6. How could the following compounds be prepared, using an alkene as one of the starting...
Show how each of the following compounds could be prepared using
the given starting materials. Please Explain
#Show how each of the following compounds could be prepared using the given starting materials, @ HCECH → M © HECH -Y © HC ECH - > D = sehr HCECH (35,4R)-4-bromo-3-hexanol and (30,45) -4- bromo-3-hexand
wing 6 Show how the following compounds could be prepared from the given starting materials. You can use any necessary organic or inorganic reagents. NHCH -NH; CH OH OH ible or an inyersible reaction? Explain.
Q 1. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. Available starting materials (source of carbon) a) .CO2Et CO2Et Ph Br CO2 or NaCN EtOH Ph CO2Et
b. How will you synthesize the following compounds starting from an alkene? Draw the structure of the alkene and the reagent(s) used for the synthesis. Он CH3CCH2CH2CH2CH3 CHз a. CH3 CH3CH2CHCHCH2CH3 он b. Он CH3CHCH2 C. Br 7. Draw one possible structure for the following. a. A hydrocarbon with formula CeH16, on hydrogenation, reacted with 1 molar equivalence of Hz2 (g) in presence of Pd catalyst. Draw any one possible structure. b. A hydrocarbon with formula CeH 12, on hydrogenation,...
Q 2. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) H CH3NO2 Available starting materials (source of carbon)
Organic Chem 142-01 2015 Dec 10 Name 6.Synthesis. Show how any THREE of the following compounds could be prepared, starting with benzene, toluene, cyclohexanol, or diethyl malonate, and any other necessary reagents. era mixture will give only the paroisomer) 18 points each CHO NHAc CO H оме Br NO2 7 of 9 Organic Chem 142-01 Name 2015 Dec 10 7. Write out THREE of the following reaction mechanisms. [10 points each] (a) Conversion of cyclopentanone to the oxime N-OH HCI...
Q 3. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. a) Available starting materials (source of carbon) CO2Et OH OPMB TM BrCH2COOEt OH OH p-methoxybenzaldehyde
Q 2. Show how each of the following compounds can be prepared from the given starting materials using retrosynthetic analysis approach. O CO2Et *CO2Et Н
Using the specified starting material and any other reagents,
show how each of the following compounds can be
prepared:
a) CH3-CH2-CH2-OH ---------> H3C-CC-H
B)CHCH------>
CH3-CH3-C-(Cl)2-CH3
c) HCCH -------->
CH2-CH2-CH(Br)-CH3
Show how each of the following compounds can be synthesized
from an alkene please help with b-f
PROBLEM 58 Show how each of the followin f the following compounds cam be synthesized from an akend lowing compounds can be synthesized from an alkene: g compounds can CH20H CH Br C. e. e. a. CHyCHOCH CH3 Br CH3 OCH3 Br