ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
10th Edition
ISBN: 9781260028355
Author: Carey
Publisher: MCG CUSTOM
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Question
Chapter 23, Problem 19P
Interpretation Introduction
Interpretation: The structure of phenacetin is to be drawn.
Concept introduction:
Phenols contain hydroxyl
Phenol is acidic in nature and in the presence of a strong base such as sodium hydroxide, the formation of phenoxide ion occurs after the abstraction of proton by hydroxide ion. The phenoxide ion acts as a nucleophile.
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34. Figure 3 shows Van Deemter plots for a solute molecule using different column inner diameters (i.d.).
A) Predict whether decreasing the column inner diameters increase or decrease bandwidth.
B) Predict which van Deemter equation coefficient (A, B, or C) has the greatest effect on increasing or
decreasing bandwidth as a function of i.d. and justify your answer.
Figure 3 Van Deemter plots for hydroquinone using different column inner diameters (i.d. in μm). The data was
obtained from liquid chromatography experiments using fused-silica capillary columns packed with 1.0-μm particles.
35
20
H(um)
큰 20
15
90
0+
1500
100
75
550
01
02
594
05
μ(cm/sec)
30
15
10
elow are
experimentally determined van Deemter plots of column efficiency, H, vs. flow rate. H is a
quantitative measurement of band broadening. The left plot is for a liquid chromatography application and the
night is for gas chromatography. Compare and contrast these two plots in terms of the three band broadening
mechanisms presented in this activity. How are they similar? How do they differ? Justify your answers.?
0.4
H (mm)
0.2
0.1-
0.3-
0
0.5
H (mm)
8.0
7.0
6.0
5.0
4.0-
3.0
T
+++
1.0
1.5
0
2.0
4.0
Flow Rate, u (cm/s)
6.0
8.0
Flow Rate, u (cm/s)
Predict the products of this organic reaction:
+
H
ZH
NaBH3CN
H+
n.
?
Click and drag to start drawing a
structure.
X
Chapter 23 Solutions
ORGANIC CHEMISTRY-PACKAGE >CUSTOM<
Ch. 23.1 - Prob. 1PCh. 23.3 - Problem 23.2 One of the hydroxybenzoic acids is...Ch. 23.4 - Prob. 3PCh. 23.5 - Prob. 4PCh. 23.6 - Problem 23.5 The compound shown was required for...Ch. 23.8 - Prob. 6PCh. 23.8 - Prob. 7PCh. 23.9 - Prob. 8PCh. 23.9 - Prob. 9PCh. 23.10 - Prob. 10P
Ch. 23.12 - Prob. 11PCh. 23 - The IUPAC rules permit the use of common names for...Ch. 23 - Prob. 13PCh. 23 - Prob. 14PCh. 23 - Prob. 15PCh. 23 - Prob. 16PCh. 23 - Prob. 17PCh. 23 - Prob. 18PCh. 23 - Prob. 19PCh. 23 - Prob. 20PCh. 23 - Prob. 21PCh. 23 - Prob. 22PCh. 23 - Prob. 23PCh. 23 - Prob. 24PCh. 23 - Prob. 25PCh. 23 - Prob. 26PCh. 23 - Choose the reaction in each of the following pairs...Ch. 23 - Pentafluorophenol is readily prepared by heating...Ch. 23 - Prob. 29PCh. 23 - Treatment of p-hydroxybenzoic acid with aqueous...Ch. 23 - Prob. 31PCh. 23 - Prob. 32PCh. 23 - Treatment of 2,4,6-tri-tert-butylphenol with...Ch. 23 - Prob. 34PCh. 23 - Prob. 35PCh. 23 - Prob. 36DSPCh. 23 - Prob. 37DSPCh. 23 - Prob. 38DSPCh. 23 - Prob. 39DSP
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