(a) Interpretation: The products formed by the treatment of CH 3 CH 2 CH 2 CH 2 OTs with the given reagent are to be drawn. Concept introduction: The strong nucleophile, and 1 ° alkyl tosylate both favors an S N 2 mechanism. The S N 2 mechanism proceeds through backside attack, and results a substitution product.
(a) Interpretation: The products formed by the treatment of CH 3 CH 2 CH 2 CH 2 OTs with the given reagent are to be drawn. Concept introduction: The strong nucleophile, and 1 ° alkyl tosylate both favors an S N 2 mechanism. The S N 2 mechanism proceeds through backside attack, and results a substitution product.
Solution Summary: The author explains that the products formed by the treatment of CH_Text3
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product.
Interpretation Introduction
(b)
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product.
Interpretation Introduction
(c)
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product.
Interpretation Introduction
(d)
Interpretation: The products formed by the treatment of CH3CH2CH2CH2OTs with the given reagent are to be drawn.
Concept introduction: The strong nucleophile, and 1° alkyl tosylate both favors an SN2 mechanism. The SN2 mechanism proceeds through backside attack, and results a substitution product. However, with strong nucleophilic bulky bases reaction proceeds through an E2 mechanism and yield elimination products.
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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