1. Draw the chemical structure of each target compound, amitriptlyline, chlorpheniramine, doxepin, chlorpromazine and papaverine. What...
1. Draw the chemical structure of each target compound, amitriptlyline, chlorpheniramine, doxepin, chlorpromazine and papaverine. What functional groups make these compounds basic in nature?
Homework Answers
The functional group in the
dotted red circle of the molecule is the reason for their basic
nature.
Add Answer to:
1. Draw the chemical structure of each target compound,
amitriptlyline, chlorpheniramine, doxepin, chlorpromazine and
papaverine. What...
1. For the following: Draw at least the MAJOR (most stable) resonance structure of each compound....
1. For the following: Draw at least the MAJOR (most stable) resonance structure of each compound. Fill in nonbonding electrons and make sure you can perfectly draw the bond-line structure of each functional group shown (nitro, aldehyde, etc) CO2Me C0 Meo CN NCCO2Me
1H-NMR: interpret the spectrum detailing chemical shifts and splittings. draw the structure of the compound and label t...
1H-NMR: interpret the spectrum detailing chemical shifts and
splittings. draw the structure of the compound and label the
hydrogens for the signals.
13C-NMR: draw the structure of the compound and label the
carbons for the signals.
IR: draw the structure of the compound and label functional
groups that are responsible for the stretches.
100 7 90 80 70 60 20 10 0 -10 2500 Wavenumbers (cm-1) 1000 4000 3500 3000 1500 2000 %Transmittance 3075.91 2937.08 2805.05 2736.70 1593.81 1575.40 1508.95...
For this assignment, the target compound that you should synthesize is 2,4,4-trimethyl-1- phenylpent-1-en-3-one. Draw the structure...
For this assignment, the target compound that you should synthesize is 2,4,4-trimethyl-1- phenylpent-1-en-3-one. Draw the structure of the target compound and retro-synthesize it. Choose the correct starting materials from chalkboard. Write the chemical equation and depict the mechanism and give the structure of all intermediates. Report the exact time needed for completing of this reaction and state the temperature. This product is a solid product. Recrystallize it and obtain its melting point. 4. Obtain H-NMR spectrum of your final product....
1. Draw the chemical structure of caffeine, diclofenac, amitriptyline and papaverine. 2. Describe the mechanism of...
1. Draw the chemical structure of caffeine, diclofenac, amitriptyline and papaverine. 2. Describe the mechanism of a mixed mode reversed phase and cation exchange SPE cartridge. 3. Describe the general layout of a UV/VIS spectrophometer.
1. For this assignment, the target compound that you should synthesize is 2,4,4-trimethyl-1- phenylpent-1-en-3-one. Draw the...
1. For this assignment, the target compound that you should synthesize is 2,4,4-trimethyl-1- phenylpent-1-en-3-one. Draw the structure of the target compound and retro-synthesize it. Write the chemical equation and depict the mechanism and give the structure of all intermediates.
2. Draw structural formulas of the following compounds. Circle and idet are present in each compound....
2. Draw structural formulas of the following compounds. Circle and idet are present in each compound. llowing compounds. Circle and identify the functional groups that a. Aspirin b. Ibuprofen c. Acetaminophen d. Caffeine 11-1
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate...
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate was formed. 2. Draw and compare the structures of acetylsalicylic acid and methyl salicylate. Circle and name the functional groups in both compounds. 3. The fragrance of apricots is due to the ester pentyl butanoate. Write the equation for the synthesis of this ester from the acid and the alcohol. 4. Give examples and names of any other compounds that contain the functional groups...
C5H1002 7. Draw the structure of the compound that correlates with this NMR. The chemical formula...
C5H1002 7. Draw the structure of the compound that correlates with this NMR. The chemical formula is given. Annotate the spectrum as we did in class, using the a, b, c scheme. O PPM 8. Tell me two IR peaks you know must be present for this compound. Draw the chemical bond and give me the approximate cm-1 value for each peak.
1. For this assignment, the target compound that you should synthesize is 2-ethyl-hex-2-enal. Draw the structure...
1. For this assignment, the target compound that you should synthesize is 2-ethyl-hex-2-enal. Draw the structure of the target compound and retro-synthesize it.
1) For the ester below, draw the structure of the two compounds needed to make the...
1) For the ester below, draw
the structure of the two compounds needed to make the ester and
give the IUPAC name for each.
2) Draw the product/s of the basic hydrolysis of the above
ester.
1. For the ester below, draw the structure of the two compounds needed to make the ester and give the IUPAC name for each ? ? + ? - wid + ? 2. Draw the product/s of the basic hydrolysis of the above ester.
1. For the following: Draw at least the MAJOR (most stable) resonance structure of each compound. Fill in nonbonding electrons and make sure you can perfectly draw the bond-line structure of each functional group shown (nitro, aldehyde, etc) CO2Me C0 Meo CN NCCO2Me
1H-NMR: interpret the spectrum detailing chemical shifts and
splittings. draw the structure of the compound and label the
hydrogens for the signals.
13C-NMR: draw the structure of the compound and label the
carbons for the signals.
IR: draw the structure of the compound and label functional
groups that are responsible for the stretches.
100 7 90 80 70 60 20 10 0 -10 2500 Wavenumbers (cm-1) 1000 4000 3500 3000 1500 2000 %Transmittance 3075.91 2937.08 2805.05 2736.70 1593.81 1575.40 1508.95...
For this assignment, the target compound that you should synthesize is 2,4,4-trimethyl-1- phenylpent-1-en-3-one. Draw the structure of the target compound and retro-synthesize it. Choose the correct starting materials from chalkboard. Write the chemical equation and depict the mechanism and give the structure of all intermediates. Report the exact time needed for completing of this reaction and state the temperature. This product is a solid product. Recrystallize it and obtain its melting point. 4. Obtain H-NMR spectrum of your final product....
1. For this assignment, the target compound that you should synthesize is 2,4,4-trimethyl-1- phenylpent-1-en-3-one. Draw the structure of the target compound and retro-synthesize it. Write the chemical equation and depict the mechanism and give the structure of all intermediates.
2. Draw structural formulas of the following compounds. Circle and idet are present in each compound. llowing compounds. Circle and identify the functional groups that a. Aspirin b. Ibuprofen c. Acetaminophen d. Caffeine 11-1
Questions 1. Draw the structure of methyl salicylate, and say what evidence indicates that methyl salicylate was formed. 2. Draw and compare the structures of acetylsalicylic acid and methyl salicylate. Circle and name the functional groups in both compounds. 3. The fragrance of apricots is due to the ester pentyl butanoate. Write the equation for the synthesis of this ester from the acid and the alcohol. 4. Give examples and names of any other compounds that contain the functional groups...
C5H1002 7. Draw the structure of the compound that correlates with this NMR. The chemical formula is given. Annotate the spectrum as we did in class, using the a, b, c scheme. O PPM 8. Tell me two IR peaks you know must be present for this compound. Draw the chemical bond and give me the approximate cm-1 value for each peak.
1. For this assignment, the target compound that you should synthesize is 2-ethyl-hex-2-enal. Draw the structure of the target compound and retro-synthesize it.
1) For the ester below, draw
the structure of the two compounds needed to make the ester and
give the IUPAC name for each.
2) Draw the product/s of the basic hydrolysis of the above
ester.
1. For the ester below, draw the structure of the two compounds needed to make the ester and give the IUPAC name for each ? ? + ? - wid + ? 2. Draw the product/s of the basic hydrolysis of the above ester.
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