CHEMISTRY-W/MASTERING CHEMISTRY ACCESS
8th Edition
ISBN: 9780135205068
Author: Robinson
Publisher: PEARSON
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Chapter 7, Problem 7.76SP
Which compound do you expect to have the stronger
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Predicting the pr
Predict the major products of the following organic reaction:
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• If there aren't any products, because no reaction will take place, check the box below the drawing area instead.
• Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are
enantiomers.
?
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propose synthesis
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.
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Chapter 7 Solutions
CHEMISTRY-W/MASTERING CHEMISTRY ACCESS
Ch. 7 - Use the electro negativity values in Figure 7.4...Ch. 7 - Conceptual APPLY 7.2 An electrostatic potential...Ch. 7 - The dipole moment of AgCI in the gas phaseis...Ch. 7 - Predict which bond has greater percent ionic...Ch. 7 - Select the correct electron-dot structure for H2S...Ch. 7 - Use the octet rule to predict the molecular...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Select the correct electron-dot structure for...Ch. 7 - Identify the correct electron-dot structure(s) for...
Ch. 7 - Prob. 7.11PCh. 7 - Which oxygen species do you predict to be most...Ch. 7 - Draw an electron-dot structure for the following...Ch. 7 - There are two molecules with the formula C2H6O...Ch. 7 - The following structure is a representation of...Ch. 7 - Draw two possible electron-dot structures for the...Ch. 7 - Called “laughing gas, nitrous oxide (N2O) is...Ch. 7 - Draw as many resonance structures as possible for...Ch. 7 - Prob. 7.19PCh. 7 - Prob. 7.20ACh. 7 - Calculate the formal charge on each atom in the...Ch. 7 - Start with the electron-dot structure for the...Ch. 7 - Calculate formal charges on the C and O atoms in...Ch. 7 - Three resonance structures for anisole (Problem...Ch. 7 - The toxicity of the organophosphate insecticides...Ch. 7 - Prob. 7.26PCh. 7 - Prob. 7.27PCh. 7 - The following structure is a representation of the...Ch. 7 - The electron-dot structure for the nerve a gentsar...Ch. 7 - Draw the new electron-dot structures indicated by...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - The following diagram shows the potential energy...Ch. 7 - Two electrostatic potential maps are shown, one of...Ch. 7 - Prob. 7.34CPCh. 7 - Which of the following drawings is most likely to...Ch. 7 - The following ball-and-stick molecular model is a...Ch. 7 - The following hall-and-stick molecular model is a...Ch. 7 - Sinapaldehyde, a compound present in the toasted...Ch. 7 - Vitamin C (ascorbic acid) has the following...Ch. 7 - Match the following descriptions with the type of...Ch. 7 - Why do two atoms come together to form a covalent...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Explain the difference in the bond dissociation...Ch. 7 - Predict which of the following bonds should be...Ch. 7 - Prob. 7.45SPCh. 7 - What general trends in electro negativity occur in...Ch. 7 - Predict the electro negativity of the undiscovered...Ch. 7 - Order the following elements according to...Ch. 7 - Order the following elements according to...Ch. 7 - Which of the following substances contain bonds...Ch. 7 - Use the electro negativity data in Figure 7.4 to...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Show the direction of polarity for each of the...Ch. 7 - Which of the substances...Ch. 7 - Which of the substances...Ch. 7 - Order the following compounds according to the...Ch. 7 - Order the following compounds according to the...Ch. 7 - Prob. 7.58SPCh. 7 - Using only the elements Ca, Cl, and Si, give...Ch. 7 - The dipole moment of BrCl is 0.518 D, and the...Ch. 7 - Prob. 7.61SPCh. 7 - Prob. 7.62SPCh. 7 - Prob. 7.63SPCh. 7 - Why does the octet rule apply primarily to...Ch. 7 - Which of the following substances contains an atom...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Draw electron-dot structures for the following...Ch. 7 - Identify the correct electron-dot structure for...Ch. 7 - Draw an electron.dot structure for the hydronium...Ch. 7 - Oxalic acid, H2C2O4 , is a mildly poisonous...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Prob. 7.72SPCh. 7 - Identify the fourth-row elements, X, that form the...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Write electron-dot structures for molecules with...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Which compound do you expect to have the stronger...Ch. 7 - Draw an electron-dot structure for each of the...Ch. 7 - Prob. 7.79SPCh. 7 - Methylphenidate (C14H19NO2) , marketed as Ritalin,...Ch. 7 - Pregabalin (C8H17NO2) , marketed as Lyric a, is an...Ch. 7 - The following molecular model is that of...Ch. 7 - Ibuprofen C 13 H 18 O 2 marketed under such brand...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can for...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Which of the following pairs of structures...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Draw as many resonance structures as you can that...Ch. 7 - Benzene has the following structural formula. Use...Ch. 7 - Draw three resonance structures for sulfur...Ch. 7 - Some mothballs used when storing clothes are made...Ch. 7 - Four different structures (a), (b), (c), and (d)...Ch. 7 - Draw an electron-dot structure for carbon...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Assign formal charges to the atoms in the...Ch. 7 - Calculate formal charges for the C and O atoms in...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Draw two electron-dot resonance structures that...Ch. 7 - Prob. 7.102SPCh. 7 - Prob. 7.103SPCh. 7 - Boron trifluoride reacts with dimethyl ether to...Ch. 7 - Thiofulminic acid, HCNS, has recently been...Ch. 7 - Draw two rcsonancc strutur for methyl isocyanate,...Ch. 7 - In the cyanatc ion. OCN , carbon is the central...Ch. 7 - Prob. 7.108MPCh. 7 - Prob. 7.109MPCh. 7 - Prob. 7.110MPCh. 7 - The neutral OH molecule has been implicated in...Ch. 7 - Prob. 7.112MPCh. 7 - Prob. 7.113MP
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- Diels 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_forwardQuestion 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_forward
- 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 0.267arrow_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_forwardCalculate 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_forward
- Problem 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_forward2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forward
- Steps 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_forwardSteps and explanationn please.arrow_forward
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