A hydrocarbon has the molecular formula C10H18. It has an unsaturation that is not terminal, a...
A hydrocarbon has the molecular formula C10H18. It has an unsaturation that is not terminal, a six carbon backbone, an ethyl substitution and a dimethyl substitution. Draw the structure and name the chemical.
Homework Answers
name-
4-Ethyl-5,5-dimethyl-2-hexyne
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A hydrocarbon has the molecular formula C10H18. It has an
unsaturation that is not terminal, a...
please explain 4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar...
please explain
4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in the unknown compound? b) How many triple bonds are present? c) How many double bonds are present? d) How many rings are present? e) Draw a structure that fits the data
4. An unknown hydrocarbon has...
1. For the molecular formula CHINO, please provide the degrees of unsaturation (DOU) and the structure....
1. For the molecular formula CHINO, please provide the degrees of unsaturation (DOU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 80 40 20 100...
For the molecular formula C9H11NO, please provide the degrees of unsaturation (DoU) and the structure. Draw...
For the molecular formula C9H11NO, please provide the degrees of
unsaturation (DoU) and the structure. Draw and label your proposed
structure for both your proton NMR table and the carbon NMR table.
Please provide a table for the proton NMR that includes the signal
label, chemical shift, multiplicity and the integration. For the
Carbon NMR please provide a table that includes the signal label
and the chemical shift
CNMR 200 180 160 140 120 80 60 40 100 PPM 20...
1. For the molecular formula C9H1NO, please provide the degrees of unsaturation (DoU) and the structure....
1. For the molecular formula C9H1NO, please provide the degrees of unsaturation (DoU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 100 PPM 80 60...
Define the terms hydrocarbon derivative, aliphatic hydrocarbon, unsaturation, and phenyl. What is the evidence for the...
Define the terms hydrocarbon derivative, aliphatic hydrocarbon, unsaturation, and phenyl. What is the evidence for the reaction of potassium permanganate with alkenes? With alkynes? What feature in its structural formula indicates whether a hydrocarbon is an alkane, alkene, alkyne, or aromatic compound? Draw the electronic structure for benzene, showing valence electrons. Write equations to illustrate the reaction of bromine with these organic compounds: ethane, C_2 H_6: ethylene, C_2H_4: and acetylene, C_2 H_2. Can the combustion test be used to distinguish...
Provide the molecular formula and Lewis structure, the expanded structural formula, for the hydrocarbon ball-and-stick model...
Provide the molecular formula and Lewis structure, the expanded structural formula, for the hydrocarbon ball-and-stick model shown. Be sure to include all hydrogen atoms in your Lewis structure. Click on the three-dimensional molecular structure of the compound and drag to rotate it, or use the controls provided. сон molecular formula: C,H Question 15 of 41 Draw the expanded, or complete, structural formula for the hydrocarbon represented by the line-angle, or skeletal, structure shown. Draw the complete structural formula. Include all...
Provide the molecular formula and Lewis structure, the expanded structural formula, for the hydrocarbon ball-and-stick model...
Provide the molecular formula and Lewis structure, the expanded structural formula, for the hydrocarbon ball-and-stick model shown. Be sure to include all hydrogen atoms in your Lewis structure. molecular formula: Click on the three-dimensional molecular structure of the compound and drag to rotate it, or use the controls provided. ICOH Draw the Lewis structure. Select Draw Rings More Erase
Determine the degrees of unsaturation and draw a possible structure for the following molecular formula (5...
Determine the degrees of unsaturation and draw a possible structure for the following molecular formula (5 points): 5. C16H24
Compound A has the molecular formula C10H14. a) Calculate the unsaturation number or IHD. b) Prov...
Compound A has the molecular formula C10H14.
a) Calculate the unsaturation number or IHD.
b) Provide the molecular ion observed in the mass spectrum,
including its units.
c) Propose a structure based on the carbon-13 NMR spectrum
given.
CH3 CH Compound A CDCl3 160 140 120100 80 60 40 20 0
CH3 CH Compound A CDCl3 160 140 120100 80 60 40 20 0
Using line structure, draw a hydrocarbon molecule that has: at least 5 carbons in the parent...
Using line structure, draw a hydrocarbon molecule that has: at least 5 carbons in the parent chain at least 1 carbon-carbon multiple bond at least 2 branches Write the correct molecular formula for your molecule (CxHy). Write the correct name for your molecule.
please explain
4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in the unknown compound? b) How many triple bonds are present? c) How many double bonds are present? d) How many rings are present? e) Draw a structure that fits the data
4. An unknown hydrocarbon has...
1. For the molecular formula CHINO, please provide the degrees of unsaturation (DOU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 80 40 20 100...
For the molecular formula C9H11NO, please provide the degrees of
unsaturation (DoU) and the structure. Draw and label your proposed
structure for both your proton NMR table and the carbon NMR table.
Please provide a table for the proton NMR that includes the signal
label, chemical shift, multiplicity and the integration. For the
Carbon NMR please provide a table that includes the signal label
and the chemical shift
CNMR 200 180 160 140 120 80 60 40 100 PPM 20...
1. For the molecular formula C9H1NO, please provide the degrees of unsaturation (DoU) and the structure. Draw and label your proposed structure for both your proton NMR table and the carbon NMR table. Please provide a table for the proton NMR that includes the signal label, chemical shift, multiplicity and the integration. For the Carbon NMR please provide a table that includes the signal label and the chemical shift. (10) CNMR 200 180 160 140 120 100 PPM 80 60...
Define the terms hydrocarbon derivative, aliphatic hydrocarbon, unsaturation, and phenyl. What is the evidence for the reaction of potassium permanganate with alkenes? With alkynes? What feature in its structural formula indicates whether a hydrocarbon is an alkane, alkene, alkyne, or aromatic compound? Draw the electronic structure for benzene, showing valence electrons. Write equations to illustrate the reaction of bromine with these organic compounds: ethane, C_2 H_6: ethylene, C_2H_4: and acetylene, C_2 H_2. Can the combustion test be used to distinguish...
Provide the molecular formula and Lewis structure, the expanded structural formula, for the hydrocarbon ball-and-stick model shown. Be sure to include all hydrogen atoms in your Lewis structure. Click on the three-dimensional molecular structure of the compound and drag to rotate it, or use the controls provided. сон molecular formula: C,H Question 15 of 41 Draw the expanded, or complete, structural formula for the hydrocarbon represented by the line-angle, or skeletal, structure shown. Draw the complete structural formula. Include all...
Provide the molecular formula and Lewis structure, the expanded structural formula, for the hydrocarbon ball-and-stick model shown. Be sure to include all hydrogen atoms in your Lewis structure. molecular formula: Click on the three-dimensional molecular structure of the compound and drag to rotate it, or use the controls provided. ICOH Draw the Lewis structure. Select Draw Rings More Erase
Determine the degrees of unsaturation and draw a possible structure for the following molecular formula (5 points): 5. C16H24
Compound A has the molecular formula C10H14.
a) Calculate the unsaturation number or IHD.
b) Provide the molecular ion observed in the mass spectrum,
including its units.
c) Propose a structure based on the carbon-13 NMR spectrum
given.
CH3 CH Compound A CDCl3 160 140 120100 80 60 40 20 0
CH3 CH Compound A CDCl3 160 140 120100 80 60 40 20 0
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