Chemistry: Principles and Practice
3rd Edition
ISBN: 9780534420123
Author: Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher: Cengage Learning
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Chapter 12, Problem 12.39QE
The density of a 3.75 M aqueous sulfuric acid solution in a car battery is 1.225 g/mL. Express the concentration of the solution in molality, mole fraction H2SO2, and mass percentage of H2SO4.
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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 12 Solutions
Chemistry: Principles and Practice
Ch. 12 - Prob. 12.1QECh. 12 - Prob. 12.2QECh. 12 - Prob. 12.3QECh. 12 - Prob. 12.4QECh. 12 - Prob. 12.5QECh. 12 - Prob. 12.6QECh. 12 - Prob. 12.7QECh. 12 - Prob. 12.8QECh. 12 - Prob. 12.9QECh. 12 - Prob. 12.10QE
Ch. 12 - Prob. 12.11QECh. 12 - Prob. 12.12QECh. 12 - Create a flow diagram, similar to those used in...Ch. 12 - Prob. 12.14QECh. 12 - Prob. 12.15QECh. 12 - Prob. 12.16QECh. 12 - Prob. 12.17QECh. 12 - Prob. 12.18QECh. 12 - Prob. 12.19QECh. 12 - Prob. 12.20QECh. 12 - Prob. 12.21QECh. 12 - Prob. 12.22QECh. 12 - Prob. 12.23QECh. 12 - Prob. 12.24QECh. 12 - Prob. 12.25QECh. 12 - Prob. 12.26QECh. 12 - Prob. 12.27QECh. 12 - What is the molality of copper(II) bromide (CuBr2)...Ch. 12 - Prob. 12.29QECh. 12 - Prob. 12.30QECh. 12 - A water solution of sodium hypochlorite (NaOCl) is...Ch. 12 - Prob. 12.32QECh. 12 - Prob. 12.33QECh. 12 - Vinegar is a 5.0% solution of acetic acid...Ch. 12 - Prob. 12.35QECh. 12 - A 2.77 M NaOH solution in water has a density of...Ch. 12 - The density of a 3.75 M aqueous sulfuric acid...Ch. 12 - Prob. 12.40QECh. 12 - Prob. 12.41QECh. 12 - Prob. 12.42QECh. 12 - Predict the relative solubility of each compound...Ch. 12 - Predict the relative solubility of each compound...Ch. 12 - Prob. 12.45QECh. 12 - Prob. 12.46QECh. 12 - Prob. 12.47QECh. 12 - Prob. 12.48QECh. 12 - Prob. 12.49QECh. 12 - The solubility of ethylene (C2H4) in water at 20 C...Ch. 12 - Prob. 12.51QECh. 12 - Prob. 12.52QECh. 12 - Prob. 12.53QECh. 12 - Prob. 12.54QECh. 12 - Prob. 12.55QECh. 12 - Prob. 12.56QECh. 12 - From the data presented in Figure 12.11, determine...Ch. 12 - Prob. 12.58QECh. 12 - Prob. 12.59QECh. 12 - Prob. 12.60QECh. 12 - Prob. 12.61QECh. 12 - Prob. 12.62QECh. 12 - The vapor pressure of chloroform (CHCl3) is 360...Ch. 12 - Prob. 12.64QECh. 12 - Prob. 12.65QECh. 12 - Prob. 12.66QECh. 12 - Prob. 12.67QECh. 12 - Prob. 12.68QECh. 12 - Prob. 12.69QECh. 12 - Prob. 12.70QECh. 12 - A solution of 1.00 g of a protein in 20.0 mL water...Ch. 12 - Prob. 12.72QECh. 12 - Arrange the following aqueous solutions in order...Ch. 12 - Arrange the following solutions in order of...Ch. 12 - Prob. 12.75QECh. 12 - An aqueous solution of sodium bromide freezes at...Ch. 12 - Prob. 12.77QECh. 12 - Prob. 12.78QECh. 12 - Prob. 12.79QECh. 12 - Prob. 12.80QECh. 12 - A 0.029 M solution of potassium sulfate has an...Ch. 12 - The freezing point of a 0.031-m solution of...Ch. 12 - Prob. 12.83QECh. 12 - Prob. 12.84QECh. 12 - Prob. 12.85QECh. 12 - Prob. 12.86QECh. 12 - Prob. 12.87QECh. 12 - Prob. 12.88QECh. 12 - Prob. 12.89QECh. 12 - Prob. 12.90QECh. 12 - Predict the relative solubility of each compound...Ch. 12 - Prob. 12.92QECh. 12 - Prob. 12.94QECh. 12 - Prob. 12.95QECh. 12 - Prob. 12.96QECh. 12 - Sketch graphs of total vapor pressure versus the...Ch. 12 - Prob. 12.98QECh. 12 - Prob. 12.99QECh. 12 - Prob. 12.100QECh. 12 - Prob. 12.101QECh. 12 - Prob. 12.102QECh. 12 - Prob. 12.103QECh. 12 - A 10.00-mL sample of a 24.00% solution of ammonium...Ch. 12 - Prob. 12.105QECh. 12 - In the 1986 Lake Nyos disaster (see the chapter...Ch. 12 - Prob. 12.107QE
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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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Solutions: Crash Course Chemistry #27; Author: Crash Course;https://www.youtube.com/watch?v=9h2f1Bjr0p4;License: Standard YouTube License, CC-BY