ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
10th Edition
ISBN: 9781260028355
Author: Carey
Publisher: MCG CUSTOM
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Chapter 22.4, Problem 7P
Interpretation Introduction
Interpretation:
Considering the resonance structure, the reason that the given compounds are weaker base than aniline corresponding to the effect of the substituent is to be explained.
Concept Introduction:
>The major factors that contribute to the basic strength are
The high percentage of
An acidic substance in a reaction donates a proton, while a base in a reaction accepts a proton.
>The elimination of a proton leads to the formation of a conjugate base. If the base accepts a proton the species formed is known as conjugate acid.
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Experiment 1
Data Table 1: Conservation of Mass - Initial Mass
Data Table 1
Data Table 2
Data Table 3
Data Table 4
Panel 1
Photo 1
Data Table 5
Reaction Mass of test tube and 5.0% HC₂H₂O2 (g)
#
(A)
(B)
Mass of NaHCO, (g) Mass of balloon and NaHCO, (g)
(C)
0.10
1
0829
14.38g
0.20
2
0.929
14.29g
0.35
1.00g
3
14.25g
0.50
1.14g
14.29
Experiment 1
Data Table 2: Moles of HC2H3O2
Reaction Volume of Mass of
Moles of HC₂H₂O₂
5.0%
Vinegar
(g)
(ML)
5.0
0.25
0042 mol
2
5.0
0.25
0042 mol
3
5.0
0.25
0042 mol
5.0
0.25
0042 mol
Experiment 1
Data Table 3: Moles of NaHCO3
Reaction Mass of NaHCO (g)
10g
20g
35g
50g
Experiment 1
Data Table 4: Theoretical Yield of CO₂
Reaction #
1
2
3
Experiment 1
Total mass before reaction (g)
(D=A+C)
15.29
15.21g
15.25g
15.349
Exercise 1
Data Table 1
Data Table 2
Data Table 3
Data Table 4
Panel 1
Photo 1
Data Table 5
Exercise 1-
Data Table 1
Data Table 2
DataTable 3
Data Table 4
Panel 1
Photo 1
Data Table 5
Exercise 1-
Moles of NaHCO
0012 mol
0025 mol
0044 mol
0062 mol…
The chemical reaction you investigated is a two-step reaction. What type of reaction occurs in each step? How did you determine your answer?
What is the relationship between the limiting reactant and theoretical yield of CO2?
Chapter 22 Solutions
ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
Ch. 22.1 - Prob. 1PCh. 22.1 - Prob. 2PCh. 22.1 - Prob. 3PCh. 22.2 - Prob. 4PCh. 22.4 - Prob. 5PCh. 22.4 - Prob. 6PCh. 22.4 - Prob. 7PCh. 22.4 - Prob. 8PCh. 22.4 - Prob. 9PCh. 22.7 - Prob. 10P
Ch. 22.8 - Problem 22.11 Three of the following amines can be...Ch. 22.9 - Prob. 12PCh. 22.10 - Prob. 13PCh. 22.13 - Prob. 14PCh. 22.14 - Prob. 15PCh. 22.15 - Prob. 16PCh. 22.15 - Prob. 17PCh. 22.17 - Prob. 18PCh. 22.17 - Prob. 19PCh. 22.17 - Prob. 20PCh. 22.17 - Prob. 21PCh. 22.18 - Prob. 22PCh. 22 - Prob. 23PCh. 22 - Prob. 24PCh. 22 - Prob. 25PCh. 22 - Prob. 26PCh. 22 - Prob. 27PCh. 22 - Arrange the following compounds or anions in each...Ch. 22 - Prob. 29PCh. 22 - Prob. 30PCh. 22 - The compound shown is a somewhat stronger base...Ch. 22 - Prob. 32PCh. 22 - Prob. 33PCh. 22 - Prob. 34PCh. 22 - Prob. 35PCh. 22 - Prob. 36PCh. 22 - Write the structure of the product formed on...Ch. 22 - Prob. 38PCh. 22 - Prob. 39PCh. 22 - Prob. 40PCh. 22 - Prob. 41PCh. 22 - Prob. 42PCh. 22 - Prob. 43PCh. 22 - Prob. 44PCh. 22 - Devise efficient syntheses of each of the...Ch. 22 - Prob. 46PCh. 22 - Prob. 47PCh. 22 - Prob. 48PCh. 22 - Prob. 49PCh. 22 - Prob. 50PCh. 22 - Prob. 51PCh. 22 - Prob. 52PCh. 22 - Prob. 53PCh. 22 - Prob. 54PCh. 22 - Prob. 55PCh. 22 - Prob. 56DSPCh. 22 - Prob. 57DSPCh. 22 - Prob. 58DSPCh. 22 - Prob. 59DSPCh. 22 - Synthetic Applications of Enamines The formation...Ch. 22 - Prob. 61DSP
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