CHEMISTRY-ALEKS 360 ACCESS
13th Edition
ISBN: 9781260994742
Author: Chang
Publisher: MCG
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Textbook Question
Chapter 10, Problem 10.31QP
Describe the bonding scheme of the AsH3 molecule in terms of hybridization.
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Consider the following nucleophilic substitution reaction. The compound listed above the arrow is the solvent for the reaction. If nothing is listed over the arrow,
then the nucleophile is also the solvent for the reaction.
Part 1 of 2
Br
CH,CN
+ I¯
What is the correct mechanism for the reaction? Select the single best answer.
@SN2
○ SN 1
Part: 1/2
Part 2 of 2
Draw the products for the reaction. Include both the major organic product and the inorganic product. If more than one stereoisomer is possible, draw
only one stereoisomer. Include stereochemistry where relevant.
Click and drag to start drawing a
structure.
X
હૈ
20.33 Think-Pair-Share
(a) Rank the following dienes and dienophiles in order of increasing reactivity in the
Diels-Alder reaction.
(i)
CO₂Et
(ii)
COEt
||
CO₂Et
MeO
MeO
(b) Draw the product that results from the most reactive diene and most reactive
dienophile shown in part (a).
(c) Draw a depiction of the orbital overlap involved in the pericyclic reaction that oc-
curs between the diene and dienophile in part (b).
(d) Is the major product formed in part (b) the endo or exo configuration? Explain
your reasoning.
20.40 The following compound undergoes an intramolecular Diels-Alder reaction to give a
tricyclic product. Propose a structural formula for the product.
CN
heat
An intramolecular
Diels-Alder adduct
Chapter 10 Solutions
CHEMISTRY-ALEKS 360 ACCESS
Ch. 10.1 - Use the VSEPR model to predict the geometry of (a)...Ch. 10.1 - What is the molecular geometry of GeCl4?Ch. 10.1 - What is the molecular geometry of BrO3?Ch. 10.1 - Which of the following geometries has a greater...Ch. 10.2 - Does the AlCl3 molecule have a dipole moment?Ch. 10.2 - Predict whether PF5 has a dipole moment.Ch. 10.2 - The molecule CF4 does not have a dipole moment...Ch. 10.2 - Carbon dioxide has a linear geometry and is...Ch. 10.3 - Compare the Lewis theory and the valence bond...Ch. 10.4 - Determine the hybridization state of the...
Ch. 10.4 - Describe the hybridization state of Se in SeF6.Ch. 10.4 - How many orbitals does a set of sp3d hybrid...Ch. 10.4 - What is the hybridization of P in PH4+?Ch. 10.4 - What is the hybridization of Xe in XeF4Ch. 10.5 - Describe the bonding in the hydrogen cyanide...Ch. 10.5 - How many pi bonds are present in CS2?Ch. 10.5 - Which of the following pairs of atomic orbitals on...Ch. 10.6 - One way to account for the fact that an O2...Ch. 10.7 - Which of the following species has a longer bond...Ch. 10.7 - Calculate the bond order of F2+.Ch. 10.7 - Determine if N2+ is diamagnetic or paramagnetic.Ch. 10.7 - Estimate the bond enthalpy (kJ/mol) of the H2+...Ch. 10.8 - Describe the bonding in the nitrate ion (NO3) in...Ch. 10 - How is the geometry of a molecule defined and why...Ch. 10 - Sketch the shape of a linear triatomic molecule, a...Ch. 10 - How many atoms are directly bonded to the central...Ch. 10 - Discuss the basic features of the VSEPR model....Ch. 10 - Prob. 10.5QPCh. 10 - Prob. 10.6QPCh. 10 - Predict the geometries of the following species...Ch. 10 - Predict the geometries of the following species:...Ch. 10 - Predict the geometry of the following molecules...Ch. 10 - Predict the geometry of the following molecules...Ch. 10 - Predict the geometry of the following molecules...Ch. 10 - Predict the geometries of the following ions: (a)...Ch. 10 - Describe the geometry around each of the three...Ch. 10 - Which of the following species are tetrahedral?...Ch. 10 - Prob. 10.15QPCh. 10 - Prob. 10.16QPCh. 10 - Prob. 10.17QPCh. 10 - The bonds in beryllium hydride (BeH2) molecules...Ch. 10 - Referring to Table 10.3, arrange the following...Ch. 10 - The dipole moments of the hydrogen halides...Ch. 10 - List the following molecules in order of...Ch. 10 - Does the molecule OCS have a higher or lower...Ch. 10 - Which of the molecules (a) or (b) has a higher...Ch. 10 - Prob. 10.24QPCh. 10 - What is valence bond theory? How does it differ...Ch. 10 - Use valence bond theory to explain the bonding in...Ch. 10 - Prob. 10.27QPCh. 10 - Prob. 10.28QPCh. 10 - Prob. 10.29QPCh. 10 - What is the angle between the following two hybrid...Ch. 10 - Describe the bonding scheme of the AsH3 molecule...Ch. 10 - What is the hybridization state of Si in SiH4 and...Ch. 10 - Describe the change in hybridization (if any) of...Ch. 10 - Consider the reaction BF3+NH3F3BNH3 Describe the...Ch. 10 - What hybrid orbitals are used by nitrogen atoms in...Ch. 10 - Prob. 10.36QPCh. 10 - Give the formula of a cation comprised of iodine...Ch. 10 - Give the formula of an anion comprised of iodine...Ch. 10 - How would you distinguish between a sigma bond and...Ch. 10 - What are the hybrid orbitals of the carbon atoms...Ch. 10 - Specify which hybrid orbitals are used by carbon...Ch. 10 - Prob. 10.42QPCh. 10 - The allene molecule H2CCCH2 is linear (the three C...Ch. 10 - How many pi bonds and sigma bonds are there in the...Ch. 10 - How many sigma bonds and pi bonds are there in...Ch. 10 - What is molecular orbital theory? How does it...Ch. 10 - Sketch the shapes of the following molecular...Ch. 10 - Explain the significance of bond order. Can bond...Ch. 10 - Explain in molecular orbital terms the changes in...Ch. 10 - The formation of H2 from two H atoms is an...Ch. 10 - Prob. 10.51QPCh. 10 - Arrange the following species in order of...Ch. 10 - Prob. 10.53QPCh. 10 - Which of these species has a longer bond, B2 or...Ch. 10 - Acetylene (C2H2) has a tendency to lose two...Ch. 10 - Compare the Lewis and molecular orbital treatments...Ch. 10 - Explain why the bond order of N2 is greater than...Ch. 10 - Compare the relative stability of the following...Ch. 10 - Use molecular orbital theory to compare the...Ch. 10 - A single bond is almost always a sigma bond, and a...Ch. 10 - In 2009 the ion N23 was isolated. Use a molecular...Ch. 10 - The following potential energy curve represents...Ch. 10 - Prob. 10.63QPCh. 10 - Prob. 10.64QPCh. 10 - Prob. 10.65QPCh. 10 - Explain why the symbol on the left is a better...Ch. 10 - Determine which of these molecules has a more...Ch. 10 - Nitryl fluoride (FNO2) is very reactive...Ch. 10 - Describe the bonding in the nitrate ion NO3 in...Ch. 10 - Prob. 10.70QPCh. 10 - Which of the following species is not likely to...Ch. 10 - Draw the Lewis structure of mercury(II) bromide....Ch. 10 - Sketch the bond moments and resultant dipole...Ch. 10 - Although both carbon and silicon are in Group 4A,...Ch. 10 - Acetaminophen is the active ingredient in Tylenol....Ch. 10 - Caffeine is a stimulant drug present in coffee....Ch. 10 - Predict the geometry of sulfur dichloride (SCl2)...Ch. 10 - Antimony pentafluoride, SbF5, reacts with XeF4 and...Ch. 10 - Draw Lewis structures and give the other...Ch. 10 - Predict the bond angles for the following...Ch. 10 - Briefly compare the VSEPR and hybridization...Ch. 10 - Describe the hybridization state of arsenic in...Ch. 10 - Draw Lewis structures and give the other...Ch. 10 - Which of the following molecules and ions are...Ch. 10 - Prob. 10.85QPCh. 10 - The N2F2 molecule can exist in either of the...Ch. 10 - Cyclopropane (C3H6) has the shape of a triangle in...Ch. 10 - The compound 1,2-dichloroethane (C2H4Cl2) is...Ch. 10 - Does the following molecule have a dipole moment?...Ch. 10 - So-called greenhouse gases, which contribute to...Ch. 10 - The bond angle of SO2 is very close to 120, even...Ch. 10 - 3-azido-3-deoxythymidine, shown here, commonly...Ch. 10 - The following molecules (AX4Y2) all have...Ch. 10 - The compounds carbon tetrachloride (CCl4) and...Ch. 10 - Prob. 10.95QPCh. 10 - What are the hybridization states of the C and N...Ch. 10 - Use molecular orbital theory to explain the...Ch. 10 - Referring to the Chemistry in Action essay...Ch. 10 - Which of the molecules (a)(c) are polar?Ch. 10 - Prob. 10.100QPCh. 10 - The stable allotropic form of phosphorus is P4, in...Ch. 10 - Referring to Table 9.4, explain why the bond...Ch. 10 - Use molecular orbital theory to explain the...Ch. 10 - The ionic character of the bond in a diatomic...Ch. 10 - Prob. 10.105QPCh. 10 - Prob. 10.106QPCh. 10 - Aluminum trichloride (AlCl3) is an...Ch. 10 - The molecules cis-dichloroethylene and...Ch. 10 - Prob. 10.109QPCh. 10 - Prob. 10.110QPCh. 10 - The molecule benzyne (C6H4) is a very reactive...Ch. 10 - Assume that the third-period element phosphorus...Ch. 10 - Consider a N2 molecule in its first excited...Ch. 10 - Prob. 10.114QPCh. 10 - Prob. 10.116QPCh. 10 - Draw the Lewis structure of ketene (C2H2O) and...Ch. 10 - TCDD, or 2,3,7,8-tetrachlorodibenzo-p-dioxin, is a...Ch. 10 - Write the electron configuration of the cyanide...Ch. 10 - Prob. 10.120QPCh. 10 - The geometries discussed in this chapter all lend...Ch. 10 - Prob. 10.122QPCh. 10 - Which of the following ions possess a dipole...Ch. 10 - Given that the order of molecular orbitals for NO...Ch. 10 - Shown here are molecular models of SX4 for X = F,...Ch. 10 - Based on what you have learned from this chapter...Ch. 10 - How many carbon atoms are contained in one square...
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- What is the reaction mechanism for this?arrow_forwardWhat is the reaction mechanism for this?arrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. + Drawing Arrows CH3ONA, CH3OH heat : Br:O Na → H H Br Na + H H H H H :0: .H + Undo Reset Done Q CH3 Drag To Pan +arrow_forward
- What is the reaction mechanism for this?arrow_forward20.19 Predict the structure of the major 1,2-addition product formed by reaction of one mole of Cl₂ with 3-methylenecyclohexene. Also predict the structure of the 1,4-addition product formed under these conditions. 20.20 Which of the two molecules shown do you expect to be the major product formed by 1,2-addition of HCI to cyclopentadiene? Explain. Cyclopentadiene + HC 3-Chlorocyclopentene (racemic) or 4-Chlorocyclopentene (racemic)arrow_forward20.35 Propose structural formulas for compounds A and B and specify the configuration of compound B. EtO₂C 250°C C14H2004 CO₂Et 1. Oso, then NaHSO3 2. HIO4 C14H2006 A Barrow_forward
- 20.21 Predict the major product formed by 1,4-addition of HCI to cyclopentadiene. 20.22 Draw structural formulas for the two constitutional isomers with the molecular for- mula C₂H,Br, formed by adding one mole of Br, to cyclopentadiene.arrow_forwardAdd substituents to draw the conformer below (sighting down the indicated bond), then rotate the back carbon to provide the conformation that will be capable of an E2 elimination. R/S stereochemistry is graded. + I I H CH3 Ph Досн Br OCH 3 Drawing Q H Atoms, Bonds and Rings Charges Tap a node to see suggestions. H H H H H Undo Reset Remove Done Rotatearrow_forward20.17 Predict the structure of the major product formed by 1,2-addition of HBr to 3-methylenecyclohexene. 3-Methylenecyclohexene 20.18 Predict the major product formed by 1,4-addition of HBr to 3-methylenecyclohexene.arrow_forward
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