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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)
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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)
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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)
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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
- Explanation O Conjugated Pi Systems Deducing the reactants of a Diels-Alder reaction Can the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one step, by moderately heating the reactants? ? Δ If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any arrangement you like. • If your answer is no, check the box under the drawing area instead. Click and drag to start drawing a structure. Xarrow_forwardDiels Alder Cycloaddition: Focus on regiochemistry (problems E-F) –> match + of thedienophile and - of the diene while also considering stereochemistry (endo).arrow_forwardHELP! URGENT! PLEASE RESOND ASAP!arrow_forward
- Question 4 Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267 First-order, k = 0.210 hour 1 First-order, k = 0.0912 hour 1 O Second-order, k = 0.590 M1 hour 1 O Zero-order, k = 0.0770 M/hour O Zero-order, k = 0.4896 M/hour O Second-order, k = 1.93 M-1-hour 1 10 ptsarrow_forwardDetermine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267arrow_forwardDraw the products of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry. Ignore inorganic byproducts. OSO4 (cat) (CH3)3COOH Select to Draw ઘarrow_forward
- Calculate the reaction rate for selenious acid, H2SeO3, if 0.1150 M I-1 decreases to 0.0770 M in 12.0 minutes. H2SeO3(aq) + 6I-1(aq) + 4H+1(aq) ⟶ Se(s) + 2I3-1(aq) + 3H2O(l)arrow_forwardProblem 5-31 Which of the following objects are chiral? (a) A basketball (d) A golf club (b) A fork (c) A wine glass (e) A spiral staircase (f) A snowflake Problem 5-32 Which of the following compounds are chiral? Draw them, and label the chirality centers. (a) 2,4-Dimethylheptane (b) 5-Ethyl-3,3-dimethylheptane (c) cis-1,4-Dichlorocyclohexane Problem 5-33 Draw chiral molecules that meet the following descriptions: (a) A chloroalkane, C5H11Cl (c) An alkene, C6H12 (b) An alcohol, C6H140 (d) An alkane, C8H18 Problem 5-36 Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How H3C CH3 many chirality centers does erythronolide B have? OH Identify them. H3C -CH3 OH Erythronolide B H3C. H3C. OH OH CH3arrow_forwardPLEASE HELP! URGENT! PLEASE RESPOND!arrow_forward
- 2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forwardSteps and explanationn please.arrow_forwardProblem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_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
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