Chemistry: Structure and Properties
1st Edition
ISBN: 9780321834683
Author: Nivaldo J. Tro
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 7, Problem 26E
Interpretation Introduction
Interpretation: How the sea model of an electron explains the conductivity, malleability and ductility of metals should be explained.
Concept introduction: Positive ions are arranged in regular fashion and valence electron (delocalized) move randomly like water in metal crystal. This electron sea model can explain many physical properties of metal. Electrons are free to move so metals conduct electricity without much resistance. In metal regular structure, positive ions are surrounded by free electrons (sea of electron) there is no specific bond like covalent or ionic bond, so it can deform easily by applying force on the metal piece.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
1.
Answer the questions about the following reaction:
(a) Draw in the arrows that can be used make this reaction occur and draw in the product of substitution in this
reaction. Be sure to include any relevant stereochemistry in the product structure.
+
SK
F
Br
+
(b) In which solvent would this reaction proceed the fastest (Circle one)
Methanol
Acetone
(c) Imagine that you are working for a chemical company and it was your job to perform a similar reaction to the
one above, with the exception of the S atom in this reaction being replaced by an O atom. During the reaction, you
observe the formation of three separate molecules instead of the single molecule obtained above. What is the likeliest
other products that are formed? Draw them in the box provided.
3. For the reactions below, draw the arrows corresponding to the transformations and draw in the boxes the reactants
or products as indicated. Note: Part A should have arrows drawn going from the reactants to the middle structure
and the arrows on the middle structure that would yield the final structure. For part B, you will need to draw in
the reactant before being able to draw the arrows corresponding to product formation.
A.
B.
Rearrangement
ΘΗ
2. Draw the arrows required to make the following reactions occur. Please ensure your arrows point from exactly
where you want to exactly where you want. If it is unclear from where arrows start or where they end, only partial
credit will be given. Note: You may need to draw in lone pairs before drawing the arrows.
A.
B.
H-Br
人
C
Θ
CI
H
Cl
Θ
+
Br
O
Chapter 7 Solutions
Chemistry: Structure and Properties
Ch. 7 - Determine the hybridization about 0 in CH3OH.Ch. 7 - Determine the hybridization about C in H2CO.Ch. 7 - According to the valance bond theory, which kind...Ch. 7 - Use molecular orbital theory to determine the bond...Ch. 7 - Use molecular orbital theory to predict which...Ch. 7 - Use molecular orbital theory to determine which...Ch. 7 - Which hybridization scheme occurs about nitrogen...Ch. 7 - Prob. 8SAQCh. 7 - Prob. 9SAQCh. 7 - Prob. 10SAQ
Ch. 7 - Which type of orbitals overlap to form the sigma...Ch. 7 - Prob. 12SAQCh. 7 - Prob. 1ECh. 7 - What is a chemical bond according to valence bond...Ch. 7 - In valence bond theory, what determines the...Ch. 7 - In valence bond theory, the interaction energy...Ch. 7 - What is hybridization? Why is hybridization...Ch. 7 - How does hybridization of the atomic orbitals in...Ch. 7 - How is the number of hybrid orbitals related to...Ch. 7 - Sketch each hybrid orbital sp sp2 sp3 sp3d sp3d2Ch. 7 - Prob. 9ECh. 7 - Name the hybridization scheme that corresponds to...Ch. 7 - What is a chemical bond according to molecular...Ch. 7 - Explain the difference between hybrid atomic...Ch. 7 - What is a bonding molecular orbital?Ch. 7 - Prob. 14ECh. 7 - What is the role of wave interference in...Ch. 7 - Prob. 16ECh. 7 - Prob. 17ECh. 7 - Prob. 18ECh. 7 - Prob. 19ECh. 7 - Prob. 20ECh. 7 - Prob. 21ECh. 7 - When applying molecular orbital theory to...Ch. 7 - In molecular orbital theory, what is a nonbonding...Ch. 7 - Write a short paragraph describing chemical...Ch. 7 - Prob. 25ECh. 7 - Prob. 26ECh. 7 - Prob. 27ECh. 7 - Prob. 28ECh. 7 - Prob. 29ECh. 7 - Prob. 30ECh. 7 - The valence electron configurations of several...Ch. 7 - The valence electron configurations of several...Ch. 7 - Draw orbital diagrams (boxes with arrows in them)...Ch. 7 - Draw orbital diagrams (boxes with arrows in them)...Ch. 7 - Prob. 35ECh. 7 - Draw orbital diagrams (boxes with arrows in them)...Ch. 7 - Which hybridization scheme allows the formation of...Ch. 7 - Which hybridization scheme allows the central atom...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Write a hybridization and bonding scheme for each...Ch. 7 - Consider the structure of the amino acid alanine...Ch. 7 - Consider the structure of the amino acid aspartic...Ch. 7 - Sketch the bonding molecular orbital that results...Ch. 7 - Sketch the antibonding molecular orbital that...Ch. 7 - Draw an MO energy diagram and predict the bond...Ch. 7 - Draw an MO energy diagram and predict the bond...Ch. 7 - Sketch the bonding and antibonding molecular...Ch. 7 - Sketch the bonding and antibonding molecular...Ch. 7 - Using the molecular orbital energy ordenng for...Ch. 7 - Using the molecular orbital energy ordering for...Ch. 7 - Apply molecular orbital theory to predict if each...Ch. 7 - Apply molecular orbital theory to predict if each...Ch. 7 - According to MO theory, which molecule or ion has...Ch. 7 - According to MO theory, which molecule or ion has...Ch. 7 - Draw an MO energy diagram for CO. (Use the energy...Ch. 7 - Draw an MO energy diagram for HCI. Predict the...Ch. 7 - Prob. 61ECh. 7 - Prob. 62ECh. 7 - Prob. 63ECh. 7 - Prob. 64ECh. 7 - Prob. 65ECh. 7 - Prob. 66ECh. 7 - For each compound, draw the Lewis structure,...Ch. 7 - For each compound, draw the Lewis structure,...Ch. 7 - Amino acids are biological compounds that link...Ch. 7 - The genetic code is based on four different bases...Ch. 7 - The structure of caffeine, present in coffee and...Ch. 7 - The structure of acetylsalicylic acid (aspirin) is...Ch. 7 - Draw a molecular orbital energy diagram for CIF....Ch. 7 - Draw Lewis structures and MO diagrams for CN+, CN,...Ch. 7 - Bromine can form compounds or ions with any number...Ch. 7 - The compound C3H4 has two double bonds. Describe...Ch. 7 - How many hybrid orbitals do we use to describe...Ch. 7 - Prob. 78ECh. 7 - In VSEPR theory, which uses the Lewis model to...Ch. 7 - The resuts of a molecular orbital calculation for...Ch. 7 - Prob. 81ECh. 7 - cis-2-Butene isomerizes (changes its structure) to...Ch. 7 - The ion CH5 + can form under very special...Ch. 7 - Neither the VSEPR model nor the hybridization...Ch. 7 - Prob. 85ECh. 7 - The most stable forms of the nonmetals in groups...Ch. 7 - Consider the bond energies of three iodine...Ch. 7 - How many atomic orbitals form a set of sp3hybrid...
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
- 4. For the reactions below, draw the expected product. Be sure to indicate relevant stereochemistry or formal charges in the product structure. a) CI, H e b) H lux ligh Br 'Harrow_forwardArrange the solutions in order of increasing acidity. (Note that K (HF) = 6.8 x 10 and K (NH3) = 1.8 × 10-5) Rank solutions from least acidity to greatest acidity. To rank items as equivalent, overlap them. ▸ View Available Hint(s) Least acidity NH&F NaBr NaOH NH,Br NaCIO Reset Greatest acidityarrow_forward1. Consider the following molecular-level diagrams of a titration. O-HA molecule -Aion °° о ° (a) о (b) (c) (d) a. Which diagram best illustrates the microscopic representation for the EQUIVALENCE POINT in a titration of a weak acid (HA) with sodium. hydroxide? (e)arrow_forward
- Answers to the remaining 6 questions will be hand-drawn on paper and submitted as a single file upload below: Review of this week's reaction: H₂NCN (cyanamide) + CH3NHCH2COOH (sarcosine) + NaCl, NH4OH, H₂O ---> H₂NC(=NH)N(CH3)CH2COOH (creatine) Q7. Draw by hand the reaction of creatine synthesis listed above using line structures without showing the Cs and some of the Hs, but include the lone pairs of electrons wherever they apply. (4 pts) Q8. Considering the Zwitterion form of an amino acid, draw the Zwitterion form of Creatine. (2 pts) Q9. Explain with drawing why the C-N bond shown in creatine structure below can or cannot rotate. (3 pts) NH2(C=NH)-N(CH)CH2COOH This bond Q10. Draw two tautomers of creatine using line structures. (Note: this question is valid because problem Q9 is valid). (4 pts) Q11. Mechanism. After seeing and understanding the mechanism of creatine synthesis, students should be ready to understand the first half of one of the Grignard reactions presented in a past…arrow_forwardPropose a synthesis pathway for the following transformations. b) c) d)arrow_forwardThe rate coefficient of the gas-phase reaction 2 NO2 + O3 → N2O5 + O2 is 2.0x104 mol–1 dm3 s–1 at 300 K. Indicate whether the order of the reaction is 0, 1, or 2.arrow_forward
- 8. Draw all the resonance forms for each of the following molecules or ions, and indicate the major contributor in each case, or if they are equivalent. (4.5 pts) (a) PH2 سمةarrow_forward3. Assign absolute configuration (Rors) to each chirality center. a. H Nitz C. он b. 0 H-C. C H 7 C. ་-4 917-417 refs H 1つ ८ ડુ d. Но f. -2- 01 Ho -OH 2HNarrow_forwardHow many signals do you expect in the H NMR spectrum for this molecule? Br Br Write the answer below. Also, in each of the drawing areas below is a copy of the molecule, with Hs shown. In each copy, one of the H atoms is colored red. Highlight in red all other H atoms that would contribute to the same signal as the H already highlighted red. Note for advanced students: In this question, any multiplet is counted as one signal. Number of signals in the 'H NMR spectrum. For the molecule in the top drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box at right. No additional Hs to color in top molecule For the molecule in the bottom drawing area, highlight in red any other H atoms that will contribute to the same signal as the H atom already highlighted red. If no other H atoms will contribute, check the box at right. No additional Hs to color in bottom moleculearrow_forward
- In the drawing area below, draw the major products of this organic reaction: 1. NaOH ? 2. CH3Br If there are no major products, because nothing much will happen to the reactant under these reaction conditions, check the box under the drawing area instead. No reaction. Click and drag to start drawing a structure. ☐ : A คarrow_forwardPredict the major products of the following organic reaction: NC Δ ? Some important Notes: • Draw the major product, or products, of the reaction in the drawing area below. • If there aren't any products, because no reaction will take place, check the box below the drawing area instead. • Be sure to draw bonds carefully to show important geometric relationships between substituents. Note: if your answer contains a complicated ring structure, you must use one of the molecular fragment stamps (available in the menu at right) to enter the ring structure. You can add any substituents using the pencil tool in the usual way. Click and drag to start drawing a structure. Х аarrow_forwardPredict the major products of this organic reaction. Be sure you use dash and wedge bonds to show stereochemistry where it's important. + ☑ OH 1. TsCl, py .... 文 P 2. t-BuO K Click and drag to start drawing a structure.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
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: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
Chemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
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
Chemistry: An Atoms First Approach
Chemistry
ISBN:9781305079243
Author:Steven S. Zumdahl, Susan A. Zumdahl
Publisher:Cengage Learning
Chemistry & Chemical Reactivity
Chemistry
ISBN:9781133949640
Author:John C. Kotz, Paul M. Treichel, John Townsend, David Treichel
Publisher:Cengage Learning
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co