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Concept explainers
(a)
Interpretation: The following incorrectly named compounds are to be drawn and named correctly.
Concept introduction: Organic compounds contain carbon and hydrogen atoms with their respective
To determine: The correct name of the given compound and its structure is to be drawn.
(a)
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Answer to Problem 111AE
Answer
The correct name of the compound is
Explanation of Solution
Explanation
The correct name of the compound is
The structure of
Figure 1
The root name hexane signifies the presence of six carbon atoms.
(b)
Interpretation: The following incorrectly named compounds are to be drawn and named correctly.
Concept introduction: Organic compounds contain carbon and hydrogen atoms with their respective functional groups. When they are named the root term, suffix and prefix are to be remembered. They are named according to the International Union of Pure and Applied Chemistry
To determine: The correct name of the given compound and its structure is to be drawn.
(b)
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Answer to Problem 111AE
Answer
The correct name of the compound is
Explanation of Solution
Explanation
The correct name of the compound is
The structure of
Figure 2
The root name is pentane which signifies the presence of five carbon atoms in a chain,
(c)
Interpretation: The following incorrectly named compounds are to be drawn and named correctly.
Concept introduction: Organic compounds contain carbon and hydrogen atoms with their respective functional groups. When they are named the root term, suffix and prefix are to be remembered. They are named according to the International Union of Pure and Applied Chemistry
To determine: The correct name of the given compound and its structure is to be drawn.
(c)
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Answer to Problem 111AE
Answer
The correct name of the compound is
Explanation of Solution
Explanation
The correct name of the compound is
The structure of 3-methyl 4-isopropylpentane with its correct name is,
Figure 3
The root name pentane signifies the presence of five carbon atoms in a chain and
(d)
Interpretation: The following incorrectly named compounds are to be drawn and named correctly.
Concept introduction: Organic compounds contain carbon and hydrogen atoms with their respective functional groups. When they are named the root term, suffix and prefix are to be remembered. They are named according to the International Union of Pure and Applied Chemistry
To determine: The correct name of the given compound and its structure is to be drawn.
(d)
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Answer to Problem 111AE
Answer
The correct name of the compound is
Explanation of Solution
Explanation
The correct name of the compound is
The structure of
Figure 4
The root name butyne signifies the presence of four carbon atoms with a triple bond in a chain and
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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
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