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OWLv2 for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th Edition, [Instant Access], 1 term (6 months)
8th Edition
ISBN: 9781305271593
Author: David W. Oxtoby; H. Pat Gillis; Laurie J. Butler
Publisher: Cengage Learning US
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Chapter 6, Problem 72AP
The stable molecular ion
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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 6 Solutions
OWLv2 for Oxtoby/Gillis/Butler's Principles of Modern Chemistry, 8th Edition, [Instant Access], 1 term (6 months)
Ch. 6 - Determine the number of nodes along the...Ch. 6 - Determine the number of nodes along the...Ch. 6 - Sketch the shape of each of the molecular...Ch. 6 - Sketch the shape of each of the molecular...Ch. 6 - Compare the electron density in the 1g and 1u*...Ch. 6 - Explain why 1g is the ground state for H2+ . By...Ch. 6 - Prob. 7PCh. 6 - Predict the ground electronic state of the He22+...Ch. 6 - Prob. 9PCh. 6 - Prob. 10P
Ch. 6 - Without consulting tables of data, predict which...Ch. 6 - Without consulting tables of data, predict which...Ch. 6 - Without consulting tables of data, on the same...Ch. 6 - Without consulting tables of data, on the same...Ch. 6 - Suppose we supply enough energy to H2 to remove...Ch. 6 - Suppose we supply enough energy to He2+ to remove...Ch. 6 - Prob. 17PCh. 6 - When one electron is added to an oxygen molecule,...Ch. 6 - Predict the valence electron configuration and the...Ch. 6 - Predict the valence electron configuration and the...Ch. 6 - Prob. 21PCh. 6 - For each of the following valence electron...Ch. 6 - For each of the electron configurations in Problem...Ch. 6 - For each of the electron configurations in Problem...Ch. 6 - Following the pattern of Figure 6.21, work out the...Ch. 6 - Following the pattern of Figure 6.21, work out the...Ch. 6 - The bond length of the transient diatomic molecule...Ch. 6 - The compound nitrogen oxide (NO) forms when the...Ch. 6 - What would be the electron configuration for a HeH...Ch. 6 - The molecular ion HeH+ has an equilibrium bond...Ch. 6 - Prob. 31PCh. 6 - Predict the ground state electronic configuration...Ch. 6 - The bond dissociation energies for the species NO,...Ch. 6 - The ionization energy of CO is greater than that...Ch. 6 - Photoelectron spectra were acquired from a sample...Ch. 6 - Photoelectron spectra were acquired from a sample...Ch. 6 - Prob. 37PCh. 6 - From the n=0 peaks in the photoelectron spectrum...Ch. 6 - The photoelectron spectrum of HBr has two main...Ch. 6 - The photoelectron spectrum of CO has four major...Ch. 6 - Write simple valence bond wave functions for the...Ch. 6 - Write simple valence bond wave functions for the...Ch. 6 - Both the simple VB model and the LCAO method...Ch. 6 - Both the simple VB model and the LCAO method...Ch. 6 - Write simple valence bond wave functions for...Ch. 6 - Write simple valence bond wave functions for...Ch. 6 - Write simple valence bond wave functions for the...Ch. 6 - Write simple valence bond wave functions for the...Ch. 6 - Formulate a localized bond picture for the amide...Ch. 6 - Formulate a localized bond picture for the...Ch. 6 - Prob. 51PCh. 6 - Draw a Lewis electron dot diagram for each of the...Ch. 6 - Describe the hybrid orbitals on the chlorine atom...Ch. 6 - Describe the hybrid orbitals on the chlorine atom...Ch. 6 - The sodium salt of the unfamiliar orthonitrate ion...Ch. 6 - Describe the hybrid orbitals used by the carbon...Ch. 6 - Describe the bonding in the bent molecule NF2 ....Ch. 6 - Describe the bonding in the bent molecule OF2 ....Ch. 6 - The azide ion (N3) is a weakly bound molecular...Ch. 6 - Formulate the MO structure of (NO2+) for localized...Ch. 6 - Discuss the nature of the bonding in the nitrite...Ch. 6 - Discuss the nature of the bonding in the nitrate...Ch. 6 - The pyridine molecule (C5H5N) is obtained by...Ch. 6 - For each of the following molecules, construct the...Ch. 6 - (a) Sketch the occupied MOs of the valence shell...Ch. 6 - Calcium carbide (CaC2) is an intermediate in the...Ch. 6 - The B2 molecule is paramagnetic; show how this...Ch. 6 - The Be2 molecule has been detected experimentally....Ch. 6 - Prob. 69APCh. 6 - The molecular ion HeH+ has an equilibrium bond...Ch. 6 - The MO of the ground state of a heteronuclear...Ch. 6 - The stable molecular ion H3+ is triangular, with...Ch. 6 - According to recent spectroscopic results,...Ch. 6 - trans-tetrazene (N4H4) consists of a chain of four...
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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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