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An unknown, non-branched saturated hydrocarbon has the mass spectrum below. What is the structure of the unknown hy...
An unknown, non-branched saturated hydrocarbon has the mass spectrum below. What is the structure of the...
An unknown, non-branched saturated hydrocarbon has the mass spectrum below. What is the structure of the unknown hydrocarbon? 100 1127 141 156 169 183 197 211 225 241 OLL 20 40 254 ihrer 80 100 120 140 160 180 200 220 240 60
2. . An unknown, non-branched saturated hydrocarbon has the mass spectrum s below. What is the...
2. . An unknown, non-branched saturated hydrocarbon has the mass spectrum s below. What is the structure of the unknown hydrocarbon? 100) 3. "19 127 141 158 189 188 107 211 225 241 20 40 60 80 100 120 140 160 180 200 220 240 An unknown compound with formula C H100, RVO negative tent with 2.4 dinitrophenylhydrazine; however, the unknown tested positive with the Jones reagent. When added to a solution of bromine dissolved in methylene, the reddin solution...
An unknown compound with formula CaHo0, gave a negative test with dinitrophenylhy drazine; however, the unknown...
An unknown compound with formula CaHo0, gave a negative test with dinitrophenylhy drazine; however, the unknown tested positive with the Jones reagent. When added to a solution of bromine dissolved in methylene, the reddi solution turned colorless. The mass spectrum of the compound is shown below. 3. 100 92 134 77 105 50 115 51 55 63 39 31 43 80 50 100 110 120 130 60 40 90 30 a. What is the structure of the unknown. b.What is...
The **C NMR and mass spectrum of an unknown compound is shown below. The unknown gave...
The **C NMR and mass spectrum of an unknown compound is shown below. The unknown gave an immediate precipitate when treated with 2,4- dinitrophenylhydrazine. When treated with the iodoform reagent, the unknown gara yellow precipitate. a. What is the structure of the unknown? What is the structure of the yellow precipitate that resulted when the compo was treated with the iodoform reagent? ita wi o mo 40 50 60 ther than ito 70 80 90 100 110 120 130 140...
4. Determine the structure of an unknown compound whose mass, IR, and 'H-NMR spectra are shown...
4. Determine the structure of an unknown compound whose mass, IR, and 'H-NMR spectra are shown below.. MS 100 43 71 Structure of the unknown compound 50 114 0 40 60 80 100 120 m/z IR H-NMR δ (ppm) 0
Student XXX-XX unknown liquid compound bumed with a sooty flame. The unknown gave an orange precipit...
Student XXX-XX unknown liquid compound bumed with a sooty flame. The unknown gave an orange precipit with 2,4-dinitrophenylhydrazine, and nega positive iodoform test. The infrared spectrum of the compound revealed a strong absorption near 1700 cm. The mass spectrum of the compound is shown below. What is the name and structure of this unknown compound, and what is the nature of the strong absorption near 1700 em? tive Schiff's and Tollens tests. The uaknown also gave a 100 50 120...
I am not understanding this assignment at all. Any assistance is very much appreciated. Mass Spectrum: Molecular Ion m/z value and structure of the Molecular Ion. Base Peak m/z value and structure of...
I am not understanding this assignment at all. Any assistance is
very much appreciated.
Mass Spectrum:
Molecular Ion m/z value and structure of the Molecular Ion.
Base Peak m/z value and structure of that ion
One other significant peak m/z value and structure of that
ion
C13 NMR Spectrum-- Draw Structure of Compound
on the C13 NMR spectrum and identify each signal with the
appropriate Carbon.
Proton NMR Spectrum-- Draw Structure of
Compound on the Proton NMR spectrum and identify...
The mass spectrum of 2,6-dimethylheptan-4-ol is shown in appendix A. a) Draw the structure of this...
The mass spectrum of 2,6-dimethylheptan-4-ol is shown in appendix A. a) Draw the structure of this compound. b) Propose structures for the fragments at m/z 87, 111 and 126. 100 80 60 abundance 40 87 20 111 126 0 10 III 100'110' 120' 130 140 150 160 20 30 40 50 60 70 80 90 m/z.
What is the structure of this compound? MASS SPECTRUM 100 Relative Intensities m/z 103-100% m/z 197-190...
What is the structure of this compound?
MASS SPECTRUM 100 Relative Intensities m/z 103-100% m/z 197-190 m/z 198-less than 1% 80 60 40 20 197 0.0t l.1 0.0 40 80 120 160 200 m/z H NMR spectrum, CDCls, 600 MHz 3.75 3.703 3.60 34 3.3 Chemical Shft (ppm) 3.65 3.55 Chemical Shft (ppm) 70 4.65 4.60 Chemical Shift (ppm) 1.26 1.24 122 120 1.18 1.16 Chemical Shift (ppm) 4.8 4.6 4.4.2 4.0 3.8 3.6 34 3.2 3.0 2.826 24 22...
Compound B only contains carbon, hydrogen and a halogen. Its mass spectrum is reproduced below. Draw...
Compound B only contains carbon, hydrogen and a halogen. Its mass spectrum is reproduced below. Draw the structure of this compound 100 60 compuesto B 80 60 40 62 20 0 40 80 120 140 160 100 -60 -20
An unknown, non-branched saturated hydrocarbon has the mass spectrum below. What is the structure of the unknown hydrocarbon? 100 1127 141 156 169 183 197 211 225 241 OLL 20 40 254 ihrer 80 100 120 140 160 180 200 220 240 60
2. . An unknown, non-branched saturated hydrocarbon has the mass spectrum s below. What is the structure of the unknown hydrocarbon? 100) 3. "19 127 141 158 189 188 107 211 225 241 20 40 60 80 100 120 140 160 180 200 220 240 An unknown compound with formula C H100, RVO negative tent with 2.4 dinitrophenylhydrazine; however, the unknown tested positive with the Jones reagent. When added to a solution of bromine dissolved in methylene, the reddin solution...
An unknown compound with formula CaHo0, gave a negative test with dinitrophenylhy drazine; however, the unknown tested positive with the Jones reagent. When added to a solution of bromine dissolved in methylene, the reddi solution turned colorless. The mass spectrum of the compound is shown below. 3. 100 92 134 77 105 50 115 51 55 63 39 31 43 80 50 100 110 120 130 60 40 90 30 a. What is the structure of the unknown. b.What is...
The **C NMR and mass spectrum of an unknown compound is shown below. The unknown gave an immediate precipitate when treated with 2,4- dinitrophenylhydrazine. When treated with the iodoform reagent, the unknown gara yellow precipitate. a. What is the structure of the unknown? What is the structure of the yellow precipitate that resulted when the compo was treated with the iodoform reagent? ita wi o mo 40 50 60 ther than ito 70 80 90 100 110 120 130 140...
4. Determine the structure of an unknown compound whose mass, IR, and 'H-NMR spectra are shown below.. MS 100 43 71 Structure of the unknown compound 50 114 0 40 60 80 100 120 m/z IR H-NMR δ (ppm) 0
Student XXX-XX unknown liquid compound bumed with a sooty flame. The unknown gave an orange precipit with 2,4-dinitrophenylhydrazine, and nega positive iodoform test. The infrared spectrum of the compound revealed a strong absorption near 1700 cm. The mass spectrum of the compound is shown below. What is the name and structure of this unknown compound, and what is the nature of the strong absorption near 1700 em? tive Schiff's and Tollens tests. The uaknown also gave a 100 50 120...
I am not understanding this assignment at all. Any assistance is
very much appreciated.
Mass Spectrum:
Molecular Ion m/z value and structure of the Molecular Ion.
Base Peak m/z value and structure of that ion
One other significant peak m/z value and structure of that
ion
C13 NMR Spectrum-- Draw Structure of Compound
on the C13 NMR spectrum and identify each signal with the
appropriate Carbon.
Proton NMR Spectrum-- Draw Structure of
Compound on the Proton NMR spectrum and identify...
The mass spectrum of 2,6-dimethylheptan-4-ol is shown in appendix A. a) Draw the structure of this compound. b) Propose structures for the fragments at m/z 87, 111 and 126. 100 80 60 abundance 40 87 20 111 126 0 10 III 100'110' 120' 130 140 150 160 20 30 40 50 60 70 80 90 m/z.
What is the structure of this compound?
MASS SPECTRUM 100 Relative Intensities m/z 103-100% m/z 197-190 m/z 198-less than 1% 80 60 40 20 197 0.0t l.1 0.0 40 80 120 160 200 m/z H NMR spectrum, CDCls, 600 MHz 3.75 3.703 3.60 34 3.3 Chemical Shft (ppm) 3.65 3.55 Chemical Shft (ppm) 70 4.65 4.60 Chemical Shift (ppm) 1.26 1.24 122 120 1.18 1.16 Chemical Shift (ppm) 4.8 4.6 4.4.2 4.0 3.8 3.6 34 3.2 3.0 2.826 24 22...
Compound B only contains carbon, hydrogen and a halogen. Its mass spectrum is reproduced below. Draw the structure of this compound 100 60 compuesto B 80 60 40 62 20 0 40 80 120 140 160 100 -60 -20
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Please help me with FLOWCHART and UML diagram for class,
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