
Physical Chemistry
2nd Edition
ISBN: 9781133958437
Author: Ball, David W. (david Warren), BAER, Tomas
Publisher: Wadsworth Cengage Learning,
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 13, Problem 13.75E
Interpretation Introduction
Interpretation:
The number of SALCs that can be constructed for
Concept introduction:
Molecular orbital diagrams are used for determining the bonding in molecules using a linear combination of atomic orbitals. The number of molecular orbitals formed is equal to the number of atomic orbitals that combine.
Expert Solution & Answer

Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
B. Classify the following amino acid. Atoms other than carbon and hydrogen are labeled.
a. acidic
b. basic
C.
neutral
C.
Consider the following image.
Which level of protein structure is shown here?
a.
primary
b. secondary
c. tertiary
d. quaternary
D.
Consider the following image.
H
RH
H
HR
H R
HR
HR
RH
Which level of protein structure is shown in the box?
a. primary
b. secondary
R
c.
tertiary
d.
quaternary
コー
R
Briefly answer three from the followings:
a. What are the four structures of the protein?
b. Why is the side chain (R) attached to the alpha carbon in the amino acids is important for the
function?
c. What are the types of amino acids? And how is it depend on the (R) structure?
d. Write a reaction to prepare an amino acid.
prod
Answe Answer A and B please
Chapter 13 Solutions
Physical Chemistry
Ch. 13 - In your own words, explain why an object that has...Ch. 13 - Identify the symmetry elements present in the...Ch. 13 - Identify the symmetry elements present in the...Ch. 13 - Prob. 13.4ECh. 13 - Prob. 13.5ECh. 13 - Prob. 13.6ECh. 13 - Prob. 13.7ECh. 13 - Prob. 13.8ECh. 13 - Any axis of symmetry Cn that rotates an object by...Ch. 13 - Prob. 13.10E
Ch. 13 - Prob. 13.11ECh. 13 - Prob. 13.12ECh. 13 - Prob. 13.13ECh. 13 - What are the number of classes and the order of...Ch. 13 - Prob. 13.15ECh. 13 - a Show that the C3v point group satisfies the...Ch. 13 - a In the Td point group, an S41 improper rotation...Ch. 13 - Determine which single symmetry operation of the...Ch. 13 - Prob. 13.19ECh. 13 - Prob. 13.20ECh. 13 - Prob. 13.21ECh. 13 - Figure 13.27 shows the structure of the molecule...Ch. 13 - Prob. 13.23ECh. 13 - Identify all the symmetry elements present in the...Ch. 13 - Point groups are called such because all of the...Ch. 13 - Determine the point groups of the following...Ch. 13 - Determine the point group of the following...Ch. 13 - Determine the point groups of the following...Ch. 13 - Determine the point groups of the following...Ch. 13 - Structural isomers can have very different point...Ch. 13 - Structural isomers can have very different point...Ch. 13 - Prob. 13.32ECh. 13 - Identify the point group of the wave functions of...Ch. 13 - Identify the point group of the wave functions of...Ch. 13 - Prob. 13.35ECh. 13 - Determine if the following species have permanent...Ch. 13 - Determine if the following species have permanent...Ch. 13 - Which of the following species will not have...Ch. 13 - Prob. 13.39ECh. 13 - Explain why a molecule with a center of inversion...Ch. 13 - a Unlike methane, bromochlorofluoromethane...Ch. 13 - Prob. 13.42ECh. 13 - Prob. 13.43ECh. 13 - Prob. 13.44ECh. 13 - Show that the irreducible representations of the...Ch. 13 - Show that any two of the irreducible...Ch. 13 - Show that any irreducible representation of these...Ch. 13 - Explain why this proposed irreducible...Ch. 13 - Prob. 13.49ECh. 13 - Prob. 13.50ECh. 13 - Why is it unnecessary to consider whether an...Ch. 13 - Prob. 13.52ECh. 13 - Prob. 13.53ECh. 13 - Prob. 13.54ECh. 13 - Prob. 13.55ECh. 13 - Prob. 13.56ECh. 13 - Prob. 13.57ECh. 13 - Prob. 13.58ECh. 13 - Reduce the following reducible representations...Ch. 13 - Determine the resulting representations for the...Ch. 13 - Prob. 13.61ECh. 13 - Without using the great orthogonality theorem,...Ch. 13 - Assume that you are evaluating the integral of...Ch. 13 - Prob. 13.64ECh. 13 - Assume that x- polarized light can be assigned an...Ch. 13 - Prob. 13.66ECh. 13 - Prob. 13.67ECh. 13 - Prob. 13.68ECh. 13 - Prob. 13.69ECh. 13 - Prob. 13.70ECh. 13 - Construct the symmetry-adapted linear combination...Ch. 13 - Prob. 13.72ECh. 13 - Prob. 13.73ECh. 13 - Prob. 13.74ECh. 13 - Prob. 13.75ECh. 13 - Prob. 13.76ECh. 13 - Prob. 13.77ECh. 13 - Suppose you use p0,p1 and p+1 along with s...Ch. 13 - Show that the individual sp orbitals, as written...Ch. 13 - Prob. 13.80ECh. 13 - What is the rough hybridization of the carbon...Ch. 13 - Determine the symmetry species of the D3h point...Ch. 13 - Determine the D3h symmetry species of the sp3d...Ch. 13 - Prob. 13.84ECh. 13 - In propene CH3CH=CH2, the first carbon has sp3...Ch. 13 - Prob. 13.87ECh. 13 - Prob. 13.88ECh. 13 - Prob. 13.89E
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
- 3. Refer to the data below to answer the following questions: Isoelectric point Amino Acid Arginine 10.76 Glutamic Acid 3.22 Tryptophan 5.89 A. Define isoelectric point. B. The most basic amino acid is C. The most acidic amino acid is sidizo zoarrow_forward3. A gas mixture contains 50 mol% H2 and 50 mol% He. 1.00-L samples of this gas mixture are mixed with variable volumes of O2 (at 0 °C and 1 atm). A spark is introduced to allow the mixture to undergo complete combustion. The final volume is measured at 0 °C and 1 atm. Which graph best depicts the final volume as a function of the volume of added O2? (A) 2.00 1.75 Final Volume, L 1.50 1.25 1.00 0.75 0.50 0.25 0.00 0.00 0.25 0.50 2.00 (B) 1.75 1.50 Final Volume, L 1.25 1.00 0.75 0.50- 0.25 0.00 0.75 1.00 0.00 0.25 Volume O₂ added, L 2 0.50 0.75 1.00 Volume O₂ added, L 2 2.00 2.00 (C) (D) 1.75 1.75 1.50 1.50 Final Volume, L 1.25 1.00 0.75 0.50 Final Volume, L 1.25 1.00 0.75 0.50 0.25 0.25 0.00 0.00 0.00 0.25 0.50 0.75 1.00 0.00 0.25 Volume O₂ added, L 0.50 0.75 1.00 Volume O₂ added, L 2arrow_forwardLeucine is an essential amino acid with the systematic name 2-amino-3-methylpentanoic acid. It has pai 2.36 and pKa2 = 9.60. H2N-C(R)H-COOH and R is -CH2-CH(CH3)2 A. Draw the condensed structure for leucine, and label all chirality centers with an asterisk. B. How many possible stereoisomers of leucine are there? C. Draw a Fischer projection of L-leucine and label the chirality center(s) as R or S. D. What is the p/ of leucine? E. Draw the structure of the predominant form of leucine at 10.00. F. Draw the structure of the predominant form of leucine at pH = 1.50. G. Leucine is described as an essential amino acid. What does this mean? H. Show the alkyl halide you would use to prepare leucine by the amidomalonate method. =arrow_forward
- a) Write out 6 completely different reactions of acetophenone (reagent, product). b) Write out 3 preparations of 1-methylcyclohexanol, using a different starting material for each one. You may use preps where you just change the functional group, and/or preps where you construct the carbon chain. c) Write out 3 preparations of 2-ethoxybenzoic acid, a different starting material for each one. You may use preps where you just change the functional group, and/or preps where you construct the carbon chain.arrow_forward12. CH3 OH OH H&C CH3 H₂C N OH H₂C CH3 H&C CH3 H₂C' CH3 H.C CH3OH H.C CH2CH3OH CH3CEN Which one of these 17 compounds is represented by this IR and this 'H NMR spectrum? IR Spectrum 3000 4000 3000 NMR Spectrum 2000 £500 RAVENUMBER 2000 1500 9 8 6 5 10 HP-00-290 ppm m 1000 500 1000 4 °arrow_forwardDraw the structure of (E,6R) 6-methoxy-4-hepten-2-one. Give the IUPAC name of this compound, including stereochemistry. Draw the most stable chair conformation of (cis) 1,3-isobutylcyclohexane. H HC=CCH₂ CH2CH3 EN(CH3)2 -CN(CH3)2arrow_forward
- 10. Write out the mechanism (intermediate/transition state) for this reaction; indicate stereochemistry in product. H3C CH₂OH CH3 SN1 Harrow_forwardWrite "most" under the member of each trio which is most stable. Write "least under the member of each trio which is least stable. b) Draw a Fischer projection of a pair of enantiomers with three chiral carbons. Which of these two would you expect to be more soluble in water? Why? 1-butanol 1-heptanol Which of these two would you expect to have the higher boiling point? Why? hexyl methyl ether 1-heptanolarrow_forwardWrite "most" under the most acidic compound. Write "least" under the least acidic compound. OH NO₂ OCH3 Br 9. Compound X, C50H84F2, reacts with excess H2/Pd to give a C50H88F2 compound. How many rings are in X? How many double bonds are in X? Show your work.arrow_forward
- 4. State whether these two are: a) the same molecule b) c) d) different compounds that are not isomers constitutional isomers diastereomers e) enantiomers CH3 CH₁₂ H OH HO H H OH HO H CH, CH₂ 5. a) How many stereocenters does this compound have? b) How many stereoisomers are possible for this compound? CH₂ OH CHCHarrow_forwardCalculating the pH at equivalence of a titration A chemist titrates 210.0 mL of a 0.1003 M hydrobromic acid (HBr) solution with 0.7550M KOH solution at 25 °C. Calculate the pH at equivalence. Round your answer to 2 decimal places. Note for advanced students: you may assume the total volume of the solution equals the initial volume plus the volume of KOH solution added. pH = ] ☑ o0o 18 Ararrow_forwardDo you do chemistry assignmentsarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning

Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher: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
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning

Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
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