show how the following compound can be synthesized from Benzene (may require 2-3 steps) c) c)...
5. Show how the following compound can be synthesized from Benzene (may require 2-3 steps) 5. Determine the order of reagents to transform benzene to the product shown. 02.0 Choose one: A. CH.COCI, AICI; LiAlH; CH.CH.COCI, AICI. B. CH.COCI, AICI; HCI, Zn(Hg); CH.CHCOCI, AICI: C. CH.CH CI, AICI; CH.CH.COCI, AICI D. CH CH.COCI, AICI: CH.COCI, AICI: HCI, Zn(Hg) E. CH.CH.COCI, AICI; CH.CH CI, AICI: 6. Determine the product for each step in the following synthetic sequence: HNO, H2SO4 Step 1...
This compound was synthesized from benzene by the scheme outlined. This compound was synthesized from benzene by the scheme outlined. CH_3CI, AICI_3 CH_3COCI, AICI_3 HNO_3, H_2SO_4 Draw the structure of the product that results from step 1 of the scheme.
Complete the equations to show how the following compound can be synthesized from cyclopentanol. C Hs Part 1 out of 5 oxidize OH 2, diethyl ether [2] H, draw structure ... draw structure ...
Tetracaine can be synthesized from benzene. The synthesis involves the following steps: Benzene + CH3Cl, AlCl3 to form product A; A + HNO3, H2SO4 to form product B; B + KMnO4, H2O to form product C; C + SOCl2 to form product D; D + HOCH2CH2N(CH3)2 to form product E; E + H2, Pt to form product F; F + CH3CH2CH2CHO to form product G; G + NaBH3CN to form Tetracaine. Draw the structures of product C and product F.
Tetracaine can be synthesized from benzene. The synthesis involves the following steps: Benzene + CH3Cl, AlCl3 to form product A; A + HNO3, H2SO4 to form product B; B + KMnO4, H2O to form product C; C + SOCl2 to form product D; D + HOCH2CH2N(CH3)2 to form product E; E + H2, Pt to form product F; F + CH3CH2CH2CHO to form product G; G + NaBH3CN to form Tetracaine. Draw the structures of product A and product G.
Show how you can synthesize the compound from a benzene Show how you can synthesize the compound from benerene COOH - Br NH2
3) Show how the following molecules can be synthesized from the starting material indicated. Draw the structure of each intermediary compound in your synthesis, and add reagents above/beneath your reaction arrows. (24 points total). c)
Show how the following compound can be synthesized from the given starting material. (Hint: Start with an acetoacetic ester. PBr HCI H20, A H2SO4 CH3CH2O We were unable to transcribe this image PBr HCI H20, A H2SO4 CH3CH2O
62. Show how the following compound can be synthesized from the given starting material. (Hint: Start with an acetoacetic ester.) OH sodinto antes O bio boogie COOH 63. Show how the following compounds can be prepared from cyclohexanone: CCH2CH2CH3 wolle CH CH.CH CH CCH boob TISU shots 0551 ollor O CH2 OH
3) Show how the following molecules can be synthesized from the starting material indicated. Draw the structure of each intermediary compound in your synthesis, and add reagents above/beneath your reaction arrows. (24 points total). Br NH2 b) acd c-o acd NHz Br