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OWLv2 with Student Solutions Manual eBook for Ebbing/Gammon's General Chemistry, 11th Edition, [Instant Access], 4 terms (24 months)
11th Edition
ISBN: 9781305864900
Author: Darrell Ebbing; Steven D. Gammon
Publisher: Cengage Learning US
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Chapter 10.4, Problem 10.7E
Dinitrogen difluoride (see Example 10.5) exists as cis and trans isomers. Write structural formulas for these isomers and explain (in terms of the
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5. A solution of sucrose is fermented in a vessel until the evolution of CO2 ceases. Then, the
product solution is analyzed and found to contain, 45% ethanol; 5% acetic acid; and 15%
glycerin by weight.
If the original charge is 500 kg, evaluate;
e. The ratio of sucrose to water in the original charge (wt/wt).
f. Moles of CO2 evolved.
g. Maximum possible amount of ethanol that could be formed.
h. Conversion efficiency.
i. Per cent excess of excess reactant.
Reactions:
Inversion reaction: C12H22O11 + H2O →2C6H12O6
Fermentation reaction: C6H12O6 →→2C2H5OH + 2CO2
Formation of acetic acid and glycerin: C6H12O6 + C2H5OH + H₂O→ CH3COOH + 2C3H8O3
Show work. don't give Ai generated solution. How many carbons and hydrogens are in the structure?
13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the
molecule depicted below.
Bond B
2°C. +2°C. cleavage
Bond A
•CH3 + 26.← Cleavage
2°C. +
Bond C
+3°C•
CH3 2C
Cleavage
E
2°C. 26.
weakest bond
Intact molecule
Strongest 3°C 20.
Gund
Largest
argest
a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in
appropriate boxes.
C
Weakest
bond
A
Produces
Most
Bond
Strongest
Bond
Strongest Gund
produces least stable
radicals
Weakest
Stable radical
b. (4pts) Consider the relative stability of all cleavage products that form when bonds A,
B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B,
and C are all carbon radicals.
i. Which ONE cleavage product is the most stable? A condensed or bond line
representation is fine.
13°C. formed in
bound C
cleavage
ii. Which ONE cleavage product is the least stable? A condensed or bond line
representation is fine.
• CH3
methyl radical
Formed in Gund A Cleavage
c.…
Chapter 10 Solutions
OWLv2 with Student Solutions Manual eBook for Ebbing/Gammon's General Chemistry, 11th Edition, [Instant Access], 4 terms (24 months)
Ch. 10.1 - An atom in a molecule is surrounded by four pairs...Ch. 10.1 - Use the VSEPR method to predict the geometry of...Ch. 10.1 - Prob. 10.2ECh. 10.2 - Bromine trifluoride, BrF3, has a nonzero dipole...Ch. 10.2 - Which of the following would be expected to have a...Ch. 10.2 - Two molecules, each with the general formula AX3,...Ch. 10.3 - Using hybrid orbitals, describe the bonding in NH3...Ch. 10.4 - Describe the bonding on the carbon atom in carbon...Ch. 10.4 - Dinitrogen difluoride (see Example 10.5) exists as...Ch. 10.4 - Prob. 10.3CC
Ch. 10.6 - The C2 molecule exists in the vapor phase over...Ch. 10.6 - Give the orbital diagram and electron...Ch. 10 - Describe the main features of the VSEPR model.Ch. 10 - According to the VSEPR model, what are the...Ch. 10 - Why is a lone pair expected to occupy an...Ch. 10 - Prob. 10.4QPCh. 10 - Explain why nitrogen trifluoride has a small...Ch. 10 - Prob. 10.6QPCh. 10 - What is the angle between two sp3 hybrid orbitals?Ch. 10 - Prob. 10.8QPCh. 10 - Prob. 10.9QPCh. 10 - How does the valence bond description of a...Ch. 10 - Prob. 10.11QPCh. 10 - What factors determine the strength of interaction...Ch. 10 - Prob. 10.13QPCh. 10 - Prob. 10.14QPCh. 10 - Prob. 10.15QPCh. 10 - Describe the bonding in O3, using molecular...Ch. 10 - Prob. 10.17QPCh. 10 - Which of the following molecular geometries does...Ch. 10 - Which of the following would be a polar molecule?...Ch. 10 - Prob. 10.20QPCh. 10 - Best Lewis Formula and Molecular Geometry A...Ch. 10 - Prob. 10.22QPCh. 10 - Prob. 10.23QPCh. 10 - Which of the following molecular models correctly...Ch. 10 - Prob. 10.25QPCh. 10 - Prob. 10.26QPCh. 10 - Indicate what hybrid orbital depicted below is...Ch. 10 - An atom in a molecule has two bonds to other atoms...Ch. 10 - Two compounds have the same molecular formula,...Ch. 10 - A neutral molecule is identified as a...Ch. 10 - Acetic acid, the sour constituent of vinegar, has...Ch. 10 - What are the bond angles predicted by the VSEPR...Ch. 10 - Predict the shape or geometry of the following...Ch. 10 - Use the electron-pair repulsion model to predict...Ch. 10 - Predict the geometry of the following ions, using...Ch. 10 - Use the VSEPR model to predict the geometry of the...Ch. 10 - For each of the following molecules, state the...Ch. 10 - For each of the following molecules, state the...Ch. 10 - Prob. 10.39QPCh. 10 - From the electron-pair repulsion model, predict...Ch. 10 - Predict the geometries of the following ions,...Ch. 10 - Name the geometries expected for the following...Ch. 10 - a The molecule AsF3 has a dipole moment of 2.59 D....Ch. 10 - a The molecule BrF3 has a dipole moment of 1.19 D....Ch. 10 - Which of the following molecules would be expected...Ch. 10 - Which of the following molecules would be expected...Ch. 10 - What hybrid orbitals would be expected for the...Ch. 10 - What hybrid orbitals would be expected for the...Ch. 10 - What hybrid orbitals would be expected for the...Ch. 10 - What hybrid orbitals would be expected for the...Ch. 10 - a Mercury(II) chloride dissolves in water to give...Ch. 10 - a Nitrogen trifluoride, NF3, is a relatively...Ch. 10 - a Carbonyl fluoride, COF2, is an extremely...Ch. 10 - a The molecule HNNH exists as a transient species...Ch. 10 - The hyponitrite ion, ONNO, exists in solid...Ch. 10 - Fumaric acid, C4H4O4, occurs in the metabolism of...Ch. 10 - Describe the electronic structure of each of the...Ch. 10 - Use molecular orbital theory to describe the...Ch. 10 - Prob. 10.59QPCh. 10 - Write the molecular orbital configuration of the...Ch. 10 - Predict the molecular geometry of the following: a...Ch. 10 - Prob. 10.62QPCh. 10 - Which of the following molecules or ions are...Ch. 10 - Which of the following molecules or ions are...Ch. 10 - Describe the hybrid orbitals used by each carbon...Ch. 10 - Prob. 10.66QPCh. 10 - Explain how the dipole moment could be used to...Ch. 10 - Two compounds have the formula Pt(NH3)2Cl2....Ch. 10 - Explain in terms of bonding theory why all four...Ch. 10 - Explain in terms of bonding theory why all atoms...Ch. 10 - What is the molecular orbital configuration of...Ch. 10 - Prob. 10.72QPCh. 10 - Calcium carbide, CaC2, consists of Ca2+ and C22...Ch. 10 - Sodium peroxide, Na2O2, consists of Na+ and O22...Ch. 10 - The oxygen oxygen bond in O2 is 112 pm and in O2...Ch. 10 - The nitrogennitrogen bond distance in N2 is 109...Ch. 10 - Using molecular orbital theory, determine the...Ch. 10 - The ionization energy of O2 is smaller than the...Ch. 10 - Prob. 10.79QPCh. 10 - Prob. 10.80QPCh. 10 - Prob. 10.81QPCh. 10 - Prob. 10.82QPCh. 10 - What is the biological importance of stratospheric...Ch. 10 - Prob. 10.84QPCh. 10 - Prob. 10.85QPCh. 10 - The bond length in C2 is 131 pm. Compare this with...Ch. 10 - Calcium carbide, CaC2, has an ionic structure with...Ch. 10 - Write Lewis formulas for the BF molecule (two with...Ch. 10 - Boron trifluoride, BF3, reacts with ammonia, NH3,...Ch. 10 - Prob. 10.90QPCh. 10 - Allene (1,2-propadicne), a gas, has the following...Ch. 10 - Prob. 10.92QPCh. 10 - The triiodide ion, I3, and the azide ion, N3, have...Ch. 10 - Hydrogen azide (also known as hydrazoic acid),...Ch. 10 - Prob. 10.95QPCh. 10 - A molecule XF6 (having no lone pairs) has a dipole...Ch. 10 - Describe the molecular orbital configurations of...Ch. 10 - Prob. 10.98QPCh. 10 - Three different compounds have the same molecular...Ch. 10 - Prob. 10.100QPCh. 10 - Prob. 10.101QPCh. 10 - Solid sulfur normally consists of crystals of S8...Ch. 10 - Prob. 10.103QPCh. 10 - Consider the bonding in nitrate ion, NO3. First...Ch. 10 - A molecular compound is composed of 52.5% Xe,...Ch. 10 - A molecular compound is composed of 58.8% Xe,...Ch. 10 - A compound of chlorine and fluorine. ClFn, reacts...Ch. 10 - Excess fluorine, F2(g), reacts at 150C with...Ch. 10 - Prob. 10.109QPCh. 10 - One resonance formula of benzene, C6H6, is What is...
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- Hi!! Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required. Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!arrow_forwardHi!! Please provide a solution that is handwritten. Ensure all figures, reaction mechanisms (with arrows and lone pairs please!!), and structures are clearly drawn to illustrate the synthesis of the product as per the standards of a third year organic chemistry course. ****the solution must include all steps, mechanisms, and intermediate structures as required. Please hand-draw the mechanisms and structures to support your explanation. Don’t give me AI-generated diagrams or text-based explanations, no wordy explanations on how to draw the structures I need help with the exact mechanism hand drawn by you!!! I am reposting this—ensure all parts of the question are straightforward and clear or please let another expert handle it thanks!!arrow_forward. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B 2°C. +2°C. < cleavage Bond A • CH3 + 26. t cleavage 2°C• +3°C• Bond C Cleavage CH3 ZC '2°C. 26. E Strongest 3°C. 2C. Gund Largest BDE weakest bond In that molecule a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest C bond Produces A Weakest Bond Most Strongest Bond Stable radical Strongest Gund produces least stable radicals b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. 人 8°C. formed in bound C cleavage ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. methyl radical •CH3 formed in bund A Cleavagearrow_forward
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