Use the References to access important values if needed for this question.NOTE:%3D1) Enter hybridization without superscripts. For example: sp = sp32) If more than one bond angle is possible, separate each with a space.A. What is the hybridization of the central atom in AlBr3?Hybridization =%3DWhat are the approximate bond angles in this substance?Bond anglesB. What is the hybridization of the central atom in SeH2?Hybridization%3DWhat are the approximate bond angles in this substance?Bond angles =

Hybridization of central atom and approximate bond angles for AlBr3 and SeH2 is shown below

A. What is the hybridization of the central atom in AlIBr3? Hybridization %3D What are the approximate bond angles in this substance? Bond angles: %3D B. What is the hybridization of the central atom in SeH2? Hybridization = %3D What are the approximate bond angles in this substance? Bond angles = %3D

A. What is the hybridization of the central atom in AlIBr3? Hybridization %3D What are the approximate bond angles in this substance? Bond angles: %3D B. What is the hybridization of the central atom in SeH2? Hybridization = %3D What are the approximate bond angles in this substance? Bond angles = %3D

Chemistry: The Molecular Science

5th Edition

ISBN:9781285199047

Author:John W. Moore, Conrad L. Stanitski

Publisher:John W. Moore, Conrad L. Stanitski

Chapter7: Molecular Structures

Section: Chapter Questions

Problem 42QRT: Methylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is (a) How many...

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The structure of amphetamine, a stimulant, is shown below. (Replacing one H atom on the NH2, or amino, group with CH3 gives methamphetamine a particularly dangerous drug commonly known as speed.) (a) What are the hybrid orbitals used by the C atoms of the C6 ring. by the C atoms of the side chain, and by the N atom? (b) Give approximate values for the bond angles A, B, and C. (c) How many bonds and bonds are in the molerule? (d) Is the molecule polar or nonpolar? (e) Amphetamine reacts readily with a proton (H+) in aqueous solution. Where does this proton attach to the molecule? Explain how the electrostatic potential map predicts this site of protonation.
Do lone pairs about a central atom affect the hybridization of the central atom? If so, how?
Give the hybridization of each central atom in the following molecules. (a) cyclohexene (b) phosgene, Cl2CO (c) glycine, H2NC(1)H2C(2)OOH (Note: Numbers in parentheses label each carbon atom.)
Minoxidil (C9H15N15O) is a compound produced by the Pharmacia Upjohn Company that has been approved as a treatment for some types of male pattern baldness. Note that in such shorthand ring structures, each point where lines meet is a carbon atom and that the hydrogen atoms bonded to the carbon atoms in the rings have been omitted. There will be four bonds to each carbon atom. a. Give the hybridization of the five nitrogen atoms in minoxidil. b. Give the hybridization of each of the nine carbon atoms in minoxidil. c. Give the approximate values for the bond angles marked a, b, c, d, e, and f. d. Including all the hydrogen atoms, how many bonds exist in minoxidil? e. How many bonds exist in minoxidil?
Methylcyanoacrylate is the active ingredient in super glues. Its Lewis structure is (a) How many sigma bonds are in the molecule? (b) How many pi bonds are in the molecule? (c) What is the hybridization of the carbon atom bonded to nitrogen? (d) What is the hybridization of the carbon atom bonded to oxygen? (e) What is the hybridization of the double-bonded oxygen?
Identify the hybrid orbitals used by antimony in SbCl5 and in SbCl6, the ion formed from the reaction of SbCl5 and Cl. Explain your choices.
The compound sketched below is acetylsalicylic acid, commonly known as aspirin. (a) What are the approximate values of the angles marked A, B, C, and D? (b) What hybrid orbitals are used by carbon atoms 1, 2, and 3ss?
The molecular orbital diagram of NO shown in Figure 10.47 also applies to the following species. Write the molecular orbital electron configuration of each, indicating the bond order and the number of unpaired electrons. (a) CN (b) CO (c) BeB (d) BC+ Figure 10.47 Molecular orbital diagram for nitric oxide (NO). The molecular orbital diagram for NO predicts a bond order of 2.5 and predicts that the molecule is paramagnetic with one unpaired electron. These predictions are verified by experimental measurements.
Why are d orbitals sometimes used to form hybrid orbitals? Which period of elements does not used orbitals for hybridization? If necessary, which d orbitals (3d, 4d, 5d, or 6d) would sulfur use to form hybrid orbitals requiring d atomic orbitals? Answer the same question for arsenic and for iodine.
In the molecular orbital mode l, compare and contrast bonds with bonds. What orbitals form the bonds and what orbitals form the bonds? Assume the z-axis is the internuclear axis.
What hybridization is required for central atoms that have a tetrahedral arrangement of electron pairs? A trigonal planar arrangement of electron pairs? A linear arrangement of e lectron pairs? How many unhybridized p atomic orbitals are present when a central atom exhibits tetrahedral geometry? Trigonal planar geometry? Linear geometry? What are the unhybridized p atomic orbitals used for? Describe the bonding in H2S, CH4, H2CO, and HCN, using the localized electron model.
Predict the valence electron molecular orbital configurations for the following, and state whether they will be stable or unstable ions. (a) Na,2+ (b) Mg,2 (c) AI,2 (d) Si,2 (e) p2+ (f) s,2 (g) F,2 (h) Ar,2 40. Predict the valence electron molecular orbital configurations for the following, and state whether they will be stable or unstable ions. (a) Na22+ (b) Mg22+ (c) Al22+ (d) Si22+ (e) P22+ (f) S22+ (g) F22+ (h) Ar22+