1)How would you synthesize the following product from the assigned reactants?
a. You have to show the shortest and most effective reaction schemes using the ONLY given compounds as carbon sources to make the product. You can use proper reagent(s) for each step.
b. Only two reactants allowed to build the carbon backbone are shown below.
c. Explain how you would confirm each step using 1H-NMR, 13C-NMR, IR, and UV-Vis spectroscopie. (no spectrums needed)
Homework Answers
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1)How would you synthesize the following product from the
assigned reactants?
a. You have to show...
4. In each reaction show how you would synthesize the product from the reactant. Show the...
4. In each reaction show how you would synthesize the product
from the reactant. Show the reagents, conditions, and the
structures of any important intermediates along the way. Any
organic reagent may be used, and more than one step may be used as
well. Include mechanism
(+-) H Br
Show how you would synthesize the following acid using carbonation of a Grignard reagent. Show how...
Show how you would synthesize the following acid using carbonation of a Grignard reagent. Show how you would synthesize the following acid using carbonation of a Grignard reagent.
Show how you would synthesize the following 3- amine in good yield using alcohols of carbons...
Show how you would synthesize the following 3- amine in good yield
using alcohols of carbons 4 or less as your only source of carbon
CH3 、CH3
Show how you would synthesize the following compounds from 1-methylene cyclopentane Q3. (i) Show how you...
Show how you would synthesize the following compounds
from 1-methylene cyclopentane
Q3. (i) Show how you would synthesize the following compounds from (Note; More than one step may be required) (8) - CH2 a). - NAPH NHPh
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps an...
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps and reagents, you do not need to show mechanisms. You must use 1-butene as your ONLY source of carbon atoms. The convergent processes have been outlined for you. for STEP 1: Show how to synthesize butyl magnesium bromide from 1-butene (5 points): BrMg STEP 2: Show how to synthesize 2-butanone from 1-butene (5 points): STEP 3: What intermediate forms below and what reagent(s) will...
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any...
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any necessary additional reagents. More than one step is needed. Br Bromobenzene, 1-Butene < Show how you woull Synthesize 4.- Nonanone, begining with 1-Butanol and any other non-organic reagents. (1-Butanol is the only Organic compouno available). only organ n
pls help 1. Your supervisor asks you to make the indicated product from the designated starting...
pls help
1. Your supervisor asks you to make the indicated product from the designated starting material. Provide a synthesis and describe how you would monitor each step using IR and NMR spectroscopy. (4 pts) он mgbr CH3 CH3 H -Br 2. Predict what the proton NMR spectrum of the two molecules below would look like by indicating the chemical shift and splitting of each peak. (4 pts) a sextet , ~ 14
1. 2. Show how you would synthesize benzylamine from each of these compounds, using the following...
1.
2.
Show how you would synthesize benzylamine from each of these compounds, using the following available reagents More than one step may be required. Enter the letters of the reagents necessary, in the order that they are to be used. Do not separate the reagents with punctuation. OH CI Reagents Available (a) NH3 (b) excess NH3 (c) H*, A (d) SOCl2 (e) N3 (f) H2, Pd/C (g) LiAlH4 then H20 (h) NaOH (i) CO, H2, heat and pressure Previous...
7. Suggest how you would synthesize the compound X shown below. Make sure that compound X...
7. Suggest how you would synthesize the compound X shown below. Make sure that compound X is the ONLY product possible! Question 7 and 8 Hint (Remember for the exam!): To answer this question, you simply need to provide the structures of the organic substrate and a reagent (in this specific case, an alkyl halide and a base or a nucleophilie and electrophile) that can be used to obtain the product X shown by using a correctly designed reaction (an...
9- Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary ad...
9- Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents. More than one step is needed. 8 Br OH Bromobenzene, 1-Butene Show hew you weulel Syntfesige 4-Nonanone, begining witA 1-Butanol and any other non- oraanie reagents.(1-Butanol is the only Organic compeonn availabe)
4. In each reaction show how you would synthesize the product
from the reactant. Show the reagents, conditions, and the
structures of any important intermediates along the way. Any
organic reagent may be used, and more than one step may be used as
well. Include mechanism
(+-) H Br
Show how you would synthesize the following acid using carbonation of a Grignard reagent. Show how you would synthesize the following acid using carbonation of a Grignard reagent.
Show how you would synthesize the following 3- amine in good yield
using alcohols of carbons 4 or less as your only source of carbon
CH3 、CH3
Show how you would synthesize the following compounds
from 1-methylene cyclopentane
Q3. (i) Show how you would synthesize the following compounds from (Note; More than one step may be required) (8) - CH2 a). - NAPH NHPh
4. Propose a synthesis to create 3,4-dimethyl-3-hexanol from 1-butene. You only need to show individual steps and reagents, you do not need to show mechanisms. You must use 1-butene as your ONLY source of carbon atoms. The convergent processes have been outlined for you. for STEP 1: Show how to synthesize butyl magnesium bromide from 1-butene (5 points): BrMg STEP 2: Show how to synthesize 2-butanone from 1-butene (5 points): STEP 3: What intermediate forms below and what reagent(s) will...
Show how you would synthesize the following a n d beginning with 1-butene, Bromma and any necessary additional reagents. More than one step is needed. Br Bromobenzene, 1-Butene < Show how you woull Synthesize 4.- Nonanone, begining with 1-Butanol and any other non-organic reagents. (1-Butanol is the only Organic compouno available). only organ n
pls help
1. Your supervisor asks you to make the indicated product from the designated starting material. Provide a synthesis and describe how you would monitor each step using IR and NMR spectroscopy. (4 pts) он mgbr CH3 CH3 H -Br 2. Predict what the proton NMR spectrum of the two molecules below would look like by indicating the chemical shift and splitting of each peak. (4 pts) a sextet , ~ 14
1.
2.
Show how you would synthesize benzylamine from each of these compounds, using the following available reagents More than one step may be required. Enter the letters of the reagents necessary, in the order that they are to be used. Do not separate the reagents with punctuation. OH CI Reagents Available (a) NH3 (b) excess NH3 (c) H*, A (d) SOCl2 (e) N3 (f) H2, Pd/C (g) LiAlH4 then H20 (h) NaOH (i) CO, H2, heat and pressure Previous...
7. Suggest how you would synthesize the compound X shown below. Make sure that compound X is the ONLY product possible! Question 7 and 8 Hint (Remember for the exam!): To answer this question, you simply need to provide the structures of the organic substrate and a reagent (in this specific case, an alkyl halide and a base or a nucleophilie and electrophile) that can be used to obtain the product X shown by using a correctly designed reaction (an...
9- Show how you would synthesize the following compound, beginning with 1-butene, Bromobenzene and any necessary additional reagents. More than one step is needed. 8 Br OH Bromobenzene, 1-Butene Show hew you weulel Syntfesige 4-Nonanone, begining witA 1-Butanol and any other non- oraanie reagents.(1-Butanol is the only Organic compeonn availabe)
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