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Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)
7th Edition
ISBN: 9780134240152
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Question
Chapter 13, Problem 41P
Interpretation Introduction
Interpretation:
The change in the degree of regioselectivity compared to the ratio of relative rates found in problem 44 has to be given.
Concept introduction:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.
Chlorine radical forms a tertiary radical five times faster than a primary radical and it forms a secondary radical 3.8 times faster than a primary radical.
Relative rates of alkyl radical formation by a chlorine radical at 125 °C.
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LABORATORY REPORT FORM
Part I. Determination of the Formula of a Known Hydrate
1. Mass of empty evaporating dish
3. Mass of hydrate
Using subtraction
or mass by difference,
find the mass of
the hydrate
76.96
-75.40
75.40g
76.968
1.568
01.56
76.90 g
2. Mass of evaporating dish + hydrate
4. Mass of evaporating dish + hydrate (after heating)
First 76.98 g
Third 76.66g
Second
Fourth (if necessary) 76.60g
5. Mass of anhydrate
6. Mass of water lost by the hydrate
7. Percent of water of hydration
(Show Calculations)
8. Moles of water
(Show Calculations)
mol
mass of water
=
MM of water (g/m)
9. Moles of anhydrate
(Show Calculations)
10. Ratio of moles of water to moles of anhydrate
11 F(Show Calculations)
11. Formula of hydrate
- Mass of water (g) x 100
% water hydration
g
g
%
Mass of hydrate (9) x IC
% = (Mass of hydrate- mass of an)
mass of hydrate (g)
% = (1.569-
× 100=
mol
1.569
mol Mol Mass of
anhydrate/MM
of anhydrate
12. What was the color of the hydrate?
blue
What was the color of the…
compared t-critical with t-calculated and 95% confidence interval to answer this question
Chapter 13 Solutions
Organic Chemistry; Modified MasteringChemistry with Pearson eText -- ValuePack Access Card; Study Guide and Student Solutions Manual for Organic Chemistry, Books a la Carte Edition (7th Edition)
Ch. 13.2 - Prob. 1PCh. 13.2 - Write the steps for formation of...Ch. 13.3 - Prob. 3PCh. 13.4 - Prob. 4PCh. 13.5 - Prob. 7PCh. 13.5 - a. Would chlorination or bromination produce a...Ch. 13.5 - Prob. 10PCh. 13.6 - Prob. 11PCh. 13.7 - Prob. 12PCh. 13.7 - Prob. 13P
Ch. 13.8 - Prob. 14PCh. 13.8 - Draw the stereoisomers of the major...Ch. 13.9 - a. How many stereoisomers are formed from the...Ch. 13.9 - Prob. 17PCh. 13.9 - Prob. 19PCh. 13.9 - Prob. 20PCh. 13.9 - Prob. 21PCh. 13.10 - Prob. 22PCh. 13.11 - How many atoms share the unpaired electrons in...Ch. 13.11 - Prob. 24PCh. 13 - Prob. 25PCh. 13 - Prob. 26PCh. 13 - Prob. 27PCh. 13 - Prob. 28PCh. 13 - Prob. 29PCh. 13 - Prob. 30PCh. 13 - Prob. 31PCh. 13 - Prob. 32PCh. 13 - Prob. 33PCh. 13 - Prob. 34PCh. 13 - Prob. 35PCh. 13 - Starting with cyclohexane, how could the following...Ch. 13 - a. Propose a mechanism for the following reaction:...Ch. 13 - What stereoisomers are obtained from the following...Ch. 13 - Prob. 39PCh. 13 - Prob. 40PCh. 13 - Prob. 41PCh. 13 - Draw the products of the following reactions,...Ch. 13 - a. What five-carbon alkene forms the same product...Ch. 13 - Prob. 44PCh. 13 - Prob. 45PCh. 13 - Prob. 46PCh. 13 - Explain why the rate of bromination of methane...Ch. 13 - Prob. 48P
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