Concept explainers
(a)
Interpretation: The type of isomerism that could be exhibited by the given formulas.
An example that illustrates the specific type of isomerism is to be stated.
Concept introduction: Organic compounds which have similar chemical formula but different structures, i.e., the atoms are in a different spatial arrangement, they are known as structural isomers. Cis and Trans isomers are also structural or geometrical isomers.
To determine: The type of isomerism that could be exhibited by
(a)

Explanation of Solution
Explanation
The structural isomer of
The given formula,
The root word hexene indicates that six carbon atoms are present in the parent chain. Double bond is present between first and second carbon.
The structure of
Figure 1
The structural isomer of
The given formula,
The root word hexene indicates that six carbon atoms are present in the parent chain. The number
The structure of
Figure 2
The structural isomer of
The given formula,
The root word hexene indicates that six carbon atoms are present in the parent chain. The number
The structure of
Figure 3
The structural isomer of
The given formula,
The root word pentene indicates that five carbon atoms are present in the parent chain. The number
The structure of
Figure 4
The structural isomer of
The given formula,
The root word butene indicates that six carbon atoms are present in the parent chain. The double bond is present between second and third carbon. Two methyl groups are attached at second and third carbon.
The structure of
Figure 5
The geometric isomer of
The structure of cis-
Figure 6
The structure of trans-
Figure 7
In the cis isomer, the two hydrogen of the double bonded carbons are adjacent to each other while in trans isomer, they are opposite to each other.
The geometric isomer of
The structure of cis-
Figure 8
The structure of trans-
Figure 9
In the cis isomer, the two hydrogen of the double bonded carbons are adjacent to each other while in trans isomer, they are opposite to each other.
(b)
Interpretation: The type of isomerism that could be exhibited by the given formulas.
An example that illustrates the specific type of isomerism is to be stated.
Concept introduction: Organic compounds which have similar chemical formula but different structures, i.e., the atoms are in a different spatial arrangement, they are known as structural isomers. Cis and Trans isomers are also structural or geometrical isomers.
To determine: The type of isomerism that could be exhibited by
(b)

Explanation of Solution
Explanation
The root word pentane indicates that five carbon atoms are present in the parent chain. Hydroxyl group is attached to first carbon.
The structure of pentan-1-ol is shown in Figure 10.
Figure 10
The structural isomer of
The root word butane indicates that four carbon atoms are present in the parent chain.
The structure of
Figure 11
The structural isomer of
The root word propane indicates that three carbon atoms are present in the parent chain.
The structure of
Figure 12
The structural isomer of
The root word butane indicates that four carbon atoms are present in the parent chain.
The structure of
Figure 13
The structural isomer of
The root word pentane indicates that five carbon atoms are present in the parent chain. Hydroxyl group is attached to third carbon.
The structure of pentan-
Figure 14
The structural isomer of
The root word pentane indicates that five carbon atoms are present in the parent chain. Hydroxyl group is attached to second carbon.
The structure of pentan-
Figure 15
(c)
Interpretation: The type of isomerism that could be exhibited by the given formulas.
An example that illustrates the specific type of isomerism is to be stated.
Concept introduction: Organic compounds which have similar chemical formula but different structures, i.e., the atoms are in a different spatial arrangement, they are known as structural isomers. Cis and Trans isomers are also structural or geometrical isomers.
To determine: The type of isomerism that could be exhibited by
(c)

Explanation of Solution
Explanation
The structural isomer of
In
Figure 16
The structural isomer of
In
Figure 17
The structural isomer of
In
Figure 18
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Chapter 21 Solutions
EBK CHEMISTRY: AN ATOMS FIRST APPROACH
- 1) Draw the correct chemical structure (using line-angle drawings / "line structures") from their given IUPAC name: a. hept-3-yne b. 5-bromo-1-fluoro-4-methylpent-2-ynearrow_forward15. How many absorptions are expected in the H-NMR spectra of fee songs? Explain your were a) CH,CH,CCH,CH, O CHUCH CHCHarrow_forwardFirefly luciferin exhibits three rings. Identify which of the rings are aromatic. Identify which lone pairs are involved in establishing aromaticity. The lone pairs are labeled A-D below.arrow_forward
- What is the [OH⁻] of a 1.80 M solution of pyridine (C₅H₅N, Kb = 1.70 × 10⁻⁹)?arrow_forwardWhat is the percent ionization in a 0.260 M solution of formic acid (HCOOH) (Ka = 1.78 × 10⁻⁴)?arrow_forwardDetermine the pH of solution of HC3H5O2 By constructing an ICE table writing the equilibrium constant expression, and using this information to determine the pH. The Ka of HC3H5O2 is 1.3 x 10-5arrow_forward
- Determine if the following salt is neutral, acidic or basic. If acidic or basic, write the appropriate equilibrium equation for the acid or base that exists when the salt is dissolved in aqueous solution. If neutral, simply write only NR. Be sure to include the proper phases for all species within the reaction LiNO3arrow_forwardAn unknown weak acid with a concentration of 0.410 M has a pH of 5.600. What is the Ka of the weak acid?arrow_forward(racemic) 19.84 Using your reaction roadmaps as a guide, show how to convert 2-oxepanone and ethanol into 1-cyclopentenecarbaldehyde. You must use 2-oxepanone as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way. & + EtOH H 2-Oxepanone 1-Cyclopentenecarbaldehydearrow_forward
- R₂ R₁ R₁ a R Rg Nu R₂ Rg R₁ R R₁₂ R3 R R Nu enolate forming R₁ R B-Alkylated carbonyl species or amines Cyclic B-Ketoester R₁₁ HOB R R₁B R R₁₂ B-Hydroxy carbonyl R diester R2 R3 R₁ RB OR R₂ 0 aB-Unsaturated carbonyl NaOR Aldol HOR reaction 1) LDA 2) R-X 3) H₂O/H₂O ketone, aldehyde 1) 2°-amine 2) acid chloride 3) H₂O'/H₂O 0 O R₁ R₁ R R₁ R₁₂ Alkylated a-carbon R₁ H.C R₁ H.C Alkylated methyl ketone acetoacetic ester B-Ketoester ester R₁ HO R₂ R B-Dicarbonyl HO Alkylated carboxylic acid malonic ester Write the reagents required to bring about each reaction next to the arrows shown. Next, record any regiochemistry or stereochemistry considerations relevant to the reaction. You should also record any key aspects of the mechanism, such as forma- tion of an important intermediate, as a helpful reminder. You may want to keep track of all reactions that make carbon-carbon bonds, because these help you build large molecules from smaller fragments. This especially applies to the reactions in…arrow_forwardProvide the reasonable steps to achieve the following synthesis.arrow_forwardIdentify which compound is more acidic. Justify your choice.arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning


