Answer:-
Step 1, is acid-catylsed addition of water molecule across the double bond of cyclohexene to produce cyclohexanol.
Step 2, is deprotonation of cyclohexanol.
Step 3, is "Williamson Ether Synthesis". This is a SN2 reaction which involves nucleophilic attack of alkoxide ion generated in step 2, over the ethyl bromide.
------------------------------
16. Starting with cyclohexene and using any other reagents of your choice, show how you would...
Part C 20.50 Starting with benzene and using any other reagents of your choice, show how you would prepare each of the following compounds: of OH N (b) (a) HO (d) (c) I-N
Practice Problem 23.50 Starting with cyclopentene and using any other reagents of your choice, show how you would make each of the following compounds: (a) (b) (c) HO OH Choose from the following list of reagents: c b d Pd[OAC)2, PPhy, BN NaOH, H20, heat H,0NaOH (xs) CH2CH2 f g e BHy-THF (xs) CHşlyZn-Cu. Et, BCOM) h Grubbs catalyst i k - BE Be Using the reagents above, list in order (by letter, no period) those necessary to provide each...
6. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 7. Starting with benzene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there may be more than one plausible answer 8. Starting with benene and using any other necessary reagents of your choice, design a synthesis for the following compound. Note: there...
Starting with nitrobenzene and using any other reagents of your choice, outline a synthesis of para-chloroaniline Using acetic acid as your only source of carbon atoms, show how could you make N-ethylacetamide:
Starting from benzene and using any other necessary reagents of your choice, design a synthesis for each of the following compounds. Some problems have more than one plausible 1. answer (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) रेर Br (i) Н-N. Br NH2 (k) Br "SoH
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
Starting with Benzene and using any other necessary reagents of your choice a synthesis for the following compound. Assume that ortho and para isomers can be There may be more than one plausible answer.
Starting from benzene and using any other necessary reagents of your choice, design a synthesis for each of the following compounds. Some problems have more than one plausible 1 answer (a) Cl. .NO2 (b) НAN. (c) H2N (d) (e) Br СООН СООН Br (g)* in this example, what can be done to minimise the amount of the meta/para isomes. NO2 (h) Br H2N Br Cl -NH2 Cl (k) Br
Starting with benzene and using any other neccessary reagents of your choice, design a synthesis for each of the following: OMe COOH Br Br NO NO (b) COOH NH Cl Cl NO2 COOH NO2 Cl NO Cl Br OEt NO2 Cl (h) C (g) NO2 Br O2N
6) Multistep synthesis from cyclohexane Using cyclohexane as your starting material, show how you would synthesize cach of the following compounds. Once you have shown how to synthesize a compound, you may use it as the starting material in any later parts of this problem.) a) bromocyclohexane (b) cyclohexene e) ethoxycyclohexane (d) 3-bromocyclohex-l-ene (e) cyclohexa-1,3-diene (1) cyclohexanol