Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
expand_more
expand_more
format_list_bulleted
Concept explainers
Videos
Textbook Question
Chapter 1, Problem 1.28P
What orbitals are used to form each bond in the following molecules?
a.
b.
c.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Which bonds allow for a large, bonded network to be more directional and why?
1. Sigma bonds
2. Pi bonds
Because
1. The orbitals overlap side-to-side to hold the bond in place.
2. The orbitals overlap end-to-end in several different directions.
3. Multiple of these bonds result in delocalized electrons.
ο ο ο ο ο ο
O 2,1
O2,2
O 1,3
O 1,2
O2,3
O 1,1
lyr
For which of the following molecules will the electron-pair geometry be different than the molecular geometry?
Draw Lewis structure for each molecule and write the electron pair and molecular geometries for each one in a separate sheet.
a.
BH3
b.
H2O
c.
CH4
d.
CO
e.
NH4+
a. One of the two known binary compounds of xenon and oxygen is XeO3. A Lewis structure is shown here, which may or may not be complete. How many lone pairs should be present on the central Xe atom?
b. What is the electron pair geometry around the Xe?
c. What is the molecular geometry of XeO3?
d. What hybrid orbitals does the Xe atom use?
Chapter 1 Solutions
Organic Chemistry-Package(Custom)
Ch. 1 - While the most common isotope of nitrogen has a...Ch. 1 - Label each bond in the following compounds as...Ch. 1 - How many covalent bonds are predicted for each...Ch. 1 - Draw a valid Lewis structure for each species. a....Ch. 1 - Draw an acceptable Lewis structure for each...Ch. 1 - Prob. 1.6PCh. 1 - Draw a Lewis structure for each ion. a. CH3Ob....Ch. 1 - Draw Lewis structures for each molecular formula....Ch. 1 - Prob. 1.9PCh. 1 - Prob. 1.10P
Ch. 1 - Prob. 1.11PCh. 1 - Prob. 1.12PCh. 1 - Draw a second resonance structure for each...Ch. 1 - Prob. 1.14PCh. 1 - Draw a second resonance structure for nitrous...Ch. 1 - Prob. 1.16PCh. 1 - Prob. 1.17PCh. 1 - Prob. 1.18PCh. 1 - Prob. 1.19PCh. 1 - Prob. 1.20PCh. 1 - Simplify each condensed structure by using...Ch. 1 - Prob. 1.22PCh. 1 - Prob. 1.23PCh. 1 - Convert each skeletal structure to a complete...Ch. 1 - Draw in all hydrogens and lone pairs on the...Ch. 1 - Prob. 1.26PCh. 1 - What orbitals are used to form each of the CC, and...Ch. 1 - What orbitals are used to form each bond in the...Ch. 1 - Determine the hybridization around the highlighted...Ch. 1 - Classify each bond in the following molecules as ...Ch. 1 - Prob. 1.31PCh. 1 - Rank the following atoms in order of increasing...Ch. 1 - Prob. 1.33PCh. 1 - Prob. 1.34PCh. 1 - Provide the following information about...Ch. 1 - Use the ball-and-stick model to answer each...Ch. 1 - Citric acid is responsible for the tartness of...Ch. 1 - Zingerone gives ginger its pungent taste. a.What...Ch. 1 - Two radioactive isotopes of iodine used for the...Ch. 1 - Prob. 1.40PCh. 1 - Assign formal charges to each carbon atom in the...Ch. 1 - Assign formal charges to each N and O atom in the...Ch. 1 - Draw one valid Lewis structure for each compound....Ch. 1 - Prob. 1.44PCh. 1 - Prob. 1.45PCh. 1 - Prob. 1.46PCh. 1 - Draw all possible isomers for each molecular...Ch. 1 - 1.45 Draw Lewis structures for the nine isomers...Ch. 1 - Prob. 1.49PCh. 1 - Prob. 1.50PCh. 1 - Prob. 1.51PCh. 1 - Prob. 1.52PCh. 1 - Prob. 1.53PCh. 1 - Prob. 1.54PCh. 1 - Draw all reasonable resonance structures for each...Ch. 1 - Prob. 1.56PCh. 1 - Rank the resonance structures in each group in...Ch. 1 - 1.56 Consider the compounds and ions with curved...Ch. 1 - 1.57 Predict all bond angles in each...Ch. 1 - Predict the geometry around each indicated atom....Ch. 1 - Prob. 1.61PCh. 1 - Prob. 1.62PCh. 1 - Draw in all the carbon and hydrogen atoms in each...Ch. 1 - Prob. 1.64PCh. 1 - Prob. 1.65PCh. 1 - Prob. 1.66PCh. 1 - Prob. 1.67PCh. 1 - Each of the following condensed or skeletal...Ch. 1 - Prob. 1.69PCh. 1 - Prob. 1.70PCh. 1 - Prob. 1.71PCh. 1 - Prob. 1.72PCh. 1 - Prob. 1.73PCh. 1 - Prob. 1.74PCh. 1 - Two useful organic compounds that contain Cl atoms...Ch. 1 - Use the symbols + and to indicate the polarity of...Ch. 1 - Label the polar bonds in each molecule. Indicate...Ch. 1 - Answer the following questions about acetonitrile...Ch. 1 - Prob. 1.79PCh. 1 - The principles of this chapter can be applied to...Ch. 1 -
a. What is the hybridization of each N atom in...Ch. 1 - 1.77 Stalevo is the trade name for a medication...Ch. 1 - 1.78 and are two highly reactive carbon...Ch. 1 - 1.79 The N atom in (acetamide) is hybridized,...Ch. 1 - Prob. 1.85PCh. 1 - Prob. 1.86PCh. 1 - Prob. 1.87PCh. 1 - Prob. 1.88PCh. 1 - Prob. 1.89PCh. 1 - Prob. 1.90P
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- Identify the molecules with a dipole moment: (a) SF4 (b) CF4 (c) Cl2CCBr2 (d) CH3Cl (e) H2COarrow_forwardAmong the following, which has the shortest bond and which has the longest: Li2, B2, C2, N2, O2?arrow_forward7.85 Consider the molecule whose structure is shown below. (a) How many carbon atoms are sp3 hybridized? (b) What is the shape of the molecule around the carbon atom marked A? (c) What is the shape of the molecule around the carbon atom marked B?arrow_forward
- Which atomic orbitals overlap to form the C−O bond of dimethyl ether, (CH3)2O? A. C 2sp3 + O 2sp2 B. C 2sp2 + O 2p C. C 2sp2 + O 2sp2 D. C 2sp3 + O 2sp3arrow_forward4. Consider the structural changes that occur in the following molecules. According to Lewis and VSEPR theory, why do these changes occur? What are the ideal bond angles for each structure, and which are expected to be а. b. distorted? BH3 CH4 NH3 H20 HFarrow_forward3. In a pi bond, A. electron density lies along the internuclear axis. B. electron density lies above and below the internuclear axis. C. electrons are more dense than they are in sigma bonds. D. more than two electrons are involved in the bond. 4. The hybridization of the central atom in CIF3 is A. sp? B. sp C. sp'd D. sp?d? 5. Determine the formal charge on the nitrogen in the Lewis structure shown below. A. +1 В. -2 C.0 D. +2 : s=C-N:arrow_forward
- 4. Draw Lewis structures for the following molecules. Describe how the bond angles would bealtered based on the Lewis structure.a. CH2Sb. SCl2arrow_forwardWhich of the following compund has same molecular geometry and electron group geometry? A. H2O B. BrF3 C. NH3 D. SO2 E. NH4+arrow_forwardWhich of the following is polar (possesses a dipole moment)? A. C6H6 B. CH4 C. H2S D. I2arrow_forward
- 1) What is the type of molecule? a. AX2E3 b. AX3E2 c. AX5 d. AX2E2 2) What is the molecular geometry of GL2-? a. Linear b. Trigonal Bypyramidal c. Bent or v-shaped d. Seesaw 3) What is the approx bond angle formed by L-G-L bond if the correct molecular geometry is followed? a. 180° b. 120° c. 109.5° d. 90° 4) Considering that L is more electronegative than G, and the en difference is 0.2, is the molecular polar? 5) What is the formal charge of G? 6) What is the formal charge of the labeled atom? (refer to the blue arrow)arrow_forward9. Show the dipole moment of each bond and then predict the overall molecule as either being polar or nonpolar? a. CH4 b. H2S c. PH3 d. SO3arrow_forwardDetermine the molecular geometry about each interior atom and sketch each molecule.a. C2H2 (skeletal structure HCCH)b. C2H4 (skeletal structure H2CCH2)c. C2H6 (skeletal structure H3CCH3)arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry by OpenStax (2015-05-04)ChemistryISBN:9781938168390Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark BlaserPublisher:OpenStax
General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage Learning
Chemistry for Engineering StudentsChemistryISBN:9781337398909Author:Lawrence S. Brown, Tom HolmePublisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781337399074
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry by OpenStax (2015-05-04)
Chemistry
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:OpenStax
General Chemistry - Standalone book (MindTap Cour...
Chemistry
ISBN:9781305580343
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Publisher:Cengage Learning
Chemistry for Engineering Students
Chemistry
ISBN:9781337398909
Author:Lawrence S. Brown, Tom Holme
Publisher:Cengage Learning
Stoichiometry - Chemistry for Massive Creatures: Crash Course Chemistry #6; Author: Crash Course;https://www.youtube.com/watch?v=UL1jmJaUkaQ;License: Standard YouTube License, CC-BY
Bonding (Ionic, Covalent & Metallic) - GCSE Chemistry; Author: Science Shorts;https://www.youtube.com/watch?v=p9MA6Od-zBA;License: Standard YouTube License, CC-BY
General Chemistry 1A. Lecture 12. Two Theories of Bonding.; Author: UCI Open;https://www.youtube.com/watch?v=dLTlL9Z1bh0;License: CC-BY