Show how you would synthesize the following compounds from 1-methylene cyclopentane
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Show how you would synthesize the following compounds from 1-methylene cyclopentane Q3. (i) Show how you...
steps invol CH2 unds from OL. ) Show how you would synthesize the followine compounds to (Note: More than one step may be required) (8) M – NHP N D raw the structure of the product (12) 1. DIBAL-H a). CH3CH2CN 2. H+/H20 1. CH3MgBI b). CH3CH2CN 2. H+/H20 1.(CH),Culi c). CH3-C 2. H+/H20 1. Liſt BuO), AIH d). CH3-CC 2. H+ / H20
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...
Show how you would synthesize the following compound starting
with acetylene and compounds containing no more than two carbon
atoms as organic starting material. You may use any additional
reagents you need
Br H H Br
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
sbow how you woukd synthesize each of the following compounds from
benzene
(a) Show how you would synthesize each of the following compounds from benzene. Br (b) (c) (d) NHA Br. Br. (e) HN NH2
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
* NH Show how you would synthesize the following compounds from toluene. OH OOH Br NBS
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)
o - and to make Use
02. Synthesize the following product from the given starting compounds. This will require more than one step. You may use any organic or inorganic reagent to carry out this synthesis. (8 pts each) (you can also use any one C reagent)
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)