We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
7. How would you perform the following syntheses using eneamines and any chloro compound you want...
How
would you perform the following synthesis using enamines and any
chloro compound you want?
5. How might you use acetoacetic ester to perform the following synthesis. (10 points). 3 om s nsonbyH o nap9byi 6. Use any reagents you wish to perform the following transformation. Hint: the first step is a chem 242L experiment.(10 points) ot stohosa y uoy dr woH 7. How would you perform the following syntheses using eneamines and any chloro compound you want to use. (8 points). olen eta se s au uoy ialin wolt.
1. Predict the products of the following reactions (18 points, 3 each) Catalytic KOH methanol/water solvent Catalytic KOH methanol/water solvent Catalytic KOH methanol water solvent Catalye KOH. 1 equivalent NaOCH.CH ethanol solvent I equivalent NaOCH.CH ethanol solvent 2. Write the product of the following reaction and the full mechanism by which it is formed. Clearly show which steps are reversible and which one step is irreversible. (8 points). 1 equivalent NaOCH CH3 cthanol solvent + excess 3. Circle the most...
7. How would you perform the following chemical transformation? OH o 8. Using acetylene as one of the starting materials, show the synthesis of the following compound.
What are the following syntheses for each compound?
7. Propose a synthesis for each of the following compounds using the indicated starting material. You may use any organic compounds, inorganic compounds, organometallic compounds, or solvents of your choice. Do not show any reactive intermediates, mechanisms, or transition states, but be sure to show each isolable compound along your synthetic route. осон steps H₂C (ra (racemic) Hoc OH Hac CH3 сна N-OH steps
3. Show efficient syntheses of each of the following from the indicated compound and any need organic or inorganic reagents. (50 pts) (a) 1-popene, from 1-bromopropane (b) 1-chloro-2-butanol, 1-bromobutane (c) 2-pentyne, from propyne (d) trans-1,2-dibromocyclohexane, from cyclohexanol (e) 2,3-hexanediol, from 2-hexene
3. Show efficient syntheses of each of the following from the indicated compound and any need organic or inorganic reagents. (50 pts) (a) 1-popene, from 1-bromopropane (b) 1-chloro-2-butanol, 1-bromobutane (c) 2-pentyne, from propyne (d) trans-1,2-dibromocyclohexane, from cyclohexanol (e) 2,3-hexanediol,...
2.Show how you would perform the multistep synthesis below. You may use any reaction taught in organic 1 and 2 and any organic compound with upto five carbon atoms. 12 points H H,C OH HO C 0 . - CH₂
Show how you would use Grignard syntheses to prepare the
following alcohols from the indicated starting materials and any
other necessary reagents. Draw the Grignard reagent and any other
organic reagents needed.
11 RUVIUWI Constans i Pendulu Part F Show how you would use Grignard syntheses to prepare the following alcohols from the indicated starting materials and any other necessary reagents. Draw the Grignard reagent and any other organic reagents needed. ОН -C-CH CH, from C-OCH.CH Draw the molecules on...
8. Show how you would accomplish the following syntheses. You may use whatever additional reagents you need. The synthesis should not take more than three or four reactions. At least one of the reactions should come from the aldehydes and ketones chapter. (6 pts) a) CO2H b)
S. Show how you would prepare the following compound using an organometallic reagent. You may use any hydrocarbons, organohalides, alcohols and/or carbonyl compounds that have five of fewer carbon atoms You may also use any needed reagents and solvents OH This one as well. He quits grading when you get two mistakes. 6. Propose a synthesis of the following compound using a Wittig reaction. You may use triphenylphosphine (Ph P) and any reagents containing five carbons or less as starting...