(a) Interpretation: The products of the dehydration reaction between the given alcohol and TsOH are to be drawn and the major product is to be labeled if the reaction results a mixture. Concept introduction: Alcohols undergo dehydration reaction in the presence of strong acids like H 2 SO 4 or p-toluenesulfonic acid ( TsOH ) and yield alkenes . The more substituted alcohols dehydrate rapidly. If an alcohol contains two or more β carbon, then dehydration is regioselective and the major product is determined by Zaitsev rule. According to this rule, the major product is more substituted alkene, when an alcohol contains two or more β carbons.
(a) Interpretation: The products of the dehydration reaction between the given alcohol and TsOH are to be drawn and the major product is to be labeled if the reaction results a mixture. Concept introduction: Alcohols undergo dehydration reaction in the presence of strong acids like H 2 SO 4 or p-toluenesulfonic acid ( TsOH ) and yield alkenes . The more substituted alcohols dehydrate rapidly. If an alcohol contains two or more β carbon, then dehydration is regioselective and the major product is determined by Zaitsev rule. According to this rule, the major product is more substituted alkene, when an alcohol contains two or more β carbons.
Solution Summary: The author explains that the products of the dehydration reaction between the given alcohol and TsOH are to be drawn.
Study of body parts and their functions. In this combined field of study, anatomy refers to studying the body structure of organisms, whereas physiology refers to their function.
Chapter 9, Problem 9.13P
Interpretation Introduction
(a)
Interpretation: The products of the dehydration reaction between the given alcohol and TsOH are to be drawn and the major product is to be labeled if the reaction results a mixture.
Concept introduction: Alcohols undergo dehydration reaction in the presence of strong acids like H2SO4 or p-toluenesulfonicacid(TsOH) and yield alkenes. The more substituted alcohols dehydrate rapidly. If an alcohol contains two or more β carbon, then dehydration is regioselective and the major product is determined by Zaitsev rule. According to this rule, the major product is more substituted alkene, when an alcohol contains two or more β carbons.
Interpretation Introduction
(b)
Interpretation: The products of the dehydration reaction between the given alcohol and TsOH are to be drawn and the major product is to be labeled if the reaction results a mixture.
Concept introduction: Alcohols undergo dehydration reaction in the presence of strong acids like H2SO4 or p-toluenesulfonicacid(TsOH) and yield alkenes. The more substituted alcohols dehydrate rapidly. If an alcohol contains two or more β carbon, then dehydration is regioselective and the major product is determined by Zaitsev rule. According to this rule, the major product is more substituted alkene, when an alcohol contains two or more β carbons.
Interpretation Introduction
(c)
Interpretation: The products of the dehydration reaction between the given alcohol and TsOH are to be drawn and the major product is to be labeled if the reaction results a mixture.
Concept introduction: Alcohols undergo dehydration reaction in the presence of strong acids like H2SO4 or p-toluenesulfonicacid(TsOH) and yield alkenes. The more substituted alcohols dehydrate rapidly. If an alcohol contains two or more β carbon, then dehydration is regioselective and the major product is determined by Zaitsev rule. According to this rule, the major product is more substituted alkene, when an alcohol contains two or more β carbons.
2H2S(g)+3O2(g)→2SO2(g)+2H2O(g)
A 1.2mol sample of H2S(g) is combined with excess O2(g), and the reaction goes to completion.
Question
Which of the following predicts the theoretical yield of SO2(g) from the reaction?
Responses
1.2 g
Answer A: 1.2 grams
A
41 g
Answer B: 41 grams
B
77 g
Answer C: 77 grams
C
154 g
Answer D: 154 grams
D
Part VII. Below are the 'HNMR, 13 C-NMR, COSY 2D- NMR, and HSQC 2D-NMR (similar with HETCOR but axes are reversed) spectra of an
organic compound with molecular formula C6H1003 - Assign chemical shift values to the H and c atoms of the
compound. Find the structure. Show complete solutions.
Predicted 1H NMR Spectrum
4.7 4.6 4.5 4.4 4.3 4.2 4.1 4.0 3.9 3.8 3.7 3.6 3.5 3.4 3.3 3.2 3.1 3.0 2.9 2.8 2.7 2.6 2.5 2.4 2.3 2.2 2.1 2.0 1.9 1.8 1.7 1.6 1.5 1.4 1.3 1.2 1.1
f1 (ppm)
Predicted 13C NMR Spectrum
100
f1 (ppm)
30
220 210 200 190 180
170
160 150 140 130 120
110
90
80
70
-26
60
50
40
46
30
20
115
10
1.0 0.9 0.8
0
-10
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