given compound is to be predicted.
Concept introduction:
Those compounds which have the same molecular formula but have different arrangements of atoms are known as isomers. The phenomenon is called as isomerism. The isomers are generally classified as structural isomers and stereoisomers. Stereoisomers are further divided into two categories diastereomers and enantiomers.
Answer to Problem 11.55E
The structural formula of the given compound is shown below as,
Explanation of Solution
The given compound is
Figure 5
The structural formula of the given compound is shown in Figure 5.
(f)
Interpretation:
The structural formula of the given compound is to be predicted.
Concept introduction:
Those compounds which have the same molecular formula but have different arrangements of atoms are known as isomers. The phenomenon is called as isomerism. The isomers are generally classified as structural isomers and stereoisomers. Stereoisomers are further divided into two categories diastereomers and enantiomers.
Answer to Problem 11.55E
The structural formulas of the given compound are shown below as,
Explanation of Solution
The given compound,
Figure 6
The structural formulas of the given compound are shown in Figure 6.
(g)
Interpretation:
The structural formula of the given compound is to be predicted.
Concept introduction:
Those compounds which have the same molecular formula but have different arrangements of atoms are known as isomers. The phenomenon is called as isomerism. The isomers are generally classified as structural isomers and stereoisomers. Stereoisomers are further divided into two categories diastereomers and enantiomers.
Answer to Problem 11.55E
The structural formula of the given compound is shown below as,
Explanation of Solution
The given compound,
Figure 7
The structural formula of the given compound is shown in Figure 7.
Want to see more full solutions like this?
Chapter 11 Solutions
Chemistry for Today: General, Organic, and Biochemistry
- Is the general formula of a cycloalkanes the same as the general formula of an alkane, CnH2n+2? Draw any structural diagram to illustrate your answer.arrow_forwardHow does the structure of a cycloalkane differ from that of a straight-chain or branched-chain alkane?arrow_forwardDistinguish between isomerism and resonance. Distinguish between structural and geometric isomerism. When writing the various structural isomers, the most difficult task is identifying which are different isomers and which are identical to a previously written structurethat is, which are compounds that differ only by the rotation of a carbon single bond. How do you distinguish between structural isomers and those that are identical? Alkenes and cycloalkanes are structural isomers of each other. Give an example of each using C4H8. Another common feature of alkenes and cycloalkanes is that both have restricted rotation about one or more bonds in the compound, so both can exhibit cis- trans isomerism. What is required for an alkene or cycloalkane to exhibit cis-trans isomerism? Explain the difference between cis and trans isomers. Alcohols and ethers are structural isomers of each other, as are aldehydes and ketones. Give an example of each to illustrate. Which functional group in Table 21-4 can be structural isomers of carboxylic acids? What is optical isomerism? What do you look for to determine whether an organic compound exhibits optical isomerism? 1-Bromo-1-chloroethane is optically active whereas 1-bromo-2-chloroethane is not optically active. Explain.arrow_forward
- What is a hydrocarbon? What is the difference between a saturated hydrocarbon and an unsaturated hydrocarbon? Distinguish between normal and branched hydrocarbons. What is an alkane? What is a cyclic alkane? What are the two general formulas for alkanes? What is the hybridization of carbon atoms in alkanes? What are the bond angles in alkanes? Why are cyclopropane and cyclobutane so reactive? The normal (unbranched) hydrocarbons are often referred to as straight-chain hydrocarbons. What does this name refer to? Does it mean that the carbon atoms in a straight-chain hydrocarbon really have a linear arrangement? Explain. In the shorthand notation for cyclic alkanes, the hydrogens are usually omitted. How do you determine the number of hydrogens bonded to each carbon in a ring structure?arrow_forwardSummarize the nomenclature rules for alkanes, alkenes, alkynes, and aromatic compounds. Correct the following false statements regarding nomenclature of hydrocarbons. a. The root name for a hydrocarbon is based on the shortest continuous chain of carbon atoms. b. The suffix used to name all hydrocarbons is -ane. c. Substituent groups are numbered so as to give the largest numbers possible. d. No number is required to indicate the positions of double or triple bonds in alkenes and alkynes. e. Substituent groups get the lowest number possible in alkenes and alkynes. f. The ortho- term in aromatic hydrocarbons indicates the presence of two substituent groups bonded to carbon- 1 and carbon-3 in benzene.arrow_forward4.2 What is an alkane?arrow_forward
- Classify each of the following hydrocarbons as alkanes, alkenes, or alkynes. (a) C12H24 (b) C7H12 (c) C13H28arrow_forwardConsider a sample of a hydrocarbon at 0.959 atm and 298 K. Upon combusting the entire sample in oxygen, you collect a mixture of gaseous carbon dioxide and water vapor at 1.51 atm and 375 K. This mixture has a density of 1.391 g/L and occupies a volume four times as large as that of the pure hydrocarbon. Determine the molecular formula of the hydrocarbon and name it.arrow_forwardAlcohols are very useful starting materials for the production of many different compounds. The following conversions, starting with 1-butanol, can be carried out in two or more steps. Show the steps (reactants/catalysts) you would follow to carry out the conversions, drawing the formula for the organic product in each step. For each step, a major product must be produced. (See Exercise 62.) (Hint: In the presence of H+, an alcohol is converted into an alkene and water. This is the exact reverse of the reaction of adding water to an alkene to form an alcohol.) a. 1-butanol butane b. 1-butanol 2-butanonearrow_forward
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage Learning
- Chemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning